DLA Renewal Success.

diolch

Tehya wrote: »

My post AGAIN.

diolch

Hubby got awarded DLA 2 years ago in May 2009, DLA MRC, HRM without a medical, this may be because he was placed in the support Group for ESA almost at the same time even though he didn't have a medical for that either. We think this may be due to the illness/condition he has.

Renewal was due in May this year so the form came Jan 2011. We sent form off on 8th March and got award letter on the 8th April (same as previous award) MRC, HRM again without a medical.

Both times the whole process took less than 5 weeks from them receiveing the forms to us getting the award letter.

So it is possible to go through both ESA and DLA claims without a medical but in 2013 everyone on DLA will go through a medical regardless of condition I believe.

OK I see where I was going wrong - thanks.

As a matter of point, I too am in the Support Group without any problems in getting it but had a medical. It was given for 4 years before it will be reviewed again.
But I tried for DLA about 5 months after and was told that I don't have any care or mobility needs. The GP's report said that he wasn't aware of any needs that I had. Strange that considering that that is the reason I am in the Support Group - Mobility all of the time and unable to care for myself most of the time.

Never mind, it would be a strange world if we all were the same.

diolch

skcollobcat10 wrote: »

If I were you I would try applying again for DLA, especially as you are in the Support Group for 4 years. I have just had mine renewed again but I had a brand new GP as the other had retired. I seem to remember years ago wasn't there a checklist on the back of the dla form so that you could let your gp know what you can do and can't do? Go through the form and photocopy it keep a copy yourself and hand one in personally to your GP so that he can read it over. This will help if the DLA send him forms to fill in. None of us want to moan everytime we go for a GP appt, so this is probably where you went wrong, not letting him know the problems you are having.

No I don't remember seeing a check list, just a place to put his name and address on.
I doubt if my GP would read the form if I gave him a copy. More likely dump it with the rest of the unsolicited mail!
It is difficult having to explain to a GP what problems people have. GP's just haven't got the time to sit and listen to someone go on about how hard it is to open a tin or what sort of pain you get when you walk. He knows whats wrong with me and treats it, that is about all.

Erme

skcollobcat10 wrote: »

Didn't know "God" had joined Atos.

Well God is the reason I'm still alive after all these years. Take it or leave it. Without him and my illness (8 years undiagnosed despite seeing medics) I'd have been 6 feet under 13 years ago...

diolch wrote: »

No I don't remember seeing a check list, just a place to put his name and address on.
I doubt if my GP would read the form if I gave him a copy. More likely dump it with the rest of the unsolicited mail!
It is difficult having to explain to a GP what problems people have. GP's just haven't got the time to sit and listen to someone go on about how hard it is to open a tin or what sort of pain you get when you walk. He knows whats wrong with me and treats it, that is about all.

Maybe try a different GP in the same practice if it's so like head banging or get someone to go with you is all I can suggest and book a double appt and go from there. Or else change surgeries.....I've had to do that a few times in the past when practices have done more harm than good and it's always been 'life or death' type stuff when I've done it (i.e. it's not to be done lightly) but always saved my life...

E

seven-day-weekend

Makes a nice change from hearing everyone talking abou the latest conspiracy to deprive them of their Benefits. Nice to hear some positive stories.

Just to say also that my son's girlfriend was awarded DLA (LRC, LRM) for the first time two years ago with no problems.

I wish everyone well.

TOBRUK

diolch wrote: »

OK I see where I was going wrong - thanks.

As a matter of point, I too am in the Support Group without any problems in getting it but had a medical. It was given for 4 years before it will be reviewed again.
But I tried for DLA about 5 months after and was told that I don't have any care or mobility needs. The GP's report said that he wasn't aware of any needs that I had. Strange that considering that that is the reason I am in the Support Group - Mobility all of the time and unable to care for myself most of the time.

Never mind, it would be a strange world if we all were the same.

Hi diolch (thankyou) The fact that you are in the 'esa support group' probably wouldn't mean anything to your GP; have you discussed your needs and difficulties with your GP - he/she needs to be made aware.

diolch wrote: »

...
It is difficult having to explain to a GP what problems people have. GP's just haven't got the time to sit and listen to someone go on about how hard it is to open a tin or what sort of pain you get when you walk. He knows whats wrong with me and treats it, that is about all.

I know GP's are busy, however, you should make an appointment to discuss your condition otherwise your GP can't help you. You really should tell your GP about the pain and difficulty you have when you walk - how can your GP treat you unless you tell him/her? I have a lot of pain in my legs when I walk but with the medication I have it does help. I have nerve pain, muscle pain, spasms etc and have different medication for the different pain.

If you have difficulties with everyday things (like opening tins etc) and are having difficulties with other things your GP could refer you to an OT who could help make your life easier.

Your GP is there to listen about your health and welfare.

diolch

Well God is the reason I'm still alive after all these years. Take it or leave it. Without him and my illness (8 years undiagnosed despite seeing medics) I'd have been 6 feet under 13 years ago...

I can fully understand that feeling. I woke up in the HDU with my vicar and family standing round me! It was a shock. I only found out much later that they had been called in because the hospital didn't think I would make it through the night. Pulled through that one (my vicar came twice a week for nearly 3 months to talk to me). Then was told that there was a 50% chance of not surviving the next 7 years) Well I'm still here at 7 years and 3 months and counting!

Maybe try a different GP in the same practice if it's so like head banging or get someone to go with you is all I can suggest and book a double appt and go from there. Or else change surgeries.....I've had to do that a few times in the past when practices have done more harm than good and it's always been 'life or death' type stuff when I've done it (i.e. it's not to be done lightly) but always saved my life...

It's not so much the GP's really when I think about it, more about feeling a 'waste of space' and believing that no one actually cares or wants to care. So why bother to try and explain myself.

diolch

Hi diolch (thankyou) The fact that you are in the 'esa support group' probably wouldn't mean anything to your GP; have you discussed your needs and difficulties with your GP - he/she needs to be made aware.

Thanks, no I don't discuss anything with them really. I don't see the point. They are busy and the last thing they need is someone to take up their time to talk about what I can't do. The thought of that depresses me.

I know GP's are busy, however, you should make an appointment to discuss your condition otherwise your GP can't help you. You really should tell your GP about the pain and difficulty you have when you walk - how can your GP treat you unless you tell him/her? I have a lot of pain in my legs when I walk but with the medication I have it does help. I have nerve pain, muscle pain, spasms etc and have different medication for the different pain.

If you have difficulties with everyday things (like opening tins etc) and are having difficulties with other things your GP could refer you to an OT who could help make your life easier.

Your GP is there to listen about your health and welfare

.

Deep down I know you are right, but knowing that is one thing, doing something about it is another. I get my medication on repeat prescriptions so I don't have to go in and ask anyone for it.
There comes a time in life when things get too big and too much to handle. It is now just a question of trying to accept life as it is for me now.

jetta_wales

skcollobcat10 wrote: »

Well please do not preach make believe on the forum.

Lol, harsh but apt