COLUMBUS, Ohio (WCMH)-Local doctor explains how Multiple Sclerosis effect the body. This is in response to actress Christina Apllegate announcing her diagnosis with he disease.
Right on. I’ve been dealing with this for months now and my doctor, the last time I went to see them, said everything was fine. But it doesn’t feel fine. I’m still dealing with the same old shit almost everyday.
@@coldblizzard5880 I’ve been told that I’m “fine” for six years. It was ME who figured out that it is probably MS. We’ll see when I see the neurologist in May. I’m pretty sure, though. I had no idea before but I knew I wasn’t “fine.” I hope you get it figured out!
Just as I started going through testing for MS, my wife of 15 years told me she's leaving. At first, I selfishly wanted to tell her so she might not leave. Now I'm glad she was able to sidestep this landmine before being permanently stuck with someone she doesn't love.
I’m so sorry. I just found out today I will be having testing done for MS. I’m very nervous because I know my husband won’t want to deal with this. Maybe we are better off ?
I think I have MS. I have a drop foot on the right side, and trick knee on the left. I have no strength in my left leg. Can not lift myself from the floor on my left leg. Numbness, tingling, pain twinges, electric shocks...I spent entire year seeing army of doctors and specialists. Had X-rays, MRIs, Brain scans, EKGs, nerve conductivity tests, 130 different blood tests...no diagnosis. No medications. Not a single doctor is in charge of this. I am just being passed from one to the next. Months go by between appointments. No one cares...I get my 15 minutes per visit and then get pushed out. I even went to ER twice determined to stay there until they find what is wrong. No, no such luck. They don't look for or treat the root cause. Only the symptoms... I am basically on my own...
my x didn't get any diag and had oper for numb arms that i thought was strange and the operation didn't help. seems he got real weak, couldn't even take out his garbage can or hook up the hose, other strange occurances also, finally years later was diagnosed with hydrocephalus, had a brain shunt put in and still not doing too well, numbness in both arms and now legs occured, just a thought
to the people here not understanding why they cannot get diagnosed with MS -- my neurologist told me there are OBJECTIVE and SUBJECTIVE symptoms. read about that...i didn't catch his meaning first time. now i do
It took almost a year and multiple ER visits for a doctor to believe me. Crying tears of joy because someone finally believed me. MRI next and blood work
So true...I literally thought all my ms symptoms were all in my head, because every doctor kept dismissing it for every other thing under the sun..It took multiple visits to ER and then outright refusal to leave until they got me an on-call neurologist and mri.
All thanks to Dr.Auchi on RU-vid for cured me completely from Multiple Sclerosis diseases, if you are there suffering from Multiple Sclerosis disease you can kind visit is RU-vid channel ru-vid.com/show-UC6tA16t1IlKx1bY93lc2rcg for a solution✅✅🙏🙏🙏
I held off getting checked for multiple years…. I’m 37, male, former bodybuilder… it took me dropping 40lbs in almost to finally go to the doctor…., I spent months in the hospital because of a car accident when I was 16….. because of that I avoided doctors…. I could have known about this probably at least 5 years ago…. It’s good timing for a diagnosis like MS but my family and myself could have been better prepared…,
All thanks to Dr.Auchi on RU-vid for cured me completely from Multiple Sclerosis diseases, if you are there suffering from Multiple Sclerosis disease you can kind visit is RU-vid channel ru-vid.com/show-UC6tA16t1IlKx1bY93lc2rcg for a solution✅✅🙏🙏🙏
@@loveydovey4u primary progressive MS…. Between muscle atrophy and muscle wasting from not using due to no energy, bowel issues on top of a small bowel reduction due to a car accident previous…. I thought I was going to die before it was figured out…..
I hope a cure can be soon found. Each time are more people with MS. Autoimmune illnesses are horrible. :-( and it's also difficult cause doctors don't believe you, don't listen, sometimes don't know them.
