Montel Williams is a real warrior. He's an inspiration to MS sufferers everywhere and he's just a model human being. An example of what strength, discipline and perseverance can do in your life.
We miss his show! Thank you for the Military family assistance and your service! I am very happy you're well and speaking out freely for years. Continue to be a hero on many fronts!
Thank you Mr. Williams. I can remember while you were walking the red carpet your wife's teared face seeing you grimace because of your pain. Thank God You & Yours have days of smiles today. As a Disabled Veteran I have copied your steps towards keeping my illness @ level 1. God Bless You & Yours as You continue such a positive journey here on earth. HeavenLee Justice
I miss seeing Montel on TV. He was a great host. I was diagnosed with ms in 2014 but had had symptoms since 1991. I've had 2 major "attacks" and quite a few reaccuring symptoms and a few new ones. I've been on the same major med for it since '14. I worked my ass off until my body yelled slow down. MS has not stopped me, only got real with me so I could be real with myself. I did ALOT of research and talked to other people with it. I was a member of a.little group that met together to talk about.their lives with ms.
@debrareibsamen4068, wow, that's a long time to go from first having symptoms to diagnosis! Thank you for sharing. May I ask how old you were when you first started having symptoms? My daughter's first symptom was age 18, 1 month (is almost 22 now, doing well) but I'm always intersted in knowing how the "long-haulers" are doing and it sounds like you're doing well. Would you recommend some specific research we could look into? I have the Wahl's Protocol, Overcoming MS, and Best Bet diet stuff and she is also on a DMT but I'm not sure how effective it is but she's tolerating it well.
@@debraindxb I would say I was in my mid 30's when I had my first major. symptom. But whenever I think really hard about it there are little signs here and there that could have also been attributed to ms. My mom has ms as well, so I have been researching since I was in Junior high. I am 55 now. I will read anything that even remotely touches on ms. I am sad to hear your daughter has developed it so young. My mom was diagnosed in the late 60's. When I decide to research more I just "start from scratch" and see if there is anything new out there. I get a magazine called MS News (I think) it has very good topics and drs answers questions. I wish I could tell you more.
Natural cures won’t make anyone rich. Montel has a valid point. Also, lots of people believe their doctor’s expensive unnatural protocols before believing that something natural, cheaper, and simpler can cure them.
Hi Montel, you look the same as the day u said goodbye on your show. Glad to hear that you are still helping people all these years later. You are such a wonderful person. I too have an autoimmune disorder and have seen how quickly doctors are to prescribe medications or steroids. U have to listen to your gut and research yourself.
I've always admired Montel Williams ever since I was a kid. I read one of his books when I was like 12. Now I'm showing symptoms of a neurological disorder like MS for about 10 yrs now. I have a Brain MRI in a couple of weeks
I also have MS nd was told the same thing 20 years ago. I am now 69 and on no meds for MS for the last 4 years and doing well.. I just loss my husband of 50 years 1 year ago, and family and friends were worried bout me having a set back. yes you nee to have a mind set to get you through. You said and I believe I have MS MS does not have me.
@user-ni2bm4io6b I am terribly sorry for your loss. Thank you for sharing how well you are doing with managing your MS. My daughter, now 21, had her first attack at 18 and I constantly think about her future.
Mavenclad has done wonders for me. I went from blind in an eye, unable to walk and no feeling from the shoulders down to playing sports and moving around freely again. It will always be my MS treatment of choice to any one with MS I meet.
My father has MS and I am now 27 and I think I am showing symptoms, it could be paranoia, but I am scared. This man however, gives me hope. Thank you Montel.
@@Numb3rs40 Go to a neuro and maybe do MRIs. It's best to catch it early so you can get the right medication. I was diagnosed in my early 20s and yes, depression hits bad especially when they give you the flyers on how to treat MS and see people in wheelchairs smiling. My thoughts were "This is my life now..." but that was BS. Though, I blame my MS for all the women I could have dated that showed interest to me but other than that what can I do? Be a better person with my MS.
@@jonplaud I had an MRI done & It’s still not confirmed what’s going on but I see a neurologist in a couple weeks so hopefully they can tell me more. It’s good to hear from others with the condition tho especially men so I can see what their experience is like. I appreciate it 🙏
Incorporate a low carb/keto/carnivore diet and fasting. Selma did stem cell therapy. When you fast for 4-5 days on just water, stem cell production goes through the roof! People who have been diagnosed with certain cancers, have water fasted their cancer away completely. Not eating sugar, processed food, and vegetable/seed oils helps when you do eat, as does eating a diet that keeps you in ketosis, which is much more clean fuel for the body and the brain.
