Advertisement

First time visiting? Register for
your free username and password

Main Menu
Forum Home
Search
 Register New User
 Books, Videos, DVDs
 Current Lyme News
 Lyme/Rife Forum
 Suggestion Box
Sponsored Links
Connie's Blog
Watch Connie Strasheim, author of "The Lyme Disease Survival Guide," on her new video blog!
Forum Stats
2716 Members
24 Forums
4570 Topics
5953 Posts

Max Online: 251 @ 12/25/10 12:01 AM
Top Posters
2069
Angls4hope
1926
LymeAngl
263
BryanRosner
178
Rich_skiweasel7
112
Steve
Request Free Info

Page 1 of 1 1
Topic Options
Rate This Topic
#4803 - 01/26/10 04:07 PM Cheeseville Lymie needs Lyme-Friends
rachel_d
New Researcher


Registered: 01/26/10
Posts: 6
Hi from Cheeseville,

I guess my story isn't much different from most others with the Lyme experience, although as you may all empathize, to be the one with Lyme around those who don't have it and are very ignorant regarding it, my story to them is alien.

In July, 2008, I spent ONE NIGHT camping in Bayfield, Wisconsin on one of the Apostle Islands, a dream come true. This night, I also was bitten by a triple-loaded tick who infected me with Lyme, Babesia and Mycoplasma. I became very very sick.

Initially, my worst symptoms were terrible abdominal pain (babesia). I had a upper endoscopy with biopsy, pH probe placed and colonscopy done which all were normal. So, they thought I was have food sensitivities and started me on chronic low doses of steroids. After a few months of that, a head CT, sleep study, EKGs, holter monitors, antidepressants, antianxiety meds, numerous other meds and TWO referrals for an inpatient stay at the nearby mental facility, I REQUESTED a lyme test.

It came back POSITIVE and I was started on doxy. Of course, I felt terrible (herxing)on it for five days until my Western Blot came back as only one band positive (because of the STEROIDS! DUH!!!) I was taken off doxy and told there was nothing they could do for me. This is ten doctors later.

The next June, my symptoms getting worse and worse, I finally was hit with the arthritic portion of our special. I knew immediately it was indeed lyme and literally guilted a friend who was a nurse practitioner to start me on antibiotics. Within five weeks, I was SYMPTOM FREE. But, as we all know, this was not the happy ending I was hoping for.

Six weeks later my symptoms returned TEN-fold. I finally found a LLMD and was diagnosed with lyme, babesia(positive titre and FISH) and mycoplasma.

After six nonresponsive weeks of doxy, amoxicillin and artemesinin, he has started me on the Jemsek Protocol of Mepron, Zithromax, Artemesinin and Flagyl. I'm currently beginning the second week and am as sick as a dying dog. Mostly, I'm nauseous and have extreme stomach upset and diarrhea. I don't really feel as if I'm herxing, more that I'm responding to the poisons in my body.

I'm now close to being very sick for two years. I'm a single mom now working 50% as a teacher. I am trying to be positive and repeat positive statements to myself every day many many times, but I have to admit, I'm going deeper and deeper into that pit of doubt and fear. Nothing seems to be working. I am alone in this fight and really need some lyme-friendly supporters.

Thanks for reading my story,
Rachel D

Top
#5408 - 09/27/10 11:07 AM Re: Cheeseville Lymie needs Lyme-Friends [Re: rachel_d]
Elle
New Researcher


Registered: 09/27/10
Posts: 2
Rachel,

I feel for you. What a horrible story. This is a horrible disease and if you don't have it, you don't understand. We all need friends. I'm about to ditch my boyfriend of 2 years because he just thinks Lyme is no big whoop and that I'm dramatizing.

I highly suggest you read Buhner's book, Healing Lyme, and a book called Cure Unknown, as well as Bryan Rosner's book on the 10 Best Lyme treatments and educate yourself as to the adjunct therapies for Lyme. Have immaculate nutrition and take the supplements recommended in these books. The key is to boost the immune system so your body can help heal itself.

Have hope, baby girl! Don't let yourself fall into the pit of despair because it'll only negatively impact your immune system. I know it's hard but work at staying positive.

Elle

Top
Page 1 of 1 1


Moderator:  Willo 
Hop to:
Bryan's Blog

Latest Forum Topics
Latest News:

 
This doctor just released the first book about Lyme written by an M.D. Learn More.

Shout Box

Newest Members
Kenny9, etkg, Sheredelight, TWDCOACH, swatz
2716 Registered Users
Who's Online
0 registered and 45 anonymous users online.
Lyme Disease Book

Generated in 0.031 seconds in which 0.015 seconds were spent on a total of 13 queries. Zlib compression disabled.

Lyme Community Forums - Discussion, Support, Friends!

 New posts in this forum since you last visited              No new posts  


Copyright © 2006 Lyme Community Forums. All rights reserved.

DISCLAIMER:  This group is for informational and educational purposes only and is not intended to prevent, diagnose, treat or cure disease.  The owners, moderators, members and contributors of this group are not doctors.  This group shall not substitute for advice from a licensed healthcare practitioner.

Links of Interest

Advertise with us       Visit our Storefront       History of Rife Technology       What is Chronic Lyme Disease?

Learn more about the Marshall Protocol      Chronic Lyme Controversy      James Schaller, M.D.

Sauna for Lyme Disease     Natural Antibiotics for Lyme Disease       Chronic Lyme Science      Pulsed Electromagnetic Fields (PEMF)

Lyme Disease in the UK (United Kingdom), Canada, Europe, and abroad     Immune Response Training

Ozone and Oxygen Treatments    Mercury Poisoning and Lyme Disease    Electromagnetic Field Sensitivity - Real or Imaginary?

Lyme Disease News    Lyme Disease Research    The Lyme Disease Solution by Ken Singleton, M.D.     The Lyme Autism Connection

The Holistic Handbook of Sauna Therapy, by Nenah Sylver, Ph.D.      The New Lyme Disease Insights Blog

Don't miss our

works in progress page

.