Monday, March 24, 2014

Pseudomonas

I missed a call this morning around 9:00, didn't hear the phone ring in my back pocket because that is the time my students are arriving, playing, and I am talking with parents as they drop off.  When we took the kids to P.E., I ducked out to listen to my voicemail.  It was Dr. Thompson, Monkey's favorite Pulmonologist from the CF Clinic.  He said he wanted to talk to me about Monkey's throat culture results, that it wasn't urgent and I shouldn't worry, and that he was in Clinic until 4:00, so would not be able to get back to me for awhile.  I shouldn't worry?  They do a throat culture every time we go to clinic (except the time he puked on me), and never call unless he is growing something.  On top of that, the doctor has NEVER called himself, it is always a nurse!  So of course I knew something was really not good, and I had all day to freak out and worry about it.

When he finally called back around 4:30 he told me Monkey is growing Pseudomonas.  I'm still fairly new to all this CF stuff, and since Monkey has been mostly healthy so far, I don't know about all the bugs our kiddos get, but I know enough to know Pseudomonas is the one you don't want your kid to have.  He went on to say that he has 3 different strands, they are all rare (of course, because everything about my Monkey is rare), and one is mucoidal.  The fact that it is mucoidal means it is likely to colonize.

Ok, deep breath Jodi, keep listening and stay focused.  Take in all the information.  Keep breathing!

He goes on to explain how they will treat it (2 weeks of oral antibiotics and a month of Tobi, an inhaled antibiotic).  If it colonizes, he will be on and off the Tobi every month to keep it at bay.  He tries to be reassuring.  Tells me some kids with Pseudomonas do just fine, while others who don't have it do poorly. It doesn't define anything, blah blah blah.

Monkey will have to start going to a different clinic, so he doesn't pass this horrible bug to other sweet babies with healthier lungs.  Monkey, up until now, was still in the newborn clinic because he was not growing anything dangerous.  Because kids with CF can easily catch these bugs from each other, they put them in clinic based on the bugs they have so they aren't sharing space with kids who can pass them a new bug they didn't already have.  He will now be going to the Tue./Thu. clinic with all the kids who have this ugly bug.  And he won't be seeing his beloved Dr. Thompson anymore.  That about broke my heart to hear!   

When I got home, I sent a message to a friend of mine who has a twelve year old son with CF.  They have  been through about everything, and she is very knowledgeable. I turn to her when facing something new with Monkey because I know she will tell me like it really is, from the perspective of a mommy, not a doctor, which is what I really need at these moments.  She is also amazing at explaining the medical stuff in a way that makes sense to me, so I really understand what is happening in Monkey's little body.

She said colonized mucoidal Pseudomonas is like a pilot light waiting to flare up.  It stays dormant, then when you get another bug, such as staph, it flares up.  Every time it flares up it causes more damage to the lung.  She says where she lives, every time a kid gets Pseudomonas, they are admitted for IV antibiotics.  Her son had mucoidal Pseudomonas before and they were able to eradicate it.     

So, with this information, I am now prepared to be my child's advocate and call tomorrow to find out how much is growing, and why they don't think it should be treated with IV antibiotics.  In the meantime, I will prepare to do whatever is best to keep my baby's lungs as healthy as possible until that cure comes along.       

8 comments:

  1. Prayers and hugs from my family to yours!

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  2. Love you guys...praying for Monkey

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  3. Hi - my daughter is 3 and has CF too. She cultured pseudomonas last year (ugh) and did 3 weeks Cipro followed by 3 months of Tobi. She still had a rare growth showing up in her next culture (rare = very minimal) so they did an additional 3 weeks of Cipro followed by 1 month of Tobi. We just got a clean culture last week. Just some other info so you can see how the oral/ Tobi thing happened...

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    1. Thank you for this info. It is always good to hear from someone who has been through it as we face each new hurdle.

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  4. Jodi you are and always will be Lex's strongest advocate. Keep asking those questions and pushing doctors to do their best.

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  5. Ok the comment section did something weird. Know that prayers and constant good thoughts come Lex's way every day.

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  6. I researched it last night before you posted to your blog. Thank you for your further explanation. Each day of life brings something new. Just about the time you have a moment where you think you can take a breath and enjoy.....something ugly raises it's head. Jodi you have my prayers and I will call others on board to pray for Lex's lungs and for mommy and daddy to somehow enjoy life in spite of LIFE.

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    1. The above comment was from Susan Hitchman Evans. <3

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