@@Numb3rs40, how did your visit to the neuro go? Sending you my positive thoughts. (Mother of a daughter with MS, Dx Oct 2021, first symptom age 18 in May 2020)
@Ozzie Crosby i was diagnosed 2 uears before my doctor started me on an infusion medication.....my balance was always off. Every time i walk in a straight line, my body will just go sideways and when go up ateps it got painful to bend my knees....i work at the gym 3-5 time weekly.....im omly 43....i am a little depressed sometimes... Because i know what can Potentially happen with this disease … but I'm going to keep the faith And pray everyday
Thank god for people like Montel Williams famous to help our military family’s my brother needs this medications after serving in active duty 9 years and tries his hardest to be healthy for his family but struggles a lot. God bless you all for serving our country like now my son 🙏🏽🙏🏽🙏🏽
Amen !!!!🙏🏻🙌 thank you for sticking up for yourself and military veterans and people who has PTSD!!!!! I have it , my sister has it not from military related
Thank you for putting him on air! So many news shows and mainstream media just put on these stupid stories without ever telling anyone what to do about it. Most, if not all, chronic disease (type 2 diabetes, Alzheimers, M.S., IBD, anxiety, depression, autoimmune, cancer, heart disease, etc…) is caused by the inflammation brought on by insulin resistance. The best and most efficient ways to decrease insulin resistance are a low carb/keto/carnivore diet and fasting. I’ve seen Montel speak before about this and he uses a ketogenic diet. At a minimum, eliminate sugar, all processed foods, and seed/vegetable oils. But to really heal, ketones are a great fuel for the body and fasting is terrific for healing, as well.
I wish I could be convinced. My daughter's first symptom, age 18, was day 5 during the month of Ramadan in which she abstained from food and drink from sun up to sun down for about 14 hrs a day. There are studies to support that fasting is not harmful but actually beneficial for MS but every year I hold my breath hoping she won't have a relapse.
Thankyou mr Williams for your inspiring words. Ill be finding out in a short time if i have ms. So far i have alot of the symptoms,and iv just been informed i have lesions on the brain. Iv just had the spinal tap,and next is the mmr of the spine.
Motels amazing there he is 3 medical universities supporting him he can afford using the P.O.Ns device $14,000 dollars to get it what normal M.s sufferer who’s health has declined badly enough to need this device can afford $14,000 on a device that will last a limited amount of time. They probably can’t even afford medication because they can’t even afford some pain relief pills. I bet the bed ridden sufferers love watching someone like montel brag about the help he gets good luck to him he’s worked and done incredibly well to get where he is but have a little compassion for those less fortunate
Please bring back your chat show well done montel you are doing great however you can afford every doctor in the world you have 3 institutions helping you and excess to the pons device that is $14,000. How can the average M.s sufferer afford that care when they can’t afford insurance? I would love you to go visit average M.S sufferers and look them in the eyes and describe how the pons can help them or how cbd can help them when they can’t even see a D.r because they don’t get enough money from disabilities health care in America only helps the rich. Have you ever considered how an average suffer feels seeing you get all this help bragging about the care they can get and hearing you telling them get up move your butt off the couch yet they live M.S without any health assistance what so ever. You have earned the right to the help you get no question but show the rest a little compassion imagine yourself in their shoes no fault of their own. Maybe do a show about care treatments for M.S or chronic illnesses that don’t cost money exercises using home equipment like chairs tins of soup as weights etc i think that would be the most helpful advice you could do.
Yeah you are right. Our healthcare system here leaves a lot of people to suffer and die and it is very sad. We are the wealthiest country in the world, but the weakest amongst us are left on their own. . .
The doctor saying you’ll need a wheelchair isn’t an insult, it’s how they protect themselves. If you get worse and the doctor promises you’ll get better, who is the first person that gets blamed?
