At the Access All Areas Now! has been very slow because we have been trying to fight for funding to build the business. Me, Jess and Andy are hoping to go on a Teaching and Management course. There will be a meeting soon to sought out what's happening. Work has been hard to get anyway due to the summer holiday but hopefully things will start picking up.
I one of many of people with learning disabilities have become MPs for the peoples' Parliament with the support of a Self - Advocacy group called Changing Our Lives who are MPs themselves.At the moment we are going through some leadership training.
During the summer my computer crashed but I still managed to do a bit of work on learning disability, friendship and relationships awareness. I have been writing a story called ' Action Speaks louder than Words'
It's about a woman with a learning disability named Jackie from Wolverhampton who goes speed dating at the Lighthouse chub building. A young man name Mark who doesn't have LD walks in, he gets told he needs to drink away from the restaurant part even though can still see the speeding dating going on. He liked the way different men were talking to different women. When the event finished at 9.00pm,Mark managed to give Jackie his phone number then walked to the bus stop. Jackey wasn't sure at first but she rang him before her speed dating results came through.
They had two dates, one on the phone and other at Jackie's house. They tried the Moon Under Water' but it was too packed out a Saturday night without any seats and they couldn't hear one another.
It turned out Mark promised Jackie the world, that he'd support her to move in with him, have his child, help her look after it and etc. As sooner as Jackie became pregnant he kicked her out of his house and decided he wanted women did have disabilities and who didn't need support, when Jackie had told him everything about her disabilities and the help she needs, he promised to give but didn't. Jackie lived with friends.
The baby was taken of her very quickly from social services and Mark. Jackie wasn't told what sex the baby was and where he or she was other than Mark putting he or she in and out of care. This led Jackie into very deep depression so badly that the friends she was living with Karen, Hana and the police saved her from taking her life at Beatles car park.
In the end she moved on, she did an English and creative at Bilston college, social services housed her in Bradmore and she found herself a new companion in life named Alex, what Alex was like is up to you readers to decide but he was a lot better than Mark.
Thursday, 26 August 2010
Saturday, 26 June 2010
LD AND HEALTHCARE FOR HEALTH STAFF AND HEALTH STUDENTS
INTRODUCTION `Access All Areas!` hope we are giving something about in the Health care of people with LD. Only because LD week is over, we still you are going to try and take as many we have raised awareness you about the Health care People with Ld have faced in our past. We hope you can do your best to better Health care. It isn't just treatment it's neglect and lives that shouldn't have been lost.
I am yet to talk to my business partner Jess about us looking Health services to see what has and hasn't got better. Myself having not been seriously ill since 1993, although it's a good thing. I don't know what has changed in the hospitals since then. This something I want see for myself without been ill.
I would like to remind you about the things we have spoke about in our training session and what I have put on my website. I may also put things on my website that we haven't spoke about.
What I have said is that people LD are more likely to die you than people with. It's up to Health to do their job how they should and putting a stop to this. Without over protecting keeping a close eye on people with LD for the sake of Health and Safety.
What we didn't make you aware of is it can be hard for people with LD to put trust into Health staff when they have had bad experiences of Health in the past. It well be hard for adult with LD to put trust in the future but if we can creative a good future for today's children we will have better future for tomorrow's adults. It's up to you to prove that you can help people Ld and the people support them to put trust in you. This can scar people away from Health care once they don't feel as if they are not been looked after and cared for. Put yourself in our shoes. Health care is better than it used to be but not good enough. Make a start of stopping bad Health care to tell past Health staff how they should have been taught even though it's not their fault that society was so in the dark in those days.
I spoke to a Gp at my doctors about Health and LD awareness. He told me that they called out most people with LD for appointments but they don't seem to make them or even turn up. I think because of Health care in the past, which I have faced myself people are scared of Health staff. Today's health staff will have a hard job to get most people with LD who have lived 20 to 40 years or more to access the Health services. For eg; I myself have changed my GPS because I wasn't happy at my last one. I stopped going for roughly 12 mouths or more, then I felt brave enough to change my GPS with a bit of help from a support worker.
How can you make Health care better for people with LD?
Me, Andy and Jess are also part of a Self Advocacy group called Our Shout supported by Mencap as well as Access All Areas NOW! even Andy isn't self employed yet. We go to lots of different meetings talking about different things, one subject is the Health care of people with Ld. We all that Health care needs to get better for people with LD. aT LOT OF health care staff find it hard to communicate with people with Ld. They need to learn about Health care we want and need. Most of us have problems with.
Talking, listening, reading, writing talking information in and explaining ourselves to people's understanding. Even a lot of people who support people with LD have problems understanding professions. It's very important for people with Ld to educate all professions. Without communicating and understand one another is useless. If you look around my website I hope I hope I have explained enough for you to understand how with Ld communicate but as different people have different disabilities we all communicate in different.
The law says that Health services need to make changes to how people LD want our Health services. People with LD believe that there are not enough changes made.
People who support people with LD find it hard to make themselves heard as well as people with LD ourselves. Things are better to what they were but we still have a long way to go. Health staff don't know enough about LD. They need to learn about you all need to learn about our needs and wants. Most people with LD find it hard to say how feel. This is why we get poor Health care, it's up to you to better it.
Sometimes Health staff can't communicate with one another.
The way you give medication out is important.
Type out medication information on the computer in size 14 to 20 font.
Easy words and pictures of people talking medication, the type of medication it is and how much.
Make as clear as possible so we understand.
Use bullet point and even numbers step by step to show us what order we take our medication. Mostly there's a lot of information many of us will find it hard to take. As many short words and sentences as possible. No jargon!
Think of the side effects most medications cause mainly when they can affect people in a big bad way. This can have dangerous affects on people's lives. Keep trying until you find the right medication for people.
If you came to our training session on Monday 21st June 2010 for LD week, you may have heard say that you must study the Mental capacity Act it's law!!!!!! I am now reminding that I have also typed it somewhere on this website if look very carefully, I think it's on the next page Learning Disability Health 2010.
What asked advised you to do in the LD week report is study the Health Action plan. There's good information but I believe there may be missing information. For eg; if someone passes out alone out and about they need records of their medication, gp, people with are supporting them, caring for them and etc.
I will also remind you, which was in our Training session and on this website on LD week report that you need to be studying Disability Discrimination Act, which law to study it if you are working in any field of LD.
PCP Person Cente Plan is also is also important to study to give people with LD our own choice and control in life.
All these things you can find websites for, put in your search engine or if you haven't got a lot of access to the internet you could search the book shops or even the libraries to see if there are books on the Health care of people with LD.
The NHS have very little training in the Health care of LD. I have put a lot of important information on this website for you to study. I hope to put new information on for you in the future.
Try to better attitudes.
Respect people with LD.
Be more patient with us.
Treat us with dignity.
Stronger action should be taken to give better Health care. Department of Health should tell all local services to do their work to the ability of LD. There are Directed Enhanced services for people with LD.
Health check ups one or twice a year.
Support for people if and when we need and want it.
Help us to communicate.
Better and clearer information for us to read and understand.
More pictures for those of us who can't read and write.
Most of us can't take information in so we may need support to do so.
I am yet to talk to my business partner Jess about us looking Health services to see what has and hasn't got better. Myself having not been seriously ill since 1993, although it's a good thing. I don't know what has changed in the hospitals since then. This something I want see for myself without been ill.
I would like to remind you about the things we have spoke about in our training session and what I have put on my website. I may also put things on my website that we haven't spoke about.
What I have said is that people LD are more likely to die you than people with. It's up to Health to do their job how they should and putting a stop to this. Without over protecting keeping a close eye on people with LD for the sake of Health and Safety.
