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Get the benefits you're entitled to: help with employment and support allowance (ESA), personal independence payment (PIP), universal credit (UC), disability living allowance (DLA). Claims...
Hi everyone,
(no pun intended in the title)
Remember me at all? I am currently writing a book (onto chapter 20) wherein one of the main characters happens to be a youngish mum who suffers from MS. I have looked around for support groups, charities and organisations so that I could get involved and meet people to have a chat and get a real feel of how things really affect those affected, but haven't had any luck. Does anyone know how I could get involved with such a group? I am in Leicester (city centre), strong and willing, without a car.
Anyway, until I can get that sorted out, I have a question for you. I hope you can help. My character, Karen, has of course MS. I have written it as a RRMS that no longer relapses or remits so much (perhaps time to alter diagnosis). As such, she has some daily difficulties with her leg, which is generally a bit naughty and unreliable. Following her WCA assessment, I have her put into the WRAG group (incorrectly) based on a belief that one day, it will all go away...
I can't speak from experience, and I absolutely would like to get this right, so could anyone who knows please help me.
What I'd like to know is: what sort of benefit would she get, realistically?
Based on what I could find out, here is what I think is correct (PLEASE tell me if this is outdated/wrong)
disability living allowance - 3month qualifying period- on no pay, then:
Assessed by two criteria:
per week:
Mobility low:
Hi
was going to ask ms nurse today about filling in dla forms but shes not coming now till 3rd nov, and the forms need to be in by the 7th . can I ask what we can get with msI am virtually housebound at the mo, hubby helps with most things as I can't do much, im not a lazy person and I am so frustrated by this just want to feel better ,. x
Okay, another question for all you helpful people, so, got my Dxon 29th Oct and it's not sunk in yet! Still in cuckoo land but am findin it quite nice here for the time being
So, havin not claimed anything at all from our wonderful system LOL since I was 20 and claimed the dole for a short period, I'm wonderin how this all works. We struggle for money but we're battling on with the mortgage and xmas looming as we do every year. Our cars an old one, not a flat screen in sight and the only sofa we have is clingin to life by its very threads! I guess what I'm gettin at is that we have always worked and stood on our own feet without credit cards and HPs and we're damn proud of it. So, now I'm hearin all these snippets of info from people 'ooohhh you'll get this benefit, that benefit and the other' so I'm tryin to find out what, the sites are a minefield with the info on and don't make much sense.
Is this something anyone can help with or is a case of waitin to see the MS nurse. Spose I'm fillin me head with ups rather than downs at the mo!
Em X
I am a recent joinee (if that is a real word?) to this forum and the reason I joined was initially to get a real view on my situation and to see if anyone can help me. I was diagnosed with relapsing remitting MS back in January 2006. Since then I have taken full advantage of DMDs such as Avonex and in January this year I moved over to Rebif as I had experienced a couple of relapses.
Throughout this time (over 2 years) I have suffered constantly from side effects and it just hasn't let off. I now take 6 ibuprofen and 6 pararcetamol a day to try and quosh the side effects. When they take hold I experience flu symptoms, headaches, muscle aches & depression. Even when I switched to the new formula Rebif in april, which was designed to be better on injection site reactions, I started getting injection sites reactions. I am extremely positive about my condition and believe very much in the power of the mind is assisting my condition. I eat healthfully, exercise in moderation but regularly and generally enjoy life. I can't help but wonder if in fact I would be better off without the treatment given that the ibuprofen alone can't be doing much for my liver.
That being said I am concerned about coming off the treatment in the fear of 'what if?' I have been offered Imuran as an alternative and as ever I am undecided because there seems to be little realistic information about people's experiences with the drug out there. Specialists nowadays have to sit on the fence which is quite frustrating and you are left to randomly search the web. There are lots of trial reports but I lost confidence in these when they told me that side effects from interferon would only last 3-6 months max, which is not the case for me.
I was wondering if anyone has taken Imuran for their condition either as a standalone treatment or a combination treatment? If so would you be so kind as to let me know your thoughts and experiences on this? I am not afraid of hearing your experiences good or bad as I need a realistic view on this.
Founded in 2004, MS People UK is a community website and discussion forum by and for people with Multiple Sclerosis as well as for friends, families, supporters and those interested in this disabling condition.
If you’re newly diagnosed or want to ask about possible first symptoms, or if you’ve had Relapse Remit, Secondary or Primary Progressive MS for some time, a welcoming group of fellow MS sufferers is here to chat with you about MS symptoms, diagnosis and treatments.
The atmosphere is friendly whilst being compassionate, supportive and caring. Members also post about a variety of subjects not related to MS, as well as share jokes, talk about their hobbies, have fun, and more.
The MS People Forum is not responsible for advice or information supplied by members. We suggest you seek medical advice before trying anything.