LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Pathologist Dr. Alan McDonald VIDEO LYME EDUCATION

 - UBBFriend: Email this page to someone!    
Author Topic: Pathologist Dr. Alan McDonald VIDEO LYME EDUCATION
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
https://www.youtube.com/watch?v=r8tESJVvM88

https://www.youtube.com/watch?v=2RATCS-3v9Q

https://www.youtube.com/watch?v=FEjNMlNM3l8

[ 06-21-2015, 11:26 AM: Message edited by: SacredHeart ]

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
https://www.youtube.com/watch?v=AmvgOfIN_8c Another good one. Wish she would have gone more in depth on mycoplasma as a separate infection.

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Here's more for you:

http://www.immed.org/

MYCOPLASMA research website

Institute for Molecular Medicine - Garth Nicolson, PhD

He is the premier researcher in the area of chronic stealth mycoplasma infections
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks. =)

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
Lymedin2010
Frequent Contributor (1K+ posts)
Member # 34322

Icon 1 posted      Profile for Lymedin2010     Send New Private Message       Edit/Delete Post   Reply With Quote 
This is BIG news for Dr. MacDonald, as his discovery for borrelia in Alzheimer's correlation has been corroborated.


This is directly from Under Our Skin:

"This is big! UNDER OUR SKIN "basement scientist" Alan Macdonald, MD is vindicated by a new study in the prestigious Journal of Alzheimer's Disease, proving a definitive link between dementia and Lyme infection in a subset of Alzheimer's patients.


"Conclusion: Pure Lyme dementia exists and has a good outcome after antibiotics. It is advisable to do Lyme serology in demented patients, and if serology is positive, to do central spinal fluid analysis with AI (intrathecal anti-Borrelia antibody index).


Neurodegenerative dementia associated with positive AI also exists, which may have been revealed by the involvement of Borrelia in the central nervous system.""


http://www.ncbi.nlm.nih.gov/pubmed/24762944

Posts: 2087 | From NY | Registered: Oct 2011  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
https://www.youtube.com/watch?v=A_01-g55fwg I found this doc in Florida that centers on the brain first. Interesting stuff.

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sacredheart,

Thanks for posting the link to the Florida doc. I had not seen that previously.

I have always been of the opinion that nutritional supplementation was almost equally as important as antibiotics or killing herbs as part of a comprehensive tickborne treatment strategy.

That particular video goes a long way toward explaining why hubby never had major pain issues. We supplemented with taurine (500 mg 3 times daily) for many years plus fish oil and phosphatidylcholine (good fats).

However, I am somewhat skeptical of supplementing to increase serotonin. Buhner has written about the alternative pathway by which serotonin precursors are converted to the neurotoxin quinolinic acid. Hubby did actually have that tested once and it was elevated. He also had low serotonin.

Resveratrol (Japanese knotweed source) allowed him to take l-tryptophan and 5HTP (activated form of b 6) for sleep and over the course of several months greatly decreased anxiety and improved sleep.

It does seem like very slowly the brain effects of lyme and tickborne illnesses are making their way into the medical journals despite the IDSA. But the majority of the research is not from the U.S. Almost anything of significance comes from foreign sources. The doc mentioned Japan and I forget which other countries.

And the lyme toxins the doc discussed have not been definitively proven by medical research as far as I know. Personally I am not sure if there are specific lyme toxins or if lyme just increases production of other normally occurring toxins such as the quinolinic acid mentioned above. And then there are the various cytokines and chemokines produced by the immune system - such as IL-2 and TNF (tumor necrosis factor).

I would love to have that doc interpret hubby's 2 brain SPECT scans.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bea and SacredHeart,

While the info from the Florida doctor may be good (I didn't look), beware:

he is NOT what he makes himself out to be. And many, if not most, of the good testimonials very much appear to be created by himself or his people.

And he seems to scrub many sites of the negative reviews.

He has duped many, many people out of a tremendous amount of money, not to mention time and energy and hope, and in many cases left them in far worse shape than when they came to him.

In those cases, they were people who were addicted to pain meds and went to him for a "rapid detox" that left them addicted to far worse opiods from his "treatment."

There is no excuse for this except greed pure and simple.

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
rumigirl,

Thanks for the head up. I was somewhat skeptical of the doc but was unaware of all the issues. I did know he was terribly expensive.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Rumigirl,

Could you please post some evidence to support your claim? It isn't good to ruin someone's name, or reputation without something to back it up. I understand that you are warning us, but there must be some kind of evidence you could post. Thanks. God Bless.

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
lpkayak
Honored Contributor (10K+ posts)
Member # 5230

Icon 1 posted      Profile for lpkayak     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ive never heard of this dr s

There is another dr s in fla that i have heard similar things about

Rumis been here a long time...so have i...i suspect she knows what shes talking about

That sort of thing is happening more and more

I think the most important thing i have learned over time is not to jump on new band wagons

When someone figures out how to deal with lyme it wont be a secret for long. We wont need a ten yr double blind study

When we see something that is really working they wont be able to keep it a secret even if they want to

--------------------
Lyme? Its complicated. Educate yourself.

Posts: 13712 | From new england | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
SacredHeart
LymeNet Contributor
Member # 44733

Icon 1 posted      Profile for SacredHeart     Send New Private Message       Edit/Delete Post   Reply With Quote 
I thought I would hit this thread again just so some of the new folks to listen to the first links on Dr. Alan Mcdonald. You can learn a lot from those three videos he has up on youtube.

--------------------
Lyme flare June, July, August of 2013. Diagnosed September 2014 Lyme, Bartonella, Mycoplasma, Mono

Posts: 595 | From Texas Crossroads | Registered: Oct 2014  |  IP: Logged | Report this post to a Moderator
Eight Legs Bad
LymeNet Contributor
Member # 13680

Icon 1 posted      Profile for Eight Legs Bad   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I agree the videos by Alan MacDonald are amazing.

Be sure to also view the one of his presentation to the Spirochaetal Alzheimers Association (SAA) in London 2014:

https://www.youtube.com/watch?v=TjfWFaIivIc

SAA can be contacted at [email protected]

Regarding the link to the French paper, Blanc et al, I agree that it vindicates Dr M in the sense that the authors admit that Lyme can cause a dementia. There were obviously a lot of honest researchers involved in that work. Sadly, Dr Jaulhac, the French "Allen Steere", was also involved and there was an assumption by the authors that serology is reliable and that all those patients who tested negative for Lyme were truly negative.

They therefore came to the wrong conclusion that "Lyme dementia" is a very rare phenomenon, and totally distinct from Alzheimer's, which is extremely common. They also considered the fact that some patients did not improve quickly with abx as further proof that it was not (or no longer) Lyme infection. Obviously they believed the current falsehoods about Lyme being easily cured.

Elena

--------------------
Justice will be ours.

Posts: 786 | From UK | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.