This is my friend's beautiful family. Their daughter, Megan, was diagnosed with Alexanders Disease...and all of a sudden their world as they knew it changed. Alexanders disease took their beautiful, happy go lucky daughter away just before Mothers Day In May 2017.
This disease is very rare and incurable at this time. Megan's mommy, Allison, had to quit her job to stay home and care for Megan as her disease progressed. Megan's daddy, Keith, continued working to support their family.
Her page is on Facebook, Mighty Miss Megs. It tells her heart-wrenching story far better than I ever could.
No parent should have to outlive their child. Megan was and is a beautiful light to everyone she encountered.
I started this go fund me to help raise money for her parents and brother to help pay their monthly bills (groceries, mortgage, utilities) and buy them more time to grieve and figure out how to function in this world without their precious little girl and not have to worry about money...they have enough to worry about right now. Keith has and will keep his job but only gets a certain amount of time off paid and unpaid.
I'm trying to raise money to ease their financial burden somewhat. They have been so strong for so long. Any donations will not help bring precious Megan back but it may help buy them a little time to figure out what their new normal is.
Rest In Peace beautiful girl. May God have mercy on your family and help them find peace.❤️