What we didn't make you aware of is it can be hard for people with LD to put trust into Health staff when they have had bad experiences of Health in the past. It well be hard for adult with LD to put trust in the future but if we can creative a good future for today's children we will have better future for tomorrow's adults. It's up to you to prove that you can help people Ld and the people support them to put trust in you. This can scar people away from Health care once they don't feel as if they are not been looked after and cared for. Put yourself in our shoes. Health care is better than it used to be but not good enough. Make a start of stopping bad Health care to tell past Health staff how they should have been taught even though it's not their fault that society was so in the dark in those days.
I spoke to a Gp at my doctors about Health and LD awareness. He told me that they called out most people with LD for appointments but they don't seem to make them or even turn up. I think because of Health care in the past, which I have faced myself people are scared of Health staff. Today's health staff will have a hard job to get most people with LD who have lived 20 to 40 years or more to access the Health services. For eg; I myself have changed my GPS because I wasn't happy at my last one. I stopped going for roughly 12 mouths or more, then I felt brave enough to change my GPS with a bit of help from a support worker.
How can you make Health care better for people with LD?
Me, Andy and Jess are also part of a Self Advocacy group called Our Shout supported by Mencap as well as Access All Areas NOW! even Andy isn't self employed yet. We go to lots of different meetings talking about different things, one subject is the Health care of people with Ld. We all that Health care needs to get better for people with LD. aT LOT OF health care staff find it hard to communicate with people with Ld. They need to learn about Health care we want and need. Most of us have problems with.
Talking, listening, reading, writing talking information in and explaining ourselves to people's understanding. Even a lot of people who support people with LD have problems understanding professions. It's very important for people with Ld to educate all professions. Without communicating and understand one another is useless. If you look around my website I hope I hope I have explained enough for you to understand how with Ld communicate but as different people have different disabilities we all communicate in different.
The law says that Health services need to make changes to how people LD want our Health services. People with LD believe that there are not enough changes made.
People who support people with LD find it hard to make themselves heard as well as people with LD ourselves. Things are better to what they were but we still have a long way to go. Health staff don't know enough about LD. They need to learn about you all need to learn about our needs and wants. Most people with LD find it hard to say how feel. This is why we get poor Health care, it's up to you to better it.
Sometimes Health staff can't communicate with one another.
The way you give medication out is important.
Type out medication information on the computer in size 14 to 20 font.
Easy words and pictures of people talking medication, the type of medication it is and how much.
Make as clear as possible so we understand.
Use bullet point and even numbers step by step to show us what order we take our medication. Mostly there's a lot of information many of us will find it hard to take. As many short words and sentences as possible. No jargon!
Think of the side effects most medications cause mainly when they can affect people in a big bad way. This can have dangerous affects on people's lives. Keep trying until you find the right medication for people.
If you came to our training session on Monday 21st June 2010 for LD week, you may have heard say that you must study the Mental capacity Act it's law!!!!!! I am now reminding that I have also typed it somewhere on this website if look very carefully, I think it's on the next page Learning Disability Health 2010.
What asked advised you to do in the LD week report is study the Health Action plan. There's good information but I believe there may be missing information. For eg; if someone passes out alone out and about they need records of their medication, gp, people with are supporting them, caring for them and etc.
I will also remind you, which was in our Training session and on this website on LD week report that you need to be studying Disability Discrimination Act, which law to study it if you are working in any field of LD.
PCP Person Cente Plan is also is also important to study to give people with LD our own choice and control in life.
All these things you can find websites for, put in your search engine or if you haven't got a lot of access to the internet you could search the book shops or even the libraries to see if there are books on the Health care of people with LD.
The NHS have very little training in the Health care of LD. I have put a lot of important information on this website for you to study. I hope to put new information on for you in the future.
Try to better attitudes.
Respect people with LD.
Be more patient with us.
Treat us with dignity.
Stronger action should be taken to give better Health care. Department of Health should tell all local services to do their work to the ability of LD. There are Directed Enhanced services for people with LD.
Health check ups one or twice a year.
Support for people if and when we need and want it.
Help us to communicate.
Better and clearer information for us to read and understand.
More pictures for those of us who can't read and write.
Most of us can't take information in so we may need support to do so.
Tuesday, 8 June 2010
Health study cases for LD week.
Study case 1. Mr Jones is eighteen years old.
He was send to a mental impairment service from the Children team nine mouths prior to his eighteenth birthday.
At the time he was living in a supported flat with 24 hour 1 to 1 support from a private run domiciliary care service, where he had resided for about one year.
He was diagnosed Autism and depression, for which he was prescribed medication by the children's psychiatrist.
At the time he was told that he had severely behavior problems, he had attacked staff several times a week.
This caused a high level of staff sickness to injury or stress.
He has had threaded members of the public.
He often went out to meet young women, that he had relationships with.
He was well known to the police service, who had been called out many times because of his violence behavior towards staff.
He was in court many times for assault and threatening behavior and been detained in young offenders institution twice.
Shortly after his referral, he was again detained in a prison which was 150 miles away from the service.
The mental impairment service attended two reviews at the prison and traveled to see him during his period of detention.
The remain prior to his eighteenth birthday was to gather information and liaise with children's' services.
It was clear that due to his level of learning disability he was not coping well in prison.
The service advised him that psychiatric assessment was done during his time of detention , with a view to finding him a hospital near his home area, and planned for a local psychiatrist to travel to the prison and carry out the assessment.
However, before he could be moved, his time of detention ended and he was released back to his old address.
He was placed on a higher level of 24 hour care with two or three staff at all times.
He has been detained on a low secure unit many times in order to treat episode of psychosis.
A few mouths later, the housing and support provider felt after many attacks, they couldn't give support any longer to Mr Jones due to his behavior.
He was evicted from the property. An emergency referral was then made to an alternative care provider which was based about 60 miles away from his home.
He was moved to another supported flat with 24 hour support from two staff.
A mouth of residing in this placement he again turned up in court following previous assaults and was remanded in prison. At this point he turned eighteen.
He was officially moved to the mental impairment service on the day of his 18th birthday.
Shortly after this, a move to this a move to a low private secure therapeutic facility was planned under section 37 of Mental Health Act. The unit is 156 miles away from Mr Jone's home.
People with LD and Mental Health problems can be misunderstood but it doesn't that everything is down to LD and Mental Health.
Some people may be unaware of what they could be saying or and doing.
There are all different kinds behavior problems.
For eg; I understand that crime can be a serous thing, I feel for people when they lose the people they love.
No is saying that people with Ld should be treated any different because of there LD but there needs to be awareness of balance if it comes to a case of a person with LD who hasn't been aware of what they may have done until they have told in a prison but at the same time we must understand the feeling of the victims loved ones.
The person with LD may be very angry with themselves to a point they could take they own life because they wouldn't be able to stand a life time in prison.
I am not saying all people with LD don't know what they are doing but for the ones don't wouldn't do such crimes if it hadn't of been for their problems.
Some causes could be done to LD, Mental problems or and the side affects of most medications. Health staff need to looking into these things so these people don't put themselves through these things.
Case 2 com pair Mr Jone's case with mine as a child.
I was on heavy medication as a child, which caused my behavior problems which didn't give me any excuse. On the other hand, I can gladly my behaviour problems weren't bad enough to commit a crime.
I found it hard to pay attention in the day time at school and I was hyperactive at night.
I think I was over tried, the medication made very dreamily and sleepily in the day time yet strangely I wouldn't rest if I had the chance of a nap.
Since I have come off those tablets I haven't those problems have stopped.
Back then I would just lose my temper any time, any place and anywhere, kick and scream the place down.
In shops I would pull the items off the shelves.
For eg; if I couldn't tie my shoes laces, I would get very angry.
I used to think that the world was more cleverer than.
I thought I was the only person couldn't cope with every day life skills. The world seemed very big to me when I was little.
