Hello,
After 6 frustratingly painful years and 3 of them actively seeking a medical answer to my constant pain and slowly worsening disabilities I was diagnosed with MS on Dec 2. The neurologist started me on Ampyra and would like me to start Tysabri sometime next year after my JCV blood test, follow up MRI and LP. I have to be honest the though of PML scares the hell out of me. I have a 7 year old son and do not want to leave my husband to raise him alone. I am looking for experiences and possibly more accurate risk information about this therapy. This is my first post and I appreciate any advice, stories or info that you may be willing to share.
Thank you.