Have you taken part in a Crohn's advocate program? What was your experience?

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Never knew this existed until now...so no.....don't think my Mom ever had any support either as I was growing up.
 
A personal friend of mine, and an attorney who suffered from severe CD, founded an advocacy program .... Advocacy for Patients with Chronic Illnesses/Advocacy for Patients. Her name was Jennifer Jaff. So yes, I was a part of that program until her death in 2012, and I have not joined another one since then.

When I was a member, I found the information and the assistance to be invaluable.
 
Not officially no but it sounds like what we basically do for each other on the forum.
 
I agree it is pretty much the same as here,from what i see on the link. Only difference is we have a whole wealth of knoweledge at our fingertips. No matter what time of day or night, because we are worldwide there is always someone awake.. and willing to help. I for one will be sticking to this site. It is the best i have come across,and the only one i use.Thanks to all of you on here. 💕💕
 
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