Blessed 🙏

Thank you very much! Hearing your positivity through all of the frustration makes this overwhelming process seem so much more approachable thank you 🙏 🧡

Hi Lauren, hope you are doing well.

You got a job again yaay I remember watching your video previously when struggling with my job because I got diagnosed with ms x

Would love to know and update!! What about ocrevus now? Thank you for sharing and blessings to you 🙏🏼

Interesting interview on KZfaq: "Oklahoma researchers find link between MS, diet"

So happy for you! You're an incredible person to do this! Knowing that it will be hard! Go for it!

I just love your soil and bubbly personality. Your positivity is infectious. I’ve been living with MS for 11 years now.

I’ve followed you for years. I hope one day if you want to have children, you are able to. You are a wonderful person and your child would be lucky to have you as a parent.

I have been an educator for 14 years and have 4 children. I don't know your age, but I was diagnosed at 35 years of age and I feel that if this is for you and God sees that you should be a Mother it shall be done.

Thank You so much for sharing your experience, Lauren. My father lived with Multiple Sclerosis. Those who are living with MS, are the unsung heroes and warriors of this world, thank you.

Do you have advice for financial help and are you receiving disability thank you I know it’s i related but I have ms and am struggling 🙏 thank you

Hi Lauren, It is so nice to see you on here. I have had MS since 2004, at 32 years old. I had my first child at age 40 and the second at 41. My fear was that I thought I would be exhausted and too tired to be with them. It wasn't the case. I felt extremely good being pregnant. I did have a relapse after each one, but even with that, for me, it was the best decision I ever made. I am on Tysabri, and that really helps with my energy levels. There are little things I would try to do when they were toddlers, which was to play games that didn't require too much moving, like dressing me up, or making me into a mummy with toilet paper, coloring, etc. My husband did the 'running around' games. Everyone is different, but it's something that you will never know the answer to unless you do it. I would say, don't let fear be part of your decision making. Lastly, I don't have family near where I live, so I used babysitters for support if I needed a rest. if you have friends and family who can support, then that would be an extra blessing and reason to go for it! Good luck with your decision! Marlo X

Ich nehme das Medikament Gilenya und bin seit inzwischen 8 Jahren Schub frei!

your great sunny attitude would make for one great parent.

Im 34 i feel too old for kids, i mean id probably be a great dad but i dont like children 😂

Hello Lauren 👋... It's nice to see you , I want to wish you the best of luck and good health in your life. ❤️🌹

Hi Lauren 👋... Sorry you had to go through that and I'm glad to know you're okay and doing well. I wish you all the best ❤🌹

I was so lucky to get rid of my Multiple Sclerosis (MS) after using DR ALAHO OLU on KZfaq herbal supplements for three weeks. He has medicine for HPV, HSV, ALS and MND.❤❤️

I was so lucky to get rid of my Multiple Sclerosis (MS) after using DR ALAHO OLU on KZfaq herbal supplements for three weeks. He has medicine for HPV, HSV, ALS and MND.❤❤️

go for it.

I think you would be a great mother. I hope that you decide on Mr. Right before you take that step. I'm sure I'm not the only one of your admirer's that have been hoping for a sign of that.

Hi Lauren, so lovely to see you post again ❤ I have had MS since 2010 and now have 2 children. One born in 2021 by c-section and one born in 2023 by vaginal birth. During my first pregnancy I came off treatment and had a minor relapse at 20 weeks so went back on treatment until 34 weeks. With my most recent pregnancy I stayed on treatment throughout the pregnancy until 34 weeks and had no relapses. I have breastfed both babies and restarted treatment within a week of giving birth and haven’t had any relapses which I am so thankful for. My consultant and nurse was very clear that MS shouldn’t hold you back from having children, and that as someone living with MS I could still successfully have a family. The toddler phase is tough but I am lucky to have a super supportive husband who can take over childcare on the days I am struggling with fatigue/pain. I am also a school teacher, working with children from age 3-12. When I returned to work after pregnancy I reduced my hours from 5 days a week to 3 which has made a real positive difference in my work/life balance. Feel free to message me with any other questions. Wishing you all the best whatever route you decide to take.

