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 » Stem cell in Mexico

 - UBBFriend: Email this page to someone!    
Author Topic: Stem cell in Mexico
bullmastiffluvr
Member
Member # 50250

Icon 1 posted      Profile for bullmastiffluvr     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has anyone been treated in Mexico with stem cell therapy successfully. I have been considering that since I feel I am no longer progressing in my treatment. Many drug allergies complicate my treatment unfortunately.
Posts: 41 | From CA | Registered: May 2017  |  IP: Logged | Report this post to a Moderator
willbeatthis
LymeNet Contributor
Member # 31111

Icon 1 posted      Profile for willbeatthis     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have you considered trying mhbot. I had at one time considered stem cell, but after my mom went through one with Amyloidosis, I decided that was not a route I was supposed to take. I have heard of success stories however. Mhbot is just a lot less invasive. You might want to read the Mhbot thread. It has been very helpful for me. Bless you.
Posts: 859 | From Southeast | Registered: Mar 2011  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks, willbeatthis...

I was also going to suggest mild hyperbaric also, as it releases your own, endogenous stem cells, and you can rent/buy/share a chamber for home treatment.

As willbeatthis mentioned, it is also less invasive and safer.

mHBOT gave me my life back; I have been well for over 5 years now from severe neuro-Lyme. Many others have since become well or are greatly improved.

Visit the mild hyperbaric thread for more information and support if you are interested.

Posts: 1880 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
Tincup
Honored Contributor (10K+ posts)
Member # 5829

Icon 1 posted      Profile for Tincup         Edit/Delete Post   Reply With Quote 
Wow, what timing! I was just dropping by to share this info and saw your post, so I'll add it here for you too!

Hope it will answer your questions! Good luck!!!

STEM CELL INFO & HOTLINE

QUOTE- "Stem Cell for Lyme Disease- The prognosis for lyme disease treatment looks brighter: stem cell lyme disease treatment involves an IV delivery system that introduces harvested stem cells into the circulatory system. The stem cells then migrate to the areas of degeneration and inflammation.

Infected cells undergo natural healing, with little or no side effects. Stem cell treatment offers relief from the painful and debilitating symptoms that accompany the disease. Patients can regain their former quality of life."

http://checkbiotech.org/stem-cell-therapy-treatment-options-call-972-800-6670-☎%EF%B8%8F/

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
Richard_F
Member
Member # 50948

Icon 1 posted      Profile for Richard_F     Send New Private Message       Edit/Delete Post   Reply With Quote 
read plenty of folks who tried MHBOT and got nowhere.

this freakin disease is so individualized you can pretty much say that about any modality!

Posts: 21 | From NJ | Registered: Oct 2017  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Richard_F...

The success of mHBOT is very much dependent on the manner in which it is used. If folks are "getting nowhere", I would first question the protocol being used.

Although it is true that Lyme manifests differently in people, there are many common denominators which mHBOT is very effective at treating. This is also why it is so healing for so many conditions.

Posts: 1880 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
We just had a member, many years ill with Lyme & co, come to our last Lyme Support meeting to report she had gone to Prague for 3 1/2 months of stem cell treatment.

She is doing amazing. She spent well over $100,000 just on tx and not housing etc.
Her experience says one must do the longer tx protocol. Saying a few weeks won't get it.

My mouth dropped open at the costs. She's a young medical student, off and on schooling because of symptoms.

We've told her some day she's going to be a LLMD.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  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.