mlkeen
Frequent Contributor (1K+ posts)
Member # 1260
posted
All three of us and the dog have lyme. Two of us have co-infections for sure. Have had it 3-5 years at least. All of us are getting better with abx, magnesium, exercise and heat.
Posts: 1572 | From Pa | Registered: Jun 2001
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posted
If you re read what the FEW of us just posted here, that is totally amazing that the medical community has a problem acknowledging this as a BIG ISSUE!!
Wow...I know there is more. I am sure that my hubby may be added to the list (with my mom, myself, and 2 girls) when he gets home.
Would love to test many others.....but so many are not open to it and there MD would probably see no need in it.
Posts: 688 | From SW Arkansas | Registered: Dec 2003
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posted
My four children, myself and my husband all tested positive, equivical, or with most significant bands positive.
My mother has classic symptoms but refuses to be tested, attributes her aches and pains, cognitive dysfunction to "old age". I think shes just hard headed.
Noy sure about other family members as I am not very close to any of them.
Cheryl
Posts: 204 | From kentucky | Registered: May 2003
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shazdancer
Frequent Contributor (1K+ posts)
Member # 1436
posted
me -- infected two years ago, no rash, positive Western Blot
my son -- probably infected 4-7 years ago, no rash, positive Western Blot
my mom -- probably infected TWENTY-FIVE years ago, diagnosed 3 months ago, is responding to oral antibiotics
my brother and niece
my sister
Posts: 1558 | From the Berkshires | Registered: Jul 2001
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posted
My father was MIS-diagnosed with Alzheimer's in the early 1980s. In 1992 at the age of 81, a LLMD in New Jersey diagnosed a very advanced case of Lyme disease - Neuro Borreliosis.
We attempted IV therapy, but stopped treatment because of our ignorance of Lyme & a multitude of complications. He spent several years in a nursing home & died of complications of Lyme disease.
I removed a tiny tick in the late 1970s or early 1980s (max attachment time: 4-6 hrs), had a 2" x 3" bull's eye rash but did not know to get treatment. No other symptoms until 1988. MIS-diagnosed with arthritis, but correctly diagnosed with Lyme & started treatment in 1992. In 2001, also diagnosed with Babesiosis & Bartonella.
Grandson, age 12 yrs, is presently being treated by Dr Jones in CT. We're pretty certain he's had Lyme since he was 7 yrs old. Almost all his symptoms were typical of ADD. Several yrs ago, his Pediatrician would not even consider Lyme, so we took him to a dr out of town. WB showed only Band 41, but since that is VERY significant in children, he was given adequate doses abx until symptoms were gone.
Symptoms flared up again. PCR was positive for Lyme. Treatment was resumed & his Lyme dr consulted with Dr Jones in CT. Since improvement was so slow, we decided to go to CT. He's had 2 appts with Dr Jones & goes back Oct 26th. Dr Jones said he's fixable, but MAY have to treat until he's 17 yrs old.
My having Lyme disease is one of the biggest blessings of my life. Without my contacts in the Lyme community (friend in NC whose son had LD & LYmeNet) my grandson never would have been diagnosed & treated.
Thanks again to all those who have so generously given their time & shared knowledge of Tick-Borne Diseases. I'll always be grateful for your help!!
Posts: 4638 | From South Carolina | Registered: Mar 2001
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posted
I have lyme disease... both my children have been exposed to it and I have to watch them per Dr. Jones.. my husband tested through Igenex and had lots of bands come up positive but his doctor said "it doesn't mean you have lyme".. yeah, right! He is a hard headed one, my husband..... my older sister has to have it, but doesn't get tested.. I believe her children have it too... my mom has symptoms, but doesn't get tested either.. probably dad too.. all have a history of bites.. but choose to be ignorant to it.. It definitely is a family disease! Posts: 802 | From Reading, PA, USA | Registered: Aug 2001
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arg82
Frequent Contributor (1K+ posts)
Member # 161
posted
All you families with Lyme, go check out the info about the camp/retreat I'm setting up for kids, families, teens, adults, or anyone else with Lyme and other TBDs. You can see it here: http://flash.lymenet.org/ubb/Forum1/HTML/026979.html.
--Annie
------------------ ``The best way out is always through.'' -Robert Frost Click to join Lyme_Camp
Posts: 2184 | From Rochester, MA | Registered: Oct 2000
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troutscout
Frequent Contributor (5K+ posts)
Member # 3121
posted
Me.... 30 some years (active) Wife....since I infected her....11 to 12 years (inactive) Girls....since birth (active)
We are all improving.
Trout
PS/////Dr Crist
Posts: 5262 | From North East Iowa | Registered: Sep 2002
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posted
Me, my husband and our 7-year-old son. I've had it for 21 yrs. but just diagnosed. Our son has congenital LD and is very sick.
Posts: 703 | From Almost Heaven | Registered: Aug 2004
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Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
Dr. Ted.. with a hurricane barrelling down on his head, as we speak.. just asked me to post this for him to help you all.
He is STILL having trouble posting at Lyme Net... but is concerned about you folks.
xxxxxxxxxxxxxxxxxxxxxxxxxxxx
1. The above posts show that the TBDs are contagious.
2. TBDs can be passed from infected mother to fetus.
3. So many tests are unreliable.
4. Diagnosis should be made on history of symptoms, family history, results of pregnancy on child, response to Abx and, most important, full clinical examination of all systems by a clinically-minded doctor if you can find one who will give you the time.
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,
NJ08534USA http://www.lymenet.org/