ScottieSue wrote:My husband was diagnosed with PPMS in 1997 and has declined to the point that he is pretty much a quadraplegic. I have read many stories from people with various stages but I am wondering if anyone else has progressed as far as my husband. I have him registered with Albany but I am afraid they may say he is "too far gone" for the CCSVI treatment. That is why I would like to hear from anyone who has the same degree of disability as my husband who may have had the treatment.
welshman wrote:We don't know what's happening to our partner, just like you don't know what's happening to yourself. In my opinion, it is very important for you to communicate to him what you feel, what is happening to you; and it's also very important that he gets to know as much about MS as he possibly can.
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