wilson's disease

In may of last year I was diagnosed with Wilsons disease which at its core means my body doesn’t dispense copper; which consequently deposits it throughout my body. With that being said it has greatly affected every part of me. including robbing me of my mobility and ability to work.  Consequently My main concern is not knowing when or if I will recover.Throughout this journey I have met with seen over twenty Dr’s; and had countless hospital visits. Though its likely begging the question, in today’s society everything cost. Naturally our healthcare system is no different.With that being said I’m am seeking any contribution large or small, to reach a goal of $10,000.