I was diagnosed with TM in December 2012. My symptoms first started in September 2012 and in the 3 months up to diagnoses I received several "it could be this". Now that I have my diagnosis, I'm told that there is a 70% chance it will be MS. I have an appointment with the MS Clinic next week for a 'education' session. I'm frustrated because I read/hear from others with TM and they almost all have mediations to take, physiotherapy, etc. I don't have anything. I don't know what I can and cannot do, or more what I should and should not do. Just really frustrated. Looking forward to this forum as I don't know anyone who has TM or MS and never heard of TM before getting it myself.