Hi, my name is Laura and I am fundraising to pay for my MALS release surgery travel expenses and recovery care. This is a rare condition so I am traveling across the country to get to my surgeon and I need to stay at a hotel for at least a couple of weeks after the surgery before it is safe for me to fly home. Since I am traveling alone, I will also need a caregiver after the surgery.

I greatly appreciate any donation you can afford. Please share this fundraiser with family and friends as I also want to raise awareness for MALS and help others who might be searching for a diagnosis for their symptoms. Although this is a rare condition, it is becoming more common with awareness. It is also linked to Postural Orthostatic Tachycardia Syndrome and connective tissue disorders like EDS.

Thank you!