I want to save my only and beloved daughter.

In 2014, my daughter was diagnosed with multiple brain sclerosis. For five years she was treated with high doses of hormones, but this only made her condition worse. She is rapidly losing strength, moves very badly and has all the classic symptoms of this terrible disease. Together we are fighting the disease, looking for new methods of treatment all over the world. A huge obstacle for us in our struggle is an acute shortage of material resources.

A month ago, we started treatment according to the method of Dr. Coimbra, having invested all our funds in this, I really want to continue the treatment and the first small results are already visible! But there are not enough funds. Please help my daughter !!! All my life I raised her alone and now we have nowhere to wait for help. Treatment according to the Coimbra method is several times cheaper than what was offered to us in our city. One course of the proposed drug (ocrelezumab) is incredibly expensive ($ 9,900 x 4), and so on every six months.

For comparison, the cost of treatment under the Coimbra protocol is approximately $ 380 per month (tests + doctor's consultation + medications) and lasts for life, but with a change in the dose of medications. I beg everyone who read our story not to leave us alone with this problem! Please help my daughter!

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