More Funds To Research a Cure for Scleroderma

Scleroderma causes tremendous physical suffering and emotional pain and there is no cure.

Congress, please support this Petition by directing the National Institute of Arthritis and Musculoskeletal and Skin Diseases at the National Institutes of Health to expand research related to scleroderma, development and evaluation of new treatments, research on the relationship between scleroderma and secondary conditions including: pulmonary hypertension, gastroparesis, Raynaud?s phenomenon, and Sjögren?s syndrome. Establishment of family and ?childhood-onset? patient registries. Support for the training of new investigators. Direct the Centers for Disease Control and Prevention to establish a scleroderma public awareness campaign highlighting disease symptoms, prevalence, related conditions, and the importance of early diagnosis.

 

This Petition is very important to patients and family members living with Scleroderma. Thank you in advance for your consideration of this Petition.

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Public Comments (6,972)
Mar 4th, 2019
Someone from Dublin, CA writes:
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Hello there, My name is Aly and I would like to know if you would have any interest to have your website here at petition2congress.com promoted as a resource on our blog alychidesign.com ? We are in the midst of updating our broken link resources to include current and up to date resources for our readers. Our resource links are manually approved allowing us to mark a link as a do-follow link as well . If you may be interested please in being included as a resource on our blog, please let me know. Thanks, Aly
Dec 17th, 2018
Someone from Brandon, MS writes:
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Please help!
Dec 17th, 2018
Someone from Morton, PA writes:
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Please help!
Dec 17th, 2018
Someone from Morton, PA writes:
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Please help!
Dec 16th, 2018
Jennifer H. from Myrtle Beach, SC writes:
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Please fund!
Dec 16th, 2018
Jennifer H. from Myrtle Beach, SC writes:
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Please fund!
Dec 11th, 2018
Alan S. from Glendale, AZ writes:
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Please help us while we are still alive
Jun 12th, 2018
Someone from Austell, GA writes:
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I was diagnosed in August 2010 of Systemic Diffuse Scleroderma. I pray that a cure is found soon. Please donate more funds to Research for a Cure for Scleroderma.
May 14th, 2018
Someone from Southfield, MI writes:
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Diagnosed in 1992, would love seeing a cure in my lifetime.
May 14th, 2018
Someone from Southfield, MI writes:
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Diagnosed in 1992, would love seeing a cure in my lifetime.

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