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Photo courtesy of Agata Day 5 of 31 This is Agata’s (@beatingmyms) story: It was 2019. My life was about to turn upside down, and I had no idea. I should’ve noticed the signs: miscarriage, anxiety, depression. I just got married to the love of my life. I…
Photo courtesy of Laurie Lambert Day 4 of 31 This is Laurie Lambert’s story: The first thing I did was worry. When my friend told me of her MS diagnosis, I thought: she has always been the sharpest member of our circle — the one with the most expansive…
Photo Courtesy of Tatiana Andjelic Day 3 of 31 This is Tatiana Andjelic’s (@tatianaandjelic/@msonthemind) story: I laughed a lot when I was diagnosed with multiple sclerosis in March 2019. My diagnosis was a tangled string of trial, error, and realism. I was lucky to work primarily with…
Photo courtesy of Zaki Farzand Day 2 of 31 This is Zaki Farzand’s (@zakifarzand) story: Hi, I’m Zaki Farzand, and I’m 33 years old. Here is my MS story, so pull up a seat, grab a coffee, and sit back. I still remember the day I got my…
Photo courtesy of Manuela Lama Day 1 of 31 This is Manuela Lama’s (@manuela.p) story: Caring for someone with multiple sclerosis can be challenging, exhausting, and stressful. As a single mother of a daughter with MS, I have been not only physically tired, but, even more…
Multiple Sclerosis News Today is bringing back its “31 Days of MS” initiative for the third year during Multiple Sclerosis Awareness Month in March. This project is aimed at raising awareness by highlighting different voices within the MS community. Every day in March, we will feature a story from…
In this installment of our “Expert Voices” series, Multiple Sclerosis News Today asked Tim Coetzee, PhD, some of your questions related to the current state of multiple sclerosis (MS) treatment and cure research. Coetzee serves as the National MS Society’s chief advocacy, services, and science officer. In this capacity, he…
In this installment of our “Expert Voices” series, Multiple Sclerosis News Today asked Allen C. Bowling, MD, PhD, to answer some of your questions related to complementary and alternative medicine (CAM) for people with multiple sclerosis (MS). Bowling is an internationally recognized neurologist and integrative medicine pioneer with…
In this installment of our “Expert Voices” series, Multiple Sclerosis News Today asked registered dietitian Mona Bostick to answer some of your questions related to diet and nutrition for people with multiple sclerosis (MS). Bostick, who has MS, works in private practice in Greensboro, North Carolina, where she helps…
In this installment of our “Expert Voices” series, Multiple Sclerosis News Today asked psychologist Gayle Lewis, PhD, to answer some of your questions related to sex and intimacy for people with multiple sclerosis (MS) and their partners. Gayle Lewis is a psychologist and psychoanalyst currently in private practice in New…
In this installment of our “Expert Voices” series, Multiple Sclerosis News Today asked Meghan Beier, PhD, a rehabilitation neuropsychologist who teaches skills and techniques to improve patients’ quality of life, to answer some of your questions related to fatigue for people with multiple sclerosis (MS). Beier is a psychologist specializing…
When I was first diagnosed with MS at 27 years old, I didn’t know everything I know now. As I’ve learned more about MS I have become an expert in my own disease and an advocate for others too. Living well with MS can bring about challenging times which are…
In the first installment of our new series, “Expert Voices,” Multiple Sclerosis News Today asked Martin Shenkman, a certified public accountant and lawyer, to answer some of your questions related to financial planning for people with multiple sclerosis (MS). Shenkman is an attorney in private practice in Fort Lee, New…
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By Biogen The introduction of disease-modifying treatments transformed what it means to receive a multiple sclerosis (MS) diagnosis, having an incredible impact on patient care. Just three decades ago, treating multiple sclerosis (MS) was limited to reducing the severity of symptoms and shortening the duration of relapses, with…
