All Posts Tagged With: "fibromyalgia"

Linda’s comment:  Misdiagnosing Lyme disease for MS is a very common thing these days,  It isn’t jut happening in Canada, it is happening world-wide. We must bring education and awareness to this serious matter.  When ignored patients are becoming sicker and sicker.  Lyme is best diagnosed clinically, as there are not that many Lyme blood tests that are accurate.  Most doctors now realize, when in doubt treat for Lyme.

Full article: http://www.calgaryherald.com/health/Doctors+misdiagnose+Lyme+disease+researcher/2908675/story.html

Excerpt:

A Manitoba researcher says some patients deemed by doctors to suffer from multiple sclerosis may be misdiagnosed.

In a recent thesis, Winnipeg researcher Kathleen Crang found that some Manitobans diagnosed with MS and other chronic conditions may actually be suffering from the borrelia bacteria, a tick-borne “biological evil genius” that causes Lyme disease.

“If I knew someone with MS, I’d be saying, ‘Let’s look at those questions,’ ” said Crang. “If their MS is coupled with heart problems, or skin rashes, or rheumatological involvement, there might be some question as to why.”

After all, the bug is dubbed “the second great imitator” — syphilis is the first.

Tests for Lyme disease can be unreliable; many of the disease’s 75 known symptoms are shared by a host of neurological conditions. Case studies have even found that Lyme can produce lesions on the brain like those seen in MS.

That in itself isn’t breaking news. Crang’s thesis, titled Knowledge and Perception of Lyme disease in Manitoba: Implications for Risk Assessment, found numerous reports in Europe and the United States of Lyme disease being initially misdiagnosed as everything from MS to ALS and fibromyalgia.

But in Manitoba, where Lyme is thought to be almost non-existent, Crang found that doctors may not be on the lookout for the disease.

Could that lack of concern lead to lasting misdiagnoses?

“There’s a bit of a disconnect there,” said Crang. “It’s an information-flow problem. The fact that individuals are hearing such low numbers of Lyme leads to a perception that Lyme isn’t there.”

In a series of interviews for the thesis, Crang found that many Manitoba public health decision-makers and clinicians didn’t perceive Lyme as a threat to Manitobans, and “did not expect they would see patients with the disease.”

Crang, 44, is living proof that the mistake can be made.

In 1999, doctors told the Fort Richmond Collegiate science teacher that she had MS; an MRI appeared to confirm the diagnosis.


Learning about Lyme disease the hard way

Linda’s comment:  Excuse me but this is very common AND TRAGIC!!  I don’t know what it is going to take to get treatments for those suffering from Lyme.  I personally treated both Lyme infections with alternatives, BUT then again I live in a state that has many licensing boards so doctors don’t have to FEAR the authorities.  The AMA can’t touch the method of treatment that alternative doctor prescribe.  The tragic part of this is insurance companies will NOT pay for alternatives…unless of course, you live in Alaska and there many of the insurance companies are paying for alternative treatments and modalities….

 
What happened to this man IS common and very TRAGIC!!!  I talk to dozens of patients on a daily basis searching for something that will help them get well.  I guide them to the FIGHT program for a beginning, THEN after reducing the total body burden of pathogens and toxins we can guide and direct folks to the right antimicrobials….Just breaks my heart that so many are suffering needlessly….
 
Regards,
Linda or Angel
Excerpt:

A month ago, Bart Fenolio was told he had Lou Gehrig’s disease and had two months to live. Doctors advised his wife, Heidi, to take him home and call a hospice. Continued

Chronic Lyme Disease: Myth or Reality?


Linda’s comment:  The FIGHT program is a perfect example of how you can fight Lyme disease.  As Dr Patricia Gerbarg, MD has found out.  She has not experienced the FIGHT program to my knowledge, but the protocols she mentioned are all part of the FIGHT program.  It is a must that we reduce the total body burden of toxins and pathogens to fight the Lyme critters.  Lyme loves heavy metals.  We are slammed every time we walk out our front doors with 500 to 600 environmental toxins.  It is a daily battle, but I found the FIGHT program made this all very easy.  I only wish I had  the knowledge of the FIGHT program with the first Lyme infection.

I have never taken any antibiotics and don’t intend to, but I focused on the lifelong daily detox program FIGHT and cleaned up my lifestyle, home and diet.  I got rid of all the GMO foods, gluten, sugar, caffeine, alcohol and my body shakes if I pass a fast-food restaurant….the smell turns my stomach.  Once you clean  up your diet and clean up your homestead, you begin to feel better….Lifestyle is probably one of the hardest things I have ever done….Yes, I cheat, but at least now I have learned to cheat. and can neutralize a toxic food if I eat it.  Once you begin to feel better it makes the journey of cleaning up much easier. Just give the FIGHT program 90 days and you too will feel the difference.

Regards, Linda Continued

Hope for Autism Conference

Here is the link to an outstanding webinar on Autism where I was the moderator   https://www2.gotomeeting.com/register/330944962.  Dr.  Renee Tocco has organized the PowerPoint with super efficiency and added graphics to many of the slides that will make this webinar very informative for patients where so much of this is news and, therefore, hard for them to comprehend when first presented.

This is a great group doing wonderful work in Autism. Please seriously look at their program and speakers, as I assure you if you get there you will be very glad you made the effort, as there is so much to learn and they have the total approach that I endorse.

Garry F. Gordon MD,DO,MD(H)
President, Gordon Research Institute
www.gordonresearch.com
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Hope for Autism Training Conference
Developed for Patients, Families and Practitioners

Register TODAY!  Only 10 days Until the Conference!

Friday, Saturday & Sunday, November 13 – 15, 2009 Registration / Exhibits Begin at 9:30 am

The Sheraton Charleston Airport Hotel
4770 Goer Drive. North Charleston, SC 29406, Phone: (843) 747-1900

This exciting, three day conference offers something for everyone.
Physicians, patients, and their families get three days of valuable information, hear inspirational success stories, and learn about successful treatment programs and approaches from knowledgeable speakers.
Chiropractic Physicians who complete the Hope for Autism Training will have the opportunity to obtain a Certificate of Proficiency and be placed on the HFA Referral Directory in addition to obtaining 20 hours of continuing education credit* ___________________________________________________________________

If you refer a chiropractor, get $100 Cash Back!
____________________________________________________________________
CLICK HERE TO REGISTER!
http://www.hopeforautism.us/Conference_Registration.html
For more information, please visit www.hopeforautism.us

Or call 843-766-1969.

Kindest Regards,
Dr. Renee Tocco
www.HopeForAutism.us