Tearful Montel Williams pleads with Oprah Winfrey to continue talk show

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Former talk-show host Montel Williams broke down to Oprah Winfrey on today's show, pleading with her to continue her successful talk show beyond its 2011 run date.

Williams -- who hosted a long-running talk show for 17 years and is battling multiple sclerosis -- said when Barack Obama was elected president in November he realized for the first time that without his show, his voice wasn't going to be heard.

"Really think hard before you say enough. You owe it to us," Williams told Winfrey. "Even if you retire from doing this everyday, we've got to hear from you everyday."

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32 Comments

Please Please help me get a copy of the Oprah show w/ Montel speaking of his life living with MS. I want to show my family what I am living with daily. I cannot explain my MS but Montel said everything I want my family to hear. I have looked and looked on Oprah sights and cannot find a place to get the video. I will pay any price to get this information to my family. Please, Please help me.

I was diagnosed in May 04. I could mot walk and remained in a hospital bed for 6 weeks and a further 6 weeks with intense physiotherapy a total of 3 months not knowing if I was going to walk again.
I live in England and like Montel I to suffer from pain.
I had nerve block treatment for the pain and it is a great shame over here in England we do not have some one like Montel who genuinely expresses how they are feeling with great empathy from deep with-in one self and that not many people could express how they are feeling.
It's a shame Montel does not come over to England as we lack education in this department along with being 10 years behind if not more with treatment/medication.
Sad really I only got to know about Montel via Multiple Sclerosis sites after looking into my own way of controlling my condition?
I pray Montel gets to hear this message as being Asian I've found my own people choose not to listen to the truth out of their own ignorance.
love you Montel.
Raj Hayer

I was diagnosed in May 04. I could mot walk and remained in a hospital bed for 6 weeks and a further 6 weeks with intense physiotherapy a total of 3 months not knowing if I was going to walk again.
I live in England and like Montel I to suffer from pain.
I had nerve block treatment for the pain and it is a great shame over here in England we do not have some one like Montel who genuinely expresses how they are feeling with great empathy from deep with-in one self and that not many people could express how they are feeling.
It's a shame Montel does not come over to England as we lack education in this department along with being 10 years behind if not more with treatment/medication.
Sad really I only got to know about Montel via Multiple Sclerosis sites after looking into my own way of controlling my condition?
I pray Montel gets to hear this message as being Asian I've found my own people choose not to listen to the truth out of their own ignorance.
love you Montel.
Raj Hayer

I was diagnosed in May 04. I could mot walk and remained in a hospital bed for 6 weeks and a further 6 weeks with intense physiotherapy a total of 3 months not knowing if I was going to walk again.
I live in England and like Montel I to suffer from pain.
I had nerve block treatment for the pain and it is a great shame over here in England we do not have some one like Montel who genuinely expresses how they are feeling with great empathy from deep with-in one self and that not many people could express how they are feeling.
It's a shame Montel does not come over to England as we lack education in this department along with being 10 years behind if not more with treatment/medication.
Sad really I only got to know about Montel via Multiple Sclerosis sites after looking into my own way of controlling my condition?
I pray Montel gets to hear this message as being Asian I've found my own people choose not to listen to the truth out of their own ignorance.
love you Montel.
Raj Hayer

I was diagnosed in May 04. I could mot walk and remained in a hospital bed for 6 weeks and a further 6 weeks with intense physiotherapy a total of 3 months not knowing if I was going to walk again.
I live in England and like Montel I to suffer from pain.
I had nerve block treatment for the pain and it is a great shame over here in England we do not have some one like Montel who genuinely expresses how they are feeling with great empathy from deep with-in one self and that not many people could express how they are feeling.
It's a shame Montel does not come over to England as we lack education in this department along with being 10 years behind if not more with treatment/medication.
Sad really I only got to know about Montel via Multiple Sclerosis sites after looking into my own way of controlling my condition?
I pray Montel gets to hear this message as being Asian I've found my own people choose not to listen to the truth out of their own ignorance.
love you Montel.
Raj Hayer

Hi Montel,

Oh how I miss you. My sister also has MS and you are just such an inspiration to many. Like MS, I really wish there was a voice for VITILIGO like you are for MS. As a black person turning white, I know that this is NOT a major illness, however, MANY suffer in silence, many contemplate suicide and many go into hiding.Yes, this is cosmetics, but the suffering is still real. There is NO perscription break and NO make up break on the purchases that we have to make.

Stay well, you are loved!

