Last year at this time I wrote about how small changes can make a big difference in the New Year. Some of the advice from that post included: developing a financial plan, changing eating habits, exercising, getting back on your schedule and setting attainable goals. I used this advice to make major changes in my […]
2016 – A Work-in-Progress Read More »
In September of 2010, I was faced with a devastating decision. I was experiencing severe spinal stenosis and a fractured C6 vertebra, which my doctors believed was a result of complications due to my initial onset of transverse myelitis five years earlier. My decision was to have an emergency cervical fusion to address the problem
Finding the Strength to Fight MS for the Holidays Read More »
Last year, Angela Haupt of US News and World Report, shared the story of ten people living their best despite having a chronic illness. I was humbled to be featured in this article. Here is what Angela wrote: Cavallo, 38, of Chandler, Arizona, was fully functioning and healthy when he went numb from the waist down
10 Lessons From Empowered Patients By Angela Haupt Read More »
**Originally posted by Matt Cavallo on MSAA Conversations on 7-24-2015 at http://blog.mymsaa.org/worth-fighting-for/** In July of 2005, I was in a deep depression. I had just been diagnosed with multiple sclerosis in June of 2005 and I was in the midst of an internal struggle trying to come to terms with being newly diagnosed. I have a
Journaling My Story (MS) – MSAA Reblog Read More »
June 10th, 2005, I remember it like it was yesterday. This was the day that I had my follow-up visit with my neurologist. During the previous month, I had lost my ability to walk, been hospitalized and had been seeing a physical therapist to learn how to walk again all due to an acute onset
Clinically Isolated Syndrome versus MS Read More »
On this day back in 1976, the Declaration of Independence was signed into law. Today, let’s look at a declaration of independence from five common symptoms of multiple sclerosis that I experienced and what it meant to me: Vision Problems Vision Problems are one of the most common symptoms associated with MS. I have had
Independence and MS Read More »
Mason, my oldest son, overheard me and my brother talking about my aunt Loretta and MS. When he asked why he had never met her, we told him that she passed away due to complications of multiple sclerosis. He became very emotional over this, not wanting to lose me the same way my cousins lost
What Being a Dad with MS Means to Me Read More »
Many of you who have read my blog over the years, know how I went blind in my right eye due to optic neuritis or my struggles before and after my anterior cervical fusion. During my rehabilitation from these events, I worked extensively with an occupational therapist (OT) to help regain the activities of daily
Occupational Therapy and MS Read More »
**Originally posted by Matt Cavallo on MSAA Conversations on 4-20-2015 at http://blog.mymsaa.org/worth-fighting-for/** Photo Citation: Wash, B. (2011, December 11). Never Never Give Up, art show 2011, MBW. Retrieved June 3, 2015, from https://flic.kr/p/b4vjd8 There was a touching moment at my last neurology appointment. You see, I have been with my same neurologist since moving to Arizona
Worth Fighting For – MSAA Reblog Read More »
Since being diagnosed with Multiple Sclerosis in 2005, the veins in my arms have been stuck well over a hundred times. My monthly Tysabri infusion alone has equaled 108 vein piercing injections once every 28 days dating back to February of 2007. Each time has been without incident. My nurses remark how I have big
Dehydration and IV Tips Read More »