BabyBeauty
New member
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>BikerEd</b></i>
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Momto2</b></i> Hmm, never heard of anyone getting special treatment in an ER before due to CF. My policy is that my health is my responsibility, and if I'm going to go anywhere where there is a high likelyhood of catching something icky, I wear a mask and wash my hands like crazy.
</end quote>
<p style="margin: 0in 0in 10pt;" class="MsoNormal"><font color="#000000" size="3" face="Calibri">Oh HEAR HEAR! I wish more parents would teach their kids how to live in a Non-CF world rather than stomp their feet anytime the world does not stop for their DD/DS w/cf. Someday they (the CFer) will find themselves in a position where the world does not revolve around CF and they will have to manage themselves in that world or isolate themselves from it.</font><font color="#000000" size="3" face="Calibri"></font>
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I look forward to the day that CF is not an issue. I pray for it each day. I fundraise my butt off for it. In the meantime, it is MY JOB as a parent to protect my daughter. If that means I ask for an isolated room. Then yes I will ask for it. I will demand it. That is my JOB. My only argument in this thread has been that my daughter should not wait in the general waiting room. Some hospitals have rooms set aside for immune compromised patients. It should be a standard of care in ER's. Should my daughter BE SEEN before an open chest wound or difficulty breathing...NO. But the hospitals should do their best to make sure immune compromised patients stay safe. We had to go to an ER in another city and had a fantastic experience. We were put in a safe room right away and yes we waiting along time to be seen, but we felt safe. No other patients were coughing on our daughter. All hospitals should strive to be better. I called the patient advocacy line and talked with a wonderful lady. She used to work in the ER at that same hospital. She said our case was handled innappropriately. She said there should be a set SOP when an immune compromised patient walks into the ER. They were going to have a meeting about my case and work on making it better. No hospital is perfect, but if they can make improvements to make sure our kids are safe, then we need to voice our opinion.
<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Momto2</b></i> Hmm, never heard of anyone getting special treatment in an ER before due to CF. My policy is that my health is my responsibility, and if I'm going to go anywhere where there is a high likelyhood of catching something icky, I wear a mask and wash my hands like crazy.
</end quote>
<p style="margin: 0in 0in 10pt;" class="MsoNormal"><font color="#000000" size="3" face="Calibri">Oh HEAR HEAR! I wish more parents would teach their kids how to live in a Non-CF world rather than stomp their feet anytime the world does not stop for their DD/DS w/cf. Someday they (the CFer) will find themselves in a position where the world does not revolve around CF and they will have to manage themselves in that world or isolate themselves from it.</font><font color="#000000" size="3" face="Calibri"></font>
</end quote>
I look forward to the day that CF is not an issue. I pray for it each day. I fundraise my butt off for it. In the meantime, it is MY JOB as a parent to protect my daughter. If that means I ask for an isolated room. Then yes I will ask for it. I will demand it. That is my JOB. My only argument in this thread has been that my daughter should not wait in the general waiting room. Some hospitals have rooms set aside for immune compromised patients. It should be a standard of care in ER's. Should my daughter BE SEEN before an open chest wound or difficulty breathing...NO. But the hospitals should do their best to make sure immune compromised patients stay safe. We had to go to an ER in another city and had a fantastic experience. We were put in a safe room right away and yes we waiting along time to be seen, but we felt safe. No other patients were coughing on our daughter. All hospitals should strive to be better. I called the patient advocacy line and talked with a wonderful lady. She used to work in the ER at that same hospital. She said our case was handled innappropriately. She said there should be a set SOP when an immune compromised patient walks into the ER. They were going to have a meeting about my case and work on making it better. No hospital is perfect, but if they can make improvements to make sure our kids are safe, then we need to voice our opinion.