Viewing 3 posts - 1 through 3 (of 3 total)
  • Author
    Posts
  • Travis Moss
    Participant
    Post count: 1

    Hi all! I’m Travis but you can call me T or Big T. I’ve had this disease for less than 2 years so I consider myself new to these issues. I’d love to hear from anyone and everyone about your symptoms and what you do to combat them. Graves and Hashimotos seems to not get much attention and I’ve had a helluva time finding this forum even. Please don’t be shy cuz I would love to talk to anyone that understands what I’m going thru. I’m really looking for anything at this point so I apologize for sounding desperate. But some days just feel like all will be, or is, lost.

    Kimberly
    Keymaster
    Post count: 4297

    Hello and welcome! Hopefully, you will get some replies here, but most of the “action” these days is over on our Facebook group. If you are on FB, do a search for @GDATF and select “Join Group”.

    You might also be interested in our monthly Zoom meetings – I’m just about to post a link to a meeting tomorrow, and we can also add you to our email list to get notification of future meetings.

    Take care!

    jeany676
    Participant
    Post count: 6

    For me, stress and sleep make a huge difference with symptoms. Also, keeping an eye on meds can be key since things seem to change all the time. Don’t worry, you’re not alone in this!

Viewing 3 posts - 1 through 3 (of 3 total)
  • You must be logged in to reply to this topic.