My daughter began spiking super high fevers (105.6!) around 9months. Â They would come on suddenly, last 2-4 days, cause a loss of appetite, nausea and vomiting and occasionally present w/swollen glands and a sore, pus-coated throat. Â My husband and I really started taking note of the frequency of these episodes when she was around 1 & 1/2yrs. old. Â Like many of you, we returned to the pediatrician time and time again with the same symptoms. Â I was lucky in that my ped. admitted it seemed strange but didn't know what it could be. Â She encouraged me to keep a calendar of onset, duration, etc. Â I also began my own search online. Â I came across many near fits but almost fell out of my chair when I read about PFAPA. Â I knew without a doubt I had found the problem and even my conservative husband (also a medicine doctor) had to agree. Â We asked our ped. about it and was referred to an ID specialist. Â Our daughter endured 8wks of bi-weekly blood draws -- she was barely 2yrs. old! Â She was a trooper but I still can't resolve having put her through that just to rule out other causes. Â Well wouldn't you know, shortly after being diagnosed w/PFAPA she began to outgrow the illness. Â The "well time" between episodes became longer, going from every 6 weeks to every 10 weeks. Â She's 4 & 1/2 now, strong, smart and so, so beautiful! Â She hasn't had an episode in over a year. Â I'm writing this now because my husband and I still think back to those days and nights of worry; not knowing what was ailing our child, unable to help and knowing only it was sure to happen again. Â We are incredibly lucky that time of uncertainty was relatively short-lived. Â Boundless thanks to those who shared their stories as one of them made for our happy ending. Â
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