Hello Montell! My name is Tina and i just wante to say it is good to see you. I didn't get a chance to see the show but my friend told me that she saw it and later went to a trigeminal neuralgia website and said that you were diagnosed with the disease.. I to have suffered with TN and it was the most horrific experience I have ever encountered. Trust and know that the Lord is with you and he will never leave you call his name and he will give you strength. I thought I was alone and God heard my cry I know he hears yours too. Just know that the pain is your testimony. He was bruised for our iniquities and transgressions.. Stay well.

I just heard that Montel was on Oprah.. I have MS and was diagnosed pretty much the exact time Montel was. I want to see this episode of Oprah. Does anyone know where I can see it?
Montel, I have watched you constantly and bought all of your books.
I feel like you are my MS Buddy.. we went through the painful diagnosis together and you kept me strong! PLEASE PLEASE if anyone knows how to see a rerun of this episode.. Let me know! I love Montel and feel like he is such an inspiration to me.

I do not understand why Montel is continuing to live with the Trigeminal neuralgia when there is a treatment available to help with that totally devastating pain. My husband was in the same place as Montel last year and we found a doctor at the University of Cincinnati who performed a micro surgery on the Trigeminal nerve and my husband is off of several of his medications and no pain in his face any longer. The pain is the worst part of MS next to the Fatigue. Dr Tew is awesome and has given my husband back to our family for the first time in 15 years. My husband is a Gulf War Veteran from Desert Storm, he is one of thousands of military who have developed this form of MS that is atypical and causes so much pain. Not sure where Montel served while in the military, but certainly I would think this could be related to his military service if he showed any symptoms during his time in the service. You can not imagine how many veterans have developed this form of MS that causes so much pain.

I also believe that families have to be considered in the treatment of MS patients as well as other patients with devastating disease. Please post this and enable others to learn more about the case management that enables families to be involved in treatment plans, keep families from falling apart and the patient feeling hopeless from the process, help them avoid suicide as an option. Doctors need to be more compassionate and willing to think outside the box to provide care for their patients that will help them have a quality of life, not just quantity. I went back to college to create a job for myself doing just this type of work, I plan to be a case manager helping people find the right treatments, regardless where the care is available and getting insurance to pay for the treatments to help the patient and their family have a quality of life.

Thank you and we love you Montel~

Thank you Montel Williams and Oprah Winfrey for openly discussing Multiple Sclerosis. I have MS, but only talk to my doctors about it. Friends and other people do not understand what it is like.

I stayed home from work to watch Montel speak about MS. I am 57 and have had MS for 18 years. I own my own business and work daily. No one understands the pain and fatigue because a lot of us look "normal" It was wonderful to see someone explain what it is like to live with this "unknown". Positive thinking is the best. Thank you Oprah and Montel for bringing this disease to the public.

Greetings from a fellow MSer.
My family a friends have all been contacting me to ask if I saw Montel on the Opra show. I regret that I am presently in a country where the power is unreliable and happened to be down when the show aired however thanks to the wonders of fibre optics from the mainland we rely VERY much on our internet service to stay somewhat informed re: world events.
I ,now age 62, along with my younger sister,was diagnosed in 1986. My MS has progressed very slowly. A few attacked have left my arms and legs numb but still mobile. My sister, on the otherhand suffers progressive desease and has been bed riden and in long term care for many years.
Our stories could fill a fair size book so I will ONLY mention for sake of space a few ways I manage to keep my core temperature cool so as not to become incredibly fatiqued and sick in the hot country I am presently in and where my husband a general surgeon live.
STAY COOL TIPS: wear wet clothes when possible and appropriate
Consume a thick slushy beverage which works wonders to keep your core cool.
Carry a spray bottle of cold water and last but NOT least DON'T, as I have learned to do,concern yourself with what anyone may think when you suddenly bolt to dive into that pool lake or ocean fully clothed,of course. Hey WE DO WHAT WE HAVE TO DO and provide along the way a few giggles from those who really don't understand.

God bless you Montel and thank you for your dedication to the MS cause.

