This is a sample guest message. Register a free account today to become a member! Once signed in, you'll be able to participate on this site by adding your own topics and posts, as well as connect with other members through your own private inbox!
Here is a study abstact I stumbled across. Many of the studies performed outside the US appear to be cost driven, but the findings are interesting.
<a target=_blank class=ftalternatingbarlinklarge...
Here is a study abstact I stumbled across. Many of the studies performed outside the US appear to be cost driven, but the findings are interesting.
<a target=_blank class=ftalternatingbarlinklarge...
Here is a study abstact I stumbled across. Many of the studies performed outside the US appear to be cost driven, but the findings are interesting.
<a target=_blank class=ftalternatingbarlinklarge...
Here is a study abstact I stumbled across. Many of the studies performed outside the US appear to be cost driven, but the findings are interesting.
<a target=_blank class=ftalternatingbarlinklarge...
Here is a study abstact I stumbled across. Many of the studies performed outside the US appear to be cost driven, but the findings are interesting.
<br /><a target=_blank class=ftalternatingbarlinklarge...
Following my sons diagnosis as homozygous for DF508, I was also tested (Ambry) and they found that I am a DF508/ poly T variant. I was told that they couldn't say I had CF, but I may (Do) have some of the milder symptoms of CF. I thought this was strange.
Following my sons diagnosis as homozygous for DF508, I was also tested (Ambry) and they found that I am a DF508/ poly T variant. I was told that they couldn't say I had CF, but I may (Do) have some of the milder symptoms of CF. I thought this was strange.
Following my sons diagnosis as homozygous for DF508, I was also tested (Ambry) and they found that I am a DF508/ poly T variant. I was told that they couldn't say I had CF, but I may (Do) have some of the milder symptoms of CF. I thought this was strange.
Following my sons diagnosis as homozygous for DF508, I was also tested (Ambry) and they found that I am a DF508/ poly T variant. I was told that they couldn't say I had CF, but I may (Do) have some of the milder symptoms of CF. I thought this was strange.
Following my sons diagnosis as homozygous for DF508, I was also tested (Ambry) and they found that I am a DF508/ poly T variant. I was told that they couldn't say I had CF, but I may (Do) have some of the milder symptoms of CF. I thought this was strange.
We currently stopped pulmozyme and are on an off month of TOBI. We are currently doing Albuterol/Pulmicort and then 7% HTS. The HTS seems to be helping. What are your initial impressions on the HTS? Thanks
We currently stopped pulmozyme and are on an off month of TOBI. We are currently doing Albuterol/Pulmicort and then 7% HTS. The HTS seems to be helping. What are your initial impressions on the HTS? Thanks
We currently stopped pulmozyme and are on an off month of TOBI. We are currently doing Albuterol/Pulmicort and then 7% HTS. The HTS seems to be helping. What are your initial impressions on the HTS? Thanks
We currently stopped pulmozyme and are on an off month of TOBI. We are currently doing Albuterol/Pulmicort and then 7% HTS. The HTS seems to be helping. What are your initial impressions on the HTS? Thanks
We currently stopped pulmozyme and are on an off month of TOBI. We are currently doing Albuterol/Pulmicort and then 7% HTS. The HTS seems to be helping. What are your initial impressions on the HTS? Thanks
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.