MALS Surgery

Hey Guys, in November of 2017 I began to get very ill and was sent to many different specialists to try and find a diagnosis. In the fall of 2018, my health was still declining to the point of not being able to eat anything without constant pain and many other symptoms which lead to me having to take the semester off from school. We were referred to Mayo Clinic but many tests later I still had no diagnosis. Thankfully I have an amazing hematologist who never gave up helping me look for answers. She had a mesenteric ultrasound and a ct scan done that suggested MALS disease. At the beginning of February, my mom and I traveled to Connecticut to see the top MALS vascular specialist. On February 20th I was officially diagnosed with MALS and will have open surgery on June 13th. Because I have a rare blood disorder surgery is a very high risk for me and  I will have to stay in Connecticut from June 11th -June 26th. I am trying to raise money to help with surgery cost and travel expenses.
Anything helps, thank you so much!