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.

Welcome to NT!

You've come to a wonderful place of support and understanding! I feel your frustration, especially when you are being told different things with no diffinitive answers.
There are many caring people here, easy to talk to, and very down-to-earth! Make yourself right at home.

Here's the link to the MS forum:

http://neurotalk.psychcentral.com/fo...aysprune=&f=17

You're sure to get good feedback there.


Just holler if you have any questions or need help in finding your way around.
I hope you will begin to get some answers very soon.

It's great to have you!

Caring,
Rae

Bayston,

It is great to have you come and be with us. You will fine a great number of dear friends to listen when you are in need of ears. Please, just let us know how we can help you out. You will find out we are supportive and relaxing place.

Please keep us up to date on your situation. Again welcome, looking forward to seeing you around. My thoughts and prayers are with you.

Welcome to NeuroTalk, there are lots of friendly folks around here to answer any questions you might have & all sorts of forums to browse, too. Not having a diffinative diagnosis can be frustrating, hoping you get some clarity on that soon.