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Andrea Taylor's Fundraiser:

Help ATS Families Travel to Specialty Clinics

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Andrea Taylor


How often to you go see your doctor? Many times it is a quick trip to the primary care doctor and you go home. Not so much for families with arterial tortuosity syndrome (ATS).

It wasn't until A Twist of Fate-ATS was started, that things started to really change in their small community of families. Research has been ignited, specialty clinics have been created and its time to help families get to these specialty clinics. These clinics are geared around ATS, patient are able to see a variety of doctors, who specialize in ATS, all in one day. 

This is different than other clinics, because often times you see a one doctor one day then the others are spread out on different days or weeks, thus wasting a lot of precious time. These clinics are not just specializing in ATS, they are also partnering to research this very rare disorder. 

Our goal is to have a one stop shop for ATS families to establish care and for the physicians to be able to support the patients doctors back home with their care. Our families deserve to be able to attend these clinics, but most have to travel across the nation and even across the world to be able to participate. 

We will never be able to create better treatment and diagnosis plans, be able to provide better support for families, or get to a "cure" without these clinics. Please look into your heart, even if it is only $5, no amount is too small. You will be helping us find the "cure" for ATS and giving new hope to many families!



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