Confirmation of diagnosis

Ratatosk

Administrator
Staff member
Yikes, I would hope that the other patients didn't have CF. When DS was in the NICU he shared a room with 3 micro preemies, then got moved to ICC (Infant Critical Care) and shared a room with a preemie, spina bifida baby and another with cranio facial issues.
<br />
<br />And when he had his bowel obstruction surgery, we were initially told by the intake person in the ER that he'd have to share a room, but the we were placed in a private room and told that all CF patients get their own room.
 

hmw

New member
Kids do have to share rooms sometimes at our hospital, but we were told that those with CF do not. Even kids that share are just the typical 2-patient rooms though- not 4. Hopefully those rooms at Hopkins are typically just for infants.
 

hmw

New member
Kids do have to share rooms sometimes at our hospital, but we were told that those with CF do not. Even kids that share are just the typical 2-patient rooms though- not 4. Hopefully those rooms at Hopkins are typically just for infants.
 

hmw

New member
Kids do have to share rooms sometimes at our hospital, but we were told that those with CF do not. Even kids that share are just the typical 2-patient rooms though- not 4. Hopefully those rooms at Hopkins are typically just for infants.
 

pipersmom

New member
Check with your CF Team, but for a long time when Piper needed to be admitted, we did the admissions through a local hospital rather than the one affiliated with our CF center (we are 2 hrs away). As long as we caught the exacerbation early, our team didn't have a problem with it at all. They knew the pediatric pulm team there, and communicated daily by phone/e-mail. It saved a lot of mileage/money for myself and my family.

Since Piper's health has gone downhill, we now do all admissions through UVa, but I would love for her to be at a place health-wise where the local admissions were an option again.
 

pipersmom

New member
Check with your CF Team, but for a long time when Piper needed to be admitted, we did the admissions through a local hospital rather than the one affiliated with our CF center (we are 2 hrs away). As long as we caught the exacerbation early, our team didn't have a problem with it at all. They knew the pediatric pulm team there, and communicated daily by phone/e-mail. It saved a lot of mileage/money for myself and my family.

Since Piper's health has gone downhill, we now do all admissions through UVa, but I would love for her to be at a place health-wise where the local admissions were an option again.
 

pipersmom

New member
Check with your CF Team, but for a long time when Piper needed to be admitted, we did the admissions through a local hospital rather than the one affiliated with our CF center (we are 2 hrs away). As long as we caught the exacerbation early, our team didn't have a problem with it at all. They knew the pediatric pulm team there, and communicated daily by phone/e-mail. It saved a lot of mileage/money for myself and my family.
<br />
<br />Since Piper's health has gone downhill, we now do all admissions through UVa, but I would love for her to be at a place health-wise where the local admissions were an option again.
 

auntcob

New member
Thanks for all the input. My hunch was staying at Hopkins, if needed, would be best. Now, how to manage that and work and other kids is a different story all together..............
 

auntcob

New member
Thanks for all the input. My hunch was staying at Hopkins, if needed, would be best. Now, how to manage that and work and other kids is a different story all together..............
 

auntcob

New member
Thanks for all the input. My hunch was staying at Hopkins, if needed, would be best. Now, how to manage that and work and other kids is a different story all together..............
 
Top