Tradução pra português eu tenho gosto de aprender mas não sei inglês 32 com esclerose múltipla tenho 60agora preciso usar cadeira mas quando vou pra algum lugar que vou demorar muiito raramente
I have ppms 33vyrs. Every time i hear anyone on internet talking about ms. Look I look ok sitting and talking too. I want to ses those same people walk for few minutes. On camera
I love Montel, but I have trouble believing thus ptsd cure us as quick and easy as he says and the US military isn't using it to keep soldiers in service
What a liar!!!!!!What kinda Ms this liar has that nothing changed in his life?I used to work as a nurse and Ms is unforgiven,he woulda been all done by now.LIAR.
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Montel Williams is a real warrior. He's an inspiration to MS sufferers everywhere and he's just a model human being. An example of what strength, discipline and perseverance can do in your life.
yes absolutely. I have friends with MS. These folks become pure warriors!
What is his way?
Glad to see Montel doing well after the many years he’s battled MS. Keep the faith Montel.
His voice is so smooth I’m glad he is doing well ❤
I grew up watching his show after middle school and hs. Glad to see he's doing well. He really hasnt aged.
I love to see Montel... my MS trip began at the same time as his- he inspired me so much- after all this time im still kicking it- thanks Montel 😁
We miss his show! Thank you for the Military family assistance and your service! I am very happy you're well and speaking out freely for years. Continue to be a hero on many fronts!
I’m giving Montez a standing ovation!
Maybe try getting his name right?!
@@bluebluesky3170 Let me guess. You’ve never hit the wrong key…ever! Must be great to be perfect or in your case, living in denial!
Thank you Mr. Williams. I can remember while you were walking the red carpet your wife's teared face seeing you grimace because of your pain. Thank God You & Yours have days of smiles today. As a Disabled Veteran I have copied your steps towards keeping my illness @ level 1. God Bless You & Yours as You continue such a positive journey here on earth. HeavenLee Justice
I'm going to be meeting him in a few hours. Very excited!!
May God bless you Montel!!!!! You are looking great.
PREACH, Montel!!! Thank you for speaking out.
Sending love to Montel 🌹❤️
So inspired for not just MS, but for anything. This is where his star shines!
He never ages.
How amazing he looks! I remember Montel sharing his journey from the beginning, He has helped so many people with his support.
Everyone needs to watch this and share this. With others that have multiple sclerosis and P. T. S.D.
Please tell me what he said in the 1.35 about something he took
I don’t understand because my English not very good
What things or medicine helps him
He could be on to something y'all. Montel you're the man. A life time of research . 🧑🎓
He used RTM for PTSD wow he is such a blessing sharing his journey with others and there families
What is RTM?
I miss seeing Montel on TV. He was a great host. I was diagnosed with ms in 2014 but had had symptoms since 1991. I've had 2 major "attacks" and quite a few reaccuring symptoms and a few new ones. I've been on the same major med for it since '14. I worked my ass off until my body yelled slow down. MS has not stopped me, only got real with me so I could be real with myself. I did ALOT of research and talked to other people with it. I was a member of a.little group that met together to talk about.their lives with ms.
@debrareibsamen4068, wow, that's a long time to go from first having symptoms to diagnosis! Thank you for sharing. May I ask how old you were when you first started having symptoms? My daughter's first symptom was age 18, 1 month (is almost 22 now, doing well) but I'm always intersted in knowing how the "long-haulers" are doing and it sounds like you're doing well. Would you recommend some specific research we could look into? I have the Wahl's Protocol, Overcoming MS, and Best Bet diet stuff and she is also on a DMT but I'm not sure how effective it is but she's tolerating it well.
@@debraindxb I would say I was in my mid 30's when I had my first major. symptom. But whenever I think really hard about it there are little signs here and there that could have also been attributed to ms. My mom has ms as well, so I have been researching since I was in Junior high. I am 55 now. I will read anything that even remotely touches on ms. I am sad to hear your daughter has developed it so young. My mom was diagnosed in the late 60's. When I decide to research more I just "start from scratch" and see if there is anything new out there. I get a magazine called MS News (I think) it has very good topics and drs answers questions. I wish I could tell you more.
This was emotional. Montel Williams is a treasure.
Natural cures won’t make anyone rich. Montel has a valid point. Also, lots of people believe their doctor’s expensive unnatural protocols before believing that something natural, cheaper, and simpler can cure them.
Hi Montel, you look the same as the day u said goodbye on your show. Glad to hear that you are still helping people all these years later. You are such a wonderful person. I too have an autoimmune disorder and have seen how quickly doctors are to prescribe medications or steroids. U have to listen to your gut and research yourself.
