About sclerodermaangel

I have Systemic Diffuse Scleroderma and after being diagnosed 1 1/2 yrs. after symptoms on 3/30/09 have been a patient advocate on social media, started a support group then Scleroderma Angel Foundation. Bringing HOPE to all who are affected by this horrible unpredictable disease and educating the public, medical and patients through all media.
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5 Responses to Events

  1. Toni says:

    Ann, you are our Hero. Thank you

  2. Rebecca McMillon says:

    Hi Ann, my mom has scleroderma and it has very rapidly taken over her body. She is coming to live with me and I would really like to get more information on scleroderma and any advice you would have for me to take the best care of her as possible . Here is my email so u can contact me I hope to hear from you soon!
    Thank you,
    Rebecca McMillon

  3. mona freeman says:

    Hi I have limited Crest system doctor hands-on told me about a seminar on Oct 14 the a bend memorial clinic , I’d like to go but not seeing were to register at ?

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