Systemic scleroderma

Discussion in 'General Chat' started by hostm, Nov 4, 2013.

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  1. #1
    My daughter who is 13 y.o. is suffering from the disease called Systemic scleroderma and needs treatment. The matter is the disease is quite new (that is an autoimmune disease) and it's rare in children and teens. So the local doctors just don't know how to treat it properly. That is why I need advice on that.

    Here is how Systemic scleroderma looks like:

    [​IMG]
     
    Last edited: Nov 5, 2013
    hostm, Nov 4, 2013 IP
  2. digitalpoint

    digitalpoint Overlord of no one Staff

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    #2
    So doctors don't know how to treat it, so you seek treatment advice on a webmaster forum?

    Makes sense I guess...
     
    digitalpoint, Nov 5, 2013 IP
  3. agung fajriadi

    agung fajriadi Well-Known Member

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    #3
    parents struggle to heal his daughter. so it should make a thread about health in webmaster forums. let's chat friend,

     
    agung fajriadi, Nov 11, 2013 IP