Welcome, Red Bank People With RSDS!

Location
Red Bank, NJ 40.35-74.07 07701US
Meetups
9 so far
Founded
October 21, 2007
Rating
No recent ratings

Meet with other local people with Reflex Sympathetic Dystrophy Syndrome (RSDS) also known as Complex Regional Pain Syndrome. Gather for support and share advice on treatment options.

Meetup Topics
Reflex Sympathetic Dystrophy Syndrome, Chronic Pain, Pain Management
Where?
This location is shown only to members
Who's coming?
1 Yes / 0 Maybe
( 14 spots left )

Want to attend?

Our first meeting went well, even though it was just a few of us, we had great conversation! Our meetings are for the sufferers of RSDS and those people who live with us and are affected by our lives. We all must support one another. I have lots of information for our next meeting along with ideas for future meet ups! Maybe even a speaker or two. Read more

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Join Red Bank Reflex Sympathetic Dystrophy Syndrome Meetup Group

You'll get invited to our Meetups as soon as they're scheduled!

What's new?

  • May 7
    • New Greeting for
       Susan, Welcome to our small but supportive group. I'm so glad that you found us and want to share your experiences with us. I look forward to chatting with you and learn about your successful treatments! 
      posted by Danielle L. Gross
  • May 6
    • New member
      Hello, I was diagnosed with RSD in 2007 and have had very successful treatments since to alleviate my symptoms. I'd love to share and help others through my experiences, but don't live in the area - so feel free to email me anytime!
  • Mar 7
    • New Greeting for
       Hey Danielle I spent the month of Feb. in Fla. so sorry I am just getting back to you. I have recently have had to deal with the spread of my RSD from my arm/hand and wrist to my rt side of my head,face,chin and my entire back. I've had to learn not to move much so my clothes don't slide on my body and cause even more burning and stinging. Thanks again for the shout and I will try to keep my posting up. 
      posted by Nancy Murtha
  • Jan 31
    • New Greeting for
       Nancy, Welcome to the group! I'm very excited to have people responding to the posting! Not for having RSDS , but for having the courage to reach out and share your experiences with others who are going through some of the same things! I look forward to seeing you soon! 
      posted by Danielle L. Gross
  • Jan 23
    • New member
      I have had RSD/CRPS since 2005 I am so tired of living in pain and coud really use support. I won't be able to attend the Feb meeting I will B in Fla. but, am looking foward to the next one.
  • Dec 4 2007
    • New Greeting for
       Hi Danielle! Thank you for the welcome! I would FIRST like to share my personal stories of CRPS. I HAVE BEEN THROUGH ALOT TO ACTUALLY GET A DIAGNOSIS. I am seeking a support group that share all types of info and treatments that work. I would eventally like to present what I know, what helps me, but ultimately I am seeking support for myself for other options! Hope to meet you all soon and share! 
      posted by Carla J. CCT, CTT
  • Dec 3 2007
    • New Greeting for
       Hi Carla! I'm so glad you signed up for our next event. So far you and I are the only members . Do you have RSD, or are you looking to present some types of treatments. Anyway, thanks for joining! 
      posted by Danielle L. Gross
  • Nov 21 2007
    • New Greeting for
       RDS/CRPS is often hard to explain. I have access to Free Groups and Free Research for others and social groups in NJ. I have my own RDS images posted on my site with research etc. I would LOVE to LEARN What HELPS Others in their "stressful" Times! http://www.cvdinc.org/Physicians.html 
      posted by Carla J. CCT, CTT