Zestfully

Arlene Turner

I cried the day that Montel Williams was on Oprah. I have a muscle Diease that I had to come too face with. It is in the MS family, Myasthenia Gravis. It turn my whole world around. At 28, years old a mother of three children, and wife. I was given this death sentence by the doctors. They gave me less than a year. I cried and I felt like my whole world was coming down all around me. I would become helpless and would have to have someone to take care of me, like a child all over again. But, as that wasn't enough to deal with, my husband of 11-years decide he couldn't handle it and walk away leaving me with it along with three children, I thought about, why me? I consider killing myself, and all kinds of things, but, my mother & father came to my bedside and said " God loves you and we do too:.You will get through this. I was down helpless for 3 1/2 years, but with God's help and taking my medciine and prayer it has been 27-years and I am going strong! I do outreach work in my small town, I am a mentor to others that suffer with illness that they don't understand. It is a good thing to come out and let others no what you may be going through.I would love to get a chance to talk with Montel Williams, I think that he touch a lot of people hearts, when he showed a side of himself that no one had seen before. Arma Woods-Montrose, AR

I am so glad that Montell spoke out on Oprah. I was diagnosed with MS 4 years ago and from the beginning, I considered Montell as the standard by which I measured my own progress. Like Montell, I will not let the disease take my quality of life or my positive attitude. The best and first advice that I got from my Doctor was that my attitude was my most powrerful weapon in this fight and I believe that 100%. I kwas so happy to see that Montell and his famiuly are living so close to my hometown of Arlington and hope that someday I might meet him. Thank you for helping to explain this disease to others - it is unpredictable and difficult for anyone who is not touched by it to really understand what it is like to live day to day without knowing what course it will take but it is a wonderful lesson in taking one day at a time and enjoying every day that we have - good or bad

Get Martha Christy's book. It will make a difference. Also, do some reaserch on Colostrum. Using this supplement will help subside the symptoms and improve your immune system.
Healthyself
Ralph

i wish i watched it....

I wanted to cry when I saw Montell on the show today. He was so emotional and I could feel his pain. I wish the best for him.

I watched the show with Montel Williams. I have MS for 12 years now. I understand the pain to the point of wanting suicide as I myself attempted it. I found myself a parapelegic. Today there is no visual sign of MS and I have many days where I can forget about it. That's what he wants. Can you give me a way to contact him to share what can make a huge difference to his life.

Gabrielle

Montel, May God ease your pain and bless you with days, months, and years free of the torment and anquish that you have endured you for so many years. No one should have suffer as you have. I watched you today telling your story,and my heart aches for you. I will continue to be apart of your life and I will pray for you to receive freedom from pain. I watched the Montel show all the time and I cannot believe how well you presented yourself to the world. I haven't really experienced pain, but I have known many that have, so I am very compassionate to those less fortunate than myself. You are a wonderful, loving and caring man. May your days be brighter!

I also found out I have MS in 1998. I continued working until 2006 (29.8 years on the same job).
In the beginning of his interview Montel mentinoned extreme facial pain and I have been trying to convince my MS doctor and regular doctor for the last year that this has to do with my MS. He had a name for this disorder and I would really appreciate getting it from you. Between both doctors I have had 4 pain pills, seizure medicine and the lastest migrain medicine even though I have explained to them both that it is not like a headache. I have also been expericing extreme pain in both my feet which I believe begain in December 2008 after falling in the show and hitting my head extremely hard in the back. I noticed the facial and feel pain became more extreme after that. Any help would be so appreciated.

Montel- I have looked up to you for almost 8 years or more. I was diagnosed with MS when I was 19, in 2001. I am now 27 and watched you every day when you were on air. I would love to meet you in person one day just to give my appreciation because when I was the one with the gun in my mouth, or in my case knife to my chest, I thought of you and my kids. I figured if you could fight through the pain than so could I. Thanks for being such a good role model to me. Maybe one day we can meet, I hope so. You did awesome on Oprah today, it was such a good show.
I don't know if I did this right but the url above is my blog. I did not know what else to put.

HI I COUGHT THE SHOW A FEW MINUTES LATE TODAY WHEN WOULD IT AIR AGAIN THE DOCTORS ARE DOING MORE TEST ON ME THERE RULING IT MS BUT NOT SURE THOSE PAINS HE CRYED ABOUT ARE THE PAINS I GET AND CRY ABOUT THEM TOO AND I ALSO AT TIMES SAY WHY ME IF IT IS IT HURTS SO BAD THE TINGALING IN MY FEET AND LEG'S ARE SO BAD I HAVE IT IN MY HANDS BUT NOT AS BAD AS MY LEG'S AND FEET .I CRYED TO SEE MONTEL CRY

I love your show!!!!! I know you went to Africa and built a school for the children,that was very kind. My grandson,Tyler Middegaal is also going to Kenya to build a new school. He is now 16 years old. 16 other kids from St.Annes school are going aswell.They are leaveing July 1st. It is going to be a nice expierence for them.They will probably come with smiles on there faces.

