Just to raise this as many are facing a renewal.
Whereas the first source of information should be your local council.
You may be interested in the Freedom Pass website run on behalf of all local councils
There are some "dead links" on this site and I have emailed them. Also I found myself being cut off before I could get to talk to someone. Just be aware if you call them.
It is worth noting that
"Q. I have a disability, can I apply for a freedom pass?
A. Disabled freedom passes are issued through your local borough council - contact them to apply. The councils follow the criteria set out by the Transport Act 2000 which outlines the 7 catagories of disability used to assess eligibility for a freedom pass.
Local councils may at their discretion issue passes to disabled people that do not meet these criteria. For further details see the Department for Transport website."
this found on this website by clicking here.
Showing posts with label Motability. Show all posts
Showing posts with label Motability. Show all posts
Tuesday, 11 March 2008
Wednesday, 27 February 2008
Freedom Passes.
Some are concerned that they might loose there entitlement to their Freedom Passes if they face a change to there Disability Living / Mobility Allowance.
Some councils do award Freedom Passes to those who may not be eligible for DLA. Doing so depending on the circumstances of individual concerned & at the discretion of the Local Council.
Check with your own Local Council if you have any concerns.
Some councils do award Freedom Passes to those who may not be eligible for DLA. Doing so depending on the circumstances of individual concerned & at the discretion of the Local Council.
Check with your own Local Council if you have any concerns.
Wednesday, 13 February 2008
Motability.
If you have any concerns about a car or vehicle you have under the Motability Scheme please call them on : 0845 456 4566 (8.30am till 5.30pm Monday to Friday).
However, as many comments & emails I have received mention worries about Motability Cars. I called them today to get some general advice. Please email me if you need any clarification.
There are two components to the Disability Living Allowance. Disability Living Allowance is awarded at three rates for personal care.
The other component is , the Mobility component also awarded at three rates. Where you are awarded the "Higher Rate". You can use your allowance to take part in the Motability Car Scheme.
I do not know how the review is impacting the Mobility component. Please email me if you have any experience to share.
However, as many comments & emails I have received mention worries about Motability Cars. I called them today to get some general advice. Please email me if you need any clarification.
There are two components to the Disability Living Allowance. Disability Living Allowance is awarded at three rates for personal care.
The other component is , the Mobility component also awarded at three rates. Where you are awarded the "Higher Rate". You can use your allowance to take part in the Motability Car Scheme.
I do not know how the review is impacting the Mobility component. Please email me if you have any experience to share.
- If your Mobility component is reviewed. And you awarded the "medium" or "lower rate". The DWP will inform you & Motability of the case.
- You then have the right to appeal that decision. An appeal can take up to three months. Inform Motability that you have made an appeal. During the appeal period you retain your car. The cost is met by Motability. You incur no extra charge.
- The DWP will write to you & Motability with the decision of the appeal.
- If your appeal is successful. You continue your contract with your car as normal.
- If your appeal is not successful. Motability will make arrangements with you to collect your car. You contract for your car ends. You will not be charged for any period of your contract that is outstanding.
Tuesday, 12 February 2008
A shared experience - Thank you.
This came in the email recently. Sorry its a long post but is complete. I have edited it to maintain confidentiality. Thanks for taking the time to email & sharing your experience & views.
Initial email :
"Thank so much for the HIV & DLA review forum. A “close relative” has had his forms hidden away for three weeks to scared to open them. A friend tidying up for him found them recently & acted quickly within the time frame allowed, we now wait anxiously for the outcome. My “close relative” understandably has an ostrich approach to life. Doesn't see it wont happen.
AT least I know what to expect when its my turn on hearing the post hits MY floor everyday............
The whole thing has become a nightmare as I am having to do all the research myself for both my “close relative” & myself. The forum has been extremely informative & so glad I found it, BUT I am still extremely anxious, having sleepless nights worrying about the outcome. Being ** y/o & diagnosed 17 years ago, 'made redundant' two weeks later?? Very suspicious but hey it was a big American take over & I suspect related.
I'm apprehensive about the future. My “close relative” has been positive for 12 years. The whole situation has had an almighty effect on all our family.
If ever there was a call for an experiment on how HIV can differently affect siblings, we will be ideal guinea pigs. My brother has had every opportunistic infection going, for ever having adverse reactions to medications, KS, PCP, to name a few. I on the other hand suffer no more serious than the occasional pneumonia or viral meningitis. Living with HIV has been more a problem for me than the physicality of the disease. I'm now diazepam dependant because of it. Oh & how my GP hates giving me repeat prescriptions for it, deal with your issues is a common response. How & with who? I've not been told despite asking.
It appears that no one really knows what's going on & what's terrifying is that when diagnosed 6 months to live 17 years ago, I made financial decisions that I now regret as I'm not eligible for Insurance or policies that would have secured my home for my HIV negative partner in the event of death, whether HIV related or not. I'm not the only one I know who made the most of a very bad situation at the time of a shortened life expectancy.
