My son has SPMS. With this he to cope with; cognitive issues, tremor, spasms, myoclonic jerks, seizures, memory loss, bladder and bowel issues, nastagmus, balance, very little ability to walk, etc etc. I am looking for NO sympathy....no time for this, thank you anyway. I would very much like to speak with another parent who is caring for an adult child with similar, if not all, issues that my son copes with everyday. We live on the west coast of Canada, near Vancouver British Columbia. My son has had 2 treatments for CCSVI. He use to have chronic pain and since the 1st CCSVI treatment he no longer lives with pain. His head fails around at times also. My son was dx with MS at age 25, he is now 41. Thank you for all and any help to connect with some one coping in the same way as my son. My email address is email@example.com. I will respond to any questions, here or at my email address. Bless all of you coping with this disease....................I have HOPE.