Support and Chronic Pain Community Group
Welcome! This room is for CP/IP survivors. This room promotes fun, family, support and compassion. No Drug Seeking Posts or Promoting of such activities are allowed here. Please, No "F" Bomb--keep swearing to a bare minimum. No posts that are "fighting" with another person/group on this board or another.

Genuine you are right about one thing what you are looking for has never been on DS. It is in research engines. You never have understood what a support group means and for that I am sorry for you.
Brandi gave this room all of her effort and her love too. Her health and lack of internet were her reasons for not being here. Once and for all why don't you quit looking for the negative in others and research your own soul.
Everyone here is in bad health. As far as I know, hers didn't worsen. She bailed on the group and didn't apologize. And if she's without regular access, I don't think she ever said that publicly.
Nobody can single-handedly research his/her way out of complex medical conditions. People need to be sharing health-related information. It's too bad the chronic pain groups get sucked into the path of friendship ahead of health improvement.
Light a candle instead of cursing the darkness.
It is usually found in our own soul anyway.
Alone.
The largest area of support we can give besides our own experiences, given that we are not doctors, is that of friendship.
For some of us, it may be the only way.
That's what drew me to DS in the first place. The ability to form relationships with people. It helps my pain, depression, and my overall health.
If you just want science, go to WebMD or Wikipedia.
miss you and others around here.
love and peace
hippy