posted
I would like to hear how people not knowing they
had lyme while starting a family and finding
out years later that they in fact do and that
it was passed to their children.
What led to their diagnose of having lyme
disease?
Does there seem to be a common pattern of
symptoms that they all seem to have?
Thanks for any help
Posts: 158 | From PA. | Registered: Jul 2006
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joalo
Frequent Contributor (1K+ posts)
Member # 12752
posted
Up.
-------------------- Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006. Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007
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Geneal
Frequent Contributor (5K+ posts)
Member # 10375
posted
I have two children with congenital Lyme.
I didn't even think to look for it until my husband and myself were diagnosed.
One child had fatigue, joint pain, and odd symptoms like feeling like she was shaking but she wasn't.
Symptoms I could easily relate to.
My other child was slow developmentally for physical milestones.
His pinnas of his ears would turn fire engine red.
He had more subjective symptoms for sure.
Both babies had colic and I nursed both of them.
My son ( with the subjective symptoms) had more positive bands on the WB via Igenex than any one else in our family.
So....I did a pretty good search for Lyme symptoms in infants and toddlers...
I posted it a couple of years ago.
It may shed some insight.
Hugs,
Geneal
Posts: 6250 | From Louisiana | Registered: Oct 2006
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