I suspected back in 199* this would happen when medical advances started to improve the quality of the lives of so many I know & so prepared myself by retraining as many of my friends did BUT have had so far had no success on the employment side. I know that a five-day 9-5 job would be a major struggle physically but I WOULD HAVE to manage. Quality of life may be financially better for some, not so sure emotionally & mentally. How the hell do you explain, without arousing suspicion, what you've been doing for the last 17 years & at what point? Advice can be taken on the right approach but I foresee problems with any employer outside of the 'gay industry that would want to employee with baggage.
There are some many unanswered questions if & when someone's DLA is taken away. Does it take effect immediately? Does that mean we can no longer pay our mortgages? How would effect other benefits i.e. Incapacity benefit? I thought that the DS1500 & DLA would at least be a security to top up a salary for low paid positions offered that I now may have to apply for as my options & time are running out. So to the Motability car which would also have enable me to seek work further a field than just locally.
Sorry I could go on & on.........
I'm not sure why I've emailed you in truth except again to thank you for the reassurance that my “close relative” & I are not alone, but maybe my email might help in giving you yet another case for the attempt at having the DLA witch hunt stopped & not just for those of us that are HIV positive.
You may use some or all of this on the forum but PLEASE NOT my details. I'm paranoid enough as it is. A white van out side the house is enough to send me into a crisis. "
I responded :
"All the issues you raise are fairly typical. The reason for the blog was to help but more to encourage dialog with those that HAD already been accessed so more of the unanswered questions could be answered. The blog can be intimidating and my direct approach on most things might make the issues somewhat daunting. I have been working on a website to try and soften the approach.
Not all stories are bad. Though if I am honest most I hear of are of a loss of some or all DLA.
Funny, we both had the forms. My partner is being reassessed and we are currently working through the form as your email arrives. I have heard nothing so far.
Your “close relative” is very much the type of person that worries me and encourages me to keep going. He is fortunate to have you. It’s the ones who don’t will suffer more adversely. If not responded to. The benefit would have been withdrawn. He would have had to apply afresh anyway.
Yes I have a post-it to call Motability to find out what the situation is. Will try and do that this week and post something. One of the problems is the more I post the more negative it can sound. Those that feel happy to email me thank me for starting the blog but are the minority. The blog has had 370 hits and on a forum elsewhere about the same. I have had about a dozen email me. I believe in “fore warned is fore armed”. I am aware the blog could look very bleak. However there are no straight answers because like HIV, everyone’s situation is different.
But the awareness is growing which is good. People are talking more openly.
I will edit & post your comments. I fully understand your confidentiality.
On the GP front. The KVN forum held a meeting about the increasing role of the GP in HIV care. This apparently has affected the Health commissions thinking. Because so many people came forward with really bad experiences.
You don’t say which area of the country you are in. Does your clinic have a patient’s forum?
Good luck with your applications. Let me know how you both get on."
Followed by :
"Thank you for replying John,
After a relatively good nights sleep for a change, mind you a couple of sleeping pills helped, I do feel a bit more positive this morning.
I live in” London ”& I must admit the services here have been excellent with the original LEAN & the Globe centre, which have now merged as POSITIVE EAST.
My “close relative” lives in Brighton, he appears to have almost a permanent bed at the hospital. He has a very good CAB woman who has helped him in the past, its just getting him to do anything that is the problem.
Just a thought....... how about trying to get our Mr PADDICK somehow on board, after all I'm sure he is hoping for a large PINK VOTE for the mayoral elections."
My last response :
"Good to hear Positive East are helping you. I will add a link to there website. I notice this issue is prominent on their website. I have called Positive East and left a message.
I would email Mr. Paddick however there is no email address on his mayoral website. Yet plenty of ways to promote his campaign."
Note: The author of this site has to remain politically neutral. Any political view expressed or implied is the view of the original author of comment / email.
Initial email :
"Thank so much for the HIV & DLA review forum. A “close relative” has had his forms hidden away for three weeks to scared to open them. A friend tidying up for him found them recently & acted quickly within the time frame allowed, we now wait anxiously for the outcome. My “close relative” understandably has an ostrich approach to life. Doesn't see it wont happen.
AT least I know what to expect when its my turn on hearing the post hits MY floor everyday............
The whole thing has become a nightmare as I am having to do all the research myself for both my “close relative” & myself. The forum has been extremely informative & so glad I found it, BUT I am still extremely anxious, having sleepless nights worrying about the outcome. Being ** y/o & diagnosed 17 years ago, 'made redundant' two weeks later?? Very suspicious but hey it was a big American take over & I suspect related.
I'm apprehensive about the future. My “close relative” has been positive for 12 years. The whole situation has had an almighty effect on all our family.
If ever there was a call for an experiment on how HIV can differently affect siblings, we will be ideal guinea pigs. My brother has had every opportunistic infection going, for ever having adverse reactions to medications, KS, PCP, to name a few. I on the other hand suffer no more serious than the occasional pneumonia or viral meningitis. Living with HIV has been more a problem for me than the physicality of the disease. I'm now diazepam dependant because of it. Oh & how my GP hates giving me repeat prescriptions for it, deal with your issues is a common response. How & with who? I've not been told despite asking.