well, do I have a story on that subtitle? but the short version. when I got my diagnosis, that I had MS, my girlfriend was devastated, because, she wanted children and she throat that was not an option anymore or soon to be, so we agreed to start making one before it was too late. we now have a boy at the age of 9. but even though I was the one with MS I had to do a lot of the work, even waking up in the middle of the night to give the bottle to our son.. short story, she had a postpartum depression, and now all so have MS, what or the odds? my advice, be a team with your partner, and it will all be fine, no matter the storm :)

I had a baby girl while I have MS … It’s not easy to do it but I succeeded to have a baby & my ex-wife was so happy. Mody😎

I don't have children of my own. I like to make Squeaky & Peanut Butter look like little kids! Squeaky plays video games. Peanut Butter loves bubble baths! He loves to take them at night. I haven't even gotten a chance to show you a picture of them! Want to see of picture of them?

I sorry, its the worst symptons for me. Was diagnosed this June, I'm embarrassed about my bladder.i go through all the pants, each morning 8 have an accident, I've destroyed t mattress. I don't go out because of it, more than the shop. I have hospital this week for my bladder. Fingers crossed they can help. Keep strong❤️

How are you doing now sweetheart?

Are you taking Nudexta ?

Hi, I'm staying up too late learning more and more about ms. When my mom and dad were here to visit last April, I was having my first bout of ms and I was tripping and falling a lot, had profound weakness in my legs and was generally exhausted. As if that wasn't bad enough, I got what I think was an ms hug. I wasn't very self-aware at the time bc ms is new to me, so I assumed it was really bad gas or indigestion. Tums and Milk of Mag weren't doing a thing to relieve it. It never once dawned on me it could be anything else, especially since I'm always constipated. The tight, sharp pangs were over my entire abdomen and shot up into my shoulders. I was also short of breath, and inhaling deeper made the pains even worse. I had not seen my parents for a few years and they were only here for a long weekend so I skipped the rest I probably needed and kept carrying on as best I could. I actually wore a loose, flowy dress out to dinner so that I wouldn't have a waist band digging into me and making me feel more miserable. I barely touched what I ordered at the restaurant and I passed on ice cream after our meal--this is very unusual for me! This horrible episode lasted into the next day before it finally started to subside. Is it safe to say I was having an ms hug or do you think it was gas like I originally thought? Any responses from the host of the video or others on here participating, please,---I'm new to this and want all the info and personal ms experiences I can get. Thank you and God bless.

You're absolutely beautiful. I'm 17 years in and in leg and four pain agony. Your videos great. Sorry I didn't see it sooner. Hope you're well. It's August of 2023.

I saved this video at some point. I went through all of the precursors to get to be able to be prescribed Provigel. My neurologist reluctantly prescribed me two scripts for generic Ritalin and that came quickly with a cease and desist trying to obtain even that for my exhaustion. And that I wouldn't be able to to even receive that for such issues. . I've had MS for 17 years. I'm in constant horrible pain in both legs feet for the last 7 years. It's getting into my arms at this point.they feel like the legs initially felt going into this amount of pain. It's gradual and painful the whole way up to it. I don't know. I'm constantly tired. I've had mono before. It's like that. I drink about 11-15 cups of coffee a dAy and I sleep for half of my day in the early afternoon. Anyways. You're cool. I know someone who takes Provigel. She's absurdly rich. I am not. It's a bummer. . No insurance wants anything to do with it being prescribed in my case for my MS exhaustion. Hope you're doing well in August of 2023. I'll try for the same.

