Support Lisa Chase’s Daughters' Battle with EDS

Hello all, I am asking for help for Lisa Chase and her 2 amazing daughters Linnea and Hannah who both have EDS. Ehlers danlos syndrome is debilitating, painful, chronic and comes with so many other disorders which makes it very complicated. These 2 girls have been through so much supported by their warrior mom who has single handedly navigated their complicated Medical care. Doctors who can treat this disease are few and far between and not at all easy to find, forcing Lisa and her girls to travel to RI, NY and now MD in search of these rare doctors who have the knowledge to help and give these kids with EDS some quality of life back. Linnea lives in constant pain, and suffers constant nausea. No pain meds work for her, all have been tried. Her quality of life has slowly been taken away. Both girls are too sick to attend school anymore. There is hope and treatments which can improve quality of life for this family. Lisa and her girls need help to navigate this difficult path. Despite Lisa facing these horrific challenges she always makes time to help and educate others with EDS. Without her support and guidance my son would be permanently paralyzed, instead he is learning to walk again. Lisa has helped so many and continues to reach out and help in any way she can while fighting for her daughters, and continuing the never ending search for providers with the knowledge to help. Please consider donating, the money goes straight to their medical care and travel expenses necessary for this journey. Thank you all so much. Even a small amount means more than you can imagine.