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 » Histamines & Mast Cell & update

 - UBBFriend: Email this page to someone!    
Author Topic: Histamines & Mast Cell & update
Mvdr
LymeNet Contributor
Member # 43034

Icon 1 posted      Profile for Mvdr     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello, everyone! I haven't been here in a long time. I have overcome Bart, Babs and Brucellosis but still fighting lyme. I am much better and functioning fairly normal about 5 days per week. I have done everything but attribute most of my healing to Colloidal silver, treating parasites, yeast, diet and exercise.

I think I have a Mast cell disorder or at least a histamine intolerance. I live on Benedryl and herbal supplements for allergies. I am just learning about HI and MC. I can't find too much on it. Where do I begin?

Where can I find diet info or sample diets? Thank you all! Be well!

Posts: 143 | From Pittsburgh | Registered: Jan 2014  |  IP: Logged | Report this post to a Moderator
hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

Icon 1 posted      Profile for hopingandpraying     Send New Private Message       Edit/Delete Post   Reply With Quote 
Here is a very informative thread poster Lymetoo started over in "General Support":

"Mast Cell Activation Disorder"
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=036299;p=0

Posts: 8981 | From Illinois | Registered: May 2006  |  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'm very sorry to hear this, mvdr.. but at least now you know what to avoid and how to treat it.
There is another VERY LONG thread I posted last year. You can search for it under my member #743.

Let me know if you need any more help.

The best link I've found is this one:

Mast Cell Disease 101

http://www.sneeze.com/allergy-resources/mast-cell-disease-101/

Great article for family and friends .. even for doctors.

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
aklnwlf
Frequent Contributor (5K+ posts)
Member # 5960

Icon 6 posted      Profile for aklnwlf     Send New Private Message       Edit/Delete Post   Reply With Quote 
MVDR-Welcome to the club! I was recently diagnosed with MCAD thanks to the wonderful info posted here on Lymenet.

Good luck in your journey to health and wellness!

[Big Grin]

--------------------
Do not take this as medical advice. This comment is based on opinion and personal experience only.

Alaska Lone Wolf

Posts: 6155 | From Columbus, GA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
Mvdr
LymeNet Contributor
Member # 43034

Icon 1 posted      Profile for Mvdr     Send New Private Message       Edit/Delete Post   Reply With Quote 
thank you all! I am learning a lot about this and already feeling better after identifying trigger foods.
Posts: 143 | From Pittsburgh | Registered: Jan 2014  |  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 
Good to hear!! I hope you have a good doctor too!

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Mvdr
LymeNet Contributor
Member # 43034

Icon 1 posted      Profile for Mvdr     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello, Lymetoo! I do not have a good doctor, sadly! I have a good herbalist and essentially treating myself at this point. I live in Pittsburgh and there is no one here!

I cannot tolerate traditional medicine and the doctors I've been to for Lyme just want to give me antibiotics which I feel have caused more harm than good.

I am pretty much on my own, like so many of us! Trying to find a traditional doctor to do MCAD testing but that is challenging, too.

Be Well, M

(breaking up the post for easier reading for many here)

[ 04-20-2017, 01:22 AM: Message edited by: Robin123 ]

Posts: 143 | From Pittsburgh | Registered: Jan 2014  |  IP: Logged | Report this post to a Moderator
Christopher J
LymeNet Contributor
Member # 46401

Icon 1 posted      Profile for Christopher J     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Mvdr:
Hello, Lymetoo! I do not have a good doctor, sadly! I have a good herbalist and essentially treating myself at this point. I live in Pittsburgh and there is no one here!

I cannot tolerate traditional medicine and the doctors I've been to for Lyme just want to give me antibiotics which I feel have caused more harm than good.

I am pretty much on my own, like so many of us! Trying to find a traditional doctor to do MCAD testing but that is challenging, too.

Be Well, M

Without antibiotics I dont think you have a chance against Lyme. I am in cycles of many antibiotics all the time and that is the only thing that has reduced symptoms and knocked down Lyme to a manageable state.

When you first start taking them, it always seems very dark and you have a worsening of symptoms. But you should absolutely NOT use that as a justification to stop. Infact it means its working.

Over the years, the ABs will have less and less of a dramatic impact and you can pop them without thinking about it. This means the Lyme is under control.

There are so many times early on that I wanted to stop, but thats the Lyme telling your brain to ease up on the killing

(breaking up the post for easier reading for many here)

[ 04-20-2017, 01:24 AM: Message edited by: Robin123 ]

Posts: 173 | From USA | Registered: Aug 2015  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some good info on here. Also some links not working yet, but this is run by volunteers

http://www.mastocytosis.ca/

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
Want to chime in here - there is no one-size-fits-all when it comes to treatment - we're all unique in our responses.

For some, longterm antibiotics is the answer. For others, not, like me, I'm allergic to antibiotics, and I go a natural treatment route.

Many are treating with herbs, like the Buhner herbs, Cowden protocol, Zhang herbs, etc. It's a matter of finding out what we respond to best.

I have elevated mast cells too and I have not figured it out for myself yet. I know there's many triggers for it. Hope to have more understanding some day about it.

Posts: 13117 | From San Francisco | Registered: May 2006  |  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 
Christopher... for some of us the initial and MAIN problem is the mast cells, not the Lyme.

Another link:

www.tmsforacure.org

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  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.