important matter, an appeal for help in the fight against muscular dystrophy for my 7-year-old son Francis.
When my son was 5 years old, genetic tests confirmed the horrible diagnosis of Congenital Muscular Dystrophy associated with the defect of the LAMA2 gene, the so-called negative merosin.
We must find strength to fight dystrophy and this power gives us stem cell therapy. The only chance at this time to stop the progress of dystrophy.
Francis was qualified by a neurologist for experimental stem cell
therapy, and the bioethical committee issued consent for five
mesenchymal stem cell applications in a dose of 30 million cells.
One application is the costs of $ 2,950.
Unfortunately, therapy is very expensive and that is why your help is needed because we know that you can do wonders. Please, help my son who has a few dreams in his life and would like them to come true. Help us maintain our hope.
Our goal is to raise funds for stem cell therapy, which can help rebuild Francis muscles and stop destroying the rest.
Each deposit is invaluable to Franciszek, because it can change his life.