It's a wonder I did not commit crimes, with the strength of the tablets I was on, it made so unaware of the world around me.
When I came off the tablets at the age of 12 because I was having less fits slowly I became aware of the world around me and my behavior problems calmed down.
My questions are to you, there's no right or wrong answers, I am just interested what you think.
How do you think my life would have ended up now if I was still on those dangerous tablets? Do you think I would have ended up like Mr Jones or not?
Lucky for me I didn't to take these tablets for the rest of my life, even they thought Health staff at that time though I was going to have to always depend on those tablets for life.
Please send me an email on sarajgorman@googlemail.com.
Phenobarbital (phenobarbitone) I think I took 3 to 500mgs One tablet three times a day,that's how dangerous the medication was for a child or any human being any age.
I read a bit of history about the tablets, the purpose was to help the soldiers sleep in the 1st or and 2nd world war.
My children was in the 1970s.
If you would like to research it on the Internet Health staff and Health students.
If you research this please send an email me to let me know what you have found out.
Case three. Mr Smith is twenty - six years old West Indian man with mild LD and psychotic disorder for which he receives prescribed medication.
He has a long history of petty offence rs for which he has been arrested and in court many times.
These include burglary, theft and minor drug offences.
He is very well known to the local police.
He had spent five years on offender register due to previous sex offenders against a girl under age sixteen.
Mr Smith resides in the area he has moved to different rented places over the years.
He often fails to keep appointments and very guarded about his whereabouts, making it hard to engage effectively with him.
He finds it hard to help himself and many of his placements have failed. His currently saying with family and is soon to be evicted.
It is known that Mr Smith does not adhere voluntary to his medication regime.
Mr Smith is very hard to house due to his history of unstable tenancies, and his offending behaviour.
He had just been arrested for burglary and his court case has been put on hold for two mouths.
There has been an ongoing issues with the police as he and his family feel that his LD is not taken into account by police or professions with the criminal justice system.
He has taken custody many times with no request for an appropriate adult, or any support from health or social services.
Why do you think Mr Smith committed the crimes he had done?
Do you think by the sounds of cases he meant to commit these crimes or not?
Make notes on the balance of the feelings of the victims and Mr Smiths feelings in case of if he didn't know what he was doing. How do you think he felt when he became aware?
In the case that he may of meant to commit these crimes what do you think should happen to him because of his LD?
What should to happen to him if he didn't know what he was doing?
What do you think caused it he didn't mean to do? LD, Mental Health problems or even the medication he's taking.
Do you think he may be misunderstood? Without excuses there may be all kinds of possibilities but we need to understand the feelings of the victims, families, lovers and friends.
Health students and Health staff, if you want to answer these questions, you may be able to research Mr Smith's LD on the internet. Please email if you want if you answer to try to answer these questions.
He was send to a mental impairment service from the Children team nine mouths prior to his eighteenth birthday.
At the time he was living in a supported flat with 24 hour 1 to 1 support from a private run domiciliary care service, where he had resided for about one year.
He was diagnosed Autism and depression, for which he was prescribed medication by the children's psychiatrist.
At the time he was told that he had severely behavior problems, he had attacked staff several times a week.
This caused a high level of staff sickness to injury or stress.
He has had threaded members of the public.
He often went out to meet young women, that he had relationships with.
He was well known to the police service, who had been called out many times because of his violence behavior towards staff.
He was in court many times for assault and threatening behavior and been detained in young offenders institution twice.
Shortly after his referral, he was again detained in a prison which was 150 miles away from the service.
The mental impairment service attended two reviews at the prison and traveled to see him during his period of detention.
The remain prior to his eighteenth birthday was to gather information and liaise with children's' services.
It was clear that due to his level of learning disability he was not coping well in prison.
The service advised him that psychiatric assessment was done during his time of detention , with a view to finding him a hospital near his home area, and planned for a local psychiatrist to travel to the prison and carry out the assessment.
However, before he could be moved, his time of detention ended and he was released back to his old address.
He was placed on a higher level of 24 hour care with two or three staff at all times.
He has been detained on a low secure unit many times in order to treat episode of psychosis.
A few mouths later, the housing and support provider felt after many attacks, they couldn't give support any longer to Mr Jones due to his behavior.
He was evicted from the property. An emergency referral was then made to an alternative care provider which was based about 60 miles away from his home.
He was moved to another supported flat with 24 hour support from two staff.
A mouth of residing in this placement he again turned up in court following previous assaults and was remanded in prison. At this point he turned eighteen.
He was officially moved to the mental impairment service on the day of his 18th birthday.
Shortly after this, a move to this a move to a low private secure therapeutic facility was planned under section 37 of Mental Health Act. The unit is 156 miles away from Mr Jone's home.
People with LD and Mental Health problems can be misunderstood but it doesn't that everything is down to LD and Mental Health.
Some people may be unaware of what they could be saying or and doing.
There are all different kinds behavior problems.
For eg; I understand that crime can be a serous thing, I feel for people when they lose the people they love.
No is saying that people with Ld should be treated any different because of there LD but there needs to be awareness of balance if it comes to a case of a person with LD who hasn't been aware of what they may have done until they have told in a prison but at the same time we must understand the feeling of the victims loved ones.
The person with LD may be very angry with themselves to a point they could take they own life because they wouldn't be able to stand a life time in prison.
I am not saying all people with LD don't know what they are doing but for the ones don't wouldn't do such crimes if it hadn't of been for their problems.
Some causes could be done to LD, Mental problems or and the side affects of most medications. Health staff need to looking into these things so these people don't put themselves through these things.
Case 2 com pair Mr Jone's case with mine as a child.
I was on heavy medication as a child, which caused my behavior problems which didn't give me any excuse. On the other hand, I can gladly my behaviour problems weren't bad enough to commit a crime.
I found it hard to pay attention in the day time at school and I was hyperactive at night.
I think I was over tried, the medication made very dreamily and sleepily in the day time yet strangely I wouldn't rest if I had the chance of a nap.
Since I have come off those tablets I haven't those problems have stopped.
Back then I would just lose my temper any time, any place and anywhere, kick and scream the place down.
In shops I would pull the items off the shelves.
For eg; if I couldn't tie my shoes laces, I would get very angry.
I used to think that the world was more cleverer than.
I thought I was the only person couldn't cope with every day life skills. The world seemed very big to me when I was little.
It's a wonder I did not commit crimes, with the strength of the tablets I was on, it made so unaware of the world around me.
When I came off the tablets at the age of 12 because I was having less fits slowly I became aware of the world around me and my behavior problems calmed down.
My questions are to you, there's no right or wrong answers, I am just interested what you think.
How do you think my life would have ended up now if I was still on those dangerous tablets? Do you think I would have ended up like Mr Jones or not?
Lucky for me I didn't to take these tablets for the rest of my life, even they thought Health staff at that time though I was going to have to always depend on those tablets for life.
Please send me an email on sarajgorman@googlemail.com.
Phenobarbital (phenobarbitone) I think I took 3 to 500mgs One tablet three times a day,that's how dangerous the medication was for a child or any human being any age.
I read a bit of history about the tablets, the purpose was to help the soldiers sleep in the 1st or and 2nd world war.
My children was in the 1970s.
If you would like to research it on the Internet Health staff and Health students.
If you research this please send an email me to let me know what you have found out.
Case three. Mr Smith is twenty - six years old West Indian man with mild LD and psychotic disorder for which he receives prescribed medication.
He has a long history of petty offence rs for which he has been arrested and in court many times.
These include burglary, theft and minor drug offences.
He is very well known to the local police.
He had spent five years on offender register due to previous sex offenders against a girl under age sixteen.
Mr Smith resides in the area he has moved to different rented places over the years.
