Chronic Fatigue Syndrome Coming on Dr. Oz -- By Jacob Teitelbaum, MD

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Mardy Ross's picture
This is directly from Dr. Teitelbaum's "endfatigue.com" e-newsletter that I was so thrilled to receive and read on Wed, Oct 15!
 

Your Comments and Posts Worked ;-)

CFS to be on the New Dr. Oz TV Show!!!

My thanks to the hundreds of readers who left a comment at the Oprah website about the Dr. Oz article in the September Oprah Magazine, which discussed fibromyalgia and recommended our treatment approach. A few weeks ago, the producers for the new nationally syndicated Dr. Oz TV show flew me to New York to tape a 12-15 minute primary segment on fatigue, with a special segment on CFS! This suggests the topics of CFS and fibromyalgia are now being tested by Oprah’s production company, and we’ll be seeing more if we keep sending in positive comments!

It will likely play as the first segment of one of the new Dr. Oz TV shows in the next 3 weeks. We’ll send an announcement of the date as soon as we hear.

Stay tuned!!!

_________________________

Here's a link to Dr. Teitelbaum's website where these letters are on file. 
www.endfatigue.com    This is a great site to keep abreast of and naturally, his book, From Fatigued to Fantastic is 'the granddaddy of them all'.  As is Dr. T!  I'm sure it will be a wonderful segment and I am very happy to see the Dr. Oz/Oprah spotlight start shining on this important and popular topic! 
I suggest everyone takes his free online symptom analyzer and receive the feedback about what you and your doctor could be doing related to where you are at with CFS/FMS and then you'll receive these e-newsletters yourselves.  He's very integrative regarding nutrition, supplements, and medications (and suggested the older/cheaper ones often are just as good or better as the newer more expensive ones!)
 
As always, we like to have people who have thoughts to share for others' reading and knowledge at our Forum area.  I have established many areas for medications and suppelements that have worked and not.  Here's the link for that area www.lumigrate.com/forum.  Thank you for helping us and others learn by writing -- thank you for allowing others to help  you by reading their contributions.  And then certainly, join us on facebook for daily discussions and some FUN if we're doing it right!  www.facebook.com/lumigrate
 
Healthy Wellness ~~Mardy
 

 

__________________

Live and Learn. Learn and Live Better! is my motto. I'm Mardy Ross, and I founded Lumigrate in 2008 after a career as an occupational therapist with a background in health education and environmental research program administration. Today I function as the desk clerk for short questions people have, as well as 'concierge' services offered for those who want a thorough exploration of their health history and direction to resources likely to progress their health according to their goals. Contact Us comes to me, so please do if you have questions or comments. Lumigrate is "Lighting the Path to Health and Well-Being" for increasing numbers of people. Follow us on social networking sites such as: Twitter: http://twitter.com/lumigrate and Facebook. (There is my personal page and several Lumigrate pages. For those interested in "groovy" local education and networking for those uniquely talented LumiGRATE experts located in my own back yard, "LumiGRATE Groove of the Grand Valley" is a Facebook page to join. (Many who have joined are beyond our area but like to see the Groovy information! We not only have FUN, we are learning about other providers we can be referring patients to and 'wearing a groove' to each other's doors -- or websites/home offices!) By covering some of the things we do, including case examples, it reinforces the concepts at Lumigrate.com as well as making YOU feel that you're part of a community. Which you ARE at Lumigrate!

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Anne J
Title: LumiGRATE Poster - Minimal
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Re: Chronic Fatigue Syndrome Coming on Dr. Oz -- By Jacob ...

 


I got my results back from my sleep study and the MD said that I morning to keep me awake during the day. He described my brain as though it is a central auditory processing kind of thing and the control panel has all the right wiring up there to do it's job but it just isn't making the right connection to get the message to my brain. I also have to undergo a nap study that was first ordered for the day after my sleep study orginally but they didn't do it, the tech felt I didn't need it. The MD says I do and was upset that a technician over rode his initial order.  So I will know more on that end as it unfolds.  As you all may have already learned and are learning just like me, when you have a chronic condition for example Fibromyalgia that you have to be patient with not only yourself, but with the health care folks out there.  The key to all of this is persistence.  I am still learning myself and probably bother Mardy more than most folks on here but she has been a source of strength and guidance for me.  I still don't have all the answers and understanding of this thing since I have only been diagnosed for a little more than a year, but I am trying and I am not going to give up.  Also, just remember that if you run across someone who doesn't believe in your condition, like I have with a neurologist, just remember that there are some folks including health care professionals are just ignorant and if they would take the time to learn more themselves then they would have a better understanding.  Granted there have been times when I really wished that the neurologist I met with could experience my good days and my bad days as well as my super bad days so that he would have a clearer understanding of the roller coaster we ride every day.  I hope you all have a great day!!

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