Photo courtesy of Pamela Neckameyer Day 16 of 31 This is Pamela Neckameyer’s story: My symptoms started in 2004. I would trip and fall for no reason. My mind would say “walk” but my legs wouldn’t move for a few seconds. I went to a neurologist who tested…
Photo courtesy of Melody Sapien Day 15 of 31 This is Melody Sapien’s (@autoimmune.wellnesswarriors) story: Eight years ago, I was diagnosed with multiple sclerosis. I was 15 years old. In a lot of ways, I am grateful for my diagnosis because, without it, I would have never…
Photo courtesy of Rennie Rankin Day 14 of 31 This is Rennie Rankin’s (@yogaren) story: My name is Rennie and I have been living with MS since the early 1990s, diagnosed on 6/2/2003. I will never forget how surreal it was hearing my diagnosis and feeling…
Photo courtesy by Michael Drohan Day 13 of 31 This is Michael Drohan’s (@mdrohan) story: I was diagnosed with multiple sclerosis at 18, right before high school graduation. I describe the 18 years since as a slow decline in my abilities. My relapsing-remitting MS has shifted to…
Photo courtesy of Inês Velosa Day 12 of 31 This is Inês Velosa’s (@inesdnobre) story: On June 6, 2021, after some confusing days, my husband was diagnosed with MS. I remember hearing this diagnosis for the first time and thinking that life, as we knew it, was…
Photo courtesy of Tyler Campbell Day 11 of 31 This is Tyler Campbell’s (@tcspeaks32 ) story: At 22, I was suffering from paralysis and even erectile dysfunction. I felt so lost and yearned to be found. I needed a friend, someone to lean on who wouldn’t judge…
Photo courtesy of Carolyn Hinds Day 10 of 31 This is Carolyn Hinds’ (@carriecnh12) story: Mild cognitive impairment, or CI for short, probably doesn’t sound as debilitating or challenging when compared to other symptoms of multiple sclerosis, but it is. The word “mild” can be very misleading because…
Photo courtesy of Cassidy Krygger Day 9 of 31 This is Cassidy Krygger’s (@cassidykrygger) story: I remember the day of my first MS symptom, more than three years ago, as clearly as if it were happening now. It was October 2018, and I realized that every time I…
In this installment of our “Expert Voices” series, Multiple Sclerosis News Today asked Kassandra Munger to answer some of your questions about the connection between vitamin D levels and multiple sclerosis (MS). Munger received her bachelor’s in biology from the University of Rochester in 1997, master’s in…
Photo courtesy of Kaci Bell Day 8 of 31 This is Kaci Bell’s (@myelinmoxi) story: Something I feel a handful of people in the disabled community have experienced but are too shy to open up about is “imposter syndrome.” Imposter syndrome and chronic illness rarely fall in the…
Photo courtesy of Alexios Touloupis Day 7 of 31 This is Alexios Touloupis’ (@alexios4real) story: I was diagnosed with multiple sclerosis in March 2016, my junior year of high school, when I was only 16. For months I struggled with one health problem after another. It was…
Photo courtesy of Kali Thomas Day 6 of 31 This is Kali Thomas’s story: Just a few months after my 21st birthday, in July 2013, I received a call that would change my life forever. I will never forget my doctor’s words: “I’m looking at your MRI, and I…
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…
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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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…
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