He often fails to keep appointments and very guarded about his whereabouts, making it hard to engage effectively with him.
He finds it hard to help himself and many of his placements have failed. His currently saying with family and is soon to be evicted.
It is known that Mr Smith does not adhere voluntary to his medication regime.
Mr Smith is very hard to house due to his history of unstable tenancies, and his offending behaviour.
He had just been arrested for burglary and his court case has been put on hold for two mouths.
There has been an ongoing issues with the police as he and his family feel that his LD is not taken into account by police or professions with the criminal justice system.
He has taken custody many times with no request for an appropriate adult, or any support from health or social services.
Why do you think Mr Smith committed the crimes he had done?
Do you think by the sounds of cases he meant to commit these crimes or not?
Make notes on the balance of the feelings of the victims and Mr Smiths feelings in case of if he didn't know what he was doing. How do you think he felt when he became aware?
In the case that he may of meant to commit these crimes what do you think should happen to him because of his LD?
What should to happen to him if he didn't know what he was doing?
What do you think caused it he didn't mean to do? LD, Mental Health problems or even the medication he's taking.
Do you think he may be misunderstood? Without excuses there may be all kinds of possibilities but we need to understand the feelings of the victims, families, lovers and friends.
Health students and Health staff, if you want to answer these questions, you may be able to research Mr Smith's LD on the internet. Please email if you want if you answer to try to answer these questions.
Wednesday, 26 May 2010
Learning disabilities' experince with the NHS.
NHS FAILS TO ACCOMMODATE PATIENTS WITH A LEARNING DISABILITY IN SINGLE SEX WARDS.
On the 12th December 2007, I read a Mencap report on the NHS not having people with learning disabilities sleeping single sex wards in the hospital. At the time there was a debate between safety and privately, which a balance between the two. We all need to be safe but also need to be private, mainly when it comes down to washing, dressing and going to the toilet for eg;. I had a meeting with Debra Edwards who was the Patient Experience leader at that time. I told her that there needs to be a balance between the two.
Back in 1993, I had an operation on my throat because I had a mild cancer lump. At the time I had been in hospital twice at the Eye, Ear, Norse and throat hospital in Shrewsbury.
The first time I was in hospital, I was in a mixed men and womens' ward, which wasn't private and I hated it.
My Mother complained about it.
When I had to go in to hospital the second time I had a private room with a alarm so I could when I wanted to go to the toilet because I had a fall the first time I was in that hospital.
Like everyone I hate hospitals but the second time I was in that hospital was better than the first. That's balanced between been private and safe.
I never got to know what has got worse or better over this report written in 2007 because it got the stage that the hospital meetings were clashing with the Accessible information meetings.
6th December 2007
A major report published today has revealed that learning disability services are failing to accommodate inpatients with a learning disability in single sex wards.
'Count me in 2007: The 2007 national census of inpatients in mental health and learning disability services in England and Wales' found that 60% of inpatients in NHS and independent learning disability hospitals and facilities were not in a single ward.
The census is a joint initiative between the Health Care Act Commission, the Care Services Improvement Partner and the National Institute for Mental Health in England.
David Congon, Mencap's Head of campaigns policy at said "It's disgraceful that the majority of patients in learning disability services were not in single sex wards.
"By treating patients with a learning disability in mixed sex wards the NHS and independent health care providers are failing to provide a service that maintains their privacy and dignity at a time when they are most vulnerable. WWW.healthcommission.org.uk
On the 12th December 2007, I read a Mencap report on the NHS not having people with learning disabilities sleeping single sex wards in the hospital. At the time there was a debate between safety and privately, which a balance between the two. We all need to be safe but also need to be private, mainly when it comes down to washing, dressing and going to the toilet for eg;. I had a meeting with Debra Edwards who was the Patient Experience leader at that time. I told her that there needs to be a balance between the two.
Back in 1993, I had an operation on my throat because I had a mild cancer lump. At the time I had been in hospital twice at the Eye, Ear, Norse and throat hospital in Shrewsbury.
The first time I was in hospital, I was in a mixed men and womens' ward, which wasn't private and I hated it.
My Mother complained about it.
When I had to go in to hospital the second time I had a private room with a alarm so I could when I wanted to go to the toilet because I had a fall the first time I was in that hospital.
Like everyone I hate hospitals but the second time I was in that hospital was better than the first. That's balanced between been private and safe.
I never got to know what has got worse or better over this report written in 2007 because it got the stage that the hospital meetings were clashing with the Accessible information meetings.
6th December 2007
A major report published today has revealed that learning disability services are failing to accommodate inpatients with a learning disability in single sex wards.
'Count me in 2007: The 2007 national census of inpatients in mental health and learning disability services in England and Wales' found that 60% of inpatients in NHS and independent learning disability hospitals and facilities were not in a single ward.
The census is a joint initiative between the Health Care Act Commission, the Care Services Improvement Partner and the National Institute for Mental Health in England.
David Congon, Mencap's Head of campaigns policy at said "It's disgraceful that the majority of patients in learning disability services were not in single sex wards.
"By treating patients with a learning disability in mixed sex wards the NHS and independent health care providers are failing to provide a service that maintains their privacy and dignity at a time when they are most vulnerable. WWW.healthcommission.org.uk
Mencap's death Indifference report.
INTRODUCTION TO MENCAP'S DEATH INDIFFERENCE REPORT.
Mencap wrote a report called 'TREAT ME RIGHT.' IN 2004.
It said that people with learning disabilities have worse health than other people.
Mencap think it's because people with learning disabilities don't get the treatment and Health care that we need.
Sometimes this can mean people with learning disabilities can die at a younger than other people. Mencap thinks it's very bad and it shouldn't happen.
'TREAT ME RIGHT.' Report said important changes need to be made to better Health care and treatment. Not enough has changed.
Since Mencap wrote ' TREAT ME RIGHT' Mencap heard that six people with learning disabilities have died because they didn't receive the right Health care and treatment.
Not only do I agree with Mencap and 'TREAT ME RIGHT' I also believe from my own experience of Health care that they were neglected.
As shocking as it is, it doesn't surprising to me when I have had learning disabilities myself for just over 40yrs since the day I was born.
It tells me that not a lot has changed for people with learning disabilities.'Come on let's get better Health care for the future of learning disability'.
EMMA. Emma has a great sense of humour.
Emma loved pulling funny faces for a laugh.
Emma had wonderful smiles that lit up the room up.
Emma died of cancer in 2004 at the age of 26.
Emma had a severe learning disability that made it hard to let people know how she felt.
Doctors thought Emma didn't agree to have the treatment for her cancer, so they didn't do anything to save her.
Mencap wants to know.
If doctors would have treated Emma, would she still be alive?
Why didn't Emma receive the right treatment and Health care?
May be Emma tried to tell the doctors but she may have found it hard to make her understood, which has happened to me and many other people learning disabilities at many times.
Why wasn't Emma given anything for the pain?
Please read the Death Indifference report on WWW.mencap.org.uk or tap Mencap's Death Indifference report in the search engine.
MARTIN. Martin loved smiling, going out and listening to music.
Martin loved to get behind the wheel of a car.
Martin died in hospital, he hadn't had any food for 26 days.
He died on the 21st December 2005.
Martin had a severe learning disability without any speech.
Martin had a Stroke and Pheumia, which was an infection in his lungs.
Martin was put on a drip, living on water and sugar.
MARK. Mark was 30 yrs of age when he died.
8 and a half wks before hand he was admitted to hospital with a broken leg (femur).
He was clearly distressed and in pain. , but he had to wait 3 days for the pain team to see him. Mark died on 29th August 2003.
I believe that the Pain team must have been to blame leaving Mark in pain for 3 days. How many people in the world died of a broken leg not very many if any.
