Rating: 3 stars 1 1 review 800
Civil Rights, Disabilities, Education, Cancer
4281 W 76th St #501 Chicago IL 60652 USA
The Fibromyalgia Association Created for Education and Self-help is commonly known as FACES. FACES was established by our founder (an African American Female Police with injury related Fibromyalgia) as a result of the healthcare and pain management disparities she personally experienced. FACES is comprised completely of volunteers - either people battling this devastating disability or friends and family members of patients. FACES participates in community collaborations of awareness campaigns, outreach projects and patient education. FACES has collaborated with disability rights associations, universities, minority health associations, and other Fibromyalgia organizations. FACES provides information and referral services, patient education and public awareness via our website www.fibrocop.org, FACES sponsored seminars and seminars of our various community partners. FACES strives to ensure that no person with Fibromyalgia, especially minorities and public safety officers (police officers, law enforcement officers, firefighters, and paramedics (EMTs)), will have to suffer the humiliating trials of misdiagnosis, inadequate treatment and disability related discrimination as our incorporating members battled.
Filter Reviews by Role
Promote This Nonprofit
Donor & Volunteer Advisory
This organization's nonprofit status may be in question. You'll need to check recent news about this organization. For more information please visit http://apps.irs.gov/app/eos/forwardToRevokeDownload.do
GreatNonprofits, as an impartial aggregator of reviews, takes no position on allegations made or issues raised by third parties. However, donors and volunteers can read recent news about this organization and determine for themselves whether such information is relevant.
Reviews for Fibromyalgia Association
7 people found this review helpful
My name is Gina and I have suffered from Fibromyalgia for about five years and not diagnosed until 15 months ago. I actually had several people suggest this before diagnosis and I hadn't heard of it before then. I'm just glad to find so many organizations out there however on this site there are no reviews, participants, patients, or fundraisers out there for this terrible syndrome. They say there is no cure, there is no result in death either, BUT it's miserable and really effects your life and the people in it as well. I continue to work daily now that I'm on pain management medicine. The dosage has gone up 3 times since I've started on it, strong pain meds to help me through the day on bad days, and sleeping meds at night so I can sleep! It's non-stop pill popping and it wears you down.! I really thought for two years I was losing my mind because every week and sometimes day to day my horrid pain was in a different spot! I just got to the point I was in tears all the time! Missing work for 3 days at times in the winter because it felt like the flu, strept throat, and like I had been in a wreck two days before that threw me across the street but yet NO FEVER! There must be something out there that can help stop this madness for us. I do exercise a lot and it helps keep me feeing good. Basically fighting it all the time. However, I always exercised daily anyway and have been a dance instructor for 25 years! but meds and exercise don't make it go away....it helps keep it under control. Every six weeks or so, I'm toast. Out of control unable to function PERIOD. Does anyone out there have luck with certain things or a certain drug?
I've personally experienced the results of this organization in...
I have not.
How frequently have you been involved with the organization?
When was your last experience with this nonprofit?