Jasmine Luce ALS Fund
Donation protected
Anyone that knows Jasmine Luce knows that she is one of the most caring and generous people they have ever met. That's why we need to give her the best quality of life possible.
On July 26th, 2018 Jasmine was diagnosed with ALS, also know as Lou Gehrigs disease, which is a nervous system disease that weakens muscles and impacts physical function. Currently there is no cure for ALS. Since then she has been to the Mayo Clinic in MN which only confirmed the diagnosis.
Muscle weakness has already been confirmed in her left arm and in her left leg. Jasmine is a wife and has 3 children who she is very involved with. At some point the muscle weakness will take over and she will not be able to do the things she can now. We need to help her and her family do things while she is healthy and able. Besides covering any medical expenses she is working on a bucket list which includes things such as home improvements and traveling. Wouldn't it be wonderful to see her check things off of her list.
Anything that you can contribute is so appreciated.
On July 26th, 2018 Jasmine was diagnosed with ALS, also know as Lou Gehrigs disease, which is a nervous system disease that weakens muscles and impacts physical function. Currently there is no cure for ALS. Since then she has been to the Mayo Clinic in MN which only confirmed the diagnosis.
Muscle weakness has already been confirmed in her left arm and in her left leg. Jasmine is a wife and has 3 children who she is very involved with. At some point the muscle weakness will take over and she will not be able to do the things she can now. We need to help her and her family do things while she is healthy and able. Besides covering any medical expenses she is working on a bucket list which includes things such as home improvements and traveling. Wouldn't it be wonderful to see her check things off of her list.
Anything that you can contribute is so appreciated.
Organizer
Kristen Telder
Organizer
Greenville, MI
