Anyone been diagnosed with polymycotis: I realise... - LUPUS UK

LUPUS UK

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Anyone been diagnosed with polymycotis

yorkshiregirl44 profile image
4 Replies

I realise iv asked this question before but because its rare i didnt have any replies.I thought at different times someone with this condition might see it. I know there are old posts about this condiion on here but they are over a year old.

Thanks

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yorkshiregirl44 profile image
yorkshiregirl44
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4 Replies
a_Scot profile image
a_Scot

[quote="yorkshiregirl44"] Anyone been diagnosed with polymycotis [/quote]

You mean polymyositis ... en.wikipedia.org/wiki/Polym...

I allege my syndrome includes something similar called dermatomyositis ,

but according to the "wonderful" NHS I'm in "limbo" , ( i.e. no official diagnosis ).

yorkshiregirl44 profile image
yorkshiregirl44 in reply to a_Scot

Yes i do mean that sorry..everytime i write the word i spell it wrong.

Im going to a rhumy soon, because its so rare im trying to find out what i can about it.

Whay kind of tests did you have if you dont mind me asking.

Renu profile image
Renu

Hi I have polymyositis. Was diagnosed about 4 years ago alongside Lupus. Yes it is rare. I struggle to climb stairs, lift arms above shoulder level, walk, stand. My thigh muscles have really weakened with it but I go aquafit and swimming regularly and have fought very hard to fight this disease and keep fit, mobile and active. I am now in remission with meds and so am happy! I have more probs with lupus rather than the polymyositis, now that it is in remission. The treatment reversed it for me so it does work! I still struggle to stand and walk any given distance but as I have lupus flares, muscle power tends to diminish further.

Renu

yorkshiregirl44 profile image
yorkshiregirl44 in reply to Renu

Thanks for your reply, You dont realise just how rare it is until you post a question on here.

I have weakness when standing and walking which makes me feel unstable like i am using all my strength to stay upright.I also have very painful burning neck and shoulder muscles.

When i am having a flare i feel very ill, like something is surging through my body, its a horrible feeling not like flu symptoms but something else.

Im going to see a rheumy and worried because it is rare that i wont have the right tests.

Of course it could be abother condition, can you relate to what i am expereincing.

Thanks

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