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 » A little more progress...

 - UBBFriend: Email this page to someone!    
Author Topic: A little more progress...
ArtistDi
Frequent Contributor (1K+ posts)
Member # 2297

Icon 1 posted      Profile for ArtistDi     Send New Private Message       Edit/Delete Post   Reply With Quote 
I thought I would post because it has taken me
years to muddle through a toxic drug protocol for
me that injured my immune system (this was documented by my drug allergist and llmd). At
any rate, I stopped having seizures in Dec. 2005
after 3 years of experiencing them, and finally,
I went on a family vacation to Maine last week.

We have not been together as a family for vacation
for six years, and I had an enjoyable time. Of
course I watched out for ticks and pretty much
stayed to the pavement.

But, this was a monumental time for me to almost
be like a "real human being."

My mcs is better, so hotels, etc. don't bother me,
and although I have miles to go before I sleep,
I am more engaged in life.

I will be having a one-person show of my artwork
this October, and that has been even longer--
exhibiting on my own!!

At any rate, it has been baby steps, steps forward
and steps back, no linear progression of health.
I still have symptoms of numbness, tingling, but
can eat better on a rotational diet and IV drugs.

I have been trying the transdermal Rifampin (very
small doses to bulid up on per drug allergist's
and llmd's orders), and I feel that it makes my
mind clearer.

So, that is the update, and I always hope that
things will quietly improve with time.

Di

Posts: 1567 | From Hatfield, MA, USA | Registered: Mar 2002  |  IP: Logged | Report this post to a Moderator
lymemomtooo
Frequent Contributor (1K+ posts)
Member # 5396

Icon 1 posted      Profile for lymemomtooo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Congratulations Di..Keep it up..hugs lymemomtooo
Posts: 2360 | From SE PA | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
Ann-OH
Frequent Contributor (5K+ posts)
Member # 2020

Icon 1 posted      Profile for Ann-OH     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am so glad you are feeling better, Di! How I would love to see your work!

What were the drugs that were toxic to you in combination?

Ann - OH

--------------------
www.ldbullseye.com

Posts: 5705 | From Ohio | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
ArtistDi
Frequent Contributor (1K+ posts)
Member # 2297

Icon 1 posted      Profile for ArtistDi     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hugs back, Lymemom, and to your daughter too.

Ann, the drugs that caused an immune injury were
Plaquenil, Biaxin and Mepron, which were used
in concert. Unfortunately, that combo caused
burning throughout my whole body--brain, limbs,
nose, mouth, etc. Moreover, a cascade of bad
events then occured when I could not tolerate
any meds orally (this is why I do IV to bypass
the gut).

It was a long, hard journey of many doctors, in
and out of state, and all kinds of therapy. I
do have autoimmune issues along with the lyme/-
infections, so that had to be addressed. I think
that the drug combo pushed me into autoimmune,
and this is my drug allergist's theory.

I just saw her in Boston with my husband a few
months ago, and she thinks it will take yet another one to two years for my body to really
settle down.

At any rate, the progress over the year has been
good, and I can at least resume some of my living.

Posts: 1567 | From Hatfield, MA, USA | Registered: Mar 2002  |  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 
HI Di!! It's been such a LONG journey for you! I'm so glad you were able to find a dr(s) who could figure all this out and help you!

Back among the living is GREAT news!! [Smile]

--------------------
--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.