sinkorswim
New member
- Joined
- Oct 8, 2024
- Messages
- 6
- Reason
- DX FIBRO
- Diagnosis
- 04/2007
Hello!
I decided to sign up today and really appreciate that there is this forum for those with FMS.
I was diagnosed in 2007 and there was nothing around by way of support. In fact I would always hope to bump into someone else with Fibro when visiting my Rheumatologist but never did. It was a lonely time and as a consequence I just went into denial and never spoke about it. It is only now that invisible disabilities are now spoken about in the mainstream, that I am willing to open up a little. It feels good to be able to find my voice. I have a choice to tell others or as the case often is, I do not bother as I will only be told...yes you guessed it, "you don't look sick...." {exaggerated eye-roll} or "..I used to have that, but I cured it by changing my diet...."
Anyway. I am really glad to be here and I am feeling uplifted already
I decided to sign up today and really appreciate that there is this forum for those with FMS.
I was diagnosed in 2007 and there was nothing around by way of support. In fact I would always hope to bump into someone else with Fibro when visiting my Rheumatologist but never did. It was a lonely time and as a consequence I just went into denial and never spoke about it. It is only now that invisible disabilities are now spoken about in the mainstream, that I am willing to open up a little. It feels good to be able to find my voice. I have a choice to tell others or as the case often is, I do not bother as I will only be told...yes you guessed it, "you don't look sick...." {exaggerated eye-roll} or "..I used to have that, but I cured it by changing my diet...."
Anyway. I am really glad to be here and I am feeling uplifted already