TED, Ted was 61 yrs of age when he died, he was dischanrged 3 after being admitted to hospital despite his condition having been assessed as 'concerning.'
He collapsed and died on 27th May 2004.
He had a severe learning disability and virtually no speech.
How can we explain Ted's unexplained death?
No one can explain how.
A hospice consultant recommended that 20 yr old Tom's pain was investigated by gastroenterologist over a year before he died.
No action was taken until it was far too late.
Tom's expression of pain wasn't listened to, he died 25th May 2004. He had profound and multiple learning disabilities.
WARREN, Warren was 30 when he died following perforation of the appendix. His Mother and Father repeatedly asked whether Warren had appendicitis or a blocked bowl when they saw the doctor.
They told them that he had a virus. Warren died on the 25th September 2004.
He had a severe learning disability and very little speech but couldn't make himself understood to his family.
Read more of this on Mencap's Death Indifference report website or search engine.
Mencap want to know.
Why didn't Martin have any food for 26 days?
Why didn't the hospital give Martin better Health care?
About this report.
Mencap wrote this report to educate and train people on learning disability and Health.
Mencap believe that people get treated unfairly in Health care services.
There's still a lot of discrimination against all races, which is wrong. Why should people stop living their lives to how they want whether they have a race or not?
People's needs aren't understood whether they have disabilities or not. People's need to be met whether they have disabilities or not. These things can happen for a long time before people know it's wrong.
People need to understand learning disability.
Mencap believes that!
People who make the decisions about Health care don't think people with learning disabilities' lives are important as theirs.
In 2006, the government said that people with learning disabilities don't always get treated equally to other people. Not many changes have been made since.
Health care professionals do not understand learning disability.
Staff aren't given enough educating or training to understand learning disability.If staff have wrong ideas about learning disability, no one tells them it's wrong.
The Disability Rights commission has found Health care professionals sometimes confuse the signs that show someone is ill when they have learning disabilities. This is diagnostic over shadowing.
Health care professions don't listen to families/ carers and they don't listen to people with learning disabilities.
People with learning disabilities don't always get our say or choices to our Health situations.
Our chooses should be supported.
It's seems that what Health staff and family/carers have control over people with learning disabilities live when they talk about our health, we need to learn how to speak for ourselves.
Even people who can't speak have another form of communication that people need to learn to understand, go along and learn to communicate in the way.
(How would you like not being understood?) Each each and everyone of us has a voice, thoughts and feelings just like you do.
Families/ carers notice if the people they care for are acting differently and can see if the person is upset or and in pain.
Only because we may find hard to make ourselves clear enough for you to understand us doesn't mean we don't feel anything.
If it's really hard to understand at least find out whether we are happy or sad, even if you can't do anything about it.
May be most us may be able to tell you the reasons why we feel like we feel. At least bare our reasons in mind if you can't help us.
In all cases Mencap looked at this report, to find out that most families/carers are ignored by Health professions knowing very well about the worries they have for the people they care for.
Families/carers should always be listened to so should people with learning disabilities main when we are in pain or whatever the situation could be.
Service providers need to learn how to balance the say of families/carer and the people with disabilities whatever the situation is.
Try to encourage the person who is supporting the person with learning disabilities to be more supportive than over protective.
Everyone who gives treatment should understand laws and consent. If they understood the laws better, people with a learning disability would get what we need and want.
Health professionals don't always see the lives of people with disabilities are just as important as everyone's.
Mencap thinks that Health staff don't think people with disabilities' lives are important to save and worth living.
The lives of people with learning disabilities should be important as much as everyone's. Health care professionals shouldn't really decide that a person's life isn't worth living just because they have learning disabilities.
What Mencap wants to happen.
Mencap wants the case reports to be looked at in an independent inquiry.
There are 6 stories about people with learning disabilities in the main report. These are called cases.
Mencap want all the 6 cases in the independent inquiry.
This means people who have not been involved in the cases will look at the cases altogether. They will try to find out the reasons behind the 6 deaths, what needs to change and what lessons need to be learned to stopped these things from happening again.
At the moment it takes too long for a complaint to be heard.
Families/carer are upset over the people who loved, looked and cared for who died.
Mencap's question why do families/carers have to wait for a complaint to be heard?
Why do people have to wait so long for a response?( Services need to find out what happened, why and how. Family/carers need clear information to their rights.
Mencap wants the Health care commission to have more money to do this job better.
We want it done easy, quick and accessible for people with learning disabilities to make complaints and to get the answers to the reason for these bad things happening.
Nothing can bring back the 6 people who died.
Their families want to know why the people who they loved died so early, when there might
have been better Heath care, they needed to be taken care of and better treatment for them.
Mencap has written this report because we want to stop people with a learning disability from dieing so early in life.
We need to train and educate Health care staff to give them the right Health care, look after them and give them the right treatment when being in hospital or anywhere they are but also for them to have equal lives with the right support.
Mencap's website is also linked to mine.
You could send me an email if you want to on sarajgorman@googlemail.com
Mencap wrote a report called 'TREAT ME RIGHT.' IN 2004.
It said that people with learning disabilities have worse health than other people.
Mencap think it's because people with learning disabilities don't get the treatment and Health care that we need.
Sometimes this can mean people with learning disabilities can die at a younger than other people. Mencap thinks it's very bad and it shouldn't happen.
'TREAT ME RIGHT.' Report said important changes need to be made to better Health care and treatment. Not enough has changed.
Since Mencap wrote ' TREAT ME RIGHT' Mencap heard that six people with learning disabilities have died because they didn't receive the right Health care and treatment.
Not only do I agree with Mencap and 'TREAT ME RIGHT' I also believe from my own experience of Health care that they were neglected.
As shocking as it is, it doesn't surprising to me when I have had learning disabilities myself for just over 40yrs since the day I was born.
It tells me that not a lot has changed for people with learning disabilities.'Come on let's get better Health care for the future of learning disability'.
EMMA. Emma has a great sense of humour.
Emma loved pulling funny faces for a laugh.
Emma had wonderful smiles that lit up the room up.
Emma died of cancer in 2004 at the age of 26.
Emma had a severe learning disability that made it hard to let people know how she felt.
Doctors thought Emma didn't agree to have the treatment for her cancer, so they didn't do anything to save her.
Mencap wants to know.
If doctors would have treated Emma, would she still be alive?
Why didn't Emma receive the right treatment and Health care?
May be Emma tried to tell the doctors but she may have found it hard to make her understood, which has happened to me and many other people learning disabilities at many times.
Why wasn't Emma given anything for the pain?
Please read the Death Indifference report on WWW.mencap.org.uk or tap Mencap's Death Indifference report in the search engine.
MARTIN. Martin loved smiling, going out and listening to music.
Martin loved to get behind the wheel of a car.
Martin died in hospital, he hadn't had any food for 26 days.
He died on the 21st December 2005.
Martin had a severe learning disability without any speech.
Martin had a Stroke and Pheumia, which was an infection in his lungs.
Martin was put on a drip, living on water and sugar.
MARK. Mark was 30 yrs of age when he died.
8 and a half wks before hand he was admitted to hospital with a broken leg (femur).
He was clearly distressed and in pain. , but he had to wait 3 days for the pain team to see him. Mark died on 29th August 2003.
I believe that the Pain team must have been to blame leaving Mark in pain for 3 days. How many people in the world died of a broken leg not very many if any.
TED, Ted was 61 yrs of age when he died, he was dischanrged 3 after being admitted to hospital despite his condition having been assessed as 'concerning.'
He collapsed and died on 27th May 2004.
He had a severe learning disability and virtually no speech.
How can we explain Ted's unexplained death?
No one can explain how.
A hospice consultant recommended that 20 yr old Tom's pain was investigated by gastroenterologist over a year before he died.
No action was taken until it was far too late.