How many times have you had steroids

I know this video is old but I wanted to let you know that I was diagnosed with Multiple Sclerosis in December of 2022 after going to the hospital because I had back surgery due to my L4 and L5 so I had a Lumber Laminectomy done July 14th but after I still was having balance, fatigue and blurry vision issues which I thought would have been fixed when I had the Surgery but it wasn't. At the hospital I told them my symptoms so the doctor ordered lab work and did a CT scan and she transferred me to another hospital where they did MRI'S and more lab work, the Nuerologist came in and said I had lesions on my brain and it looked like Multiple Sclerosis. Well, fast forward I have had been having more issues with balance, walking and Cognitive issues so I kept researching everything and I have to let you know I was a Medical Assistant and my mother is a retired Nurse, well I heard about taking Vitamin D3 in high doses to help with Multiple Sclerosis it started with a Doctor in Brazil and it is called the Coimbra Protocol. I don't take the high doses like it was talking about because you really need to be in close care with your doctor to do that but I have been taking 5,000 IU of D3 and 600mg Calcium with 125mcg D3 and I have been seeing a big difference in my fatigue, cognition and walking so I wanted to share and also I am not on any DMT yet.

Do what worksl😢 😢 fit you 🎉

Also, my neurologist told me that I am better in the morning or the evening.. For me, I like to do everything and finish it before 2 p.m.

Temperature affects me too, I am better when I am cool.

waxxines have caused M.S. forever. the guinea pigs got played the buyer remorse is endemic SADS but true 🐑💉🧪🦠🧬⏱💣💥

I love catching up with you. Despite your trials and setbacks, you fight like a champ and always stay hopeful. You are awesome.

This didn’t age well

I get botox injection

kzfaq.info/get/bejne/qJZgd9GDp7u1hY0.html

Pain

I wish I found this years ago I was in an accident too in 2012. It caused a relapse. I wasn't diagnosed until 2017.I have the same issues with mascara, walking drinking talking and shaking. Thank you for posting this.

hi are you still doing videos?

For me personally, this particular symptom is hands-down the #1 Most distressing, uncomfortable, and nefarious of symptoms (of many) that I experience w/ MS. In my personal journey with the MS hug, it's not just a singular sensation of feeling like I'm being squeezed. And most specifically, my MS hugs have evolved to the point where there's a tendency for this symptom to encompass the entire area from just below the clavicle, down to my groin area. As the 'episode' intensifies, it get's to the point where I almost feel like I'm going to explode. The best way to describe it is the sensation that my entire chest and mid section is expanding to the point of bursting. Much like what happens when you fill a balloon with too much helium. And this sounds silly, but I become instinctually driven to remove clothing in the attempts to relieve pressure. 1. The chest pain unto itself is terrifying. And I've lost count how many times the Doctors have ordered chest x-rays, EKG's/ECG's, Troponin blood tests (a blood test used to see if you've had a heart attack), CT scans, etc. It got to the point where I told them, " My EKG/ECG is going to be normal. My Troponin levels are going to be unremarkable, and If you guy's give me one more chest x-ray and ct scan I'm going to become radio active." 2. My MS hug episodes will peak. And at this peak of any given episode I'll start getting intense pinching electrical shock sensations throughout various parts of my body. They're so startling and painful that it takes my breath away. Compared to the feeling of getting the wind knocked out of you. Complete w/ dizziness, near syncope, and my leg buckling at the knee. 3. I start getting cognitively confused and unable to concentrate. 4. The epic pins and needles sensation starts creeping in and spreading. And although it's an almost constant symptom of mine with MS = During an MS Hug episode in particular, it Intensifies. Frankly, during an MS Hug episode, labeling it 'Pins and needles' puts it mildly. It's more comparable to the velocity of a torrential down pour of rain impacting the ground (or your car windshield). It stings. One day during an MS hug episode, I literally felt it creep up from the front base of my neck up to (and around) the underneath of my chin and head. Followed by numbness. Again, It's hands down the most insidious sensation I've ever had the misfortune to endure. 5. You intuitively understand that it's ravaging your body.

kzfaq.info/get/bejne/eZOogMqrqNbNd3k.html

I was diagnosed while trying to conceive, less than a month before I conceived my first. My neurologist was optimistic and told me that pregnancy was protective for MS. I had two children three years apart, breast fed both for a year, and only got on medication after my second child weaned, so that was at least 4 years after diagnosis. I was lucky not to have any relapses after birth, but have been pretty lucky in general with my MS. (And the oral medication I take now is working for me.)

Glad ur ok. Has your doctor ever talked to you about vitamin B1 deficiency and effects on Myelin Sheath?

💪💪💪