MS wheelchair fun
I was hospitalized for five months last year, and one month in Rusk Rehabilitation. Which I highly recommend to anyone who needs helps
"Specialists at Rusk Rehabilitation at NYU Langone Orthopedic Hospital provide the care and resources you need to reach your treatment goals. U.S. News & World Report's “Best Hospitals” ranks Rusk Rehabilitation among the top 5 programs in the nation for rehabilitation."
Since being their unfortunately, I've had more bad days than good due to Ozai (invsible best friend MS) autoimmune disease. In May 2024 I started practicing with my new wheelchair after losing function in my legs for three weeks but haven't been the same since. What's surprising I'm the first in my family to have Multiple sclerosis! How does even happen? Why I have MS, I have millions questions but taking a day at a time. But on a positive note, I've met some great people at NYU Langone, I've started a cool aid collection, and I get to take a lot of naps due to fatigue. I've also made a fun video of myself using my wheelchair.
Paramore- hard times: was o n e of many songs that really helps
https://linktr.ee/StoneDreamersllc
💙Theres major factor with Multiple Sclerosis
Multiple Sclerosis (MS) is a complex and multifactorial disease. While the exact causes of MS are still not fully understood, research has identified several major factors that contribute to the development and progression of the disease. Here are some of the key factors:
# Environmental Factors
1. *Vitamin D levels*: Low levels of vitamin D have been linked to an increased risk of developing MS.
2. *Sun exposure*: Reduced sun exposure, particularly during childhood and adolescence, may increase the risk of developing MS.
3 *Infections*: Certain infections, such as Epstein-Barr virus (EBV), may trigger the onset of MS in susceptible individuals.
# Immune System Factors
1. *Autoimmune response*: MS is characterized by an abnormal autoimmune response, in which the immune system mistakenly attacks the protective myelin sheath surrounding nerve fibers.
2. *Imbalance of immune cells*: An imbalance of immune cells, including T cells and B cells, can contribute to the development and prog
Embracing a new chapter with MS, especially when it involves adapting to a wheelchair, brings a unique set of challenges and triumphs. After my time at Rusk Rehabilitation, which truly offered incredible support and resources, I've been navigating what 'Domo Daily Life Living with Multiple Sclerosis' truly means for me. It’s not just about mobility; it’s about rethinking every aspect of daily existence. One of the biggest hurdles has been getting comfortable with my wheelchair. It's more than just a tool; it's an extension of my independence. Initially, I felt a mix of frustration and freedom. Simple tasks like navigating my home or going out became an adventure. I’ve learned to scope out accessible routes, advocate for myself, and even discover new ways to stay active. For anyone just starting their wheelchair journey, my advice is to embrace every small victory and don't be afraid to ask for help or modifications that make your space work for you. Little changes, like rearranging furniture or installing a ramp, can make a world of difference. Another constant companion with MS is fatigue. It's not just feeling tired; it's an overwhelming exhaustion that can derail a whole day. I’ve found that listening to my body, like taking those much-needed naps, is crucial. Pacing myself, breaking tasks into smaller chunks, and prioritizing what truly matters have helped me manage my energy levels. It’s a continuous learning process, and some days are better than others, but establishing a rhythm that respects my body’s limits has been key. The emotional toll of MS can be just as challenging. There are days filled with questions and frustration, wondering 'why me?' and pondering the unpredictability of it all. During those times, I lean on the positive connections I've made, like the wonderful people at NYU Langone. Finding a community, whether online or in person, where others understand what you're going through is invaluable. Sometimes, just knowing you’re not alone makes a huge difference. I also find comfort in music; songs like Paramore’s 'Hard Times' can be surprisingly uplifting, reminding me that even through struggles, there’s strength to be found. Living with MS disability means a constant dance of acceptance and adaptation. It's about finding joy in the small moments, celebrating personal achievements, and remembering that every day is an opportunity to learn something new about myself and my body. It's a journey, not a destination, and I'm committed to finding ways to live it fully, one day at a time.





































































