Living With Aggressive MS at 24 - Q&A 

You are so inspiring to me Izzy, your attitude is so positive and beautiful 💓💓💓

So glad I found this video! I have MS too I was diagnosed in December 2016

Don't have ms but have a rather nasty chronic nerve condition known as CIDP, enjoy watching your videos - you have the right attitude for dealing with this. I Myself have went vegan, and hammer the gym, has transformed how i have been able to handle this problem with no relapses.

Funny I did same too when first diagnosed. Researched and bought all kinds of supplements, therapies, etc etc. Now 5 years in i realised that no 2 people with MS have the same symptoms. So i just do me. I am toying with going vegan. I eat “clean”, raw, organic. I’ve just started going back to gym with a trainer 🏋🏽‍♂️- who’s speciality is rehab training. You’ve got to keep moving (or your muscles waste away, hence weakness in the body). Exercise is good for the brain 🧠. I use cannabis oil (don’t care whether legal or not - I know where to get it). I’m not on DMTs. Never taken because I believe it’s “poison”. I do drink alcohol now and again. It gives me confidence and I actually walk better (go figure). I also fast. And try to stay away from stress. Also i do the same as u when on holiday. I eat anything within reason because my tastes have changed, burgers, fries, cocktails (i love cocktails 🍸🍹). I’m doing good. I’m going to do oxygen therapy (Walthamstow). Anyhoo, I’m staying positive and loving life! 💕🤸🏽‍♂️

Thank you Izzy, I too was diagnosed With MS for a long time since 2006 until now. I am 54 gonna be 55 next month. I like your videos 👍

Hi! I love watching your videos! So much good advice. Happy holidays!

you have really kept me sane through my diagnosis Izzy! Sending you a huge hug. Who know's, maybe one day we will meet in the oxygen tank! (i think its a mask actually isn't it!)

Thanks for doing this video. It’s really great🧡

Love your videos,especially your 'what I eat in a day' x

This was such a fantastic video you covered so many subjects

Combivir or Duovir, probably only $50-100 a month or $300-600 a year.

Hey how do you know you had MS? I have anxiety but I’ve had a few tremors when waking up and had an episode a few weeks back where my left arm and leg were numb/tingly. I’m 18 and worried I have MS x

Thanks for sharing and it's always great to hear from others with MS. Have you had any other relapses? Are there any symptoms you see more frequently you deal with?

omg i missed the opportunity to ask a question! how long after your first relapse did it take you to fully be recovered? i also was paralyzed in my arm and leg like you!

Izzy do you struggle with muscle spasticity at all? Mine has become so painful daily. I exercise everyday which does help and I eat a healthy diet. Is there anything you find helps? I feel like I’ve run a Marathon every morning that I wake up. Great to hear you are doing well on the Lemtrada. I have had MS for 2 years this month, and I’ve been on Tysabri infusions since then which has been working really well. X

Very informative Thank you for sharing All the best

Have you have any relapses since the last one that got you admitted? I'm considering suggesting lemtrada to my doctor but he say's my ms is too mild to go on it.

Try Plant based lifestyle You will be suprisse how your body will responde Vegan for the animals ❤️ A lots of love for you ❤️

Will the doctor aprove stamcell if lemtrada have been a positive outcome? In Sweden they only accept it for patients that are really bad

Lemtrada here is 165,000+usd

The best vitamin for me is Mykind

Ok I would just say it you look good and I appreciate everything you're saying♡😱👻🤧🤓

Thanks for posting

If you like travel you must come to Portugal n1 destinstion on the world

Does ms affect your relationship or your sex life I've only been with my boyfriend for 5 months and I'm in the stage of seeing if I have it I have a lot of symptoms

Love this video. Its great to know more of how you feel about everything

It's always the most attractive