Montel Williams rocks.
What a wonderful real hearted person.

"Former" should not be a consideration for either. What a loss to the public should such happen.

sincerely,
a consumer
:)


THANK YOU MONTEL FOR GOING ON THE OPRAH SHOW AND TELLING IT AS IT IS!!!!!I WENT WITH A GENTLEMAN THAT HAD MS. I READ UP ON HOW THE MYLIN GETS EATEN AWAY AND THE EFFECTS IT CAUSES, THE SIDE EFFECTS FROM THE MEDICINE, HOW THE HEAT IS NOT GOOD FOR YOUR CORE, ETC.. . . .THE DEPRESSION WOULD COME ON LIKE A CLOUD OVER HIM AND HE WOULD HAVE TO WORK ON GETTING PAST IT. HE WAS 30 YRS OLD WHEN HE GOT MS. BEFORE THAT HE WAS A GO, GO PERSON. I WOULD WATCH HIM SLEEP AND FEEL HIS LOSS. I WAS SO ANGRY THAT NO ONE WOULD LET OUT THE TRUETH ABOUT MS AND HOW REAL PEOPLE DEAL.
MS HIT MEN IN THE 30-40 RANGE. AT THAT AGE THEY
HAVE NOT PUT ALOT OF MONEY AWAY AND MUST END UP
(IF THEY ARE LUCKY)LIVING WITH THEIR PARENTS. MEN ARE DOERS AND PROVIDERS AND AT THIS POINT IN THEIR LIVES THEIR ARE JUST TRING TO DEAL. IF THEY ARE ON SSI FOR HELP, THEY ARE NOT ALOUD TO EARN EXTRA MONEY ELSE THEY WILL LOSE THE BENIFITS.IT IS A CATCH 22. ANYWAY I WOULD SAY ABOUT 1998 I CALLED THE DIFFENT TALK SHOW TO GET THE VOICE OF NORMAL PEOPLE WITH MS AND THE SHOWS
TOLD ME. THEY DO NOT WANT TO DO THAT (DEPRESS THE AUDIANCE) WHEN I HEAR THAT YOU HAD MS. . . I KNEW THAT THE WORD WOULD GET OUT!!!!!! I HEARD YOU TALK AND I RELIVED IT ALL AGAIN. . .PLEASE NEVER SILENCE YOUR VOICE. . . PLEASE. . .

I am writing in hopes that this information may be helpful for Montel. My mother suffered from Trigeminal Neuralgia for years along with Parkinsons disease. For years she was in severe pain and was treated with alcohol injections to the nerve and in extreme cases admitted to hospital and put on morphine. She was finally sent to a specialist in Winnipeg, Manitoba where the neurologist performed surgery. He lifted the trigeminal nerve and placed a swab underneath to prevent friction. My mother required one more alcohol injection and after that never had pain again. After listening to the show today it makes me wonder why that can't be done around the nerves in the legs as well. You may have heard of this surgery before but I want you to know that after so many years of pain my mother finally had relief.
My Best to You!

Montel
Thank you so much for being on Oprah. People need to know about MS. I have had MS since Oct 1974. I have a lot of the symptoms you have. Like you said everyone is different. I have constant pain that I have learned to live with it. When I was diagnosed there was nothing but very little information. I was also told that I would be in a wheelchair. Thank God I had a mother & father that would not let me give up at all. Right now I am dealing with seizures from my MS. This is a difficult time for me. Like you I have MS but MS does not have me. Thank you again for your fighting & love for everyone

It sadden me to see the pain that Mr. Montel Williams was in as I watched him on Oprah today.

I am not sure if you are able to get Mr. Williams a message but I would love for him to look and try MonaVie. The acai berry is a superfruit from Brazil that has helped people in a number of ways. 2 oz in the morning and 2 oz in the evening is equivalent to 13 servings of fruit in a day. This is an amazing product. I am not sure if this will help Mr. Williams but I would even purchase the product for him if there is a possibility for him to stop his pain.

Thank you for your time.

Denise Bullock

SWEET POISON! A MUST READ!

In October of 2001, my sister started getting very sick. She had stomach spasms and she was having a hard time getting around.

Walking was a major chore. It took everything she had just to get out of bed; she was in so much pain.

By March 2002, she had undergone several tissue and muscle biopsies and was on 24 various prescription medications. The doctors could not determine what was wrong with her. She was in so much pain, and so sick she just knew she was dying.

She put her house, bank accounts, life insurance, etc., in her oldest daughter's name, and made sure that her younger children were to be taken care of.

