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 » Clinic in Beverly Hills that does Stem Cell for Lyme

 - UBBFriend: Email this page to someone!    
Author Topic: Clinic in Beverly Hills that does Stem Cell for Lyme
etb6855
Member
Member # 48383

Icon 1 posted      Profile for etb6855     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has anyone been to this clinic in Beverly Hills? They also have one in Germany.

A state Lyme Disease Assoc posted info about them and a testimonial video of a girl who was helped by them. They apparently collect stem cells from your adipose tissue and then give them back to you as well as do hyperbaric treatments.

I looked at their website offering "medical treatments in a spa like atmosphere" and they offer all other types of treatment modalities as well. Of course they charge anywhere from $20-30,000!

Has anyone been here?

Does anyone have any links to the success of this treatment for Lyme?

Posts: 86 | From LA | Registered: Jul 2016  |  IP: Logged | Report this post to a Moderator
lapis29
Member
Member # 47626

Icon 1 posted      Profile for lapis29     Send New Private Message       Edit/Delete Post   Reply With Quote 
hold on, let me check behind the couch, I might have dropped 30k back there last tuesday...
Posts: 90 | From Wisconsin | Registered: Mar 2016  |  IP: Logged | Report this post to a Moderator
etb6855
Member
Member # 48383

Icon 1 posted      Profile for etb6855     Send New Private Message       Edit/Delete Post   Reply With Quote 
HAHA Seriously its unbelievable I mean the supplements we have to take for years are outrageous enough.

wonder how long I would be well once I returned to living in a card board box under a bridge if I would even be able to pay for that kind of treatment.

Posts: 86 | From LA | Registered: Jul 2016  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I would pass on that one.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

Icon 1 posted      Profile for Bartenderbonnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ah, the age old story of the haves and the have nots. . .

Human sufferring on a massive scale and no one will help us
unless you have money.

I m just wishing for insurance coverage for Lyme doctors and treatment, better testing , and basic human compassion.

I don't begrudge people that have money, as they have worked hard for it.

My distain is with the CDC and the IDSA for keeping us ill and unable to provide for ourselves.

Lord, hear our prayers !

Posts: 2978 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Also disdain for those who promise cures and offer none.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
lymehope
Member
Member # 48581

Icon 1 posted      Profile for lymehope     Send New Private Message       Edit/Delete Post   Reply With Quote 
I went to a similar clinic in Germany. It did not help. I actually got worse after that. I am currently in treatment with Dr. S from DC and every day I see improvements. My brain is coming back. She has been my Angel. If I was you I would use that money in getting best Dr. that follows the Burrascano method. I spent a lot of money in Germany and here in NY in alternative treatments. I was afraid of long term antibiotics, but they are working for me. It is not even one year and so much better.
Good luck with any decision you make. We are all different so you never know. This has just been my experience.

Posts: 68 | From new york | Registered: Aug 2016  |  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 
Stem cell treatment will not help long-term (or even much short-teem) if you haven't taken care of the infections---that's infections plural.

That kind of $$$ for something that may not even help is userous in my view---even if someone had the $ or came up with it. And if someone came up with it through crowd-funding, etc. and then found out that what they really needed was treatment for the infections and all the related issues?? Then what?

Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
randibear
Honored Contributor (10K+ posts)
Member # 11290

Icon 1 posted      Profile for randibear     Send New Private Message       Edit/Delete Post   Reply With Quote 
uh oh sure. by the time I saved that I'd be dead anyway.

--------------------
do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
Badtick
LymeNet Contributor
Member # 9794

Icon 1 posted      Profile for Badtick     Send New Private Message       Edit/Delete Post   Reply With Quote 
It's places like this that give Lyme treatment a bad reputation and undermine the credibility of those providing reasonable and effective therapies.
Posts: 184 | From CT | Registered: Aug 2006  |  IP: Logged | Report this post to a Moderator
etb6855
Member
Member # 48383

Icon 1 posted      Profile for etb6855     Send New Private Message       Edit/Delete Post   Reply With Quote 
AGREED!
Posts: 86 | From LA | Registered: Jul 2016  |  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.