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Brief look into my life since having Chronic Inflammatory Demyelinating Polyneuropathy or CIDP, a rare neurological disorder that affects about 1 in every 100,000 persons (US figures), which means not many people know much about it, including most doctors.
1 comment:
I just found your blog. My husband has CIDP also. Was diagnosed in Oct. of 2006. Very difficult to get the IvIG on a steady basis. Would love to talk with your more. My husband is completely disabled. I am amazed to see that you are working. I will be checking your blog regularly now that I have found someone who has the same syndrome as my husbands.
I wish the best for you.
Sharon HH
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