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...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...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...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...reactions3repliesAwarenessSide EffectsTreatment
The Experience and the Explanation: MS Numbness...Numbness has been a symptom I have dealt with since the very beginning of my MS journey. It was one of the...reactions76comments
Insight in my symptoms please....Hi all, I (F 43) don’t have a diagnosis and at the moment I don’t know whether I hope to never get...reactions4repliesUndiagnosed/Seeking Diagnosis
My New Focus on Well-Being and Managing Daily Movement...So often, living with chronic conditions like MS, we learn how to manage medications, manage doctor appointments, manage lifestyle choices, manage time...reactions17comments
Tremors...Hi! I've had tremors for a few months. Started in my hands, but now it's also in my arms and legs. It's...reactions1replySymptomsUndiagnosed/Seeking Diagnosis
Unique Considerations About Sex for Men With MS...Being a man who has been diagnosed with multiple sclerosis can lead to questions about changes in sexual activity. Maybe you are...reactions6comments
Unsolicited Advice..."You should try bee therapy or acupuncture." "You should just smile more." "We're never given more than we can handle." "You're really...reactions95repliesTips & AdviceCopingFriends & Family
On Deaf Ears and People Who Are Helpless...Here is the thing. I tell my loved ones the total truth about how I am feeling about my physical and or...reactions1comment
How I Talk Myself Through My MS Journey Using Transactional Analysis...Many people with chronic illness benefit from practicing some form of psychotherapy. It can easily be added to drug and physical therapies...reactions9comments
Area Postrema Syndrome!...I know it's very uncommon but I am really desperate to find someone who can relate! A little history about my case:...reactions2replies
The Latest on MS Clinical Trials...Clinical trials are the process we use to test new treatments. Most of the drugs and treatments we use exist because of...reactions7comments
HMO or PPO...I have been on a PPO plan for last ten years. This has allowed me to travel out of my small county...reactions1replyInsurance & DisabilityTips & Advice
Livin my best life...Diagnosed in 2004 at age 27 I realized just how strong I really am. I had lost all feeling from the chest...reactions2repliesCoping
Handicap Accessories...You know, it always makes me wonder why any devices that can help MSers live a bit easier of a life always...reactions8repliesAssistive Devices
Living with ms...The heat is terrible my legs get tight and starts aching then i have to take a pain pill and raise my...reactions1replyCopingSymptoms
The Inhumane Disability System: Part 2...Recently, I wrote about some experiences that I’ve (as well as many people I have spoken with) had with the disability process...reactions47comments
Advice...I really feel crappy. My bones hurt. My muscles hurt. My brain is all 'KMAGYOYO' and I'm tired and wired. I can't...reactions7repliesCopingMental Health
