My Lyme Disease (Autoimmune Diseases/Disorders) Story
LymeOrNot asked:
Could I have Lyme disease from birth as autism fist, then became selective mutism, Epilepsy, Bipolar, Depression, Influenza Flu/Cold, MRSA(Staph)infection at left wrist and gum areas, Obesity, Tumors/blisters at brain and uterus areas, Alzheimer's, Parkinson's, Arthritis, Fibromyalgia, Meniere's disease, Lupus, Multiple Sclerosis, Chronic Fatigue Syndrome…??? …
Susy
March 28th, 2009 at 9:36 pm
Patti
Please stay strong and look at the progress, and not the symptoms….it may be a very long process…
March 31st, 2009 at 2:06 am
Franny
Thanks. Hope your are doing better each day, one day at a time…
April 1st, 2009 at 11:59 pm
Christopher
Google…..”Low Dose Naltrexone Homepage.” And also here on You tube…”Controlling Lyme Disease,” and see the LDN videos by “TropicalDawg” here as well. I have been using LDN, for just over a week now, and feel the need to pass the buzz. This is a drug that helps with the immune system, inflammation and endorphins. Eat as if you had a yeast problem, because Lyme loves what yeast loves. And no sugars of any kind…”Including Fruit!”
April 4th, 2009 at 11:24 pm
Jane
ive just been diagnosed with lymes & am experiencing mass symtoms although i too look rather well most of the time, i can relate to all that you,ve said, thanks i think im begining to understand maybe whats happening to me xx
April 8th, 2009 at 6:56 am
Annemarie
Bless your strong will and spirit!
April 9th, 2009 at 2:31 pm
Jane
IMPORTANT NOTICE FROM On The Marc Media:
We’d like to share some really important news. Two weeks ago Oprah’s Dr. Oz interviewed Andy Abrahams Wilson, director of Under Our Skin and Washington D.C. ABC-7′s Medical Reporter Kathy Fowler. They talked for about 45 minutes about the film and the controversy surrounding Lyme disease….
Dr. Oz wants to hear from people with Lyme disease. Please visit Oprah web site and email Dr. Oz.
April 12th, 2009 at 11:48 pm
Vichelle
You are a beautiful woman,wife,mother,sister,aunt and best friend anyone in this world could have and I will stand by you until the day I go to heaven.
My sons symptoms and daughters do get worse in the afternoon and yes the microbes are regrouping or moving. I have watched them move on my sons face.I myself get these symptoms of alzheimers in the late afternoon and midafternoon.. Keep up the good work!
THE CURE UNKNOWN!!!!! great book
April 14th, 2009 at 12:15 am
Samantha
Yes! I probally have Lyme and my children were infected by me. Then my 8yr son re-infected. Then came my little girl in 04. Her father was born with listera and i’m sure Lyme. He grew ip on 350 acres and hunted. We know live on 10 acres. surronded by hunting clubs. Thank you sooo much for your bravery.
April 17th, 2009 at 5:55 am
Violette
Thanks, Elaine, for sharing your experiences.
When we continue to share our stories, the others may avoid the colossal errors/mistakes made by the medical professionals/scientists. Have you considered posting your brochure as a Video Response? 
April 18th, 2009 at 11:59 pm
Janet
Thanks, the same to you. Please stay well.
April 21st, 2009 at 3:26 pm
Sherri
I sympathize with you 100 %.On a much smaller scale, my experience was similar. Had a perfect bulls-eye rash,positive Western-blot, and a lot of symptoms. Still I was told that Lyme disease does not exist in my area. I found help 6 hours away and went through an extensive IV therapy program. This doctor does pulse therapy. IV and oral antibiotics are given to you rotationally. I wrote a Lyme brochure for my area with the Lyme specialist’s help. Will email to anyone interested.
Elaine in VA
April 23rd, 2009 at 9:47 pm
Violet
Thanks and take care.
April 27th, 2009 at 4:05 am
Joan
LymeOrNot, my heart goes out to you. You are a fighter and I am so proud of you and it gives me hope to keep on fighting. A big hug and smile from me.
April 27th, 2009 at 2:40 pm
Sandy
No way in hell Steere or any of that gang will ever admit they are wrong. Their egos are way too big for that. There is a book thats kinda new (forget the name), but apparently proof is there that Steere is doing all this because he was angry that in the 1970′s in CT.. they would not name the lyme spirochette after him, and Willy B got that credit instead. Havent read this book yet.. my Lyme Dr just told me about it last week. Will get the name and post it tho when I see her again next week.
April 29th, 2009 at 4:50 pm
Louise
I am so sorry for what you have been through… My gosh you have been through a lot… I am pretty much going through the same thing right now. If you have time you could watch my videos… Thank you and keep making these very informative videos!!