Welcome to My Personal Page: Team Love For Lynn
Well it’s that time of year again where we gather together and remember my sister Lynn. She lost her life 11 years ago to this devastating and incurable disease. She has missed so much these past 11 years and oh how I wish she was here to see it all. She now has two grand babies and an upcoming wedding for her son. So many milestones have been reached with her children and so many more to come. I know you are celebrating somewhere Lynn! We all miss you so much it hurts. We think of you all the time and we will always walk in honor of you and in hope that one day we can find a cure for the disease that took you away from all of us. DFT 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, and presently there is no known cause or cure.
That's why I'm walking. To change the statistics. To bring help and hope to those living with the disease. To ensure that no one ever hears the words: "You have ALS" again.
The past two years have brought incredible advancements in ALS research, expanded access to care for people living with ALS, and enabled legislation that impacts the quality of life of people with ALS and their families.
But we can't stop now. The key to a cure begins with you.
Please consider walking with me or sponsoring me. With your help, we will be able to make a difference in the lives of people affected by this disease.
I Made a Difference!
I supported this event with a personal donation.
Fundraising Honor Roll
Mrs. Deborah Gibian
LOVE FOR LYNN TEAM
Ms. Lisa Iezzi
Love for Lynn
Fay G. Lohr
Mrs. Valerie Goodyear
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