Support Group Meetings

The Support Group was established in Charlotte 4 years ago. We meet the 2nd Saturday of each month.  Each month we discuss a different subject – topics are suggested by group members. Topics range from: traveling with CRPS; helping through the holidays; alternative treatments; etc. We bring in guest speakers, have workshops, and more. 

 

Our members are very diverse. We have members who have had CRPS for 6 months – 30 years; men/woman; some right here from Charlotte, and others who drive almost 3 hours for each meeting. We have new people join us almost each session.  At every meeting, caregivers (spouses, partners, etc) are always welcome to be a part of our meetings. The location is subject to change but will always be announced in emails and social media.

Contact Us For More Information

Henry Evans

CEO

Adele Crawford

Designer

Where Can I Find Out More? 

Each of these external sites holds additional information about CRPS. 

01

Overall CRPS Information

If you are in need of additional general information about CRPS, Burning Nights can be a  great help!         Click Here

02

Questions about CRPS?

Dr. Hooshmand’s RSD (now called CRPS) puzzles can help answer many questions you might have.             Click Here.

03

Chronic Pain?

The National Pain Report has a lot of wonderful articles on various chronic pain issues. Click Here.  

04

More Information on Rare Diseases

National Organization for Rare Disorders advocates and funds research, education, and networking among service providers. Click Here

The NIH provides information from the government and is in charge of  biomedical  and public health research. Click Here

Social Security & Workers Compensation


There are many questions when you have CRPS and want to file for Social Security and/or Workers Compensation. If you need assistance with either of these, please see the links provided for more information.