GBS/CIDP
ClaytonGirl
Community member Posts: 3 Listener
I have CIDP. Is there anyone who has CIDP or GBS. Thinking of moving to wales
Comments
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Hi @ClaytonGirl & welcome to the forum.Just in case others don't understand the abbreviations (I certainly had to look up CIDP), it seems you have Chronic Inflammatory Demyelinating Polyneuropathy. The other related condition you mention is Guillian-Barre Syndrome which seems to be more the acute counterpart of your disorder.I hope others who may have these conditions may reply. I'm very sorry you have this problem & if you have any other questions, please just ask.
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Hi I was diagnosed with CIDP last week.
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Oh so sorry. Don’t give in to it. It’s not the end of the world.
I have had CIDP for 10 years now. Yes there are times when I struggle but that’s when I let my head take over or when I don’t take my medication when I should.
My medication is Lyrica Pregabalin 25mg 50mg and 150mg.
Nightime is my problem BUT that’s when I have chopped down trees or have been Line Dancing. I am not stopping either of these. They are my life.
My Hospital and staff are fantastic. Stay away from stress they say BUT that’s easier said than done.
Please keep in touch.
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Hi thanks for your reply. I start ivig treatment monday ..I seem generally always weak but still have better days ..stress! Well pip just said no so i am very stressed. IRS incouraging that you still.seem to do stuff ....
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Sorry its encouraging you still remain active..my problem is being jot able to work.
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Let me know how you go on. We are off to Devon to mind the family dogs while they go off enjoying themselves. My husband loves the village it has 2 shops AND 2 pubs. So we master walking down to the village and then up the hill to the pub. The hill is harder going home . Many short stops but we do it. Keep your chin up. Truly you can live your life. Don’t give in. If I get low I think of my daughter-in-law who is young and has MS. She’s brilliant and lets me sit on her knee on her golf buggy when we are checking the horses. The only thing is her legs kick out and I end up with my chin on the handle bar. ?
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Thanks have a lovely trip..all the best x
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Hi @ClaytonGirl pleased you & jonno have 'met.' Hope you have a great 'dog sitting' holiday.@jonno1971 if you start a new thread about your recent PIP claim, others here will be able to help with their advice if you're looking to go for a Mandatory Reconsideration.
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Hi jonno and Clayton girl.....I hadnt heard of CIPD either...but seeing the full name makes me think about when I was diagnosed (wrongly) with MS...demylination plays a major role, doesn`t it?
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Did you move? I'm in Wales too and left with residuals from GBS. I bet you're finding the NHS and whole care system a bit archaic compared to England x
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