Medical Expenses for Megan Pederson

We are starting a Go Fund Me for Courtney and Megan Pederson to help pay for medical and travel expenses for Megan, who is just 19. For the past 4 years, Megan has been struggling with the rare syndromes SMAS and MALS. It has caused her to be unable to get nutrition into her body in any form. In April of 2021 she underwent SMAS surgery and MALS surgery in November 2021. Unfortunately, the results were short-lived and now she is unable to get nutrition at all even through feeding tubes and TPN (Total Parenteral Nutrition), which is a last resort. The family has exhausted all options for doctors treating this rare condition in the Midwest. Luckily they have found Dr. Sherisa Warren, in Oklahoma City, who may be able to help Megan. We are hoping to help the family pay for any medical and travel expenses related to the care of Megan. Megan is hoping to spread awareness of these rare syndromes which many know little about. Thank you for any contribution to help the Pederson family!

https://kfor.com/news/local/she-is-wasting-away-in-front-of-our-eyes-teen-on-the-road-to-recovery-after-rare-diagnosis/

Here is the Caring Bridge website to follow along on Megan's journey

https://www.caringbridge.org/visit/meganpederson/journal/view/id/649f22c682357a23115b68b9