I was diagnosed in April this year, although have had symptoms for many years.
I work full time but finding things are getting difficult lately.
I had a fare up that lasted about 4 months then things seemed to settle down, just had what I call background pain.
Then the last two days things have become bad again, struggling to get up from sitting position, climbing the stairs, even walking around the house.
Was wondering if I could claim PIP so that I could possibly reduce my hours in work.
Also has anyone had their symptoms get worse?
Sorry for long post.
Thanks in advance for any support
Written by
Col123
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11 Replies
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Helo col Iv had fibro for 10 years and was told at the beginning they get worse , So all you can do is sort out your medication and do the best you can I have had loads of help from this Foram and you will too with the great people on this site to help you Good luck to you
Hi col and welcome hope you get lots of help and advice off here.not sure about pip but I think you can claim it while your working but would advice you to phone welfare right they will tell you also I got told fibromyalgia would only get worse. You won't be sorry you've joined us on her friendly people who all suffer together ☺Carol x
Hello and welcome! Not a long post at all. So sorry you're struggling with another flare so soon. As I understand it, PIP is assessed according to how your condition impacts on living a 'normal' (whatever normal is) life and things you cant do because of it. The Forum has it's own benefits advisor, whose name escapes me but I'm sure someone will know. Perhaps message TheAuthor, or post it. You have nothing to lose by trying. I do wish you well!
Got a feeling am going to be a regular on this site as I don't really have anyone to talk to about the dreaded fibro....don't like to talk about it at work.
I know what you mean. I don't have many people I can talk to about it either. But fortunately my partner has been amazing in supporting me though. But everyone else don't seem to understand it much. I'm tired of having to explain in detail what I go through daily. Sometimes just saying "I hurt and I'm tired all the time" (or something to that effect) just doesn't cut it. You feel compelled to go into every detail, even though that's exhausting in itself, just to try and stop people from looking at you as if you're a lazy beggar or something!
What treatment or exercises have you tried? My doctor has recommended swimming as its a good all-over body exercise.......so it definitely sucks that I have a fear of water! Lol.
Welcome to the forum and it is wonderful to make your acquaintance. I have pasted you a link below to our mother site, FMA UK which hosts loads of useful Fibro information:
I am so gneuinely sorry to read that you are struggling with work, and it is always worth applying for PIP. I have pasted you a link below to the GOV.UK cache on applying for PIP:
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