June is National Scleroderma Awareness Month

What is Scleroderma?

Scleroderma is a rare and debilitating autoimmune disease which there is no cure for. It’s often progressive and sometimes, fatal. It affects every age and gender and it’s neither preventable or contagious. It confuses the best of the medical field by making it difficult to diagnose. Scleroderma attacks the Vascular System, cutting off blood flow to extremities, resulting in Gangrene and amputation. It affects the Gastrointestinal Tract, Heart, Kidneys, Lungs, and Esophagus. Scleroderma causes hardening, thickening, and tightening of the skin which oftentimes, causes devastating results to one’s facial appearance and one’s mobility. Scleroderma has no cure.

Scleroderma steals lives, families, friends, jobs and so much more.

For more information about Scleroderma, please visit the Scleroderma Foundation @

http://www.scleroderma.org.

For more information about Juvenile Scleroderma, please visit the Juvenile Network @

http://www.jsdn.org.

To donate to the Scleroderma Research Foundation, please visit the Scleroderma Research Foundation @ http://www.srfcure.org.

Please help us “Raise Awareness” of Scleroderma, by sharing this information with family, friends, and co-workers.

Raising awareness of Scleroderma is one of the “Greatest Gifts” you can give to those who have Scleroderma.

Please accept my invitation, to visit my Scleroderma Facebook Pages. The names of the my Pages are as follows:

Help End Scleroderma † and Support Scleroderma Awareness: WE NEED A CURE

Thank you for your time.

In † Christian Love, Susan Osten

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