I am a musician and vocalist it’s been a battle to get back to things hanging on

I’d love to see how Kerry and Paul are doing now.

Your podcast was most informative. I am South African and was diagnosed with MS six years ago. I might really have had it for many years before. As I shall be turning 80 in 2024 my MS diagnosis, after many frustrating years and many doctors appointments, was a relief, and even though at the moment it is difficult to walk, talk or write, I'm able to look after myself and my four dogs, who are my constant companions. What I find distressing is listening to young people who are dealing with with this disease and I really hope that there will be a treatment breakthrough in the near future. I prefer not to take prescription drugs but CBD drops seem to help me. Good luck Gareth and hope things go well for you.

All thanks to DR ALAHO OLU on KZbin Channel who finally cured me and my wife from MS and ALS. He cures HPV, HSV, Lungs Disease, Cancer, HIV and many more.🌱🌱

All thanks to DR ALAHO OLU on KZbin Channel who finally cured me and my wife from MS and ALS. He cures HPV, HSV, Lungs Disease, Cancer, HIV and many more.🌱🌱

Thank you for sharing your journey. My husband has not been diagnosed but he has many symptoms and is waiting for another MRI (reverse) & will be referred to an MS clinic for a second opinion. Praying for you 🙏♥️

Doesn't breast milk contain endocannabanoids ?

Dave Watson worked for GW pharmaceuticals and gave them the genetics that make up Sativex. Dave Watson is also known as "Skunk Man Sam" . A Doctor really shouldn't use the term "Strains" when it comes to cannabis . Variety or cultivar is far more applicable. Eric is excellent and he's correct in his knowledge on terpenes. Terpenes modulate the cannabanoids, so some could make you more sleepy or some more energy, or some could make you hungry or less hungry etc. It's complex as it's not one size fits all. Some patients will respond differently to various cannabanoid and terpene ratios

How much is a monthly prescription for Sativex ?and how much would it cost a patient to grow plants with a profile that suits them the best ?

Going on 13 yrs with rrrms...not fun..hope the best for you.

Snooker

Thank you for video. Very informative. Yes, buy a bungalow. I know you don’t want to think of being disabled, but living in a bungalow will make your life easier and make you more independent, if, God forbid you ever need to use a walker. I have fibromyalgia and have flare ups where I can’t get up stairs. The least amount of steps or stairs you have to deal with as you get older, the better. It just makes everyone’s life easier. Good luck for the future. You have a very positive attitude, so you will do fine. ❤️🇨🇦

Thank you for sharing.

Please watch living proof with Matt Embry. God bless you 💜

KZbin Alan MacDonald : MS is a parasitosis

I can totally rely on what you says, Emma..! It's the same to me

kzbin.info/www/bejne/e3m5iX2meaeWo7c

In this video, Alan Macdonald, FCAP, A pathologist from Florida, and a well respected researcher goes over some impressive findings regarding Spinal Fluids of patients with Multiple Sclerosis. In particular, nematode worms observed under Dark Field microscopy, or even with the naked eye. kzbin.info/www/bejne/e3m5iX2meaeWo7c

KZbin Alan Macdonald: MS is a parasitosis kzbin.info/www/bejne/e3m5iX2meaeWo7c

Hello from New Zealand 🇳🇿

Thank you, Naomi! I have been diagnosed a couple weeks ago, am 47, and have the same experiences with my arm. I take what you said about the impact of stress on MS very seriously. Best from Germany

Very inspiring! Thank you!

I just want to say to all the people who say look into diets for MS, there is no actual scientific backing that says that diet will definitely change MS. As someone with MS myself, 29 years old and my brother and my mother also have MS, it is actually mildly annoying to hear people tell me to look at my diet for MS. I for one, do not appreciate being told by someone who is not medically qualified, telling me to change my diet to help my disease. It also makes me feel worse about having the disease. It makes me feel as though I should be so desperate and feel so hopeless as to crave someone's advice who is not even a medical professional about my disease. The truth is, we don't know what causes MS and we don't know what helps it apart from stopping new lesions on the brain and spine with medications. Some people have benefited from diet, some have not. I don't want you to try and fix me, I want you to realise that medications today stop new lesions on my brain and my spine and that being a young person with MS is not like it used to be. I don't want to be a burden placed upon you and my family, I don't want you to pity me and feel sorry for me. I just want you to say "that must have been hard to be told that you have a disease." Yes it was very, very hard... but other people get told much harder things, for example that they may not live to see a future. MS is a disease, yes, but it does not mean that we have no future, it does not mean we will be in a wheelchair, and it does not mean that we will be a burden on society and our families. MS is changing rapidly and MS does not define anybody. MS is not the worst thing that can happen to somebody. Please help me change this stigma about MS in that not everyone who is diagnosed with Multiple Sclerosis is going through the same thing or is going to undergo the same journey. People with MS are people like anyone else. There is no direct path for them. We experience the hurdles of life just like anyone else. We will have up's and downs, but we are just people like anyone else.