Tom's expression of pain wasn't listened to, he died 25th May 2004. He had profound and multiple learning disabilities.
WARREN, Warren was 30 when he died following perforation of the appendix. His Mother and Father repeatedly asked whether Warren had appendicitis or a blocked bowl when they saw the doctor.
They told them that he had a virus. Warren died on the 25th September 2004.
He had a severe learning disability and very little speech but couldn't make himself understood to his family.
Read more of this on Mencap's Death Indifference report website or search engine.
Mencap want to know.
Why didn't Martin have any food for 26 days?
Why didn't the hospital give Martin better Health care?
About this report.
Mencap wrote this report to educate and train people on learning disability and Health.
Mencap believe that people get treated unfairly in Health care services.
There's still a lot of discrimination against all races, which is wrong. Why should people stop living their lives to how they want whether they have a race or not?
People's needs aren't understood whether they have disabilities or not. People's need to be met whether they have disabilities or not. These things can happen for a long time before people know it's wrong.
People need to understand learning disability.
Mencap believes that!
People who make the decisions about Health care don't think people with learning disabilities' lives are important as theirs.
In 2006, the government said that people with learning disabilities don't always get treated equally to other people. Not many changes have been made since.
Health care professionals do not understand learning disability.
Staff aren't given enough educating or training to understand learning disability.If staff have wrong ideas about learning disability, no one tells them it's wrong.
The Disability Rights commission has found Health care professionals sometimes confuse the signs that show someone is ill when they have learning disabilities. This is diagnostic over shadowing.
Health care professions don't listen to families/ carers and they don't listen to people with learning disabilities.
People with learning disabilities don't always get our say or choices to our Health situations.
Our chooses should be supported.
It's seems that what Health staff and family/carers have control over people with learning disabilities live when they talk about our health, we need to learn how to speak for ourselves.
Even people who can't speak have another form of communication that people need to learn to understand, go along and learn to communicate in the way.
(How would you like not being understood?) Each each and everyone of us has a voice, thoughts and feelings just like you do.
Families/ carers notice if the people they care for are acting differently and can see if the person is upset or and in pain.
Only because we may find hard to make ourselves clear enough for you to understand us doesn't mean we don't feel anything.
If it's really hard to understand at least find out whether we are happy or sad, even if you can't do anything about it.
May be most us may be able to tell you the reasons why we feel like we feel. At least bare our reasons in mind if you can't help us.
In all cases Mencap looked at this report, to find out that most families/carers are ignored by Health professions knowing very well about the worries they have for the people they care for.
Families/carers should always be listened to so should people with learning disabilities main when we are in pain or whatever the situation could be.
Service providers need to learn how to balance the say of families/carer and the people with disabilities whatever the situation is.
Try to encourage the person who is supporting the person with learning disabilities to be more supportive than over protective.
Everyone who gives treatment should understand laws and consent. If they understood the laws better, people with a learning disability would get what we need and want.
Health professionals don't always see the lives of people with disabilities are just as important as everyone's.
Mencap thinks that Health staff don't think people with disabilities' lives are important to save and worth living.
The lives of people with learning disabilities should be important as much as everyone's. Health care professionals shouldn't really decide that a person's life isn't worth living just because they have learning disabilities.
What Mencap wants to happen.
Mencap wants the case reports to be looked at in an independent inquiry.
There are 6 stories about people with learning disabilities in the main report. These are called cases.
Mencap want all the 6 cases in the independent inquiry.
This means people who have not been involved in the cases will look at the cases altogether. They will try to find out the reasons behind the 6 deaths, what needs to change and what lessons need to be learned to stopped these things from happening again.
At the moment it takes too long for a complaint to be heard.
Families/carer are upset over the people who loved, looked and cared for who died.
Mencap's question why do families/carers have to wait for a complaint to be heard?
Why do people have to wait so long for a response?( Services need to find out what happened, why and how. Family/carers need clear information to their rights.
Mencap wants the Health care commission to have more money to do this job better.
We want it done easy, quick and accessible for people with learning disabilities to make complaints and to get the answers to the reason for these bad things happening.
Nothing can bring back the 6 people who died.
Their families want to know why the people who they loved died so early, when there might
have been better Heath care, they needed to be taken care of and better treatment for them.
Mencap has written this report because we want to stop people with a learning disability from dieing so early in life.
We need to train and educate Health care staff to give them the right Health care, look after them and give them the right treatment when being in hospital or anywhere they are but also for them to have equal lives with the right support.
Mencap's website is also linked to mine.
You could send me an email if you want to on sarajgorman@googlemail.com
Sunday, 9 May 2010
UNDERSTANDING ANXENTYAND DEPRESSION.
Anxiety and depression can be linked to learning disabilites.
Some people have anxiety, depression and epilespy, which can link together.
If people get stressed very easily stuffer Panic attacks it can bring epilespy but it doesn't affect everyone the same.
Change can be a big thing for a lot of people with Autism.
People can have these conditions whether they have disabilities or not. Health problems can link to disabilities or be without disabilities.
Anxiety and depression is bad for enough anyone.
New things which is change whether it's good or bad can make people nervus. When some people get nervus they can have Panic attacks but Panic attacks can be brought by other things like for example; stress other reasons or no reason at all like depression.
Change can be a big thing for of people whether they are nervus about something or someone.
Whatever is going on in peoples' lives and minds some people can sleep for thinking all the while others sleep to all the while to avoid the sitations whether it's a good bad change in their lives.
Some people can find it hard to contrate on other things they only cope with one thing at a time.
Some people may worry more than they should, which is part of their condition what seems a mole hill to you feels like a mountain to them. You just need to be patient until the person realises that things may not be as bad to what it seems to them.
Everyone suffers from Anxiety and depression one way or another.
Sadly there's not enough said about stress I think we need to raise Stress awareness for everyone, that includes people with LD and Health problems.
Some people don't know that some people stuffer LD and Health problems together, that's what I have otherwise I wouldn't have known that.
Anxiety and depression are forms of stress in every ones' lives.
Many things can get on top of people, paying bills, not enough work, too much work, marriage, relationships, children and even loneliness.
It's very hard to make a balance to keep healthily and happy.
This can be why a lot of people can turn to smoking, drugs and etc.
When you have learning disabilities there can be a lack of support off society because we are slow and find it harder to cope with our lives than other people yet we are more easy ill than other people.
Stress, Depression and Anxiety can last short term or for life.
If you think about it we can all stuffer stress one way or another.
It's so easy to worry about things that you didn't need to but with somethings you were right doing so.
If you would like to have more understanding with the Mind.
You may learn whats, whys and hows the Mind is or can be affected.
Tap Mind in the Google engine or whatever you have got.
WWW.mind.org.uk
Save it in your favorites or Bookmarks.
Whatever Health problems and disabilities are we have enough stress with that on it's own.
We understand for eg; that we have to pay our bills like everyone else but with the problems we have already, we have double stress.
You feel tense.
You panic and worry about things that aren't as bad as they seem.
For eg; when I leave home to go anywhere I check my bag and my front door to make sure I have locked the door, remember my keys, bus passed and etc.
Touch wood I only forgot my money and phone once and had to travel from town back home to get, lucky I wasn't working at the time.
It seems like the end of the world when someone in your life dies or when your relationship breaks down.
You feel as if the world is controlling you.
I panic when I walk into services, load of people give me different answers to one question.
For eg; Is this benefit right for me?
I can't cope with too much jargon and too much information.
To be truthful the answer is either yes or no not both.
Managers need to inform all staff on what the rules are otherwise it confuses people.
Sometimes crowds can panic me where there are too many people around me.
I am a bit better than I used to be.
It can depend where I am and how many people there are.
When I really worry about things, it causes me to have Peta Mal fits.