She also wanted her last hooray, so she planned a trip to Florida (basically in a wheelchair) for March 22nd.


On March 19 I called her to ask how her most recent tests went, and she said they didn't find anything on the test, but they believe she had MS. I recalled an article a friend of mine e-mailed to me and I asked my sister if she drank diet soda?


She told me that she did. As a matter of fact, she was getting ready to crack one open that moment.


I told her not to open it, and to stop drinking the diet soda! I e-mailed her article my friend, a lawyer, had sent.


My sister called me within 32 hours after our phone conversation and told me she had stopped drinking the diet soda AND she could walk!
The muscle spasms went away. She said she didn't feel 100% but, she sure felt a lot better.
She told me she was going to her doctor with this article and would call me when she got home.


Well, she called me, and said her doctor was amazed! He is going to call all of his MS patients to find out if they consumed artificial sweeteners of any kind.


In a nutshell, she was being poisoned by the Aspartame in the diet soda...and literally dying a slow and miserable death.


When she got to Florida March 22, all she had to take was one pill, and that was a pill for the Aspartame poisoning! She is well on her way to a complete recovery. And she is walking! No wheelchair! This article saved her life.

If it says 'SUGAR FREE' on the label; DO NOT EVEN THINK ABOUT IT! I have spent several days lecturing at the WORLD ENVIRONMENTAL CONFERENCE on 'ASPARTAME,' marketed as 'Nutra Sweet,'

'Equal,' and 'Spoonful.'

In the keynote address by the EPA, it was announced that in the United States in 2001 there is an epidemic of multiple sclerosis and systemic lupus. It was difficult to determine exactly what toxin was causing this to be rampant. I stood up and said that I was there to lecture on exactly that subject.

I will explain why Aspartame is so dangerous: When the temperature of this sweetener exceeds 86 degrees F, the wood alcohol in ASPARTAME converts to formaldehyde and then to formic acid, which in turn causes metabolic acidosis. Formic acid is the poison found in the sting of fire ants.
The methanol toxicity mimics, among other conditions, multiple sclerosis and systemic lupus.

Many people were being diagnosed in error.
Although multiple sclerosis is not a death sentence, Methanol toxicity is!


Systemic lupus has become almost as rampant as multiple sclerosis, especially with Diet Coke and Diet Pepsi drinkers.
The victim usually does not know that the Aspartame is the culprit. He or she continues its use; irritating the lupus to such a degr ee that it may become a life-threatening condition.


We have seen patients with systemic lupus become asymptotic, once taken off diet sodas.
In cases of those diagnosed with Multiple Sclerosis, most of the symptoms disappear. We've seen many cases where vision loss returned and hearing loss improved markedly.


This also applies to cases of tinnitus and fibromyalgia.
During a lecture, I said, 'If you are using ASPARTAME (Nutra Sweet, Equal, Spoonful, etc) and you suffer from fibromyalgia symptoms, spasms, shooting, pains, numbness in your legs, Cramps, Vertigo, Dizziness,Headaches, Tinnitus, Joint pain, Unexplainable depression, anxiety attacks, slurred speech, blurred vision, or memory loss y ou probably have ASPARTAME poisoning!'
People were jumping up during the lecture saying, 'I have some of these symptoms. Is it reversible?'


Yes! Yes! Yes!
STOP drinking diet sodas and be alert for Aspartame on food labels! Many products are fortified with it!

This is a serious problem.
Dr. Espart (one of my speakers) remarked that so many people seem to be symptomatic for MS and during his recent visit to a hospice; a nurse stated that six of her friends, who were heavy Diet Coke addicts, had all been diagnosed with MS. This is beyond coincidence!

Diet soda is NOT a diet product! It is a chemically altered, multiple SODIUM (salt) and ASPARTAME containing product that actually makes you crave carbohydrates. It is far more likely to make you GAIN weight!
These products also contain formaldehyde, which stores in the fat cells, particularly in the hips and thighs. Formaldehyde is an absolute toxin and is used primarily to preserve 'tissue specimens.'

Many products we use every day contain this chemical but we SHOULD NOT store it IN our body!

Dr. H. J. Roberts stated in his lectures that once free of the 'diet products' and with no significant increase in exercise; his patients lost an average of 19 pounds over a trial period.

Aspartame is especially dangerous for diabetics.
We found that some physicians, who believed that they had a patient with retinopathy, in fact, had symptoms caused by Aspartame. The Aspartame drives the blood sugar out of control.


