Thank you for sharing your story!

Hi there Izzy, great to hear from you again. May God bless and keep you and all those who suffer from this condition.

Hi Izzy, thank you so much for uploading your videos. Just seeing another person in a similar situation being so upbeat through it all helps immensely. I hope you're doing well.

Hi Izzy!! Thank you so much for sharing your story with us! You've been incredibly helpful.

Thank you for posting this. After a downhill battle with my Ms this year, I was moved on to tecfidera previously from Copaxone and they've just taking me off the tec, planning to put me on tysabri. Went to the MS Clinic yesterday and my wonderful neurologist has decided along with me that lemtrada is the best course of action for me. Just waiting for bloodwork to come back and I'll be getting signed up for my first round of treatment.

You are beautiful inside and out. My niece was just diagnosed at 48 with this form of MS, and I have been trying to get some information. You are so candid and honest. We all have different journeys. Thank you for being so vulnerable to share your story to help others. A true angel.

Thank you for your transparency. This is very helpful with my choices.

Thanks for the upload!

I also wanted to say thank you for sharing this, I realized most people don't talk about their experiences with ms meds so it was difficult when the neurologist told me to research them and choose one, especially when they all are known to have some form of nasty side effects. I appreciate it!

You are such a beautiful person inside and out, thank you for helping me feel like I'm not alone ☺

Thank you so much for these videos.

Continued and great success and blessings to you.

Even with a rash you are quite beautiful and insightful. You're so uplifting I like watching your video because it keeps people strong. I was diagnosed with Multiple Sclerosis back in December so it's hard, but you make things great : )

Thank you for sharing your story.

Your so inspiring thank u for the videos they are helping a lot of people

I didn't respond to the steroid infusions and now my acne is so severe! Your videos help me a lot! Thank you for sharing!

I've had my first dose of lemtrada and due my second in November. Can't notice any difference atm still feel rubbish hope things get better ☺ ♡ coping with life being a single mum we can do it !!!

Thank you for sharing you’re amazing

i have to have an mri im sooo scared i keep getting excruiatingly painful optic neuritus in my right eye i get numbness onset suddenly in my left leg now and again i have chronic fatigue to the point all i want to do is sleep mood swings irritability depression anxiety which has been going on many years the eye thing has only started this year i have chronic back pain and get cramps in my stomach and legs and feet all of a sudden your such a brave young lady im 39 will be 40 this year my mum had a stroke and died at 44 my dad a heart attack my grandad a stroke my grandma heart failure god bless u going through all of this and thankyou for helping make me and many other people aware your so brave xx

Omg thankss befor one week i did the mri and the lp test it was really hard!!! It’s probably ms so it’s the beginning

Brilliant video - I admire you for uploading it :)

The BEST DMT out there PERIOD! I'm 6 months post round 1 feeling great. Keep up the great work

@19:21 was a nice cheerful surprise for you I bet. I really hope you get better.

Hi Izzy , looking at your videos , your looking so so much better each one , glad the lemtrada is working for you , mine started in July 2017 , and its feb 2018 and still waiting for treatment and meds . !!! where in the country are you that you managed to get treatment so quickly ?? glad its working out for you .

Hey Izzy! Thankyou so much for sharing your experiences with us. I just had lemtrada last week, as like you I got the rash and tiredness but wasnt half as bad as I thought. How did you feel after the week? I've been wondering around a bit dazed/drunk/ not quite with it I guess due to the drugs. How long did you still have your rash for? X

Lawrence here from Dinsmore Colony in Saskatchewan Canada I've received Lemtrada to it helped me big time

My year 2 is a bit late but can’t wait

Very informative! Thank you for sharing your story. I got diagnosed a month ago not too long after my 22nd birthday, and I recently started on tysabri. Best of luck!

Did you ever have infectious mononucleosis (also called glandular fever or mono) before you were diagnosed with MS?

Hi Izzy I also did Lemtrada and got 2 admit no change and only did the 1 treatment but have continued with blood and urine!

Did they use your stem cells too after nuking your immune system? I am looking for better treatment than tecfidera, and any advice would be amazing

I've been diagnosed 12 months and already been in a wheelchair my Ms is aggressive to I'm now waiting for my lemtrada which should be this month sometime really hoping it makes a difference x x

it's been 6 years since you uploaded this video. let us know if you okay please.

I seem to have VERY aggressive MS.. disabled at 27 with severe difficulty speaking and am not able to walk without a walker. I'm on Ocrevus now and it doesn't seem to be helping honestly

Hi is the treatment available in Uk where did you get the treatment Hugs

I heard that it’s the weeks after was pretty bad how was it for you

My doctor started talking about that yesterday day

Why exactly does it cause heavy legs?

Did injection is good to control ms or no?

Hi, did it affect your hair?

Hi Izzy. I just wanted to share my story... *I HATED MY M.S. AND MY LIFE* My classmates in college started bullying me coz they don't believe I do chemo or even have MS, all because "I look okay" I don't "look sick". Like, they expect me to waltz in class in a wheelchair with an IV strapped to me or something. I get taunted for having PWD perks since again, I appear okay. I have a high body pain tolerance and I'm pretty expressionless to begin with, so it didnt help. I was branded a Sociopath by my friends, and school became more difficult while recovering. I almost felt an inclination to EXAGGERATE my pain and sickness just to end the badgering. But, I'm a terrible actress so I kinda added more to the Sociopath assumptions. I love makeup and dressing nice, I like it since it makes me feel like I was never ill and a PWD, but they took this as a proof I lied saying "NO SICK PERSON WOULD CARE ABOUT LOOKING PRETTY OR HAVE THE ENERGY TO". I've had my seat poured with juice, my wallet emptied in my bag, getting shoved "accidentally", teased, punched or kicked "accidentally", etc. And it all started when I got diagnosed and I couldn't attend school as much since my body is weak but I still pass my subjects. I hated how I have something I couldn't CONTROL or even STOP. I lost friends and got enemies. I can't swim or do sports anymore (but I stubbornly tried but really cant). I just hated my life, I got more and more depressed and it made matters worse. My mother never had much to brag about me to her friends, but now when she finally mentions me it's that I do chemo, like it's a girl's night topic. My Dad had lower standards for me ever since I failed a subject once in college, now he just expects nothing of me because he says my illness is so spontaneous he doesn't want to get his hopes up. The only "good" thing I kept getting since M.S. was PITY like my sister does, but I never wanted it. I wanted people to think I'm strong instead, but I feel like I'm getting weaker each day. My symptoms are just getting worse each year, and the chemo is working less and less. Honestly, I'd settle with just being completely invisible. I thought of ending it all, but I remember how much loans my parents got for my treatments and chemo and felt like they've invested for nothing if I go. Healthcare here sucks, I went to an org that aids patients for discounts, and saw a Stage 2 Cancer patient get yelled at and intimidated by the interviewer all because she had messy paperwork. I realized I dont hate living, or my M.S. Its simply the unique bad circumstances that are consistently happening to me. And I cant control that. And it's okay to have things we can't control, it's not a punishment it's a challenge for willpower. I wanna believe that is true. That's all that's left that's keeping my sanity. Thank you as well for sharing. You look so healthy and well too. And I feel like I'm less alone in this.

Fasting ... for MS..Serrapeptase also .. research it✌️

Lemtrada doesn't work my girlfriend did it and she gained 25lbs in two days and she hasn't been the same since.