I am easy misunderstood mainly when I am accessing services, when information doesn't seem straight forward to me.
I always have to have things going on in my life, otherwise I get very angry,depressed and bored.
My Gran died in 2007 and my last relationship broke down for the last time.
If it hadn't of been for Employment Pathways getting me on to Mencap, I don't know how I would have coped with my life now.
The first longest my relationship broke up at the end of 1996, which was two and a half years.
Now when I think about it wasn't that long yet after been apart 4 years, I gave him a second chance that lasted seven years.
Now there's no going back.
I couldn't stand sitting in the house alone but I wasn't in the mood to talk to people either.
I just used watch the world go by.
At that point I used to drink very heavy, which lasted six to twelve mouths.
I then worked it that couldn't go on like this forever yet I was still having a break down and even feeling as if I wanted to end my life.
Never the less I cut the drinking down and I started writing poetry to get things off my chest.
Some people have anxiety, depression and epilespy, which can link together.
If people get stressed very easily stuffer Panic attacks it can bring epilespy but it doesn't affect everyone the same.
Change can be a big thing for a lot of people with Autism.
People can have these conditions whether they have disabilities or not. Health problems can link to disabilities or be without disabilities.
Anxiety and depression is bad for enough anyone.
New things which is change whether it's good or bad can make people nervus. When some people get nervus they can have Panic attacks but Panic attacks can be brought by other things like for example; stress other reasons or no reason at all like depression.
Change can be a big thing for of people whether they are nervus about something or someone.
Whatever is going on in peoples' lives and minds some people can sleep for thinking all the while others sleep to all the while to avoid the sitations whether it's a good bad change in their lives.
Some people can find it hard to contrate on other things they only cope with one thing at a time.
Some people may worry more than they should, which is part of their condition what seems a mole hill to you feels like a mountain to them. You just need to be patient until the person realises that things may not be as bad to what it seems to them.
Everyone suffers from Anxiety and depression one way or another.
Sadly there's not enough said about stress I think we need to raise Stress awareness for everyone, that includes people with LD and Health problems.
Some people don't know that some people stuffer LD and Health problems together, that's what I have otherwise I wouldn't have known that.
Anxiety and depression are forms of stress in every ones' lives.
Many things can get on top of people, paying bills, not enough work, too much work, marriage, relationships, children and even loneliness.
It's very hard to make a balance to keep healthily and happy.
This can be why a lot of people can turn to smoking, drugs and etc.
When you have learning disabilities there can be a lack of support off society because we are slow and find it harder to cope with our lives than other people yet we are more easy ill than other people.
Stress, Depression and Anxiety can last short term or for life.
If you think about it we can all stuffer stress one way or another.
It's so easy to worry about things that you didn't need to but with somethings you were right doing so.
If you would like to have more understanding with the Mind.
You may learn whats, whys and hows the Mind is or can be affected.
Tap Mind in the Google engine or whatever you have got.
WWW.mind.org.uk
Save it in your favorites or Bookmarks.
Whatever Health problems and disabilities are we have enough stress with that on it's own.
We understand for eg; that we have to pay our bills like everyone else but with the problems we have already, we have double stress.
You feel tense.
You panic and worry about things that aren't as bad as they seem.
For eg; when I leave home to go anywhere I check my bag and my front door to make sure I have locked the door, remember my keys, bus passed and etc.
Touch wood I only forgot my money and phone once and had to travel from town back home to get, lucky I wasn't working at the time.
It seems like the end of the world when someone in your life dies or when your relationship breaks down.
You feel as if the world is controlling you.
I panic when I walk into services, load of people give me different answers to one question.
For eg; Is this benefit right for me?
I can't cope with too much jargon and too much information.
To be truthful the answer is either yes or no not both.
Managers need to inform all staff on what the rules are otherwise it confuses people.
Sometimes crowds can panic me where there are too many people around me.
I am a bit better than I used to be.
It can depend where I am and how many people there are.
When I really worry about things, it causes me to have Peta Mal fits.
I am easy misunderstood mainly when I am accessing services, when information doesn't seem straight forward to me.
I always have to have things going on in my life, otherwise I get very angry,depressed and bored.
My Gran died in 2007 and my last relationship broke down for the last time.
If it hadn't of been for Employment Pathways getting me on to Mencap, I don't know how I would have coped with my life now.
The first longest my relationship broke up at the end of 1996, which was two and a half years.
Now when I think about it wasn't that long yet after been apart 4 years, I gave him a second chance that lasted seven years.
Now there's no going back.
I couldn't stand sitting in the house alone but I wasn't in the mood to talk to people either.
I just used watch the world go by.
At that point I used to drink very heavy, which lasted six to twelve mouths.
I then worked it that couldn't go on like this forever yet I was still having a break down and even feeling as if I wanted to end my life.
Never the less I cut the drinking down and I started writing poetry to get things off my chest.
Saturday, 1 May 2010
Employment
Back in 1999, there were a lot of employers sued for discriminating disability, sex and race.
People with disabilities feel more of a Health and Safety Hazard at home than work. A lot of us stuffer from Anxiety and depression, we need to keep our bodies and minds busy.I spent 13 yrs signing on, which made me very down in myself. Since I have been working 3yrs ago, helping others like myself, I can take anything that life throws at me. My work can at the right time for me just a little before my Nan died and as my last relationship was breaking up.Everyone has the rights to a life, you wouldn't like sitting at home staring at the wall all day long, why should people with disabilities and Health problems. I like to end the days knowing that I have made differences to people's lives.
If you read my report on Access All Area Now and Our Shout I have written about how I am willing to help people like myself to gain a career of their choice whether they want to be employed or Self employed. Baring in mind that Access All Areas Now! has only just started and it need time to build, we have a lot to learn ourselves just yet. We are just on our business plan at the moment.
People with learning disabilities are treated better than they used to be but we still have a long way to go. People's attitudes still need to get better towards people with disabilities. A lot of people with LD, such as myself didn't learn anything at school mostly due to lack of communication and understanding with teachers. A lot of us didn't leave school with qualifications, which made us feel useless.
A lot of us went to college after school, achieving qualifications, not getting job for years or not at all. No one gave us enough support to get work, which meant not giving us enough time or and not enough chances. Not many of us had paid work or we were on training schemes, which was very low pay. Most of us had to spend our time st airing at the four walls at home doing nothing. The people were lucky enough to do something were messed about place to place through discrimination in the work placements or and at college achieving qualifications but not knowing what our future was. We just had to enroll every September, which were mostly the same ones for eg; English and maths. Most people didn't find the course very interesting. Society didn't seem to think many of us were very clever. All we needed was the right support. Why have most of us been given the job all day long when we have been on placements?
This has made us feel like dog's bodies.
Support and attitudes needs to get better. Jobs need to be more interesting, we need to spend our days doing different jobs not the same. Those people like myself with dyslexia need more support. People with LD should train people without LD. We should be given the right support for the LD we have got. No one should be left out no matter what.
There's still too much information and too much jargon. The government or and managers should all staff what our rights so we don't get different information off different people.
There are a lot us with LD who are creative so we should create creative jobs. There still isn't enough people with LD with jobs at all but it's better than it was. Mencap works hard to battle with with government to see that people with LD get our rights. We believe a future for all people with LD when we see it.
People with high support needs need their benefits more than people with mild needs. The government should spend money on the people who need it most otherwise they are also costing themselves too much money. With the right support people with mild LD should get a wage like everyone else. With the right support people with LD accept good and bad in life like everyone. For eg; having to pay tax.
We should be given the right support to learn Health and Safety. We should be given the right support be healthily and safe in all areas of life, which includes the work placements.
Back 2008, Our Shout Self - Advocacy were talking about a Travel Buddy Social Enterprise. This is what Andy and myself from Our Shout read at the Learning Disability Employment play.
