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I don't know how old your daughter is and if she would be able to take this, but when I was younger and oral meds were making me feel sick to my stomach, my mom would give me Mylanta before each dose and it would coat my stomach and help with the nauseousness. The downside is that Mylanta tastes...
I don't know how old your daughter is and if she would be able to take this, but when I was younger and oral meds were making me feel sick to my stomach, my mom would give me Mylanta before each dose and it would coat my stomach and help with the nauseousness. The downside is that Mylanta tastes...
I don't know how old your daughter is and if she would be able to take this, but when I was younger and oral meds were making me feel sick to my stomach, my mom would give me Mylanta before each dose and it would coat my stomach and help with the nauseousness. The downside is that Mylanta tastes...
I wouldn't go to a support group either...for the same exact reasons as saveferris, I work so hard everyday to maintain my health and I wouldn't want to put that at risk. This is why I never go to Great Strides meetings either. I think it's just another cruelty of CF, to have a disease that...
I wouldn't go to a support group either...for the same exact reasons as saveferris, I work so hard everyday to maintain my health and I wouldn't want to put that at risk. This is why I never go to Great Strides meetings either. I think it's just another cruelty of CF, to have a disease that...
I wouldn't go to a support group either...for the same exact reasons as saveferris, I work so hard everyday to maintain my health and I wouldn't want to put that at risk. This is why I never go to Great Strides meetings either. I think it's just another cruelty of CF, to have a disease that...
I wouldn't go to a support group either...for the same exact reasons as saveferris, I work so hard everyday to maintain my health and I wouldn't want to put that at risk. This is why I never go to Great Strides meetings either. I think it's just another cruelty of CF, to have a disease that...
I wouldn't go to a support group either...for the same exact reasons as saveferris, I work so hard everyday to maintain my health and I wouldn't want to put that at risk. This is why I never go to Great Strides meetings either. I think it's just another cruelty of CF, to have a disease that...
Just to clarify, are you saying it takes 6 weeks to get your synergy testing results? I know it takes longer than a normal culture but my results are usually back within 7-10 days, 2 weeks at most. Is that not the norm?
Just to clarify, are you saying it takes 6 weeks to get your synergy testing results? I know it takes longer than a normal culture but my results are usually back within 7-10 days, 2 weeks at most. Is that not the norm?
Just to clarify, are you saying it takes 6 weeks to get your synergy testing results? I know it takes longer than a normal culture but my results are usually back within 7-10 days, 2 weeks at most. Is that not the norm?
Just to clarify, are you saying it takes 6 weeks to get your synergy testing results? I know it takes longer than a normal culture but my results are usually back within 7-10 days, 2 weeks at most. Is that not the norm?
Just to clarify, are you saying it takes 6 weeks to get your synergy testing results? I know it takes longer than a normal culture but my results are usually back within 7-10 days, 2 weeks at most. Is that not the norm?
I agree that the synergy testing would be much more helpful at the beginning of an exacerbation. My sensitivities to drugs vary from culture to culture. Definitely push for this in the future! And I would absolutely push for the desensitization to the drug you are sensitive to!!!! If your CF...
I agree that the synergy testing would be much more helpful at the beginning of an exacerbation. My sensitivities to drugs vary from culture to culture. Definitely push for this in the future! And I would absolutely push for the desensitization to the drug you are sensitive to!!!! If your CF...
I agree that the synergy testing would be much more helpful at the beginning of an exacerbation. My sensitivities to drugs vary from culture to culture. Definitely push for this in the future! And I would absolutely push for the desensitization to the drug you are sensitive to!!!! If your CF...
I agree that the synergy testing would be much more helpful at the beginning of an exacerbation. My sensitivities to drugs vary from culture to culture. Definitely push for this in the future! And I would absolutely push for the desensitization to the drug you are sensitive to!!!! If your CF...
I agree that the synergy testing would be much more helpful at the beginning of an exacerbation. My sensitivities to drugs vary from culture to culture. Definitely push for this in the future! And I would absolutely push for the desensitization to the drug you are sensitive to!!!! If your CF...
My doctor always sends my cultures out for synergy testing when they come back as being intermediate. My understanding was that an antibiotic could be intermediate when tested individually, but have an entirely different result when tested in conjunction with a 2nd and/or 3rd antibiotic. Also...
My doctor always sends my cultures out for synergy testing when they come back as being intermediate. My understanding was that an antibiotic could be intermediate when tested individually, but have an entirely different result when tested in conjunction with a 2nd and/or 3rd antibiotic. Also...
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