Memories and Support

A beautiful friend of mine has an 7 years old Boy who has just been diagnosed with Lymphangioma, a type of vascular birthmark due to malformed and dilated lymphatic vessel. It’s a rare congenital tumor with very few treatment options.

Once the symptoms present, the degeneration can be quite aggressive. Despire being benign, the tumor develops as child grow, and it can cause a lot of pain and restrict some actions. Time is precious and crucial.

After undergoing ineffective therapies in Angola, Brazil, Cuba, Namibia, South Africa, and Germany, we renew the hope of getting new treatment to him in USA, but unfortunely his family has no funds to pay for the procedure, valued at £15.000.

I feel beyond helpless. We’ve tried so much with alleviation of his pain and symptoms that are getting more frequent and worse.

I am at loss to get this child the help and treatment he needs! We already have £5k in medical bills not including his most recent hospital stays. This has been hard for the Child!

Time is of the essence,

Thank in advance for your support.

Link: NORD (National Organization for Rare Disorders)