Sjogren’s Syndrome – Introduce yourself and meet others
I have been diagnosed with this and I'm in pain most days and would like to have discussions.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
I have been diagnosed with this and I'm in pain most days and would like to have discussions.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
I’m so deeply sorry. How is your sleep?
My therapist is excellent. She will return at end of December from LOA for surgery. She had her thyroid removed due to cancer. She told me only because it is the same CA that I had in my thyroid. Otherwise, I attend NAMI support group every Thursday. My family tries but do not understand my issues with depression.
Decent because I take several meds that sedate. Neurontin was the most effective because I no longer wake up with arm pain.
I am glad that they are now calling it "Sjogren's Disease" and not Syndrome, which never made sense...
As we all know this is not an easy thing to have...
Where is your pain? Does your doctor have you on any meds for this?
How do you sleep?
I sent you another message, but you answered it already, thanks. Please disregard the last msg.
some nights I sleep well and others I don't
It is awful. I. am not be treated. Do you have this and how are you treated?
yes but the drugs used for Sjogrens aren't the best as there is so little research into autoimmune diseases..
Do you have it too!?