Going through this now I have every symtopm that says MS asked my doctor first this he said is its due to weight gain and a ear infection, I'm like I have numb and tingling toes ,They don't believe you sometimes, Gave me a blood lab for diabetes
Doubtful a cure will be found as most of its sufferers are women. Which can keep the flare-ups at Bay apparently but what's the damage is done apparently it's done and because Ms presents differently in every single person it's really hard to pin down and diagnose the most you can do is get an MRI of your brain and spine. I'm 47 I was diagnosed a year or two ago and it took being so bad that they thought I was having a stroke they did the right tests and realized it's not a stroke it's MS and I've had symptoms for decades
How I wish more videos and media would educate doctors, nurses and the everyday public about MS. It’s surprising how many healthcare professionals are clueless about this disease. Back in February, I had surgery for Thyroid cancer. Anesthesia does a number on the brain, especially post-op. I had severe tremors, and a group of nurses accused me of being an alcoholic: completely humiliating. Even though I kept emphasizing I have MS, they wouldn’t stop. I don’t want special treatment, just for medical personnel to educate themselves, and for others to realize we’re not lazy.
I also have Multiple Sclerosis I am a male and this is something that is no joke at all and dose need to be taken serious by all walks of life Noone needs to have it and the cure of it needs to be made more .I would want you to deal with something that will hinder you in your life at all this sickness 😷 is something but a thing that is and needs to be dealt with .thank you
“In MS, the CSF total white blood cell (WBC) count is normal in about two thirds of patients and less than 50 cells/µL, with rare exceptions.” According to AMA Journal of Ethics.
I need big data on the stories of people experiencing MS symptoms. There's a little stuffy on symptoms, a little bit on medications, but nearly nothing on causes. What makes our immune system attack what it should leave alone?
I have had all of these symptoms and my doctors have been saying there is nothing wrong with me. At one point they said I have Hypothyroidism and put me on thyroid meds but honestly those havnt helped. How can I get my doctors to test me for this?
Auto-Immune Hashimotos Thyroiditis can truly mimic MS so they definitely need to also rule out this disease before assuming it is only the low thyroid causing all your symptoms!!
I’m so tired of the medical field. I’ve had something wrong with me for years here lately it’s gotten really bad I go to the hospital they told me there’s nothing wrong with me. It’s anxiety about four years ago. I was having really bad stomach pains and I went to the doctor told me there’s nothing wrong I went to another doctor told me there’s nothing wrong. Finally I went to emergency room and they were getting ready to release me and I broke down and started crying and said I’m gonna die. I don’t know what the Hells wrong with me oh this woman did a blood test on me and they found it, my heart was being damaged. I had troponins in my blood so long story short they put me on blood pressure medicine which made me feel even worse. I start doing my own research and found that anemia and vitamin deficiencies can cause heart issues so I’ve started taking vitamins and I started getting better, but my symptoms of being tired I’ll be walking and my leg just feels like it disappears for a few minutes and I’ll try not to fall. I get tingling in my hands and the doctors keep telling me there’s nothing wrong with me and I know the difference between anxiety and something being wrong but apparently doctors don’t so I’m starting to suspect MS and I need to figure out how to approach a doctor so they’ll actually Tessman listen because you can’t just go get tested on your own you have to get a referral.
Walking myself was difficult for me because of my parkinson health situation but am happy that Dr Madida medicine on youtube I was able to get cured. Now I can walk properly🙏🙏
@@tomfletcher2345 this isn't a scam, if you have ran into someone who scammed you I will really say sorry that you had to pass through that but Dr Madida I know and that helped me is never a scammer and I have never seen anyone complain about him negatively. If anyone did anything bad to you, you should face that person alone instead of involving others that know nothing about it like Dr madida because he is a good man. YOU SHOULD STOP SPOILING OTHER PEOPLE'S NAME YOU HAVE NEVER SPOKE TO OR DID ANY BUSINESS WITH COS I DID CALLED DR MADIDA ABOUT YOUR COMMENT ON MY WRITE UP AND HE SAID HE DON'T KNOW YOU AND HAS NEVER IN HIS LIFE TALK TO YOU OR CHAT WITH YOU. YOU REALLY NEED TO STOP ALL THIS YOU ARE DOING.
It takes 6 months to see a neurologist. You regular doctor just wants to give you drugs. I waited 2 months and I still haven't been scheduled to see the neuro doc. It's really criminal.
