When Marypat Velasco was diagnosed with Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig’s disease) near the end of 2024, what she thought would be the golden age of her life quickly took an unexpected turn. The plans she had made for this next phase were abruptly altered, and new plans had to be made.
In the face of such adversity, she and her family created a bucket list. They would stop at nothing to make sure that everything was completed and checked off. But one item was proving a bit more difficult.
One of her daughters, Molly Velasco, took to Threads and tagged the New York Knicks directly:
“@nyknicks: My amazing mother Marypat, nurse of 47 years, my best friend, & everyone’s favorite person just finished her last clinical trial for ALS, also known as Lou Gehrig’s Disease. The last item on her bucket list is to see her favorite team, the New York Knicks, play at @thegarden, but all your accessible tickets are sold out. Is there ANYTHING you can do? Please help me make this happen. I have completed every other item on her bucket list. This is her last item & the last szn she has.”

Spike Lee entered the chat
As luck would have it, notoriously devoted Knicks fan Spike Lee entered the chat almost immediately. He even signed off on his post as though it were a letter: “DM me. Spike Lee.”
Molly jumped on the offer, replying, “OH MY GOSH! Yes! Just sent you a message!” Lee later followed up, saying he had reached out and was “waiting to hear back.”
Just his appearance in the comment section was enough to get the proverbial ball rolling. Other celebrities, including actress Yvette Nicole Brown, chimed in, tagging New York Mayor Zohran Mamdani and others. The outpouring of love was beautiful. Thousands of comments flowed in, as one might imagine.
One Threader noted the speed at which Lee chimed in: “Can we talk about how FAST Spike Lee responded? All these huge billion-dollar companies and organizations are silent, and this man is on it. Great job. No notes, Spike!”
Raising awareness for ALS
Molly shared additional updates, using them to raise awareness about ALS and highlight the disease’s rapid progression. In one post, she expressed gratitude to the many people who had reached out:
“For those of you who have been touched by ALS, my heart breaks for you. It is truly the cruelest disease. Thank you for sharing and understanding. I look forward to replying to you over the next few days and hearing about the amazing people you love.”

Then came the update everyone had been waiting for:
“UPDATE: WE ARE GOING TO NYC BABYYYY!!!! Thriends, WE DID IT!! Thanks to all of you & especially Trish Fuller ✨ (@trishmfuller) ✨, our new friend & fairy godmother from the original post, mere days before the last regular game of the season, THE @nyknicks reached out to us & have generously offered us tix & the opportunity to come watch warm-ups courtside! We will cross off my mom’s last bucket list item: ‘I have always wanted to see my New York Knicks at Madison Square Garden.’ Sunday, Knicks vs. Hornets!!”

Upworthy reached out to Molly to learn more about the family. As she packed for New York, she took the time not only to answer questions, but also to ask whether ALS had touched my family. That’s the kind of caring advocate she is.
Marypat, the “favorite” Velasco
Upworthy: Tell us anything you’d like to share about your mom.
Molly: “She is the sweetest, funniest most stubborn person you will ever meet. We all say she’s everyone ‘favorite Velasco’ because she is. She is the most incredible friend, nurse, and mom. She loves to read and instilled a love of reading in all of us. She has a green thumb so has a garden every summer and house plants year round. She adopts senior golden retrievers. Her current pup is Javier, a ten year old golden she’s had for 5 years. He’s completely blind and was formally a street dog in Istanbul, Turkey.

