❤Thank You for sharing this. I am waiting for my MRI date and very possibly I have Ms. A lot of what you mentioned I have experienced Thank you.

My daughter was just recently diagnosed and her MS started with eye problems too. But they didn't diagnose MS for about 6 - 8 months after that when she was having issues feeling things like orgasms and her legs. May I ask if you had Covid? Unfortunately, she had it several times and I've been reading that they're finding more people are getting diagnosed with MS that had a lot about Covid because it attacks the spinal fibers? You probably know what I'm talking about. I don't really know what I'm talking about. I'm just learning.

My daughter was just recently diagnosed and her MS started with eye problems too. But they didn't diagnose MS for about 6 - 8 months after that when she was having issues feeling things like orgasms and her legs. May I ask if you had Covid? Unfortunately, she had it several times and I've been reading that they're finding more people are getting diagnosed with MS that had a lot about Covid because it attacks the spinal fibers? You probably know what I'm talking about. I don't really know what I'm talking about. I'm just learning.

im happy you are feeling better.

my MS is getting a little worse too. My heartbeat will beat fast at random times, too much walking and walking too fast leads to wobbly knees. I cognitive gets bad. i can't think properly, I am so forgetful. we have the same symptoms. :(

Were you sore at all? My whole upper body is sore. Jaw, throat, neck, eyes, shoulders , arms.

I went into the ER with messed up vision that had been going on for a week at that point, then the doctor looked my left eye and said "oh ... that's weird" called in and eye specialist and then another one that's how I found out I had MS

I am 43 years old now, I was diagnosed when I was 33, now I look at people with the same diagnosis, I do not have the worst course of the disease.I have trouble with diction and coordination.but it seems to me that it's better than spasticity always

Thank you for sharing your story. I teach anatomy and like to put a personal tone to some of the anatomy lessons. This video will be helpful for my students to understand the diagnosis and progression of MS.

You are so positive and this is such a great video.

Dr Aaron Boster, is an MS Specialist who practices is Ohio and has a very active KZbin channel. He has monthly livestreams when he answers questions viewers may have youtube.com/@aaronbostermd?si=3HSrJ6iYYZHcCgeW

Hi! You are so beautiful and inspiring! Thank you for this video. Did you lose your vision like completely or just peripheral? Was it like tunnel vision?

I've had leg spasms, facial issues & panic attacks for on & off about 10 yrs. No one seems to think it's real, because it's not happening to them.

Thank you for this 🧡

I am relating to this so much! I had double vision during the pandemic and numbness of course so that was my fun. Used to want to be in dentistry myself. Do folks with MS love teeth? Jk but girl I am relating so much with the misdiagnoses for such a long time. In the process of being diagnosed with MS but the tests are showing pretty much.

i love that you're fine and you update that you're fine. please keep updating. its good to know that someone with your type of symptoms can do so well after a few years!!

Look into lion's mane mushroom as well.

I was given 75 prednizone tablets to take across 3 days when my brain was swollen and causing my eyes to cross amongst other things. That's how I found out I had MS. Great video, thanks!

I was diagnosed this year and I personally just love to see someone whos well and thriving. Love your videos, really informative and I can relate. I hope you are still well 😃

Thankyou so so much for this video

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You are so strong! I’ve been sick 18 months and I’m waiting on funding for a wheelchair so I can get out more. Just know that all you got through is incredible and I really appreciate you sharing. Off to check out more of your channel x

I have to say: MS was nowhere on my radar. It wasn’t until an (ongoing) episode of what we think is optic neuritis happened, from my second opinion doctor. I have all these weird symptoms that I’ve been attributing to medication side effects, that very well could be either. It’s crazy how widespread the symptoms can get, whether I end up having it or not

I know this is an old video but I did have a question: How were you able to work every day with your situation? I’m having symptoms and, after four months- I finally see a neurologist in 2 weeks. But in the meantime I can only get through maybe 4 hours at work. I’m a nurse and on my feet constantly and need to be sharp. But with this 😢, it’s very hard. Also, it’s hard to concentrate at work because I’m all consumed with how I’m feeling. Also- I feel alone and isolated and a burden on my husband. Thank you for your inspiring story. ❤

Will you continue to keep up updated throughout the 6 months MRIs? I have MS and I watch your happy result videos every time after I get my results, they make me feel better ❤

Numbness! Wow!

God Bless You!

