hope for Aurora♡

We are trying to raise funds to take a very special little girl to Florida to see a prader-willi syndrome specialist. Aurora is 5 years old and was diagnosed with pws at the age of 3. Pws has many impacts on aurora and her everyday life. She desperately needs to see this doctor! The specialist in Florida can provide us with not only care for aurora but also very important care plans for every care giver in her life.

This is my baby girl who i worry about every second of every day. There are no cures for pws, she will live with this for the rest of her life. The only thing i can do for her is to ensure in properly providing the care she needs which is 24 hours a day, 7 days a week. Pws takes no breaks and gives no down time. Please help us get our special girl to the doctor she desperately needs to see! We appreciate any and all support!

Below I've provided a little information on pws.
http://www.mayoclinic.org/diseases-conditions/prader-willi-syndrome/basics/definition/con-20028982