I am in the positon of having symptoms of MS and my Doctor has said like you have that the symptoms are similar in several other conditions. However, he has referred me to an Neurologist and am awaiting an appointment for an MRI and Catscan. Thank you for posting this video. It made me feel better knowing that the infromation I have been told is right.
I'm 21 and the same is for me right now. Ive been getting tested for thing like RA and Ankylosing Spondylitis. Anytime I've mentioned a possibility of MS i've been kind of shrugged off...I used to work around solvent based chemicals in a wood finishing booth and have used wood and model solvents since I was a child. We didnt always use the most worksafe of techniques, i now regret every second of not wearing a vapour mask. I have even told them this and they will not listen.
@jessica164 I know how it feels and I'm 39! It sucks when they think it's all in your head. Thankfully I now finally have a dr who listens and is trying I think even if she keeps harping on saying it's depression lol
If you’re diagnosed with Multiple Sclerosis, cheer up because the cure for MS is already discovered, and it’s called “CCSVI,” or “The Liberation Treatment!” This cure was discovered by “Dr. Zamboni!” You can search this here on You Tube. Just search: “CCSVI,” and/or “The Liberation Treatment,” and/or “Doctor Zamboni!” You can also log on Facebook and check”CCSVI in Multiple Sclerosis!” Feel better!
I'm pretty sure I have MS. I've been having so many problems that have been associated with MS for the past year and I've just been told I'm faking it for attention because I'm only 17. I am just so frustrated with all of this but my only chance for a diagnosis is seeing a neurologist which is over 4 hours away.
Thank you for making this video. I don't know what I have, but I finally found a general practice doctor that said if I don't have MS, then I definitely have a neurological problem going on. On top of my symptoms, she was able to see from the tremors in my hands, and a test she did on my eyes. She told me my pupils flutter, and said I need to see a Neuro asap. It has taken me a long time just to find a doctor that is showing some compassion to what I'm going through.
@Mojosfire yeah i know the feeling, some Dr's are heartless gits! My Dr i have now is amazing, even texting me to see how i feel! wishing you all the luck!
@stopbeingnasty Thank you for your response. Well the doctor I have was very different the next time I saw her, even though I hadn't seen the neuro or anything then. She was rude, and wanted to rush me out the door. I think it has to do with being on state health insurance. Anyhow, I finally got to see a nuero. He ordered an MRI, not a spinal though. He said my reflexes are abnormally brisk, whatever that means. Anyhow, he was very unfriendly as well. I'm tired of cold hearted doctors!
I thought I had sciatica, but ended up diagnosed with RRMS. Then, 3 years later, I was diagnosed with sciatica after all ha ha. They think maybe the MS caused it. I've made a video about this. The waist-down symptoms are very similar...
I thought you was 17 :) hey its nice to see a new Video from you, It's also very good that you explain (and try to avoid hypochondriac people, jumping on this). I sympathize with you with respect to medical people/Doctors/Practitioners not having a clue, or misdiagnosis. Its live a never-ending fight (in more ways than one) .
Well, You are still very Beautiful, and I wish you strength, from one who knows "what it feels like" I can only share my love and heart with you.
thank you for the video.. I only had an MRI 2 years ago and never had a spinal test. my neuro sent my MRI off to a MS speacialist hospital. Should i ask my neuro for Spinal tap?
WebMD is a horrible place to go for information. They tell you to ask your Doctor about medications. WebMD accepts no treatment advice that doesn't involve being on a drug. When will America wake up and see that the people teaching us about our ailments and how to fix them are tied directly to the multi-million dollar drug companies. Our future med students are being taught to sign a script and get you on medication.
Good video sweetie {{{{{{{HUG}}}}}}}, sorry, it's just been so long since ive seen you. You mean a lots to me, i found you on here when i first was dx'ed with MS and you pointed me in some good directions so thank you. As for spinal taps, never again will I do that, and I have told my Doc(s) that. It went bad for me.
Do you get it where your friends.notice possible symptoms in themselves and then grill you on MS? I think in some cases it's an attempt at connection. I've gone to handing out my Neuro's card when they ask.
You don't have MS.
Your doctors and brain are telling you that you have it but you don't
You have mercury + other heavy metals in your body.
EVERYONE DOES. It's in our food, land air, ect.
Get a full heavy metal test @ a wellness centre and you will be SHOCKED at the results as heavy metals are causing your symptoms.
Why do you think I would take so much time out of my life to help people?
Because, I care and I know I can help you.
Just go and get it done? It's so simple!
vancouverislandbass 3 months ago
These are real MD's doing this research and not quacks by the way.
Do a google search on the Wheldon protocol and then do a google search on
Paolo Zamboni MS
SevenThunderful 4 months ago
I wanted to post a possible cure but you tube won't allow it sorry.
SevenThunderful 4 months ago
I am in the positon of having symptoms of MS and my Doctor has said like you have that the symptoms are similar in several other conditions. However, he has referred me to an Neurologist and am awaiting an appointment for an MRI and Catscan. Thank you for posting this video. It made me feel better knowing that the infromation I have been told is right.
TFS
Tracy x
Paganmaiden 5 months ago
I'm 21 and the same is for me right now. Ive been getting tested for thing like RA and Ankylosing Spondylitis. Anytime I've mentioned a possibility of MS i've been kind of shrugged off...I used to work around solvent based chemicals in a wood finishing booth and have used wood and model solvents since I was a child. We didnt always use the most worksafe of techniques, i now regret every second of not wearing a vapour mask. I have even told them this and they will not listen.
