Bionews Staff,  writers and editors—

Bionews, the owner and publisher of this site, employs science writers and editors, most of whom have PhDs in the life sciences, as well as veteran journalists, who ensure stories are well-written and easy to understand. Our stories undergo a comprehensive fact-checking and editing process to confirm accuracy, objectiveness, and thoroughness in order to best serve our audience of patients and caregivers.

Articles by Bionews Staff

With MS, strength has nothing to do with being OK

Michelle Lesmeister posed for this headshot in February 2025. (Photos courtesy of Michelle Lesmeister) Day 23 of 31 This is Michelle Lesmeister’s story: “You’re the strongest person I know — you will be OK.” Lesmeister takes her dog Barrett for an afternoon walk. Who wants to be just…

My day, interrupted by MS

Ena Salcinovic celebrates her birthday three years after her MS diagnosis. (Photos courtesy of Ena Salcinovic) Day 22 of 31 This is Ena Salcinovic’s story: Saturday. Finally. A good day. I still believe that even though I overslept and missed the Red Cross and our weekly international cooking. I…

Having RRMS has taught me how to live one moment at a time

Ross Libby smiles for a photo. (Photos courtesy of Ross Libby) Day 22 of 31 This is Ross Libby’s story: I was diagnosed with relapsing-remitting multiple sclerosis (RRMS) in 2007 when I was a senior in college. I had been very sick with vertigo and gastrointestinal issues…

Learning from others in the MS community empowers me

Jenn Powell wears her MS ambassador shirt with pride. (Photos courtesy of Jenn Powell) Day 20 of 31 This is Jenn Powell’s story: Hosting The Multiple Sclerosis Podcast has been eye-opening, exposing me to the diverse and inspiring voices within the multiple sclerosis (MS) community. Every guest I…

How I’ve embraced a holistic approach to living with MS

Latifa Janahi takes a five-day course of corticosteroids to reduce inflammation in her body. (Photos courtesy of Latifa Janahi) Day 19 of 31 This is Latifa Janahi’s story: I am a woman from Bahrain Island who’s passionate about technology and baking. After working in the tech field for 10…

Sharing my truth as one of many stars in the MS universe

Tom Anderson, 67, was diagnosed with multiple sclerosis at about 30 years old. (Photos courtesy of Tom Anderson) Day 16 of 31 This is Tom Anderson’s story: I may be the dimmest star, but don’t get all hokey on me. There are lots of us. The following are the…

My dad with MS teaches me to live wholeheartedly

Sterling Hofmeister is pictured here at 6 months, carried in a backpack by his father Ben Hofmeister. (Photos courtesy of Ben Hofmeister) Day 15 of 31 This is Sterling Hofmeister’s story: Sterling Hofmeister, far right, is pictured with his brothers and father in 2018. My name is Sterling…

With or without MS, we are all unique people — from A to Z

Christy Hoffman poses for a picture with her husband Mike, who has MS. (Photos courtesy of Christy Hoffman) Day 13 of 31 This is Christy Hoffman’s story: Anxious. Blessed. Curious. Daring. Excited. Frustrated. Gregarious. Happy. Isolated. Jovial. Kind. Loving. Moody. Numb. Opinionated. Pumped. Quiet. Restless. Strong. Trusting. Underrated. Valiant.

Finding workarounds makes it easier to navigate an MS flare

Nanette Lai locks eyes with her chihuahua Fanny. Lai says mutual gazing between humans and dogs can cause synchronization in areas of the brain. (Photos courtesy of Nanette Lai) Day 12 of 31 This is Nanette Lai’s story: My name is Nanette, and I have lived with relapsing-remitting…

Even after my MS diagnosis, camping is still the best medicine

Izzy Abbas loves to go camping, but he also enjoys traveling internationally, Here, he is shown visiting Turkey. (Photos courtesy of Izzy Abbas) Day 11 of 31 This is Izzy Abbas’ story: Camping — being out in the woods and mountains — is something I’ve always loved. Despite all…

Living with MS means adapting to a new normal

Sarah Zichterman poses for a photo one year after her MS diagnosis. (Photos courtesy of Sarah Zichterman) Day 10 of 31 This is Sarah Zichterman’s story: Getting diagnosed with MS was not something I thought would happen to me at age 24. One day in January 2024, I woke…

MS has changed my course but it hasn’t taken my dreams

Naty Caez shares about her life with MS on Instagram. (Photos courtesy of Naty Caez) Day 9 of 31 This is Naty Caez’s story: In September 2024, I was diagnosed with multiple sclerosis (MS). Everyone’s diagnosis story is going to look a little different, but for me, it took…

My 10-year-old tattoo speaks to me and my life with MS now

Brittany Boudreau attends the MS Dream Center of Rhode Island’s An Evening to Remember gala. (Photos courtesy of Brittany Boudreau) Day 5 of 31 This is Brittany Boudreau’s story: In August 2021, my life was going according to a plan I’ve had since I was 10. However, two days…

My sister’s MS journey made me a better person

A young Michael Lama Jr. poses with his sister, Desiree Lama, at Christmastime years ago. (Photos courtesy of Michael Lama Jr.) Day 3 of 31 This is Michael Lama Jr.’s story: Growing up, my sister Desiree and I used to play video games and sports in our grandma’s backyard.

A special night with Lady Gaga changed everything for us

From left, Michael Lee Martinez and Feliciano Velazquez celebrate the holiday with their cats, Korra and Cleo, on Dec. 23, 2024. (Photos courtesy of Michael Lee Martinez) Day 2 of 31 This is Michael Lee Martinez’s story: Picture this: After stanning one of the biggest pop stars of our…

From diagnosis to determination: My MS journey of hope

Sanam Saeedi resolved not to allow a diagnosis of MS to determine the course her life could take. (Photos courtesy of Sanam Saeedi) Day 1 of 31 This is Sanam Saeedi’s story: For years, I lived with numbness and tingling in my toes, but dismissed it as a result…

MS taught me the importance of being kind to yourself

It took years for Gregory Sonn to receive an MS diagnosis. He first noticed symptoms while traveling in his 20s. (Photo courtesy of Gregory Sonn) Day 31 of 31 This is Gregory Sonn’s story: My name is Gregory and I’m currently living in the unincorporated area of Roseville, near…

As an MS warrior, I advocate for myself and take things slowly

Lynne Denise, right, and her dad, Don Collins, attend last year’s MS walk in Edwardsville, Illinois. (Photos courtesy of Lynne Denise) Day 30 of 31 This is Lynne Denise’s story: Hello, multiple sclerosis (MS) warriors! My name is Lynne Brush, and I was diagnosed with relapsing-remitting…

We love each other, but we hate multiple sclerosis

Day 29 of 31 This is Mike and Jenn Powell’s story, as a conversation: Jenn and Mike Powell stand with their dog, Skye, in Laguna Beach in November 2023. (Photo by Vicki Shequin) Jenn Powell: My husband, Mike, hates multiple sclerosis (MS). There was a…

I’m coping with MS the best way I can

Kelly Earley teaches family and consumer sciences at a middle school. (Photos courtesy of Kelly Earley) Day 28 of 31 This is Kelly Earley’s story: I have been living with multiple sclerosis (MS) since I was 17 years old but was only officially diagnosed when I was 24…

Creating a new normal in life with relapsing-remitting MS

Rochelle waits for a virtual appointment with her doctor in 2020. (Photos courtesy of Rochelle) Day 25 of 31 This is Rochelle’s story: I’m writing this on the anniversary of “that day.” I was diagnosed with relapsing-remitting multiple sclerosis, or RRMS, in March 2020. How fitting that I…