The symptoms I have are tingling in my 4 limbs on really bad days. But always my left foot that goes up my shin I’m either freezing or sweating When I wake up I’m ok. When I start moving the pain starts. I can feel it spreading. It feels like I have razor cuts all over me and someone’s poured acid on me I have no strength in my hands and some days I can hardly walk I am exhausted when I try to eat breakfast. So tired I can’t feed myself. I’ve had insomnia for years but thought that was always bc of my other meds. I have double vision when I look at lights. Street lights. Screen savers. Etc My drs have been saying it’s neuropathy from diabetes for the past 2 yrs. I don’t think it is. It started over night. I was fine. I work up the next day and my feet were burning My drs keep pushing me off and just say take more of the pain meds you have if needed :(
All thanks to Dr.Auchi on RU-vid for cured me completely from Multiple Sclerosis diseases, if you are there suffering from Multiple Sclerosis disease you can kind visit is RU-vid channel ru-vid.com/show-UC6tA16t1IlKx1bY93lc2rcg for a solution✅✅🙏🙏🙏
I have been diagnosed with fibromyalgia however I’m getting nerve flicks in neck tinging in 👄 I can’t use left arm properly and struggling with balance and tripping it’s now effecting my work unable to get pip forgetful with my appointments what’s the difference in ms and fibromyalgia as I do think I have ms
MS symptoms are weird. They vary from person to person and they come and go. It’s crazy making and doctors are unlikely to put it all together, in my experience.
My sister is 32 years old and she has suffered from meniere disease for years and she always complains to me that I had to bought her Dr Madida herbs I saw on RU-vid and she is telling me last month that she is cured completely and don’t long have the symptoms like vertigo or dizziness, feeling of fullness in the ear or ringing, hearing loss, imbalance, motion sickness, nausea, or nystagmus
I was in the middle of sexual intercourse with my girlfriend while she was on her back on I started feeling numb all over my body and I laid back and could feel or move anything while feeling the tingling and needle type sensations in my lower body and legs. My lower spine had this numbing sensation and I was panicking while I felt cognitively dysfunctional like I could think and my vision felt weird but was fine for the most part. Im a healthy 22 year old and praying I don’t have such a scary disease. And feedback would be welcome
Could be spine related, sounds like you need an MRI, maybe lumber puncture. The MRI will likely be a contrasting one to look for white lesions related to MS as well as looking for issues in your spine. ❤
There is a possible connection between EBV, MS and hashimotos disease. I have just been diagnosed with EBV and hashimotos and undergoing testing for MS after 15 years of issues which have been misdiagnosed several times. I believe research for the connection is ongoing
People have been getting MS way before fraudulent people with no medical background started blurting out "iTs the jAb!" like they have tourrette syndrome.
Due to the limited studies on Coof vax, specifically, it's too early to tell. And if there were, doubtful it would be made public en masse. Censorship of other qualified virologists without anything to gain or maintain but clear consciences, have been silenced.
Hi I would like to know why we don't see more research with foods and supplements, once we can find in Pubmed, basic research about MS, in animal models, etc. , still without scientific foundation, but that deserves trials in humans, once are foods and natural supplements, that can have side effects, but under medical supervision, in controlled trials. the doctors can do safe research, (and randomized double blind) i with ginger, genistein ( or even soy), curcumin, etc. (in the site of Pubmed or even in Google, when we do some search with the words multiple sclerosis and ginger, or genistein and multiple sclerosis, or curcumin and MS, or Boswellia Serrata and multiple sclerosis, we can find the research articles. But all these supplements can have antiplatelets mechanisms, and can causes coagulation disorders, between others side effects. Please, this is not a prescription and in no way a suggestion to use such things. It is only a question to the doctors of this channel. Do not takes none supplements, once all can cause side effects and have interactions with medicine drugs that the patient is taking , etc. No one never would try to treat so serious disease as multiple sclerosis with such foods or supplements without medical supervision and prescription. Only the doctor of the patient can gives the prescription of foods, supplements and drugs to patients with any disease, and mainly MS.
With natural supplements I was Cured totally from ( M.S ) within 17 days of taking DR RORPOPOR HERBAL on RU-vid medications. Thank you for saving me.......