People with LD are being encouraged to access community facilities but this will be hard and too much money for those who don't travel independently.
Isolation is a feeling that most people with LD face in the evenings and weekends. There's very little help for these people to get out and about to see, they have never had the chance to achieve this without Families/carers. Many could travel independently with the right support.
A ' Travel Buddy' will help people with LD to travel on pubic transport to get to where they want to go. This will help build Self-stream and potentially lead them becoming independent travellers in the future.
To promote Health and Wellbeing of people with LD by increasing involvement in community based work and activities.
Intensively trained adults with LD to set up a City wide team of paid ' Travel Buddies.'
The proposed service will help encourage social inclusion, promote independence, and give paid work chances.
Many people with LD do not like traveling on ' Special buses to the Day Centres. To up date this report to 2010, we have found out the work we have been doing for the last year that prices have gone up on the Day centre buses. Now many a people with LD who go to these Day Centres could have learned with the right support to travel independently. These people often spend a long time on the transport while others get picked up.
Since 2008 myself and Jessica Bromley have started a business 'Access All Areas Now!' in December 2009. At the moment Access All Areas Now! is just a LD Awareness Training service, which trains all services around LD awareness. We also hope to create a service to support people with LD with all areas of life. We are not building our hopes up but never say never. It will be a long time if it ever does happen. We will work our hardest to see that the Travel Buddy service does happen.
Often people are travelling to Day Centres before going to college in the morning. This means people are taking two journeys instead of one.
Background.
In the past people such as myself from Our Shout Self Advocacy group haven't had any good luck in employment this why we wanted to work for ourselves. At the moment there's only myself and Jess. We hope all of Our Shout be with us but it's a case of more support and funding. One of our areas now we hope to achieve is employing people with LD and creating jobs for people with LD.
Transport has always been a big issue for many people with LD and it was highlighted that there was a need for a travel service to support people with LD to access the communities when people with LD need to and want to.
Aims
The Travel service will give proper paid jobs for people with LD with 1 to 1 support with who wants to use pubic transport to get around.
To help social inclusion people with LD help them to become confident and independent.
To give Wolverhampton a unique bus sevice that supports people with LD help given by people with LD. there are many egs; in other areas of the country where this is working well.
In 2008, Mencap put together a bid for some Eurpopean funding and are continuing to look for other funding chances in case we are successful.
Jess's boyfriend Andy Howell is working with myself and Jess at Access All Areas Now! but he isn't Self - Employed yet but he will soon will be.
People with disabilities feel more of a Health and Safety Hazard at home than work. A lot of us stuffer from Anxiety and depression, we need to keep our bodies and minds busy.I spent 13 yrs signing on, which made me very down in myself. Since I have been working 3yrs ago, helping others like myself, I can take anything that life throws at me. My work can at the right time for me just a little before my Nan died and as my last relationship was breaking up.Everyone has the rights to a life, you wouldn't like sitting at home staring at the wall all day long, why should people with disabilities and Health problems. I like to end the days knowing that I have made differences to people's lives.
If you read my report on Access All Area Now and Our Shout I have written about how I am willing to help people like myself to gain a career of their choice whether they want to be employed or Self employed. Baring in mind that Access All Areas Now! has only just started and it need time to build, we have a lot to learn ourselves just yet. We are just on our business plan at the moment.
People with learning disabilities are treated better than they used to be but we still have a long way to go. People's attitudes still need to get better towards people with disabilities. A lot of people with LD, such as myself didn't learn anything at school mostly due to lack of communication and understanding with teachers. A lot of us didn't leave school with qualifications, which made us feel useless.
A lot of us went to college after school, achieving qualifications, not getting job for years or not at all. No one gave us enough support to get work, which meant not giving us enough time or and not enough chances. Not many of us had paid work or we were on training schemes, which was very low pay. Most of us had to spend our time st airing at the four walls at home doing nothing. The people were lucky enough to do something were messed about place to place through discrimination in the work placements or and at college achieving qualifications but not knowing what our future was. We just had to enroll every September, which were mostly the same ones for eg; English and maths. Most people didn't find the course very interesting. Society didn't seem to think many of us were very clever. All we needed was the right support. Why have most of us been given the job all day long when we have been on placements?
This has made us feel like dog's bodies.
Support and attitudes needs to get better. Jobs need to be more interesting, we need to spend our days doing different jobs not the same. Those people like myself with dyslexia need more support. People with LD should train people without LD. We should be given the right support for the LD we have got. No one should be left out no matter what.
There's still too much information and too much jargon. The government or and managers should all staff what our rights so we don't get different information off different people.
There are a lot us with LD who are creative so we should create creative jobs. There still isn't enough people with LD with jobs at all but it's better than it was. Mencap works hard to battle with with government to see that people with LD get our rights. We believe a future for all people with LD when we see it.
People with high support needs need their benefits more than people with mild needs. The government should spend money on the people who need it most otherwise they are also costing themselves too much money. With the right support people with mild LD should get a wage like everyone else. With the right support people with LD accept good and bad in life like everyone. For eg; having to pay tax.
We should be given the right support to learn Health and Safety. We should be given the right support be healthily and safe in all areas of life, which includes the work placements.
Back 2008, Our Shout Self - Advocacy were talking about a Travel Buddy Social Enterprise. This is what Andy and myself from Our Shout read at the Learning Disability Employment play.
People with LD are being encouraged to access community facilities but this will be hard and too much money for those who don't travel independently.
Isolation is a feeling that most people with LD face in the evenings and weekends. There's very little help for these people to get out and about to see, they have never had the chance to achieve this without Families/carers. Many could travel independently with the right support.
A ' Travel Buddy' will help people with LD to travel on pubic transport to get to where they want to go. This will help build Self-stream and potentially lead them becoming independent travellers in the future.
To promote Health and Wellbeing of people with LD by increasing involvement in community based work and activities.
Intensively trained adults with LD to set up a City wide team of paid ' Travel Buddies.'
The proposed service will help encourage social inclusion, promote independence, and give paid work chances.
Many people with LD do not like traveling on ' Special buses to the Day Centres. To up date this report to 2010, we have found out the work we have been doing for the last year that prices have gone up on the Day centre buses. Now many a people with LD who go to these Day Centres could have learned with the right support to travel independently. These people often spend a long time on the transport while others get picked up.
Since 2008 myself and Jessica Bromley have started a business 'Access All Areas Now!' in December 2009. At the moment Access All Areas Now! is just a LD Awareness Training service, which trains all services around LD awareness. We also hope to create a service to support people with LD with all areas of life. We are not building our hopes up but never say never. It will be a long time if it ever does happen. We will work our hardest to see that the Travel Buddy service does happen.
Often people are travelling to Day Centres before going to college in the morning. This means people are taking two journeys instead of one.
Background.
In the past people such as myself from Our Shout Self Advocacy group haven't had any good luck in employment this why we wanted to work for ourselves. At the moment there's only myself and Jess. We hope all of Our Shout be with us but it's a case of more support and funding. One of our areas now we hope to achieve is employing people with LD and creating jobs for people with LD.
Transport has always been a big issue for many people with LD and it was highlighted that there was a need for a travel service to support people with LD to access the communities when people with LD need to and want to.
Aims
The Travel service will give proper paid jobs for people with LD with 1 to 1 support with who wants to use pubic transport to get around.
To help social inclusion people with LD help them to become confident and independent.
To give Wolverhampton a unique bus sevice that supports people with LD help given by people with LD. there are many egs; in other areas of the country where this is working well.
In 2008, Mencap put together a bid for some Eurpopean funding and are continuing to look for other funding chances in case we are successful.
Jess's boyfriend Andy Howell is working with myself and Jess at Access All Areas Now! but he isn't Self - Employed yet but he will soon will be.
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