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! 💕🤸🏽♂️
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!)
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.
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?
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
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!
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
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
![Lp. Сердце Вселенной #60 РОЖДЕНИЕ ЛОЛОЛОШКИ [Финал] • Майнкрафт](http://i.ytimg.com/vi/YoR0pAV9FVQ/mqdefault.jpg)
So glad I found this video! I have MS too I was diagnosed in December 2016
You are so inspiring to me Izzy, your attitude is so positive and beautiful 💓💓💓
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.
Hi! I love watching your videos! So much good advice. Happy holidays!
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 👍
Thanks for doing this video. It’s really great🧡
Very informative
Thank you for sharing
All the best
Love your videos,especially your 'what I eat in a day' x
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! 💕🤸🏽♂️
This was such a fantastic video you covered so many subjects
Aw yay so glad you enjoyed it!
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!)
Combivir or Duovir, probably only $50-100 a month or $300-600 a year.
Will the doctor aprove stamcell if lemtrada have been a positive outcome? In Sweden they only accept it for patients that are really bad
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.
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?
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
Add me on Instagram or something I'm also 18 and in the same worrying stage as you
My insta is abbiehoole
Abbie Crompton sure it’s auttxx xx
The best vitamin for me is Mykind
If you like travel you must come to Portugal n1 destinstion on the world
Thanks for posting
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!
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
Some people say that it does. For me it has affected my mental more when feeling confident during sex.
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
Try Plant based lifestyle
You will be suprisse how your body will responde
Vegan for the animals ❤️
A lots of love for you ❤️
Ok I would just say it you look good and I appreciate everything you're saying♡😱👻🤧🤓
Lemtrada here is 165,000+usd
😮😮😮
Good thing I have a great insurance
I got diagnosed when I was 16 I am now 24 and just heard of lemtrada last year
Because your health care sucks ass
Eric Brown what were your first signs and symptoms before your diagnosis
Love this video. Its great to know more of how you feel about everything
What's your favorite unhealthy meal?
It's always the most attractive