Evelyn Haggerty Family Medical Fund

Hi Friends Near & Far,

Evelyn Ruth has been battling an unknown sickness for almost 2 weeks. Today a diagnosis was given of a very rare disease called Wolman Disease.

The geneticist at our children's hospital has never seen a case in his 30 year career. There is no cure at this time. There is however, a enzyme medicine (given IV) that will provide her body the missing enzymes that her body does not produce. This medicine/treatment is stated to be very expensive (cost unknown at this time). There are clinical trials that she may qualify for. There is bureaucratic red tape that must be torn down in order to receive this rare enzyme treatment. Evelyn needs this ASAP because her liver and spleen are failing more every day. This precious 2.5 month old needs your prayers for a miracle! The journey of treatment and healing will be long and very costly. Megan and Dylan are willing to pay anything to save their baby. We also know that this path will lead to immense financial stress. Many in this world have been blessed with wealth or the heart to help others, so if you feel lead to donate you'll be apart of saving Evelyn's life!

Thank you for your generosity ❤️