It appears that no one really knows what's going on & what's terrifying is that when diagnosed 6 months to live 17 years ago, I made financial decisions that I now regret as I'm not eligible for Insurance or policies that would have secured my home for my HIV negative partner in the event of death, whether HIV related or not. I'm not the only one I know who made the most of a very bad situation at the time of a shortened life expectancy.
I suspected back in 199* this would happen when medical advances started to improve the quality of the lives of so many I know & so prepared myself by retraining as many of my friends did BUT have had so far had no success on the employment side. I know that a five-day 9-5 job would be a major struggle physically but I WOULD HAVE to manage. Quality of life may be financially better for some, not so sure emotionally & mentally. How the hell do you explain, without arousing suspicion, what you've been doing for the last 17 years & at what point? Advice can be taken on the right approach but I foresee problems with any employer outside of the 'gay industry that would want to employee with baggage.
There are some many unanswered questions if & when someone's DLA is taken away. Does it take effect immediately? Does that mean we can no longer pay our mortgages? How would effect other benefits i.e. Incapacity benefit? I thought that the DS1500 & DLA would at least be a security to top up a salary for low paid positions offered that I now may have to apply for as my options & time are running out. So to the Motability car which would also have enable me to seek work further a field than just locally.
Sorry I could go on & on.........
I'm not sure why I've emailed you in truth except again to thank you for the reassurance that my “close relative” & I are not alone, but maybe my email might help in giving you yet another case for the attempt at having the DLA witch hunt stopped & not just for those of us that are HIV positive.
You may use some or all of this on the forum but PLEASE NOT my details. I'm paranoid enough as it is. A white van out side the house is enough to send me into a crisis. "
I responded :
"All the issues you raise are fairly typical. The reason for the blog was to help but more to encourage dialog with those that HAD already been accessed so more of the unanswered questions could be answered. The blog can be intimidating and my direct approach on most things might make the issues somewhat daunting. I have been working on a website to try and soften the approach.
Not all stories are bad. Though if I am honest most I hear of are of a loss of some or all DLA.
Funny, we both had the forms. My partner is being reassessed and we are currently working through the form as your email arrives. I have heard nothing so far.
Your “close relative” is very much the type of person that worries me and encourages me to keep going. He is fortunate to have you. It’s the ones who don’t will suffer more adversely. If not responded to. The benefit would have been withdrawn. He would have had to apply afresh anyway.
Yes I have a post-it to call Motability to find out what the situation is. Will try and do that this week and post something. One of the problems is the more I post the more negative it can sound. Those that feel happy to email me thank me for starting the blog but are the minority. The blog has had 370 hits and on a forum elsewhere about the same. I have had about a dozen email me. I believe in “fore warned is fore armed”. I am aware the blog could look very bleak. However there are no straight answers because like HIV, everyone’s situation is different.
But the awareness is growing which is good. People are talking more openly.
I will edit & post your comments. I fully understand your confidentiality.
On the GP front. The KVN forum held a meeting about the increasing role of the GP in HIV care. This apparently has affected the Health commissions thinking. Because so many people came forward with really bad experiences.
You don’t say which area of the country you are in. Does your clinic have a patient’s forum?
Good luck with your applications. Let me know how you both get on."
Followed by :
"Thank you for replying John,
After a relatively good nights sleep for a change, mind you a couple of sleeping pills helped, I do feel a bit more positive this morning.
I live in” London ”& I must admit the services here have been excellent with the original LEAN & the Globe centre, which have now merged as POSITIVE EAST.
My “close relative” lives in Brighton, he appears to have almost a permanent bed at the hospital. He has a very good CAB woman who has helped him in the past, its just getting him to do anything that is the problem.
Just a thought....... how about trying to get our Mr PADDICK somehow on board, after all I'm sure he is hoping for a large PINK VOTE for the mayoral elections."
My last response :
"Good to hear Positive East are helping you. I will add a link to there website. I notice this issue is prominent on their website. I have called Positive East and left a message.
I would email Mr. Paddick however there is no email address on his mayoral website. Yet plenty of ways to promote his campaign."
Note: The author of this site has to remain politically neutral. Any political view expressed or implied is the view of the original author of comment / email.
Labels:
Emailed Comment,
Motability,
Positive East
Thursday, 31 January 2008
Motability.
Some may have a car provided by the Motability Scheme as they receive the High Rate of the Mobility Component of DLA.
I have searched the website and have found no information on the process or what happens if this review impacts the rate you receive should it fall.
If you have any concerns call Motability and ask their advice. I have added "getting this information" to my to list and write it up when I have it.
For many the use of car allows them to attend medical appointments, get out of the house, encourage independence & live as normal a life as possible.
I have searched the website and have found no information on the process or what happens if this review impacts the rate you receive should it fall.
If you have any concerns call Motability and ask their advice. I have added "getting this information" to my to list and write it up when I have it.
For many the use of car allows them to attend medical appointments, get out of the house, encourage independence & live as normal a life as possible.
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