Cystic Fibrosis Forum (EXP)

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Recent content by canilucas

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    Methotrexate anyone?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>mysticrose</b></i> I was curious if any one here had any experience with this medication? As I had posted before my DD's joints are swelling. After a long drawn out time we finally got into see a rheumatologist. They put her on...
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    Methotrexate anyone?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>mysticrose</b></i> I was curious if any one here had any experience with this medication? As I had posted before my DD's joints are swelling. After a long drawn out time we finally got into see a rheumatologist. They put her on...
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    7% saline nebulizer- any help here?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Printer</b></i> Canilucas: Have you discussed this question with her CF Doctor? Bill</end quote> No, I didn't want to bother them with a simple question like this.. wanted to ask around first, and see what other's experiences have...
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    7% saline nebulizer- any help here?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Printer</b></i> Canilucas: Have you discussed this question with her CF Doctor? Bill</end quote> No, I didn't want to bother them with a simple question like this.. wanted to ask around first, and see what other's experiences have...
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    7% saline nebulizer- any help here?

    Thank you for this reply! I didn't even think of that because she is using her Pari and alternating with the ones that were clean (disposable) kind, and those ones suck! Thank you-I didn't realize the particle size made a difference, however, the rep pf Pari told me that it takes 5 minutes to...
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    7% saline nebulizer- any help here?

    Thank you for this reply! I didn't even think of that because she is using her Pari and alternating with the ones that were clean (disposable) kind, and those ones suck! Thank you-I didn't realize the particle size made a difference, however, the rep pf Pari told me that it takes 5 minutes to...
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    7% saline nebulizer- any help here?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Rebjane</b></i> How old is your daughter? My daughter started 7% saline around 4 years old. It did make her cough alot. Under her nose would get irritated, I guess it took a few weeks for her to get used to it. Do you use albuterol...
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    7% saline nebulizer- any help here?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Rebjane</b></i> How old is your daughter? My daughter started 7% saline around 4 years old. It did make her cough alot. Under her nose would get irritated, I guess it took a few weeks for her to get used to it. Do you use albuterol...
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    7% saline nebulizer- any help here?

    question: started my daughter on 7% saline via nebulizer, and she says her mouth, nose are "itchy" and "scratchy" and "hurt her" and are "dry" during the treatment, and right after. It goes away after she wipes her face, but She says she hates it. She trialed the 3% and didn't notice it at all...
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    7% saline nebulizer- any help here?

    question: started my daughter on 7% saline via nebulizer, and she says her mouth, nose are "itchy" and "scratchy" and "hurt her" and are "dry" during the treatment, and right after. It goes away after she wipes her face, but She says she hates it. She trialed the 3% and didn't notice it at all...
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    Anyone with single mutation w/CF symptoms?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>BarbaraW</b></i> My kids each have 1 mutation - s1235r. They both have a lot of pancreatic stuff going on, as well as some respitory issues. DS tends to get pnuemonia a few times a year, and DD has a lot of sinus issues. Right now...
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    Anyone with single mutation w/CF symptoms?

    <div class="FTQUOTE"><begin quote><i>Originally posted by: <b>BarbaraW</b></i> My kids each have 1 mutation - s1235r. They both have a lot of pancreatic stuff going on, as well as some respitory issues. DS tends to get pnuemonia a few times a year, and DD has a lot of sinus issues. Right now...
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    Anyone with single mutation w/CF symptoms?

    WHAT IS CRMS?
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    Anyone with single mutation w/CF symptoms?

    WHAT IS CRMS?
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    Anyone with single mutation w/CF symptoms?

    Swallowtail66, can you explain to me a bit more about allelles? I know each parent contributes one CFTR gene but do they also contribute variants? We have rampant autoimmune disease in our family. I have Grave's, my sister has SLE (Lupus) and my cousin has some unusual eye disease (going blind)...
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