SamuelRICHARDable 9 months ago
If you suspect you have MS? Insist that you need an MRi scan! so there will be no dought. YOU NEED TO KNOW THIS?
Richie979 9 months ago
@jessica164 I know how it feels and I'm 39! It sucks when they think it's all in your head. Thankfully I now finally have a dr who listens and is trying I think even if she keeps harping on saying it's depression lol
MissKrisNails 11 months ago
This has been flagged as spam show
If you’re diagnosed with Multiple Sclerosis, cheer up because the cure for MS is already discovered, and it’s called “CCSVI,” or “The Liberation Treatment!” This cure was discovered by “Dr. Zamboni!” You can search this here on You Tube. Just search: “CCSVI,” and/or “The Liberation Treatment,” and/or “Doctor Zamboni!” You can also log on Facebook and check”CCSVI in Multiple Sclerosis!” Feel better!
MSpinalcord 11 months ago
I'm pretty sure I have MS. I've been having so many problems that have been associated with MS for the past year and I've just been told I'm faking it for attention because I'm only 17. I am just so frustrated with all of this but my only chance for a diagnosis is seeing a neurologist which is over 4 hours away.
Jessica164 1 year ago
can you take hot showers when you have multiple sclerosis?
JonathanJGuevara 1 year ago
I'm worried that I may have MS and if I do, it really screws me up because I'm trying to prepare for a career in the Royal Marine Commandos.
proudwesterner2 1 year ago
@proudwesterner2 If you have it I suggest you don't inform them and you still go for your career.
guitarobsessed85 1 year ago
Thank you for making this video. I don't know what I have, but I finally found a general practice doctor that said if I don't have MS, then I definitely have a neurological problem going on. On top of my symptoms, she was able to see from the tremors in my hands, and a test she did on my eyes. She told me my pupils flutter, and said I need to see a Neuro asap. It has taken me a long time just to find a doctor that is showing some compassion to what I'm going through.
Mojosfire 1 year ago
@Mojosfire yeah i know the feeling, some Dr's are heartless gits! My Dr i have now is amazing, even texting me to see how i feel! wishing you all the luck!
stopbeingnasty 1 year ago
@stopbeingnasty Thank you for your response. Well the doctor I have was very different the next time I saw her, even though I hadn't seen the neuro or anything then. She was rude, and wanted to rush me out the door. I think it has to do with being on state health insurance. Anyhow, I finally got to see a nuero. He ordered an MRI, not a spinal though. He said my reflexes are abnormally brisk, whatever that means. Anyhow, he was very unfriendly as well. I'm tired of cold hearted doctors!
Mojosfire 1 year ago
borreliosis is sometimes confused with MS,and pple are treated like for MS!all the best
elEmulator 1 year ago
Thank god i don't have this, its lamer than cancer because it can't even be prevented, or can it?
HellFireUlisses 1 year ago
I thought I had sciatica, but ended up diagnosed with RRMS. Then, 3 years later, I was diagnosed with sciatica after all ha ha. They think maybe the MS caused it. I've made a video about this. The waist-down symptoms are very similar...
lovingfatalist 1 year ago
I think i have MS and my doctors play 2 many game
BELLA3905 1 year ago
I thought you was 17 :) hey its nice to see a new Video from you, It's also very good that you explain (and try to avoid hypochondriac people, jumping on this). I sympathize with you with respect to medical people/Doctors/Practitioners not having a clue, or misdiagnosis. Its live a never-ending fight (in more ways than one) .
Well, You are still very Beautiful, and I wish you strength, from one who knows "what it feels like" I can only share my love and heart with you.
Take care, K...
Innersymbiance 2 years ago
Hi,
thank you for the video.. I only had an MRI 2 years ago and never had a spinal test. my neuro sent my MRI off to a MS speacialist hospital. Should i ask my neuro for Spinal tap?
Oh im scared of having a spinal tap :P
Thanx
Omario
omexmc80 2 years ago
Nice to see a new video from you. Great advice.
Andrea
MSVlogSupport 2 years ago
You NEED a spinal tap.
Prissie28 2 years ago
WebMD is a horrible place to go for information. They tell you to ask your Doctor about medications. WebMD accepts no treatment advice that doesn't involve being on a drug. When will America wake up and see that the people teaching us about our ailments and how to fix them are tied directly to the multi-million dollar drug companies. Our future med students are being taught to sign a script and get you on medication.
ChucknMcNuggets 2 years ago
Great video Kelli!
vbeachy 2 years ago
Good video sweetie {{{{{{{HUG}}}}}}}, sorry, it's just been so long since ive seen you. You mean a lots to me, i found you on here when i first was dx'ed with MS and you pointed me in some good directions so thank you. As for spinal taps, never again will I do that, and I have told my Doc(s) that. It went bad for me.
WORRO01 2 years ago
Do you get it where your friends.notice possible symptoms in themselves and then grill you on MS? I think in some cases it's an attempt at connection. I've gone to handing out my Neuro's card when they ask.
jesterspace 2 years ago
MS symptoms are always different. What we have cannot be explained fully.
CyberPirate83 2 years ago
well my moms MS is getting worse now its her arms!
ionrocket 2 years ago
Yes I have MS since 1986. I commented on your previous video so go look.
zekest 2 years ago