Life Beyond the Relapse: Real Stories of Living with SPMS
If you are living with secondary progressive multiple sclerosis (SPMS), you know that life feels different from how it used to be. For years, you might have lived in the RRMS world...
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If you are living with secondary progressive multiple sclerosis (SPMS), you know that life feels different from how it used to be. For years, you might have lived in the RRMS world...
By Nicole Robinson Living with multiple sclerosis has taught me a lot, especially when it comes to protecting my mental and emotional well-being. When I was first diagnosed, I did...
Rafael Lara, who goes by Macho, shares his experience living with multiple sclerosis fatigue, including how it affects his daily routines, energy levels, and ability to spend quali...
If I can help even one person get a correct diagnosis of their own, meaning they can get started with treatment, it’ll be worth it.You know your body better than anyone – but what...
Dear family and friends, Over the years, I have wondered how my diagnosis of relapsing-remitting multiple sclerosis has impacted your worlds, as well. Just as I am unable to convey...
In an extract from her new book, Susan Bennett tells how she and her husband had long dreamed of adventure, until dual multiple sclerosis diagnoses finally forced their hand.
By Dr. Eva Jackson Holistic wellness plays a critical role in improving the quality of life for individuals affected by multiple sclerosis (MS). This approach, recognized and studi...
Between my tours with the Army, a new course was added to the curriculum for me to teach — a two-week basic combat skills course for support personnel. The logic was that if a mech...
Declan Watson outlines how myeloma, a blood cancer notoriously difficult to diagnose, offers symptoms so vague that many patients only learn the truth in an emergency.
By now, I’ve spent at least 70 hours inside an MRI machine. That’s three days of my life spent lying perfectly still while magnetic resonance imaging (MRI) searched my brain, spine...
I had never known anyone personally who had been admitted to a psychiatric hospital. Walking my husband, Rhead, through those doors was one of the strangest moments of my life — no...
Navigating the Slow Climb: Our Journey with PPMS Living with Primary Progressive Multiple Sclerosis (PPMS) can often feel like we are navigating a different world than our peers wi...
During my sophomore year of high school, my class schedule was changed against my wishes, resulting in me having to enroll in a theater class for the semester. Although I had dabbl...
This article was provided by our partner, Can Do MS. It has been reviewed by Bionews for accuracy and relevance. The views and opinions expressed are those of the author and do not...
How recent drug, coverage and digital execution changes reshape cash flow, fiduciary structure and protective planning.
Alan Osmond, a member of The Osmonds, has died after 19 years of living with Multiple Sclerosis - here is what you need to know about the incurable condition
While Multiple Sclerosis (MS) Awareness Month is observed in March, we recognize World MS Day on May 30 to honor individuals around the world living with MS, as well as their famil...
Talking openly with your care team about your multiple sclerosis treatment goals can help personalize your care, improve symptom management, and support your long-term quality of l...
Lindsay Kelly shares how recognizing subtle symptoms and speaking up helped guide her husband’s progressive MS care. The post A caregiver’s role in recognizing progressive MS appea...
A 12-week intervention combining breathing exercises, cold exposure, and meditation — known as the Wim Hof Method (WHM) — or a lifestyle intervention aimed at improving physical ac...
By Dr. Eva Jackson One of the most meaningful quotes I have read this year is, “Nothing amazing happens inside our comfort zone.” When you first hear that tests confirm a diagnosis...
Aranzazu Calzadu shares why speaking up about care expectations is essential to finding your ideal treatment approach. The post MS is your disease — own your care appeared first on...
If I sit for over three minutes, it takes almost that long to regain movement in my legs when I stand. Even then, my limbs must fight the relentless pressure of immobility. Focused...
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