Could it be MS?...Hi all, I'm new here but am hoping I can get some input from those who have secured a diagnosis. Over the last 5-6 years, I've been having increasingly troubling...reactions1reply
The MS Age Restriction...When I received my diagnosis, I was 22 years old. In the world of MS, the onset typically falls between 20-40 years of age. As you might imagine, getting diagnosed...reactions15comments
The Villainous MS...Being a victim of theft can make you feel worried, sad, frustrated, scared, or angry. Years ago, I hosted a birthday party at my home for a close friend. The...reactions2comments
Ask Me Anything Giveaway Terms and Conditions...Official Rules, Terms and Conditions for the KoldTec Giveaway NO PURCHASE NECESSARY TO ENTER OR WIN. A PURCHASE DOES NOT INCREASE YOUR CHANCES OF WINNING. VOID WHERE PROHIBITED. The KoldTec...reactions6comments
America living in Australia - worth it to come home?...Hello. I was recently diagnosed with Relapsing-remitting multiple sclerosis (RRMS). Luckily for me it was caught early and I was able to leap onto medication before the lesions had a...reactions10repliesAwarenessCopingCostTreatment
I Have MS But It Doesn't Have ME!...I have been diagnosed with Relapsing-Remitting Multiple Sclerosis since September 2020, and I can only describe my life as a roller coaster ride since then. The days leading up to...reactions2comments
Info please...I'm in the process of finding out what is going on with me. I am going on my 4th neurologist. No one takes me seriously because my Mri came back...reactions12repliesUndiagnosed/Seeking Diagnosis
Stories...How long does it take for stories to be approved? I submitted my story and haven't had an update...reactions1reply
Anyone living with NMOSD/ Devics Disease? We want to hear from you 💚...Hey there! Jada here, I help run Neuromyelitis-Optica.net and where we support so many living with NMO. We know SO many people have had the NMO misdiagnosed as MS. Sadly...reactionsrepliesAwarenessUndiagnosed/Seeking DiagnosisSymptoms
A Day-in-the-Life With MS...What does a typical day look like for someone living with multiple sclerosis (MS)? In some ways, the days are the same as anyone else. In some ways, our days...reactions1comment
The Effect of MS: Me vs Dog...“You don’t get MS until you get MS” is a common quote among people who live with the disease. The difference between our appearance and our abilities (as well as...reactions16comments
HELP bloody feet...At the end of my tether!!!my bloody feet do this weird thing and uncontrollable my toes and thighs ligaments tense up. Nothing eases it. Keeping my feet ice cold will...reactions1replySymptomsPain
MS and Knee Surgery: My Total Knee Replacement Adventure, Part 1...Symptoms of multiple sclerosis are rarely fun or enjoyable. Many times they can be downright debilitating. One of my more worrisome MS symptoms in recent years has been spasticity in...reactions9comments
I’m Positive: MS, COVID-19 & 2/18 Are About More Than Me...I looked to my right and watched Dan standing dumbfounded as the woman in a hospital-issued hazmat suit rushed me and my power wheelchair through the metal door. “But, but...reactions2comments
Another Icky Flare up!...Currently going through a flare up being treated with a 5 day solu-medrol treatment. We had to halt my last two dosages due to my sugars going too high now...reactions4repliesCopingMental HealthSide Effects
Six Ways to Earn Money After an MS Diagnosis...Just been diagnosed with MS and worried it will affect your earning ability? Medically retired on disability and need to make some extra money? There is no time like the...reactions15comments
Lightheadedness off and on ...Hello Warriors! I have been suffering from moments of lightheadedness. I can't put my finger on what's going on. I just completed my dmt Mavenclad in December. I'm very well...reactions3repliesSymptomsTreatment
Pride and the Tale of Two Devins...My life before being diagnosed with multiple sclerosis was one that filled me with an incredible sense of pride. I worked very hard and was fairly successful. I was proud...reactions20comments
Marti Hines...In late 2019, Ms. Hines launched the platform Marti’s MS Life as a transparent way to share her journey with Multiple Sclerosis. Ms.Hines was first diagnosed with the immune disorder...
Problems with memory...Hi, I'm new to the site since I kind of suspect I may have MS and I wanted to see if someone could help me. I have had some weird...reactions11repliesDiagnosisMental HealthSymptoms
