June 2022 my mom, Sandy Mougin was diagnosed with ALS. She started with a drop foot in 2019 and started losing strength in that leg. We were sent to the Univ of Iowa Neurology, after an EMG she was diagnosed with ALS. Currently, she has lost mist of strength in her right leg and has drop foot and losing strength in left leg. She has a power wheelchair that allows her to get a round. We are blessed to have the support and resources from the ALS Association. The equipment closet has been a lifesaver, you can borrow equipment to help keep her in her home. It is truly amazing and things like this would not be possible with donations.
Thank you for helping me reach my Walk to Defeat ALS fundraising goal! The Walk to Defeat ALS raises funds to support those affected by ALS and to spread awareness of the urgency to find treatments and a cure.
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.
Thanks
Diane