Sara McCall McDaniel can't be sure when her symptoms of amyotrophic lateral sclerosis began, but she received her diagnosis of Lou Gehrig’s Disease, or ALS toward the end of October. It has been just 3 months since that diagnosis, and her infectious smile confirms the fact that she is still embracing happiness. In the photo, Sara is with her physical therapist and cheer leader, Sierra, who has become more than a PT to Sara and is an integral part of Sara's life. Another wonderful source of encouragement comes from Team Gleason who has gifted her a wheelchair and offers her signs of hope. Please help us support Team Gleason by making a contribution to this fundraiser and sharing this page with your family and friends. Every dollar we raise will advance Team Gleason's great cause! The mission of Team Gleason is to improve life for families with ALS by delivering innovative technology and equipment, as well as providing and empowering an improved life experience. The mantra of Team Gleason is “No White Flags”.
Together, we can make a difference for Team Gleason and Sara. Make your donation a Valentine for Sara and for your other special someone, too.
FEB 13
2-12-2024 The Dallas ALS Specialist Trip. Sara McCall McDaniel with Gary McDaniel and Shirley King in Wichita Falls.
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