mbrandazzo
New member
Hi Sarah,
You are NOT alone! I can completely relate to you... My son is not yet two, and has cultured both MRSA and recently pseudo...
He cultured MRSA when he was just three months old... It was right after he was diagnosed and they admitted him right away - We were scared, devastated, and SO new to the whole CF world that it didn't seem real or possible! He was in the hospital for two weeks on heavy IV antibiotics, and then when we were sent home, we had to do a daily cleansing of his nose area... That was when he was 3 months, now he is 21 months and he HAS NOT cultured it since! So the good news is that it is POSSIBLE to get rid of it, or at least keep it at bay...
Now, the whole pseudo thing is still kind of new, and that was a BIG blow to us because we had thought he was doing so well. Like you, we don't send him to daycare and are VERY careful with his exposure to germs... We couldn't understand why it happened, when it seemed we were doing everything we could to prevent it. I was bawling my eyes out when I got the call... Anyway, we have since learned that there really is NO WAY to prevent exposure to PA, and that it is very treatable with the TOBI, so in other words it is not the beginning of the end!
So, please do not lose hope, and please know that you are not alone at all! I felt the EXACT same way you do, I thought that it must mean that Logan has a "severe" case because he seems to catch everything possible, but now I really try and focus on the positives - That he is being treated and given EXCELLENT care... That he is LOVED more than any other little boy I know... and that we believe in the future (hopefully not too far out there) that our little guy will be one of the first to see people like him with CF live full lives. Maybe it is a little idealistic, but we want him to feel positive about things, and pass that spirit on to others...
You are NOT alone! I can completely relate to you... My son is not yet two, and has cultured both MRSA and recently pseudo...
He cultured MRSA when he was just three months old... It was right after he was diagnosed and they admitted him right away - We were scared, devastated, and SO new to the whole CF world that it didn't seem real or possible! He was in the hospital for two weeks on heavy IV antibiotics, and then when we were sent home, we had to do a daily cleansing of his nose area... That was when he was 3 months, now he is 21 months and he HAS NOT cultured it since! So the good news is that it is POSSIBLE to get rid of it, or at least keep it at bay...
Now, the whole pseudo thing is still kind of new, and that was a BIG blow to us because we had thought he was doing so well. Like you, we don't send him to daycare and are VERY careful with his exposure to germs... We couldn't understand why it happened, when it seemed we were doing everything we could to prevent it. I was bawling my eyes out when I got the call... Anyway, we have since learned that there really is NO WAY to prevent exposure to PA, and that it is very treatable with the TOBI, so in other words it is not the beginning of the end!
So, please do not lose hope, and please know that you are not alone at all! I felt the EXACT same way you do, I thought that it must mean that Logan has a "severe" case because he seems to catch everything possible, but now I really try and focus on the positives - That he is being treated and given EXCELLENT care... That he is LOVED more than any other little boy I know... and that we believe in the future (hopefully not too far out there) that our little guy will be one of the first to see people like him with CF live full lives. Maybe it is a little idealistic, but we want him to feel positive about things, and pass that spirit on to others...