Our sister, Janet Linehan, was officially diagnosed with ALS in February of this year. This came as a shock to us all. Janet is a vibrant person, full of life and spunk. She was an outstanding athlete in high school and college. Until her symptoms progressed, Janet strived for the “trifecta” every day. That meant three forms of exercise daily, whether it be tennis, pickle ball, paddle, paddle boarding, golf, biking, or just plain walking. Janet is extremely competitive; second best is never good enough. She is battling this disease just like she has battled every athletic event.
Janet is the mother of three incredible children. Katharine, Dan, and Ned have been the light of her life, her reason for living. Janet’s husband Mark has always been the best husband and is constantly by her side, taking care of her every need. Janet also has two wonderful daughters-in-law, Julie and Louisa, who have dropped everything to support Janet and their spouses. Janet has the cutest grandson, Jack, who has become her greatest joy. Janet is one of seven children. She was absolutely adored by our parents and is truly loved by all of us and our spouses.
We are forming this team for one of the greatest people we know. Janet, like everyone else diagnosed with ALS, does not deserve this cruel sentence. Our goal is to have 100 participants on our team and to raise $25,000.00 in support of Janet, other ALS patients, ALS research and ALS caregiver support. We want to find a cure for this horrific disease so the future becomes bright for all those afflicted.
Please join us on October 20, 2024 for the ALS Walk in Boston or contribute to a member of our team as we honor the most incredible person, Janet McManama Linehan. Remember, POSITIVE VIBES ONLY!!
ABOUT ALS
Amyotrophic lateral sclerosis (ALS) is a progressive, fatal neuromuscular disease that slowly robs the body of its ability to walk, speak, swallow and breathe. The life expectancy of a person with ALS averages 2 to 5 years from the time of diagnosis.
ALS can strike anyone. Presently there is no known cause of the disease, yet it still costs loved ones an average of $250,000 a year to provide the care people living with ALS and their families need. Join the movement to provide help and hope today!
