
When Rob Pontes was diagnosed with ALS the guys over at REAL Skateboards did a lot more than just another ice bucket challenge to help their good friend pay for the outrageous medical costs he needs to fight the disease. They actually threw a skate event and made special decks, shirts and gear to help raise money for Rob to beat it.
ALS is a progressive neurodegenerative disease, meaning that after only a few months of symptoms Rob went from popping nollie heels to having to have a friend piggyback him to the skateshop. His treatment is long and expensive, so his friends in the industry have teamed up to throw a series of benefit demos around the East Coast to help get Rob and his family through it.
Rob is a pillar of the New England skate scene who’s done more for shops, skaters, and skateparks there than can be summed up in a sentence, but in short he’s the definition of what’s best about skating – strength and a ‘never say die’ attitude.
The first event of the year took place on a wintry night in Rob’s hometown of Boston to a totally packed house at Subliminal Skate Shop. As the weather raged outside, the crowd watched some legendary skaters (Ellington, Shetler, Westgate and more…) #rollforrob. Check out some of the photos from the event, and, better yet, help fight Rob’s ALS by buying an Actions REALized benefit board, donating to the cause, or by keeping your eyes out for a Roll for Rob event near you.
We got a video recap about the event and the campaign too! Check it out below:
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June 4, 2021 4:22 pm
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July 21, 2026 1:03 pm
My wife (55) was diagnosed with Motor Neuron Disease (ALS) in February 2026. She started displaying symptoms in July 2025. We were referred to an ALS clinic and began all the blood tests, MRI”s, etc. our neurologist stated that this looked more like an autoimmune than ALS but all of the autoimmune treatments were not effective. Referred to another ALS clinic were they confirmed diagnosis of sporadic limb onset ALS. In November 2025, she was using a cane to walk due to foot drop and leg weakness. She had fasciculations in her arms and back, clonus in her left leg, and weakness in her right arm and hand. Currently, she was 100% dependent on me for her care. She had virtually no use of her arms, hands and legs. She struggled with more things that have time to list here. This year our family physician suggested using Limitless Natural Wellness ALS/MND protocol, which my wife has been receiving for a few months now. and it has changed everything., she no longer requires a feeding tube, sleeps soundly, works out frequently, and is now very active. We got the ALS/MND herbal formula from ww w. limitless natural wellness. c om. Don’t give up hope.