Photo courtesy of Katie Collett Day 31 of 31 This is Katie Collett’s story: “You have multiple sclerosis” were words that struck fear in my heart nine years ago. I thought my life and my dreams were over. As I learned more about my diagnosis and met…
Photo courtesy of Sam Mizzelle Day 30 of 31 This is Kathy Reagan Young’s story: I’m Kathy Reagan Young. I was diagnosed with MS 13 years ago. I was so blindsided when I got the diagnosis, I don’t think I truly processed it for a couple…
Photo courtesy of Joanna Hammond Day 29 of 31 This is Joanna Hammond’s story: I was diagnosed with MS back in January 2018, and I felt like my world had fallen apart. One of the very best things I did very quickly was to attend my local…
Photo courtesy of Carter Stough Lowe Day 28 of 31 This is Carter Stough Lowe’s story: I first noticed extreme blurriness in my right eye when I was home for my grandfather’s funeral and informed my mother of my vision problems. She sent me to her eye…
Photo courtesy of Stephanie Wiley Day 27 of 31 This is Caroline Craven’s story: This year marks 20 years since my MS diagnosis, yet every day brings something new. Every day reminds me of some shift in life that I chose to make so that thriving with MS is…
Photo courtesy of @JackieHicksFondMemories Day 26 of 31 This is Stacy Barton’s story: I’m Stacy Barton, and this is my story: In 2005, I was married with two children, including an autistic daughter, and working on Capitol Hill. I had grown accustomed to walking around…
Photo courtesy of Colin Hirst Day 25 of 31 This is Colin Hirst’s story: Hello, I’m Colin and I have relapsing-remitting MS. Simply put, MS is an auto-immune disease that makes your body’s own cells break down the myelin around your nerves because it believes they are…
Photo courtesy of Matthew Embry Day 24 of 31 This is Matthew Embry’s story: Hi! My name is Mathew Embry, and I was diagnosed with multiple sclerosis in 1995. More than 25 years later, I am living symptom-free and making the best of…
Photo courtesy of Dawn Morgan Day 23 of 31 This is Dawn Morgan’s story: Hi! I’m Dawn Morgan. I have been living with relapsing-remitting MS since 2000, when I was 25. It was a complete shock. At the time, I was just beginning my professional career as…
Photo courtesy of Caroline Gellatly Day 22 of 31 This is Marissa Green’s story: I am Marissa, a fundraiser, drama therapist, and mental health practitioner who loves the outdoors, cooking, music, and any excuse for a party. My original diagnosis, Balo’s concentric sclerosis, happened…
Photo courtesy of Rebecca Anton Day 21 of 31 This is Rosani Christy’s story: My name is Rosani Christy, and I have been living with MS for over 20 years. I have always been a class clown. Making those around me laugh gave me a high, and…
Photos courtesy of Esme Robinson Day 20 of 31 This is Bron Webster’s story: Multiple sclerosis is unpredictable and volatile. I got my diagnosis in 1996. I adapted. I gave up my 20-year financial services career in 2008 to focus on my daughter. I retrained…
Photo courtesy of Conor Devine Day 19 of 31 This is Conor Devine’s story: I have been living with MS now for more than 15 years, which I would summarize as follows: 2006–2011. The first five years were horrendous. I gave up, felt awful most…
Photo courtesy of Amy Thompson Day 18 of 31 This is Amy Thompson’s story: In April 2018, just after my 21st birthday, I was diagnosed with relapsing-remitting MS. My whole world was turned upside down and I couldn’t find anyone I could relate to. That…
Photo courtesy of Jess Faulds Day 17 of 31 This is Jess Faulds’ story: My name is Jess, and I am a 28-year-old woman from Alberta, Canada. Ask anyone who knows me and the two things in life that I am most passionate about are food and…
We consulted some of our community contributors at MS News Today and came up with 12 questions people should consider asking their doctors after an MS diagnosis.
Check it out by clicking here.
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