Scleroderma Research Archives - Raynaud's Association

Patients With Scleroderma Wanted for Clinical Trial

We have been contacted by a pharmaceutical company to help recruit patients for a clinical trial being conducted in patients with Raynaud’s phenomenon secondary to scleroderma/systemic sclerosis. The study medication is a topical cream that will be applied to the hand. Participation will require travel to a clinical site. The first site is in Encinitas,

Frostie2015-04-03T19:23:33-04:00November 17th, 2014|In The News|Comments Off on Patients With Scleroderma Wanted for Clinical Trial

New Jersey Presentation on Clinical Trials

Dr. Vivien Hsu, Medical Director of Clinical Research Center at Robert Wood Johnson Medical School, will be speaking about upcoming clinical trials for scleroderma and Raynaud’s phenomenon patients on Saturday, November 13, 2010 1:00-3:00 p.m. at the Hackensack University Medical Center in New Jersey.

Frostie2010-11-11T23:16:21-05:00October 2nd, 2010|In The News|2 Comments

Announcing a New Raynaud’s Support Group in Southern NJ!
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…relieved to know what it is…comforted to know there are other folks that have this condition…nice to have a place to share what works for us. by J.J. (VA)

A Place to Share What Works for Us

This nonprofit made me realize I wasn’t alone, and referred me to some great gloves that have changed my life!! by Anonymous

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I had no idea there was a name for what I’d been experiencing…found the Raynaud’s Association. THERE I found useful information & was connected with a network of support. I’ve learned so much & am so grateful to have this resource. by S. F. (Facebook Fan)

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It’s a fantastic opportunity to be able to voice opinions and learn of new advancements in the medical treatment of this horrible affliction…Thank you for creating a page that helps. by N.L. (UK)

Fantastic Opportunity to Voice Opinions & Learn of New Advancements

Thank you so much for having your Facebook page. It’s comforting to know that people understand the pain. That we are not alone. by L.M. (Facebook Fan)

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The Raynaud’s Association provides a lot of essential tips and resources to help me manage my day to day symptoms. I’m able to manage much better thanks to this Association. by Anonymous

Able to Manage Much Better Thanks to This Association