Lymphangioleiomyomatosis

The story of Nancy

My daughters was diagnosed with LAM three years ago. Lymphangioleiomyomatosis Is a very rare lung disease that affects women in there child bearing years. Currently there is no cure for her disease! Unfortunately the disease not only affects my daughters  life it affects her whole family ❤️ I thought I would share a picture and wish my sweet 8 year old granddaughter made for her Mom. Thank you to NIH and all the Drs. and scientists who work endlessly for a cure LAM and all Rare Disease❤️

 

*Find others with Lymphangioleiomyomatosis on RareConnect, the online platform for people affected by rare diseases