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Yeah I have gotten those. It is VERY random and does not happen often but lasts for no more than 10 seconds. It is SUPER sharp and I can not take a breathe in. It is so bizarre and comes out of nowhere. I wonder if it is the mucus moving and that just can cause a pain. I would say if it does not...
Yeah I have gotten those. It is VERY random and does not happen often but lasts for no more than 10 seconds. It is SUPER sharp and I can not take a breathe in. It is so bizarre and comes out of nowhere. I wonder if it is the mucus moving and that just can cause a pain. I would say if it does not...
I never go. I actually only went one time when I was suffering from terrible vertigo. But otherwise I do not go and have not had any sinus surgery. I would imagine anyone that have had the surgeries would go regularly to keep things going good
Jennifer 38 with CF and CFRD
I never go. I actually only went one time when I was suffering from terrible vertigo. But otherwise I do not go and have not had any sinus surgery. I would imagine anyone that have had the surgeries would go regularly to keep things going good
Jennifer 38 with CF and CFRD
I never go. I actually only went one time when I was suffering from terrible vertigo. But otherwise I do not go and have not had any sinus surgery. I would imagine anyone that have had the surgeries would go regularly to keep things going good
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<br />Jennifer 38 with CF and CFRD
Those of you using the pari pro nebs for sure get a new compressor if the HTS and PUlmozyme is taking longer than 20 mins. the compressor fan gets clogged up with the medicine that is released in the air and a new one will put you back down to the 15-20 minute mark for those drugs. I noticed...
Those of you using the pari pro nebs for sure get a new compressor if the HTS and PUlmozyme is taking longer than 20 mins. the compressor fan gets clogged up with the medicine that is released in the air and a new one will put you back down to the 15-20 minute mark for those drugs. I noticed...
Those of you using the pari pro nebs for sure get a new compressor if the HTS and PUlmozyme is taking longer than 20 mins. the compressor fan gets clogged up with the medicine that is released in the air and a new one will put you back down to the 15-20 minute mark for those drugs. I noticed...
I have been using the eflow since jan and yes I do like it but I had to stop using the HTS and Pulmozyme in it cause it was cloggingh up the metal head and then defeated the purpose of using it for fasssst treatments. Kinda bummed. So now I use it for Albuterol and Tobra and Colistin. And then...
I have been using the eflow since jan and yes I do like it but I had to stop using the HTS and Pulmozyme in it cause it was cloggingh up the metal head and then defeated the purpose of using it for fasssst treatments. Kinda bummed. So now I use it for Albuterol and Tobra and Colistin. And then...
I have been using the eflow since jan and yes I do like it but I had to stop using the HTS and Pulmozyme in it cause it was cloggingh up the metal head and then defeated the purpose of using it for fasssst treatments. Kinda bummed. So now I use it for Albuterol and Tobra and Colistin. And then...
My voice is kinda hoarsy and sounds like child. When I answer the phone they ask if my mom or dad is home! HA
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<br />Jennifer 38 with CF and CFRD
Have him do an ultrasound of your gallbladder cause the pain your described and location could be gallstones. Ultrasound is ALOT less invasive than colonoscopy too. Ask him about gallstones.
Hope you feel better soon and find some relief!
Jennifer 38 with CF and CFRD
Have him do an ultrasound of your gallbladder cause the pain your described and location could be gallstones. Ultrasound is ALOT less invasive than colonoscopy too. Ask him about gallstones.
Hope you feel better soon and find some relief!
Jennifer 38 with CF and CFRD
Have him do an ultrasound of your gallbladder cause the pain your described and location could be gallstones. Ultrasound is ALOT less invasive than colonoscopy too. Ask him about gallstones.
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<br />Hope you feel better soon and find some relief!
<br />
<br />
<br />Jennifer 38 with CF and CFRD
I have found using Abreva the second you feel a tingle and then constantly reapplying through out the day helps speed up the recovery. I also find icing it does ALOT of good! But it is a virus so you gotta just wait for it to pass. But if it is infecting your whole mouth maybe the doc has...
I have found using Abreva the second you feel a tingle and then constantly reapplying through out the day helps speed up the recovery. I also find icing it does ALOT of good! But it is a virus so you gotta just wait for it to pass. But if it is infecting your whole mouth maybe the doc has...
I have found using Abreva the second you feel a tingle and then constantly reapplying through out the day helps speed up the recovery. I also find icing it does ALOT of good! But it is a virus so you gotta just wait for it to pass. But if it is infecting your whole mouth maybe the doc has...
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