Sharing my thoughts, feelings, and experiences.
So sorry to learn about CIPD and its devastating effects. Is ti a form of MS? I will pray for you. I promise.
Thanks Susan. It affects the peripheral nervous system instead of the spine and brain.
Oh gosh, hope it improves for you...take care.
I hope you perk up soon! In the meantime, take it easy.
I'll try not to let it get me down.
I feel like that poor dog sometimes. He looks uncomfortable.
I'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?
I give myself subcutaneous injections of human immune globulin each week. It usually helps but for the past two weeks I've been getting worse.
Hope things improve for you.Take care John.All the best Jan
Thank you Jan
Take care and stay positive. Best wishes John.
I'll try, thanks.
I enjoy reading your comments.I'll visit your blog.