Lyme Disease Support Group

Group Leader

Lyme Warrior!

Lyme & MSIDS (Multi-Systemic Infectious Disease Syndrome)

I am not a doctor. Any information offered is based on my experience and personal knowledge. Please always refer to your doctor or other healthcare professional for medical advice.

My story can be found on my profile.

nan

I am not a doctor, nor have I ever been. All comments are based on my personal experience or opinion.

IgM
41+

IgG
41+
31 IND
39 IND

Currently treating Lyme & Babesiosis.
Have many Bart symptoms.

Blessings! :)

Group Leader

Lyme Warrior!

Lyme & MSIDS (Multi-Systemic Infectious Disease Syndrome)

I am not a doctor. Any information offered is based on my experience and personal knowledge. Please always refer to your doctor or other healthcare professional for medical advice.

My story can be found on my profile.

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.

I have a policy that I only share my experience with Lyme Disease & coinfections.

I also, share some of what I have learned from my own research. I sometimes give friendly advice.

If you need medical advise please see a MD or other medical professionial.

Group Leader

Lyme Warrior!

Lyme & MSIDS (Multi-Systemic Infectious Disease Syndrome)

I am not a doctor. Any information offered is based on my experience and personal knowledge. Please always refer to your doctor or other healthcare professional for medical advice.

My story can be found on my profile.

Was diagnosed with Autonomic Disorder, POTS, Interstitial Cystitis, and Fibromyalgia. True story is I have late stage Lyme which has caused these things. Just began the fight in October 2011 (have been full-blown Lyme since Sept. 5, 2010), and WILL be victorious! Positive bands: IgG 41 and 60; IgM 23 and 41. CDC positive!

Not a doctor, not anyone of any legal standing... just someone on the search.
(Translation: Please do not take anything I say as medical advice. Always see your doctor when needing medical advice.)

GlitchyMomma

I am not a doctor, nor do I play one on TV. All comments are based on my personal experience or opinion.
______________________________
Only major "bites" I remember were chigger bites in June 2000 and flea bites in early 2001.

First weird symptom was a panic attack w/ tachycardia in 2001. My husband brought me to the ER, and I was released when everything showed normal.

~June 2001 - Possible VERY early miscarriage, 10 EPTs were positive then I had a heavy menses a few days later. ER said I was never pregnant.

Hashimoto's Thyroiditis dx July 2003
Cholecystectomy March 2010
Vit D3 Deficiency 2011
Progesterone Deficiency 2011
Adrenal Fatigue September 2011
January 2012 Labcorp: IgG 41 Positive, IgG 18 Positive, IgG 23 Positive, IgM 39 Positive, IgM 41 positive
CD57 - 32

ABX: Doxy 28 days, Minocycline 30 days, Ceftin 37 days, 4/16/2012 started Azithromycin

P23 and P41 bands positive, IBS like symptoms caused by possible candida, herbal and antiobiotic treatment, gluten free, candida diet.

I do not have a medical license so my suggestions are limited to personal experience and research. Also I am not a lawyer so if I offer advice relating to school issues it is only from my experiences as a special education teacher, my own disabilities real or Lyme induced, and research.