JennifersHope
New member
Mayo does do a good job finding mutations if you get the full gene study done.. They have to look at the whole gene.. It took them a little over four weeks but they found my second mutation..
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Seeking some advice
- Thread starter MaeFlower
- Start date
Thanks for the info. Vivi's pediatrician called me this afternoon, she has "infiltrates" on her lungs for the 4th time since birth. She also had a c. diff test that did show a toxin, he wants to repeat a stool culture this week. I will keep you all posted. Please pray for Vivien that the Pulmonologist will have the complete panel tested. With no diagnosis of anything, some days I feel as if I'm chasing Unicorns.
Thanks for the info. Vivi's pediatrician called me this afternoon, she has "infiltrates" on her lungs for the 4th time since birth. She also had a c. diff test that did show a toxin, he wants to repeat a stool culture this week. I will keep you all posted. Please pray for Vivien that the Pulmonologist will have the complete panel tested. With no diagnosis of anything, some days I feel as if I'm chasing Unicorns.
Thanks for the info. Vivi's pediatrician called me this afternoon, she has "infiltrates" on her lungs for the 4th time since birth. She also had a c. diff test that did show a toxin, he wants to repeat a stool culture this week. I will keep you all posted. Please pray for Vivien that the Pulmonologist will have the complete panel tested. With no diagnosis of anything, some days I feel as if I'm chasing Unicorns.
T
tarheel
Guest
The beginning of your story- failure to thrive, jaundice, GERD- sounds like the beginnings of my story. I was below birth weight until I believe 3 months. My sweat test, however, was very high. I would keep pushing for the full pannel- I was almost diagnosed with biliary atresia (misspelling I think) before they did the sweat test. (The genetics test wasn't even available when I was diagnosed)
T
tarheel
Guest
The beginning of your story- failure to thrive, jaundice, GERD- sounds like the beginnings of my story. I was below birth weight until I believe 3 months. My sweat test, however, was very high. I would keep pushing for the full pannel- I was almost diagnosed with biliary atresia (misspelling I think) before they did the sweat test. (The genetics test wasn't even available when I was diagnosed)
T
tarheel
Guest
The beginning of your story- failure to thrive, jaundice, GERD- sounds like the beginnings of my story. I was below birth weight until I believe 3 months. My sweat test, however, was very high. I would keep pushing for the full pannel- I was almost diagnosed with biliary atresia (misspelling I think) before they did the sweat test. (The genetics test wasn't even available when I was diagnosed)