Thus diabetics may suffer acute memory loss due to the fact that aspartic acid and phenylalanine are NEUROTOXIC when taken without the other amino acids necessary for a good balance.


Treating diabetes is all about BALANCE. Especially with diabetics, the Aspartame passes the blood/brain barrier and it then deteriorates the neurons of the brain; causing various levels of brain damage, Seizures, Depression, Manic depression, Panic attacks, Uncontrollable anger and rage.


Consumption of Aspartame causes these same symptoms in non-diabetics as well.

Documentation and observation also reveal that thousands of children diagnosed with ADD and ADHD have had complete turnarounds in their behavior when these chemicals have been removed from their diet.
So called 'behavior modification prescription drugs' (Ritalin and others) are no longer needed. Truth be told, they were never NEEDED in the first place!

Most of these children were being 'poisoned' on a daily basis with the very foods that were 'better for them than sugar.'


It is also suspected that the Aspartame in thousands of pallets of Diet Coke and Diet Pepsiconsumed by men and women fighting in the Gulf War, may be partially to blame for the well-known Gulf War Syndrome.


Dr. Roberts warns that it can cau se birth defects, i.e. mental retardation, if taken at the time of conception and during early pregnancy.
Children are especially at risk for neurological disorders and should NEVER be given artificial sweeteners.
There are many different case histories to relate of children suffering grand mal seizures and other neurological disturbances talking about a plague of neurological diseases directly caused by the use of this deadly poison.'


Herein lies the prob lem: There were Congressional Hearings when Aspartame was included in 100 different products and strong objection was made concerning its use. Since this initial hearing, there have been two subsequent hearings, and still nothing has been done. The drug and chemical lobbies have very deep pockets.

Sadly, MONSANTO'S patent on Aspartame has EXPIRED! There are now over 5,000 products on the market that contain this deadly chemical and there will be thousands more introduced. Everybody wants a 'piece of the Aspartame pie.'

I assure you that MONSANTO, the creator of Aspartame, knows how deadly it is.

And isn't it ironic that MONSANTO funds, among others, the American Diabetes Association, the American Dietetic Association and the Conference of the American College of Physicians?


This has been recently exposed in the New York Times.


These [organizations] cannot criticize any additives or convey their link to MONSANTO because they take money from the food industry and are required to endorse their products.

Senator Howard Metzenbaum wrote and presented a bill that would require label warnings on products containing Aspartame, especially regarding pregnant women, children and infants.
The bill would also institute indepen dent studies on the known dangers and the problems existing in the general population regarding seizures, changes in brain chemistry, neurological changes and behavioral symptoms.

The bill was killed.


It is known that the powerful drug and chemical lobbies are responsible for this, letting loose the hounds of disease and death on an unsuspecting and uninformed public. Well, you're informed now!
YOU HAVE A R IGHT TO KNOW!


Please print this out and/or e-mail To your family And friends.
They have a right to know too!


I found you site 'Montel Live' and I sent an email to you, Mr. Williams. I hope you get it. It was an explanation of why I am attempting to write you at this time.
Have you heard of Sunrider International? If not please dial up the address: Sunrider.com. This a whole food company, that properly mix food and herbs in such a way that assist the bodies natural process in cleansing, nurishing and balancing itself to good health. Many have found success with the foods and I believe you will find it also.
The owner expertise of the Sunrider company is credited to it's owners Dr. Tei-Fu Chen and Mrs. Dr. Oi-Lin Chen. Please look into it, right away!


I found you site 'Montel Live' and I sent an email to you, Mr. Williams. I hope you get it. It was an explanation of why I am attempting to write you at this time.
Have you heard of Sunrider International? If not please dial up the address: Sunrider.com. This a whole food company, that properly mix food and herbs in such a way that assist the bodies natural process in cleansing, nurishing and balancing itself to good health. Many have found success with the foods and I believe you will find it also.
The owner expertise of the Sunrider company is credited to it's owners Dr. Tei-Fu Chen and Mrs. Dr. Oi-Lin Chen. Please look into it, right away!


I love you Montel - You are a trooper and an inspiration - My best girlfriend's sister has MS and we walk each and every time we can - I include your name in each one of our walks - Stay strong we surely miss ya each and every day - THANKS for just being you :)

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This page contains a single entry by Mark Bieganski published on March 17, 2009 11:21 AM.

Oprah Winfrey sports new 'do -- do we like? was the previous entry in this blog.

One of Oprah's adopted puppies dies over weekend is the next entry in this blog.

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