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I've cultured staph off and on (it seems to be my only bug that disappears and then reappears, though I'm pretty sure it's always in there) for as long as I can remember. They treated it with Bactrim as a young child, and I had an allergic reaction to the drug, so then I believe I treated it...

I've cultured staph off and on (it seems to be my only bug that disappears and then reappears, though I'm pretty sure it's always in there) for as long as I can remember. They treated it with Bactrim as a young child, and I had an allergic reaction to the drug, so then I believe I treated it...

I've cultured staph off and on (it seems to be my only bug that disappears and then reappears, though I'm pretty sure it's always in there) for as long as I can remember. They treated it with Bactrim as a young child, and I had an allergic reaction to the drug, so then I believe I treated it...

I've cultured staph off and on (it seems to be my only bug that disappears and then reappears, though I'm pretty sure it's always in there) for as long as I can remember. They treated it with Bactrim as a young child, and I had an allergic reaction to the drug, so then I believe I treated it...

I've cultured staph off and on (it seems to be my only bug that disappears and then reappears, though I'm pretty sure it's always in there) for as long as I can remember. They treated it with Bactrim as a young child, and I had an allergic reaction to the drug, so then I believe I treated it...

I'd do it, absolutely. $1600 is a lot of money, I know, and esp. right now. But absolutely nothing is more worth it than knowing 100% for sure that your child does not have cystic fibrosis. As Harriet said, your child is without a doubt a carrier of the D508 gene, and if your husband has any CF...

I'd do it, absolutely. $1600 is a lot of money, I know, and esp. right now. But absolutely nothing is more worth it than knowing 100% for sure that your child does not have cystic fibrosis. As Harriet said, your child is without a doubt a carrier of the D508 gene, and if your husband has any CF...

I'd do it, absolutely. $1600 is a lot of money, I know, and esp. right now. But absolutely nothing is more worth it than knowing 100% for sure that your child does not have cystic fibrosis. As Harriet said, your child is without a doubt a carrier of the D508 gene, and if your husband has any CF...

I'd do it, absolutely. $1600 is a lot of money, I know, and esp. right now. But absolutely nothing is more worth it than knowing 100% for sure that your child does not have cystic fibrosis. As Harriet said, your child is without a doubt a carrier of the D508 gene, and if your husband has any CF...

I'd do it, absolutely. $1600 is a lot of money, I know, and esp. right now. But absolutely nothing is more worth it than knowing 100% for sure that your child does not have cystic fibrosis. As Harriet said, your child is without a doubt a carrier of the D508 gene, and if your husband has any CF...

I was actually on the Pulmozyme (aka DNase) study back when it was first introduced. I forget when that was, but it was sometime in my middle schoolish years, and I'm now 28. I've been on it non-stop ever since. This was, I believe, the second drug EVER to be developed specifically for the...

I was actually on the Pulmozyme (aka DNase) study back when it was first introduced. I forget when that was, but it was sometime in my middle schoolish years, and I'm now 28. I've been on it non-stop ever since. This was, I believe, the second drug EVER to be developed specifically for the...

I was actually on the Pulmozyme (aka DNase) study back when it was first introduced. I forget when that was, but it was sometime in my middle schoolish years, and I'm now 28. I've been on it non-stop ever since. This was, I believe, the second drug EVER to be developed specifically for the...

I was actually on the Pulmozyme (aka DNase) study back when it was first introduced. I forget when that was, but it was sometime in my middle schoolish years, and I'm now 28. I've been on it non-stop ever since. This was, I believe, the second drug EVER to be developed specifically for the...

I was actually on the Pulmozyme (aka DNase) study back when it was first introduced. I forget when that was, but it was sometime in my middle schoolish years, and I'm now 28. I've been on it non-stop ever since. <br /> <br />This was, I believe, the second drug EVER to be developed specifically...

I've had pseudo for as long as I can remember. I won't sugarcoat it, b/c it is a nasty bug, but it is absolutely not the end of the world. I agree with everyone here that with all the new drugs your son has a good chance of getting rid of this bug, at least for now, but just in case, I think...

I've had pseudo for as long as I can remember. I won't sugarcoat it, b/c it is a nasty bug, but it is absolutely not the end of the world. I agree with everyone here that with all the new drugs your son has a good chance of getting rid of this bug, at least for now, but just in case, I think...

I've had pseudo for as long as I can remember. I won't sugarcoat it, b/c it is a nasty bug, but it is absolutely not the end of the world. I agree with everyone here that with all the new drugs your son has a good chance of getting rid of this bug, at least for now, but just in case, I think...

I've had pseudo for as long as I can remember. I won't sugarcoat it, b/c it is a nasty bug, but it is absolutely not the end of the world. I agree with everyone here that with all the new drugs your son has a good chance of getting rid of this bug, at least for now, but just in case, I think...

I've had pseudo for as long as I can remember. I won't sugarcoat it, b/c it is a nasty bug, but it is absolutely not the end of the world. I agree with everyone here that with all the new drugs your son has a good chance of getting rid of this bug, at least for now, but just in case, I think...