A.L.S. Family

Join us for the first Cape Cod beach party of the season in Mashpee, MA. Food, drinks, live music, and a great time will benefit the Patient Programs of ALS Family Charitable Foundation.

August is almost over! Purchase a $2.50 reusable Community Bag at the @StopandShop located at 20 Teaticket Highway, Falmouth MA before the end of the month and ALS Family Charitable Foundation will receive a $1 donation! #giveback

We are very fortunate to benefit from independent fundraisers, which come in all shapes and sizes. One example is the Kittery Rib Cookoff, held June 22nd in Maine. How did it happen? Kittery Police... facebook.com/alsfamilyfound…

Did you see our post about the Lawrence wedding & donation? Here’s another of the Lawrence brothers and another way the Lawrence family pays it forward—Ben is running for our Falmouth Road Race team for a second... facebook.com/208776328952/p…

Congratulations to Zach & Hannah Lawrence on your wedding. We have known and loved the Lawrence family for many years, first having met when Zach and his brothers were just boys and their father had been... facebook.com/208776328952/p…

Aging celebrities get botox to avoid wrinkles, I got botox directly into my salivary glands to ease the amount of excess saliva in my mouth. That is ALS. It's a monster that never stops attacking. If you see me, don't be surprised if I look younger! 🤣#Quinn4theWin #FightingALS

@AlsDads <3

Hi my name is Juan and I have .... ALS!?! It started with a twitch, just a twitch man. Next thing I'm into the hard stuff, spasms, muscle loss, falling...I hit rock bottom when using wheelchair man.Thats when I needed help... help with everything man don't do ALS man. Thank you

Every night we go to sleep and dream. Every morning we wake up and have a chance to make those dreams real. Last night I dreamed that #TalkALSToMe was trending on twitter. Not sure if I can make that happen tomorrow, but I’m sure as hell gonna try...

@DavidWalkerSr2 We'll be in touch in the next few days.

davidwalkerracing@gmail.com 207-890-3085

@DavidWalkerSr2 David, we have patient programs for PALS in New England. We can be reached at 508-759-9696--please give us a call or tell us how we can get in touch.

Brian Wallach of I AM ALS giving an emotional plea to Congress to fund research to find a cure for him and thousands of others who are living with ALS. youtube.com/watch?v=ZOHaL8…

A very big thank you to Fran Spitaleri for thinking of our patients and families as she honors her husband, Bob, on the 5th anniversary of his passing from ALS. We are forever grateful, Fran. xoxo facebook.com/alsfamilyfound…

The A.L.S. Family Charitable Foundation is looking for a few more runners for the Falmouth Road Race! Great non-profit that helps so many families & patients in NE. facebook.com/alsfamilyfound…

The Real Deal will be back for our 23rd Annual Cliff Walk For ALS on Sunday, September 8, 2019! But if you don't want to wait until September to see them, come on down to Dino's Sports Bar - Dino's on Deck in Mashpee this Saturday night, April... facebook.com/alsfamilyfound…

Insurance Coverage: We're here to help! bit.ly/2HCpDG4

Thank you to Chris Jennings for thinking of our patients and their families! facebook.com/alsfamilyfound…

A big thank you to Andrew Christopher for thinking of our Foundation and supporting our patients and families! We are forever grateful! facebook.com/alsfamilyfound…

Thanks so much to our dear friend and long time supporter, Lenny Ferrara for thinking of our Foundation for his upcoming birthday. Funds raised will be directed to our Jan Ferrara "Get Away For A Day" Fund... facebook.com/alsfamilyfound…