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 » ALS and Doxy

 - UBBFriend: Email this page to someone!    
Author Topic: ALS and Doxy
2young2dieMom
LymeNet Contributor
Member # 25434

Icon 1 posted      Profile for 2young2dieMom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Anyone else with an ALS diagnosis try Doxycycline? I've heard this drug kills ALS patients very quickly.

I took a new version of it, Doryx, for about a month before I started having trouble breathing. I was so scared that my diaphram was being paralyzed already. I'm going for a pulmonary test next week to see if any damage was done.

Too bad, the doryx really seemed to be helping. I had so much more energy and actually an increase in muscle function.

--------------------
Dxd ALS 3/2010
Dxd cllinical Lyme 4/2010
Positive for Protomyxzoa but absolutely nothing else in Igenex

Posts: 417 | From central ct | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
joalo
Frequent Contributor (1K+ posts)
Member # 12752

Icon 1 posted      Profile for joalo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Up.

--------------------
Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006.

Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
LymeLogged
Member
Member # 36494

Icon 1 posted      Profile for LymeLogged         Edit/Delete Post   Reply With Quote 
I'm so sorry for your troubles.

I only wanted to add that Doryx is timed release Doxy. Way more espensive than regular Doxy, but it's easier on most peoples stomachs.

I hope you get an answer soon.

Posts: 74 | From NEPA | Registered: Mar 2012  |  IP: Logged | Report this post to a Moderator
jackie51
Frequent Contributor (1K+ posts)
Member # 14233

Icon 1 posted      Profile for jackie51     Send New Private Message       Edit/Delete Post   Reply With Quote 
Your shortness of breath could be caused by a co-infection.
Posts: 1374 | From Crazy Town | Registered: Dec 2007  |  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 
that is so scaarey and so sad

im taking regular doxy with not trouble

my son got the othere one and it was easy on his stomach

i hope you get answers and get well

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

Posts: 13712 | From new england | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
Sammi
Frequent Contributor (1K+ posts)
Member # 110

Icon 1 posted      Profile for Sammi     Send New Private Message       Edit/Delete Post   Reply With Quote 
I recently started Minocycline. My shortness of breath has increased since starting it, but I have Babesiosis.

Do you have Babesiosis?

Do you think it could be a herx since this happened after you took it for about a month?

Posts: 4682 | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
steve1906
Frequent Contributor (1K+ posts)
Member # 16206

Icon 1 posted      Profile for steve1906   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lyme Disease Found in 100 Percent of 150 ALS Patients>
http://floridadetox.com/lyme-disease-found-in-100-percent-of-150-als-patients

_________________________________________________

--------------------
Everything I say is just my opinion!

Posts: 3529 | From Massachusetts Boston Area | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
lyme-o
LymeNet Contributor
Member # 35115

Icon 1 posted      Profile for lyme-o     Send New Private Message       Edit/Delete Post   Reply With Quote 
Anyone that I have talked to has never heard of this Florida Detox. I actually got the info from them. But they only treat with mega doses of Vitamin C. And I've heard thats not good with Lyme
Posts: 305 | From United States | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
Caniggia
Member
Member # 30479

Icon 1 posted      Profile for Caniggia     Send New Private Message       Edit/Delete Post   Reply With Quote 
HBOT, you got to try that. It's gonna make you feel better.

--------------------
My blog about my condition - http://borreliawenttofar.wordpress.com - Diagnosed with cellular activity for Borrelia, Ehrlichia, Chlamydia Pneu. Also have the herpes simplex virus.

Posts: 52 | From Sweden | Registered: Feb 2011  |  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.