Gold Coast Take Steps

Twin Power


Please help us reach our team goal of $6,000.00 for Take Steps Gold Coast by donating or registering and fundraising. Your support will help the Foundation invest in cures for the future, while providing support to patients today.

My name is Matthew Cozier. I was diagnosed with Crohn's Disease right before my 16th birthday. I had begun to rapidly lose weight and was finding myself sleeping for hours upon hours and I couldn’t keep up with my friends and teammates. I just kept thinking to myself what was wrong with me? Once I was diagnosed, I began treatments of Remicade and slowly my body began to respond to it.

I am now 18 years old and a freshman at Farmingdale State College. If you were to look at me now you would never know I live with this disease. When I first found out I had Crohn's Disease I felt a sense of relief mixed with a sense of dread because after a long journey. I had finally found out what was wrong with me, but I was still unsure of what was to come. My doctors gave me an informational packet about the Crohn’s & Colitis Foundation, and it was a game changer for us. Through the foundation we have gotten so much support and guidance about how to navigate life with Crohn’s Disease. My family and I ‘Take Steps’ in the hopes of finding a cure for this invisible disease which has an effect on my, my families and patients’ daily life. I am hopeful that with all the great work that the Crohn’s & Colitis Foundation does that a cure will be found in the near future.


My name is Jennifer (Jenna) Cozier. I was diagnosed with Crohn's disease 6 months after my twin brother was diagnosed. For a while, I had joint pain and stomach problems but attributed it to growing pains and food issues. As I became sicker, mundane tasks such as showering or unloading the dishwasher became harder and made me easily tired. When my brother was diagnosed, I then realized that the symptoms that I was having weren't normal. I was finally diagnosed in February 2020. I was also diagnosed with IBD arthritis due to my Crohn's disease.

When I first got sick, I was afraid I would always feel this way and it would never get better, but after getting started weekly on Humira, I felt so much better. Although I still have bad days, my medications make the good days even better and the bad days not so bad. The Crohn’s & Colitis Foundation is a huge support system in my life. By working together as a team, I am positive that more treatment options and possibly even a cure will be achievable in the future.

Do you know someone who is affected by Crohn's disease or ulcerative colitis? Join our team and share our fundraising page to spread awareness in the community!


Check Donations can be sent to me at:


Crohn's & Colitis Foundation LI Chapter 
Attention: Suzanne Beck / Team, Twin Power
585 Stewart Avenue, Ste 304
Garden City, NY 11530

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