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Hey guys, I saw in a post about weight lifting, someone mentioned MS warrior program. Can somebody explain this to me please😊

I recently got diagnosed January 2021 after 10 years of symptoms and lost use of my legs. After a lengthy stay at the hospital and many pt appointments I can get around with my cane or walker.

Anti Inflammatory?

I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.

Hello fellow Warriors! I’m one, like many others, who enjoy a variety of autoimmune afflictions; MS, Type 1 Diabetes, Fibromyalgia, Pernicious Anemia, Hypothyroidism and a bout of Autoimmune Gastritis. As a veteran diabetic (33 years) and an MS’r since 2010, I find that these two impact me the most ...

I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.

Hi! MS warriors...I'm Stacy new to the group

Hello everyone, I wanted to ask you all what it takes to be a MS warrior? Now more than ever it seems we need to draw on all of our resources and wondered what these are? I'm newly diagnosed, new to this site and looking for some inspiration to help me cope over the next few weeks and months. Thanks...

Hopefully many of you have seen my fellow MS team mate (from CPISRA World Champs) and all round inspirational girl Kadeena Cox breaking the World Record at the World Championships in Doha this week in the 100M sprint. Kadeena is an outstanding athlete and a most humble, caring and loving character t...

I'm just sharing some thoughts here and I'm curious about other people's opinions! So, we may all know that Christina Applegate did a red carpet in the past couple days with a cane that had "FUMS" all over it. Which I respect but it's not for me. The "MSWarrior/Fighter" and the " FUMS" mentality isn...

I recently decided to start telling people I have MS. I have been very private about my diagnosis since I was diagnosed about 3 years ago. I felt like a huge weight was lifted off my chest! My friends encouraged me to go further with sharing as a healing tool. I decided to create a blog about mother...

Hi everyone I wanted to invite you all to my Beneath the Tracksuit socials, as an MS Warrior, a published Author and now I'm an approved artist, I wanted to share it all with you https://instagram.com/beneath_the_tracksuit?igshid=ZDdkNTZiNTM= https://www.facebook.com/Beneaththetracksuit https://t...

Hey Shift.ms community 👋 We'd love to hear from you about how you identify with multiple sclerosis. Do you consider yourself a "person with MS," or do you prefer terms like "MS warrior" or "MS survivor?" How do these labels make you feel, and do you feel like they accurately represent your experie...

I stumbled across this on Instagram, I’m hoping to connect with others that have this illness. I share my journey on TikTok @mswarriorantonio if you’re interested :-) I’m hoping to hear back from you all!

So in Nov 2021 I woke up with a numb bottom and foot, brushed it off that I had slept funny. Next morning symptoms worse so went to Doctors, sent to my local hospital and given an mri they did no see Anything and sent me home. Next morning woke up wobbly legs pins needles in legs, went back to hospi...

Hi everyone, I’ve had RRMS for over 20 years. I was diagnosed during a time when Australian TV was flooded with commercials of young women with MS in wheelchairs. So, when I was diagnosed naturally I assumed this was what my future held. Thankfully, I had a tribe of supporters who would not allow ...

Hi everyone! My name is Alex. I'm an MS Warrior diagnosed in 2015. I'm sure you all understand these were not the easiest 7 years of my life. After getting my diagnosis, I was almost mindlessly trying every approach and solution I could find online. Different MS medications, homeopathy, countless di...

Hi everyone! I am a new member and I look forward to making connections here. I have been diagnosed with Primary Progressive MS just over a year ago. I used to work as a Dental Hygienist (DH) and a DH educator with a college downtown. Since my diagnosis I have noticed an increase lack of balance and...

I recently found this group and am happy to be part of a community who will understand the every day life of MS. I am the daughter of an MSWarrior. My father has had MS as long as I can remember (27 years +) and I am the only support system he has. I have been struggling for the past few years as hi...

Hi fellow MSers! I was recently introducing myself on a Facebook group for a course I am doing, and wanted to let them know about my MS as it's just as much a part of me as my job. I was going to write 'ms sufferer' but that sounds so selfpitying so I put 'ms warrior' instead, but I don't really lik...