Please donate in Liv’s honor.
When Liv was 2 we noticed a lump on her head. It took a couple months to figure out the diagnosis. By the time we knew it was Langerhans Cell Histiocytosis it was the size of a golf ball. It was surgically removed and the docs told us it won’t come back!
In May of last year, Liv started losing weight rapidly and she was thirsty all the time. It happened so quickly, the next thing I knew we were in the hospital for 10 days. The LCH that wasn’t supposed to come back did, and things got serious very quickly. Liv has irreparable damage to part of her brain (luckily not cognitive) and she will be on medication forever.
Liv is responding very well to treatment and if everything goes according to plan she will finish her last treatment on May 4.