LymeNet Flash: The Agony of Mast Cell Activation Syndrome

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

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.

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 » Questions and Discussion » General Support » The Agony of Mast Cell Activation Syndrome

UBBFriend: Email this page to someone!

Author

Topic: The Agony of Mast Cell Activation Syndrome

Lymetoo
Moderator
Member # 743

posted

https://www.lymedisease.org/lyme-sci-mcas-agony/

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

Posts: 96227 | From Texas | Registered: Feb 2001 | IP: Logged |

Silverwolf
Frequent Contributor (1K+ posts)
Member # 9196

posted

Hi <<<<< Lymetoo >>>>>,

Thanks for the link, very helpful, I still feel this is what is happening to me.

Jus' Silverwolfi here

--------------------
2006,May-August2006 Dx w/ Lyme/Bartonella/White Matter Lesion Disease on Brain.
[ Clinical Dx w/ two positives and several IND's on the tests from Igenex ], Prior Dx of CFIDS/CEBV 1992, and FMS '93-'94
Diabetes*2 Dx 10/'08

Posts: 3581 | From SE Idaho | Registered: May 2006 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Most likely. [Frown]

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

Posts: 96227 | From Texas | Registered: Feb 2001 | IP: Logged |

Ann-Ohio
Frequent Contributor (1K+ posts)
Member # 44364

posted

https://www.lymedisease.org/lyme-sci-mcas-agony/ is a good article and very thorough. I am bringing it back up to emphasize it.

--------------------
Ann-OH

Posts: 1621 | From Ohio | Registered: Aug 2014 | IP: Logged |

lpkayak
Honored Contributor (10K+ posts)
Member # 5230

posted

Wow. Excellent. So much...easy to understand...organized. Good yo give to those who don't understand

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

Posts: 13712 | From new england | Registered: Feb 2004 | IP: Logged |

TrekCoord
LymeNet Contributor
Member # 48888

posted

Good article and I agree with Silver - I think this may be a root to her issues (besides the LD).

--------------------
I still have a good time wherever I go!

Posts: 138 | From Lost Wages | Registered: Oct 2016 | IP: Logged |

aklnwlf
Frequent Contributor (5K+ posts)
Member # 5960

posted

Really good info TuTu!

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

Alaska Lone Wolf

Posts: 6222 | From Columbus, GA | Registered: Jul 2004 | IP: Logged |

TX Lyme Mom
Frequent Contributor (1K+ posts)
Member # 3162

posted

Here's are links to parts 2 and 3 of this article, written by the same author. Part 3 talks about healing from MCAS.

Awe shucks. It won't let me copy the URL for the link to Part 2, but the part 2 link can be found inside the third part of this article (link below).

https://www.lymedisease.org/lyme-sci-more-mcas/

I'm in a hurry to try to beat LymeToo to the draw on posting this. (Hint: I signed up for updates from the website, so Part 3 arrived in my in-box just a few minutes ago.)

Posts: 4563 | From TX | Registered: Sep 2002 | IP: Logged |

Printer-friendly view of this topic

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
http://www.lymenet.org/