I've always admired Montel Williams ever since I was a kid. I read one of his books when I was like 12. Now I'm showing symptoms of a neurological disorder like MS for about 10 yrs now. I have a Brain MRI in a couple of weeks
Just wondering how your results came Back ?
That’s the Montez we all know and love God bless him in his fight for his health ❤️🙏
Seriously, if you know and love him, why can't you spell his name right?!
I also have MS nd was told the same thing 20 years ago. I am now 69 and on no meds for MS for the last 4 years and doing well.. I just loss my husband of 50 years 1 year ago, and family and friends were worried bout me having a set back. yes you nee to have a mind set to get you through. You said and I believe I have MS MS does not have me.
@user-ni2bm4io6b I am terribly sorry for your loss. Thank you for sharing how well you are doing with managing your MS. My daughter, now 21, had her first attack at 18 and I constantly think about her future.
I wish you good health .. my daughter 22 years old had ms and always tired
Mavenclad has done wonders for me. I went from blind in an eye, unable to walk and no feeling from the shoulders down to playing sports and moving around freely again. It will always be my MS treatment of choice to any one with MS I meet.
I miss his voice on tv 😭 those were the days!
First thing that hit 👋 me… his voice 👐🏾
This man is an inspiration! God bless you Montel and please continue your positive journey!
My father has MS and I am now 27 and I think I am showing symptoms, it could be paranoia, but I am scared. This man however, gives me hope. Thank you Montel.
I’m 26 and possibly have it as well. It’s scary but I know things can be done and try to stay positive for the future
@@Numb3rs40 Go to a neuro and maybe do MRIs. It's best to catch it early so you can get the right medication. I was diagnosed in my early 20s and yes, depression hits bad especially when they give you the flyers on how to treat MS and see people in wheelchairs smiling. My thoughts were "This is my life now..." but that was BS. Though, I blame my MS for all the women I could have dated that showed interest to me but other than that what can I do?
Be a better person with my MS.
@@jonplaud I had an MRI done & It’s still not confirmed what’s going on but I see a neurologist in a couple weeks so hopefully they can tell me more. It’s good to hear from others with the condition tho especially men so I can see what their experience is like. I appreciate it 🙏
Incorporate a low carb/keto/carnivore diet and fasting. Selma did stem cell therapy. When you fast for 4-5 days on just water, stem cell production goes through the roof! People who have been diagnosed with certain cancers, have water fasted their cancer away completely. Not eating sugar, processed food, and vegetable/seed oils helps when you do eat, as does eating a diet that keeps you in ketosis, which is much more clean fuel for the body and the brain.
@@Numb3rs40, how did your visit to the neuro go? Sending you my positive thoughts. (Mother of a daughter with MS, Dx Oct 2021, first symptom age 18 in May 2020)
He looks wonderful! I miss his show!❤
i loved watching montel, his show was the best chat show , he is such a nice man glad to see him again xx
I have MS for almost 10 years and the source of my strength is the Lord. I don't know how I would've cope with MS without Him.
Favourite day time talk show host of all time! Love Montel Williams. ❤
I love this man!!!
Love you Montel 🎉🎉🎉
He's looking fantastic. ❤
He looks so good!
I was diagnosed on the 22nd of this year in March so he is an inspiration to me
Im going for a spinal tap on tomorrow. I'm hoping I don't have it. What were some of your symptoms?
@Ozzie Crosby i was diagnosed 2 uears before my doctor started me on an infusion medication.....my balance was always off. Every time i walk in a straight line, my body will just go sideways and when go up ateps it got painful to bend my knees....i work at the gym 3-5 time weekly.....im omly 43....i am a little depressed sometimes... Because i know what can Potentially happen with this disease … but I'm going to keep the faith And pray everyday
Montel, you look wonderful! God bless you!!!
Thank god for people like Montel Williams famous to help our military family’s my brother needs this medications after serving in active duty 9 years and tries his hardest to be healthy for his family but struggles a lot. God bless you all for serving our country like now my son 🙏🏽🙏🏽🙏🏽
Amen !!!!🙏🏻🙌 thank you for sticking up for yourself and military veterans and people who has PTSD!!!!! I have it , my sister has it not from military related
Thank you ❤️
Thank you for putting him on air! So many news shows and mainstream media just put on these stupid stories without ever telling anyone what to do about it. Most, if not all, chronic disease (type 2 diabetes, Alzheimers, M.S., IBD, anxiety, depression, autoimmune, cancer, heart disease, etc…) is caused by the inflammation brought on by insulin resistance. The best and most efficient ways to decrease insulin resistance are a low carb/keto/carnivore diet and fasting.