We share a passion for culinary and food. Her favorite song is Ventura Highway by America and she always had music playing in our house growing up. She has always been open hearted and minded. She believes everyone deserves food, safety, medical care and shelter. And has taken in any of my friends who need a family. Definitely a more the merrier person. She says adorable things like ‘holy smokies!’ And ‘wowie zowie’. And…has been a fierce advocate for mental health care.”
Always loved the Knicks
Upworthy: Has she always been a Knicks fan?
Molly: “YES! She is from Hyde Park, NY, and she and her 4 brothers all played basketball. Since she was a little girl, she had a poster of Walt Frazier on her wall. She became a fan watching the Knicks with her dad, my Pop, and her brothers.”
Upworthy: Who ended up hooking you up with the tickets?
Molly: “One of the women who saw my post—Trish—used to work at MSG. She DM’d me and asked for my email and had friends that still worked there. She followed up with them over and over until her friend Tony, who works for the Garden, passed along the message to the Knicks Social Impact team, where a member of their team, Isaiah, emailed me. I sobbed immediately when I read the email!”
The bucket list
Upworthy: What else was on her bucket list?
Molly:
“-See America in Concert
-Pet Harpita (seriously spicy cat)
-Make the kids make each others Xmas gifts for fun
-Eat David’s Halibut from the Cape
-See brothers all together in one place
-Stay in a house that opens up to the beach like a Diane Keaton/Diane Lane movie
-Eat really good New York Rye Bread
-Go back to Hyde Park and see my childhood house my dad built
-Try Korean BBQ
-Eat Crème Brulee for the first time
-See the New York Knick’s Play at Madison Square Garden
The beautiful thing about this so that she traveled with traveling nurse and lived so much her whole life she didn’t have huge things on her bucket list. She had already jumped out of a plane skydiving and got a tattoo at 50, traveled all over the US minus 4 states. She lived her whole life 💛
There are also 3 things she said would be too hard, go to Santa Fe Art galleries, see orcas in the wild, go to the inside passage, and go on safari so she made me promise I would go when she’s gone and that way she can come with me.”
How quickly life changed
Upworthy: How has her diagnosis impacted your family?
Molly: “It turned our life upside down. My mom was set to retire from nursing after an amazing 47 years in May 2025 but was diagnosed the previous December 30, 2024. She was really looking forward to her next chapter—had planned to move closer to my sister, who is in PA, from MA.
Wanted to have a garden and volunteer helping animals and just enjoy her retirement. I was working for a local nonprofit that fights food insecurity in North Central Massachusetts. I had built our youth program from the ground up and recently got some funding to grow my fun farm days, where I bring at-risk youth to historically excluded farmer organic farms, where we help out, do projects, and learn about the food system.
When we got her diagnosis, everything changed. My entire perspective shifted, and my first thought post-shock was we need to go to the beach more. She had been rapidly deteriorating in ability starting the June prior, so we knew this was a possibility. The diagnosis process is truly the beginning of the nightmare. She got her first EMG in September, and then you just have to wait three months to get tested again. All the while, she’s getting worse and worse. It was terrifying. She was getting so weak that I begged them to let her get in earlier because she was getting so much worse we were confident they would see a change.

By the time you’re diagnosed, you are so behind already on everything. Her ALS started with arm weakness and her core muscles, which means her breathing was impacted really early. She is a stubborn nurse, though, so she kept saying she was totally fine.”
What others should know
Upworthy: What would you want other families who have received this diagnosis to know?
Molly: “Our doctors and team at the Sean Healy ALS Clinic out of Massachusetts General Hospital told us early on that the three things that cause you to progress even quicker are losing weight, falls, and feeling hopeless. So I would say to them, eat what feels good and tastes good. If that’s mashed potatoes and chocolate cake for 12 meals in a row, do that! Lean into what sounds yummy to you. Embrace equipment. It’s so hard because ALS doesn’t give you time to breathe or grieve. The sooner you embrace the tools, the more living you can do. And the hardest one, in my opinion, is trying to find hope with a disease that not only has no cure but also is so scary—you have to find a reason to keep going.”
Finding glimmers of good
Molly: “You have to find some joy in humor in these impossible circumstances. We started searching for glimmers. Some are big, like being able to go to the New York Knicks, but also sometimes it’s just an exceptionally good cup of coffee in the morning.
Or my very grumpy cat, who hates everyone, choosing to lay on my mom, purring so loudly, or right now, as I send this, my mom is sitting outside basking in the sun.
Every night before bed, we say what our glimmers were from that day. It’s helped us focus on not only the big good things but also the small good things, like three amazing songs playing in a row on shuffle or one of our many house plants I’m trying not to kill growing a new leaf. Even in my next chapter, I can’t imagine not spending the rest of my life collecting glimmers.
Not every day is good, but there is something good in every day.”




















