When I was digging into the information the lab tests gave
me, I noticed issues with LH levels in children can be due to chronic
illnesses. When I was around a year old I had a seizure while my mom was
napping with me. She felt me get warm and as she was rousing herself I seized
and stopped breathing. She called my dad at work while performing CPR on our
kitchen table and was able to rouse me before the ambulance found the house
(our house is the last on a dirt drive way nearly a mile off the paved state
road – and back when I was a baby there was no GPS to help find the location).
I checked out fine in the hospital and the seizure was blamed on a sudden spike
in my temperature. For the next 3 years I was constantly getting fevers and sore
throats, to the point that when my parents felt me getting warm they would take
me fully clothed and jump into a tepid shower – children’s Tylenol did not work
fast enough to stop the fever from building and causing another seizure. I was
prescribed bubblegum flavored penicillin on a regular basis until I had my
tonsils out at 4 years old. Then the fevers and sore throats stopped. It was
all blamed on my tonsils, but in my searching recently I believe I was
misdiagnosed. Or maybe this diagnosis didn’t exist when I was a child. I
believe I suffered from periodic adenitis pharyngitis aphthous ulcer syndrome
(PFAPA). Basically, what this mouthful means
is that I would have cyclical bouts of high fevers accompanied by sore throats,
mouth sores (which I don’t remember) and body aches for seemingly no reason.
Between episodes I was symptom free. In my reading I discovered often times
having the tonsils and adenoids (I still have my adenoids) removed, for reasons
unknown to the medical community, can stop the cycle. If not, most children
grow out of PFAPA by the time they hit double digits.
How strange to read about a syndrome and see it describe
your life to a T but never having been applied to you by a medical professional.
The sad part is, I was doused with antibiotics to the point where penicillin
does little for me when this would not have been necessary, according to my
research. I did not uncover the answer to my original question, if this has
anything to do with pushing my body out-of-line with certain hormones, but the
discovery was notable regardless. The other thing to note is that this syndrome
is genetically connected, so if I had been able to have children they might
have had the same issues. I know my father had his tonsils out as a child but
the doctor had claimed his were truly infected, at least from what my
grandmother recalls. So, did my dad unknowingly pass this along to me? I guess
it’s possible. It seems unlikely there is any link between PFAPA and PCOS so,
theoretically I had two separate syndromes affecting my life and my health. If
the precluding syndrome (PFAPA) kicked off the future syndrome (PCOS) due to chronic
fever/inflammation in my body, it might explain why my sister doesn’t seem to
struggle with the same weight/menstrual issues that I do and follows more
closely to our mother’s experience. Genetics are a big old bowl of crazy and
the combinations and possibilities often times seal our fate even before we
were born. Academically, it is interesting to learn, but emotionally, it’s hard
to think I might never have stood a chance. I’m curious as to what the
Nutritionist RN will say about what I’ve uncovered.
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