When I was twenty eight years old, I seemingly had everything I ever wanted in life. I was married to my college sweetheart, Jocelyn. We had a 1950’s ranch house in Weymouth, Massachusetts close to friends and family. I was on my way up the corporate ladder as an analyst for a real estate development. […]
Newly Diagnosed Fears Read More »
As soon as I wrote the blog about how to handle high prescription costs for specialty drugs, my inbox got flooded with emails about natural cures for Multiple Sclerosis. When I was first diagnosed with MS, it seemed that everyone I knew had some sort of Homeopathic cure. One of my friends even told me
Supplements, Diet and Multiple Sclerosis Read More »
The Patient Protection and Accountable Care Act, aka Obama Care, lacks accountability when it comes to drug costs. A Sacramento Bee report, identified that to keep insurance premiums low some insurers are being allowed to charge patients hefty copays for specialty drugs. This includes many MS and Cancer patients that need this medicine to help
Overcoming High Copays for Specialty Drugs Read More »
I wanted to start by wishing Happy Mother’s Day to all the mom’s out there! I especially wanted to wish my wife a Happy Mother’s Day for bringing my two beautiful boys, Mason and Colby into this life. I also wanted to send a big Happy Mother’s Day out to Moms with MS and Caregiver
Happy Mother’s Day! A Tribute to Moms with MS and Caregiver Moms Read More »
According to a study by Dr. Kleinewietfeld, an increased salt intake could lead to triggering an autoimmune reaction which could lead to Multiple Sclerosis. The frustrating thing is about Multiple Sclerosis is there is no single cause. MS can be triggered by any number of factors including environment, genetics, diet and location. As researchers narrow
Skip the Salt? Trial and Error Approach to Living with MS. Read More »
When my Aunt Loretta was diagnosed with MS in the early 1970’s, Multiple Sclerosis was thought to be the wheel chair disease. In fact, my only memories of my Aunt Loretta were that she was in a wheelchair and could only mumble and moan. When I was lying in my hospital bed with an acute
Living with a chronic illness, like Multiple Sclerosis, is tough to talk about. Often times we shut out the people we love because we don’t know how to communicate how we feel. Chronic illness impacts how we communicate with our loved ones, friends and co-workers. Instead of talking openly about how we feel, we tend
Radio interviews about living well with MS Read More »
The question of why I write has many layers. My first memories of writing date back to second grade. My mom was in a fight with my dad. She swore she was going to pack up and move to Vermont. As I sat and cried in my room, I took a pencil and blue wide-lined
Being follow by a Moon Shadow (MS) Read More »
It is the dog days of summer. No one knows this better than the MS crowd. The hotter it gets, the harder it gets on the MS population. There have been a lot of blogs that touched upon this subject lately, so here is my two cents. It’s all scientific. A study conducted by Uhthoff
Cool Fashion: MS and Heat Read More »
This presidential campaign is an interesting match-up of first lady candidates and their relationship to Multiple Sclerosis. In one corner you have the incumbent, Michelle Obama. At the Olympics the first lady talked about her father’s battle with MS. According to the Washington Post, Obama, who said she was “just in awe” of their company,
MS and the White House: Michelle Obama vs. Ann Romney Read More »
