My CIDP is acting up. It was fine a couple of weeks ago, then last week I felt it coming back. Now I'm so weak and both my calves ache when I rest in bed.
I'll have to be patient. It should improve. If it gets much worse I'll have to call my doctor.
Sharing my thoughts, feelings, and experiences.
So sorry to learn about CIPD and its devastating effects. Is ti a form of MS?
ReplyDeleteI will pray for you. I promise.
Thanks Susan. It affects the peripheral nervous system instead of the spine and brain.
DeleteOh gosh, hope it improves for you...take care.
ReplyDeleteThank you.
DeleteI hope you perk up soon! In the meantime, take it easy.
ReplyDeleteI'll try not to let it get me down.
DeleteI feel like that poor dog sometimes. He looks uncomfortable.
ReplyDeleteHe does.
DeleteI'm so sorry to head your CIDP is flaring up. You might remember I've told you my cousin has it too. It's a challenge, for sure. I hope you get some strength back soon. Are you still getting treatments for it?
ReplyDeleteI give myself subcutaneous injections of human immune globulin each week. It usually helps but for the past two weeks I've been getting worse.
DeleteHope things improve for you.
ReplyDeleteTake care John.
All the best Jan
Thank you Jan
ReplyDeleteTake care and stay positive.
ReplyDeleteBest wishes John.
I'll try, thanks.
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