I’ve seen Montel speak before about this and he uses a ketogenic diet. At a minimum, eliminate sugar, all processed foods, and seed/vegetable oils. But to really heal, ketones are a great fuel for the body and fasting is terrific for healing, as well.
I wish I could be convinced. My daughter's first symptom, age 18, was day 5 during the month of Ramadan in which she abstained from food and drink from sun up to sun down for about 14 hrs a day. There are studies to support that fasting is not harmful but actually beneficial for MS but every year I hold my breath hoping she won't have a relapse.
God bless u bro.....
Montel. you inspire me…..
This man hasn’t changed since the 90’S how doesn’t he get old?! lol
Thankyou mr Williams for your inspiring words. Ill be finding out in a short time if i have ms. So far i have alot of the symptoms,and iv just been informed i have lesions on the brain. Iv just had the spinal tap,and next is the mmr of the spine.
Motels amazing there he is 3 medical universities supporting him he can afford using the P.O.Ns device $14,000 dollars to get it what normal M.s sufferer who’s health has declined badly enough to need this device can afford $14,000 on a device that will last a limited amount of time. They probably can’t even afford medication because they can’t even afford some pain relief pills. I bet the bed ridden sufferers love watching someone like montel brag about the help he gets good luck to him he’s worked and done incredibly well to get where he is but have a little compassion for those less fortunate
Please bring back your chat show well done montel you are doing great however you can afford every doctor in the world you have 3 institutions helping you and excess to the pons device that is $14,000. How can the average M.s sufferer afford that care when they can’t afford insurance? I would love you to go visit average M.S sufferers and look them in the eyes and describe how the pons can help them or how cbd can help them when they can’t even see a D.r because they don’t get enough money from disabilities health care in America only helps the rich. Have you ever considered how an average suffer feels seeing you get all this help bragging about the care they can get and hearing you telling them get up move your butt off the couch yet they live M.S without any health assistance what so ever. You have earned the right to the help you get no question but show the rest a little compassion imagine yourself in their shoes no fault of their own. Maybe do a show about care treatments for M.S or chronic illnesses that don’t cost money exercises using home equipment like chairs tins of soup as weights etc i think that would be the most helpful advice you could do.
Yeah you are right. Our healthcare system here leaves a lot of people to suffer and die and it is very sad. We are the wealthiest country in the world, but the weakest amongst us are left on their own. . .
For someone who has it. For decades, you would
Never know it
The doctor saying you’ll need a wheelchair isn’t an insult, it’s how they protect themselves.
If you get worse and the doctor promises you’ll get better, who is the first person that gets blamed?
I was diagnosed when I was 21
❤❤❤
Just like u said Montel. It's called greed
Tradução pra português eu tenho gosto de aprender mas não sei inglês 32 com esclerose múltipla tenho 60agora preciso usar cadeira mas quando vou pra algum lugar que vou demorar muiito raramente
I thought this was about MS and his health journey but it sounds more like a sales pitch for a PTSD holistic treatment protocol?
💯💕
I have ppms 33vyrs. Every time i hear anyone on internet talking about ms. Look I look ok sitting and talking too. I want to ses those same people walk for few minutes. On camera
He has MS also? 😮
yes...now it is spms...
Hey Montel do you Remember that Sylvia Browne predicted ALL THESE TRAIN WRECKS BEFORE SHE DIED🙄💔?!?!?!?!?!
2 Peter 1:3
Just a note, it's the height of ignorance to point at someone while in company.
Does he even age?
I love Montel, but I have trouble believing thus ptsd cure us as quick and easy as he says and the US military isn't using it to keep soldiers in service
MS doesn't affect his speech.
Cha-ching $$$$
Lmao 😂
Looks like instead of jumping in 2 feet, he jumped 6 feet in lol
What a liar!!!!!!What kinda Ms this liar has that nothing changed in his life?I used to work as a nurse and Ms is unforgiven,he woulda been all done by now.LIAR.
I love this guy he’s so informative & he did his research..Now look at him living proof to health wealth…