My daughter had been diagnosed with autoimmune multiple sclerosis. She's been hospitalised for the 2nd time and today She had seizures and was taken to the ICU. They did MRI and ICU doctor said they found a blood clot on one of the vessels in the brain so now they going to do a CT scan to zoom to the exact place and start my girl on blood thinning medication. I am going through so much and can't stop my tears and I have been praying for her. I love my daughter very much!

My daughter had been diagnosed with autoimmune multiple sclerosis. She's been hospitalised for the 2nd time and today She had seizures and was taken to the ICU. They did MRI and ICU doctor said they found a blood clot on one of the vessels in the brain so now they going to do a CT scan to zoom to the exact place and start my girl on blood thinning medication. I am going through so much and can't stop my tears and I have been praying for her. I love my daughter very much!

I am from the US, but its so encouraging to know there are people like me out there. Thank you for sharing your story. You’re an inspiration to me.

Niami is there any Natural help for MS at your side of the world

Lawrence Hofer here from Dinsmore Hutterite Colony in Saskatchewan Canada Naomi looks like you Ms Beautiful are not from North America

I absolutely love the idea. Thank you for bring awareness. Having an ‘’invisible’’ disease isn’t easy. I totally would set up something like this, here in Alaska! If anyone has any advice on how to take something like this on- I’m all ears 😊 Thanks in advance!

😃 Great video!

Irish bloodline is strong.

Avances bio médicos regenerativos facebook.com/896399837043074/posts/3519697718046593/?d=n Esclerosis múltiple Caso liz Villanueva facebook.com/cientificomarioncamacho/videos/1767590836590632?vh=e&d=n&sfns=mo facebook.com/cientificomarioncamacho/videos/1911795905503457?vh=e&d=n&sfns=mo Refresh neuronal facebook.com/cientificomarioncamacho/videos/1902015503148164?vh=e&d=n&sfns=mo facebook.com/cientificomarioncamacho/videos/1924172514265796?vh=e&d=n&sfns=mo facebook.com/cientificomarioncamacho/videos/1924156850934029?vh=e&d=n&sfns=mo facebook.com/kary.camacho.52831

Ian O'Reilly, loved the Zoo film. What beautiful eyes you have. My daughters fallen in love with you.Hope to see you in more films.

Every symptom of MS occurs with Neuroborreliosis. The MRI of the brain in MS and Neuroborreliosis are identical. Proper testing confirms the infection. Appropriate antibiotics CURES !!!

Did you coming here?

Actually, the isolation of alpha tocopherol was the biggest mistake in nutritional history. The following video describes this mistake in detail as well as why it failed as an antioxidant and causes higher mortality rates.kzbin.info/www/bejne/jGrdeZmJfrWXidE

This centre means everything to me i love going there and I've made so many friends enjoy every minute of my stay

I was diagnosed at 12 ....It was the hardest thing to deal with but im finally at a stage where I've come to terms with it and I'm learning to live with it ....my way...it gets easier and better :)

Margaret and Deirdre will be sadly missed.

so Lady how do you manage fatigue

Zidovudine keeps EBV in check: www.sciencedirect.com/science/article/pii/S2211034818300828

Thank you for this video ❤

A woman talks about the natural method by which she cure multiple sclerosis. kzbin.info/www/bejne/nWa9fJV-abFja5Y

Thank you, Kerri

I have had MS since 2002 and Im still walking praise God!! Not so stable somedays. Yes working out is the best. I use to teach and learned that it is a cool for your body and swimming is excellent for my MS! I no longer teach, im grateful I learned about it. It helps my modify my life, learned to slow down and not rush!

Me no superhero like u dear. Lend me some of ur spirit. My surrounding is all ignorant not helpful. Feel like I am alone :'-(

It is hell yeah . Life gone to waste unfortunately

yea bizarre is right tell me about it. over 3 years of intertractale hiccups 24\7 with all the Joy's of little sleep, puking into my mouth every 10 mins, having to eat my sick till it digested and being unable to breath at times and passing out when they went into machine gun multi spasm per second mode . Yes MS can do "anything" to you symptom wise . all good for now for now after i stopped them myself .

HSCT

I’m