The Tisch MS Research Center of New York

The Tisch MS Research Center of New York is an independent nonprofit 501(c)(3) organization dedicated to finding the cause of and cure for multiple sclerosis. By conducting groundbreaking medical investigations, Tisch MSRCNY accelerates the pace at which research discoveries translate from lab bench to bedside. The Center aims to discover the cause of MSelucidate mechanisms of disease progression, develop translational research programs that will lead to new therapies, and investigate regeneration and repair in MS while offering patient access to the best and most advanced treatment possible. The Center's medical research is designed to understand all aspects of MS, including experimentation at the cellular and molecular levels, in order to treat and cure MS. 

Allison Laidlaw's Experience with Tisch MSRCNY

It's a few friends and family that can say they have known me for 19 years.  I can't even say I've known my husband for that long.  But 19 years ago, my circle of long time friends and family grew when I was diagnosed with Multiple Sclerosis (MS).  I sometimes laugh when someone I've known for years learns I have MS and says "how did I never know that?".  It's because of a promise I made 19 years ago.  As Dr. Sadiq welcomed me (and a good part of my family) into his office that day, we discussed my diagnosis and next steps.  After hearing what seemed like a death sentence to a 22 year old that was single and recently unemployed, he made me an offer.  He said if I do everything he tells me to do, when he tells me to do it, he will make sure I live a normal/regular life, able to bear children, and a future without a wheelchair (fortunately my MS type allowed him to make me that promise).  I signed on the line that day.  Fast forward to April 2nd, 2020, days into a global pandemic where NYC was basically shut down.  I was set to go in for my infusion treatment.  I called the office expecting them to reschedule, but no.  What I got was "Dr. Sadiq wants you to come in.  We will keep you safe.".  I remembered my promise to him 19 years ago.  Even after most all of his promises had come true; I was married, had two healthy girls, and was living the most regular life anyone could ask for, I knew I still had to keep my end of the deal.  Into NYC I went (with my mom even more worried than she already is) and I got my infusion from the AMAZING nursing staff at the Tisch MS Center.  A year into the pandemic and I continue to go in for my treatments each month.  His promise holds true.  The care and treatment I have received over the past 19 years has been nothing less than remarkable.  I wish I could give more to him and this practice.  Until I win the lottery though, I'll continue to support him in efforts and fundraising like this.  Remember this name.  Big things are coming for them, I truly believe. 

The Jenny's Experience with Tisch MSRCNY (In Alex's Perspective)

April 20, 2012. The day I found out my dad had Primary Progressive Multiple Sclerosis. I was 8 and couldn’t even remember the name Primary Progressive Multiple Sclerosis. He had been diagnosed January 20, 2012 -- 2 days before I turned 8. I had overheard my parents talking about a problem with my dad a few months prior, all I heard was dehydration. Immediately I was concerned and tried to make my dad drink Gatorade and water to make sure he was ok. I wanted to help him be ok. Little did I know the battle was larger than electrolytes. The tricky thing about a progressive disease is it catches you by surprise, through the little things. The sudden declines start to add up and continue to build. It wasn’t before my dad became a patient at Tisch MS that we truly began to feel hope. Not even just for him, but for the future of MS. We felt a part of the community right away. In addition to the understanding and brilliant mind of Dr. Sadiq, everyone was so welcoming and kind. There is comfort knowing in the everyday fight my family has with MS, people are right there fighting with us. This is why Tisch MSRCNY is so important in the fight against MS. Hope. Hope instilled in the patients and hope for the families who watch their loved ones battle MS every single day. The fact that one day someone just like me will not have to write a post like this - because a cure will exist for their father is the reason for this fundraiser. The title of this race is Trailblaze for Team Tisch MS, meaning we are trailblazing to the cure. By entering and/or donating to Tisch, you are trailblazing toward a cure and will be helping countless people now, and many more to come. You are running or walking for someone who cannot because of MS. Someone just like my dad. Trailblazing to the cure is also very important because we are not just running or walking for the cure, anyone can participate with any support they need. Whether you are running, walking, using assistance such as a walking stick, walker, scooter, etc. … you are helping create a future without MS. Thank you so much for your support of the amazing things happening at Tisch MSRCNY and I cannot wait to trailblaze for Team Tisch MS with all of you!!!

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