We need Spinraza in pakistan, A treatment for rare disease Spinal Muscular Atrophy
0 have signed. Let’s get to 100!
Spinal Muscular Atrophy is now curable in the world, SPINRAZA is now available all over the world, "THE CURE" for SMA . SMA type 1 is No. one genetic killer of infants & SMA type 2 & 3 are making people wheel chair bound with progessive muscle weakness or no movement..
Help raise awareness if you want this country (Pakistan) to be disabled free. sign the petition HELP ME & OTHERS WITH SPINAL MUSCULAR ATROPHY to have SPINRAZA in PAKISTAN & in their country too !
Javaria Malik (SMA TYPE 3 Warrior)
Today: Javaria is counting on you
Javaria Malik needs your help with “Biogen Idec: We need Spinraza in pakistan, A treatment for rare disease Spinal Muscular Atrophy”. Join Javaria and 79 supporters today.