Lou Gehrig’s Disease
I don’t think there is a more devastating illness than ALS (Lou Gehrig’s Disease). This neurodegenerative treachery robs its victims of muscular control. First it limits and then eliminates leg and hand movements, then finally it impedes the ability to swallow and breath. But it leaves the mind intact- fully aware of its body’s condition.
ALS affects the sufferers’ family/caregivers as well. It levies a ponderous emotional and financial toll. Once diagnosed, the average lifespan for someone with ALS is two to five years. It is always fatal.
Organizations like the ALS Foundation are working to support ALS sufferers and their families while also funding research for treatments and a cure.
For the past eight years Nicole Roy and Team Roy have participated in the Ride to Defeat ALS to raise much-needed funds for the ALS Foundation. She lost her father Paul to ALS over 20 years ago. He was a great man and a good friend of mine whose smile was infectious. As I’ve said in a previous blog , smiling may be the bravest thing you can do when you have ALS.
Nicole is looking for your support to help raise money for the ALS Foundation. If you are able to give, please go here to donate: :https://www.facebook.com/donate/1191671207873585/10219707843141627/.
And as Nicole says “Every little bit helps”.