New to this site but not to MS

[LarryG]

Hello everyone! Texas resident and 23 years living with PPMS here. Hopefully I can contribute something here.

[lyndacarol]

Hello everyone! Texas resident and 23 years living with PPMS here. Hopefully I can contribute something here.

Welcome to ThisIsMS, Larry (LarryG). We are glad to have you join us.

[ElliotB]

Welcome! Perhaps you can share some of your insights?

[justKathy]

Hello Larry - same here, but only 21 years
I've never joined a fórum before, but I'd like to talk to some of my own now...

[lyndacarol]

I've never joined a fórum before, but I'd like to talk to some of my own now...

Welcome to ThisIsMS, Kathy. We are good listeners – you found the right place.

[robnanza3]

I just found you. I am looking to help a friend that has MS. Over 2 years ago I was beginning to experience tremors and since I am a vietnam vet right away my thoughts were Agent Orange. Any way I am looking to continue to research and see who has found natural help to recover their health.

[lyndacarol]

I just found you. I am looking to help a friend that has MS. Over 2 years ago I was beginning to experience tremors and since I am a vietnam vet right away my thoughts were Agent Orange. Any way I am looking to continue to research and see who has found natural help to recover their health.

Welcome to ThisIsMS, robnanza3.

Since you are a military veteran, you may find people with similar experiences and questions posting in the "Veterans and MS" sub forum (http://www.thisisms.com/forum/veterans-and-ms-f51/)

There is lots of information here at TIMS. If you can't find a particular subject, just ask (the General Discussion thread is good for these questions) – we may not always have the answers, but we are glad to share our opinions.

[LarryG]

Hello Larry - same here, but only 21 years
I've never joined a fórum before, but I'd like to talk to some of my own now...

This is new to me as well. Up until now, I have never joined a forum before. In fact, I have always purposely avoided talking to anyone with MS. My way of avoiding the issue and trying to feel normal, I guess. I need to change that.