New symptom (again)...I was wondering if any of my MS warriors have or had this sensation. Without warning, I'll get this very warm feeling around my head. It feels like warm water...reactions27repliesSymptomsSide EffectsUndiagnosed/Seeking Diagnosis
How Did I Even Get Here and What's Next...On my 50th birthday, which was 2 years ago almost to the day. I felt like I was on top of the world! I spent it backcountry camping at Lake...reactions19comments
Medical Review Board...The Health Union Medical Review Board is made up of board-certified healthcare professionals with extensive experience in their respective fields. They review and ensure that our content is accurate and...
A Service Call to Dog Lovers With MS...There was a reason why I named him Bean. In the award-winning book Ender’s Game, there was a character named Bean. This character was genetically modified to be incredibly smart...reactions63comments
I feel angry most of the time or tired...Ive always been a little grumpy at times, but these days i feel angry/annonyed. Just getting out of my chair again to grab a drink/cook dinner/shower/feed the dog can make...reactions3replies
"I think it's shingles or MS."...January 26th 2001 I went to the doctor because my right leg was numb. After some time he said that I have 1 of 2 things: MS or shingles. It...reactions1replyDiagnosis
Another Day, Another Diagnosis: Cervical Dystonia and MS...I have dealt with essential tremors for as long as I can remember. They began in my hands, but my hand tremors lessened in college, and I began noticing an...reactions19comments
Editorial Team...The Editorial Team works with its Medical Review Board and experienced medical writers to provide Health Union's Community Team with reliable, easy-to-understand information about a host of chronic health conditions...
COVID and ms...I recently tested positive for covid and I have pprms and they put me on some medication to take for like 5 days but I'm really concerned and I'm really...reactions4repliesCoping
OMG Moments...So many indignities, so little time. MS is comical at the best of times. My gait resembles a drunken Roomba, my speech is stunted and choppy, and everything in my...reactions5comments
Community Team...Welcome to Health Union's Community Team. Our Community Team is made up of a diverse group of employees of Health Union who bring you engaging, accurate information about living with...
PPMS...Hi everyone. I am new to this group. I was diagnosed with RRMS in 2017 and informed that I now have PPMS. I have been on Ocrevus for 5 years...reactions1replyPPMSCopingTreatment
An Advocate Without a Ribbon...This past March was another multiple sclerosis awareness month of lost opportunities. Each year I have lofty goals to participate in every activity available. I want to support my chronic...reactions9comments
Happiest Day Turns Into the Worst...It was back February 23, 2010. I was admitted to labor and delivery, and February 24th at 12:30 am my son came into this world via emergency C-section! I wasn't...reactionscomments
Handicap Accessories...I have read a little bit about device that helps bladder leaks especially for women. Cant help wondering if it would help the urgency problems for me with ppms. Any...reactions1replyAssistive Devices
MS and the holiday season: What's your experience?...The holiday season can be a difficult time for many people, MS or not. Living with MS doesn't make that any easier, in fact, it can create additional issues during...reactions99repliesFriends & FamilyMental HealthTravel
MSAA Webinar: Living with MS as an LGBTQIA+ Person...On September 29th, the Multiple Sclerosis Association of America (MSAA) is hosting a digital educational program dedicated to raising awareness and understanding about living with MS as an LGBTQIA+ person...reactionscomments
Parents with Multiple Sclerosis...School has started up again for most kids, which means an insane amount of running around, extra-curricular events, organizing breakfasts while getting kids ready for school, trying to get lunches...reactions4repliesCopingFriends & FamilyTips & Advice
My First Summer with MS in Australia...Hi, i live in Australia, and the weather is starting to warm up, cant say im looking forward to summer. My feet already drive me crazy, hot cold hot cold...reactions5repliesWeatherSymptomsTips & Advice
Wat does Immune Compromised mean?...I was diagnosed in February 2022, and am still learning about my new MS life. I am on the Tysabri 6months, just been tested for JCV, and awaiting results. I...reactions3repliesAwarenessSide EffectsTreatment