Heat and stress

Thank u for this. I have Ms and I'm only 23 years old. I struggle to walk as I have lost my balance and I'm always dizzy all the time especially when turning around and my left hand has no co - ordination . Although I'm happy that I can walk myself around the house to do things without assistance I can't ignore the fact that my life has changed completely I no longer go out by myself. I need to have someone with me. That time I have zero support, it's just me and this thing. My mother is too busy with her own life, plus she doesn't take this disease seriously and my friends have distance themselves from me. I can't even get a job to sustain myself. Couldn't do my fitness test for the job I had applied for before falling sick and it broke my heart because it was a really well paying job. I'm from South Africa btw(African female). I just wish that I could recover completely and go back to my normal life like it was before 😢

skills

I just got diagnosed with MS. I am 23 years old and my entire right side of my body and my entire face is still numb. It is very inspiring to see that your story has a good outcome.

I'm so happy that you are in a good place! No change is good change. I'm very curious about how dentistry is going! I'm a dental Hygienist who was planning on going to dental school. Having issues with my body though... (which is how I found you haha).

Please keep us updated with your journey,i'm almost at my decade mark but i still love learning about other people's MS journeys.

Just gone through all of your MS videos and wow. I am so happy for you and agree with the other commenters, you could just upload 2 min video updates from time to time so we can celebrate it together with you here 🎉🎉🎉🎉. Really happy for you ❤!

I was officially diagnosed yesterday and am going to be beginning treatment as soon as all the referrals and scripts and bloodwork gets sent out and done. Thank you so much for posting and documenting your journey. I like the realness with which you discuss these things in your videos. I'm struggling a lot with memory issues, fatigue and anxiety. It is so scary to think that my memory may not improve but listening to what happened with your hand gives me hope that treatment could change things despite the doctor saying its likely permanent at this point. The grief I feel now is immeasurable, but there is hope where there otherwise may not have been because of hearing stories like yours. Thank you, Sarah! Also, for the record your crying face looks better than mine haha so points for you on that end too XD

Thanks my son was diagnosed a few months ago. Not knowing what to expect is heartbreaking. He is 51 President of our family business. Lot of pressure.

Thanks!

I was diagnosed in 2009 at 41. I started having symptoms after my mother’s death, but during my divorce i went partially paralyzed. I regained my strength after years. Stress is the biggest trigger.

I’m in the process of getting diagnosed due to having optic neuritis. Question has anyone here had their diagnosis just with a regular MRI or do I really need to get an MRI with constrast?

Hi. I know you aren’t a doctor but curious to get your opinion. I’ve had two episodes now (one which I’m currently having) where I lose sensation and have pain on the left side of my body... leg and face mostly but also arm and neck. I’m having a hard time walking and I’m switching between a cane and a walker. I went to the ER both times, and this time they found a lesion on my spine. I only have one though so do you think this could be MS? I also have a weird left-sided face stuff and my smile is off and my left eye hurts and can go lazy.

I have all the symptoms. What should i do. It's scary.

Can you please make an update. Let us know your symptoms and what youve been feeling. Are your hands and legs still numb. Also, did you take anything for anxiety like antidepressants? Please give us an update

i get the symptoms and the doctos send me for MRI's and scans and at the same time i was combatting a concussion and stress from a car accident and it was covid tim eso i totally get you with the anxiety Sarah , It was such craz times. Doctor see the lesions on my brain and upper spine but dont' want to say i have MS yet .. (not sure how many times i have to wet myself when i all of a sudden have to pee. the spasms the vision blurring and then fine and then blurred in only 1 eye lol people taht do'nt know about it dont get the variety of symptoms... heck i donlt even get them all if something fees weird i often think is this a symptom or not and then go find a group to see if anyone else has it. lol I havent really openly spoke about MS because they can't say for sure i have it but i combat what is there with healthy holistiv alternatives and thats what messes the doctors up. beat the inflamation for sure.

Parasites cleanse and heavy métal cleanse needed on m'y God wake up people!!!

Stumble on your video...and 1) I thought I was the only one who sleeps in MRI!?...but the technicians when finding out its me, warn me not to sleep cause i twitch and I mess things up.🤣🙄 2)I like your gap, plus you seem to have good oral hygiene, which seriously dont understand why is it so hard for others. 3) good video. Wish you well, good fortune....go nutts, enjoy life, have fun...oh plus some advice -- dont be afraid to laugh and voice your opinions.

What a brave lady - thanx 4 sharing ur difficult journey with us & may God Bless You with His Healing Hands❤

sexy.

Imagine how funny an MS couple would look together trying to do stuff for each other.

Did people ignore you and try to downplay your symptoms at first? Doctors not actually doing their jobs, "it's just stress", youre just depressed. I'm pretty sure I have MS or ALS for 9 months at least. I have weird muscle firings all over my body. They started in my face. Most of them are small single pops or flutters but sometimes they get set into a muscle. I get so tired quixk sometimes.