Austin Nesties
Dear Community,

Our tech team has launched updates to The Nest today. As a result of these updates, members of the Nest Community will need to change their password in order to continue participating in the community. In addition, The Nest community member's avatars will be replaced with generic default avatars. If you wish to revert to your original avatar, you will need to re-upload it via The Nest.

If you have questions about this, please email help@theknot.com.

Thank you.

Note: This only affects The Nest's community members and will not affect members on The Bump or The Knot.

Another update

Again your nestie dust and prayers are so appreciated.  I can not thank you enough.  This is all very overwhelming for me and watching my husband in so much pain is heartwrenching.  Our one year anniversary is next month.  I guess if we can get through this in our first year of marriage we will be able to get through anything!

Since surgery, the one thing we don't seem to have any concerns with is the heart.  The heart surgeon, has come and seen him several times and he keeps saying that everything sounds good.  Another cardiologist who Michael has history with, has also came and seen him and he too believes Michael's heart is doing just fine.  They started him back on his flecanide medication, one that Michael has taken for years, to watch out for the arrhythmia to make sure everything is ok.  Apparently some time last night, Michael did have some arrhythmia with his heart for the first time post surgery, but it was small and must not have been that bad because Michael never noticed and never said anything about it.  The cardiologist said that was normal and we still needed to give the flecanide more time to work.

Every since Michael came out of surgery, we have been monitoring his blood pressure.  It has been really low and is still somewhat of a concern.  Since yesterday afternoon it is steadily a little higher but still not where it should be.  Every now and then though, we will get a read on it and it will be a really good blood pressure rate.  So, there's hope it is going back up.  We just need it to get up and stay up.

Another thing we have been dealing with is Mike's bladder.  His catheter was taken out yesterday afternoon because he seemed to be putting out enough fluids.  Since then, he has not been able to urinate on his own for some reason.  Last night around midnight, the nurse had to put in a temporary catheter where they put it in, drain his bladder, and then pull it back out. They also did some tests to try and figure out what is going on.  It seems that his kidneys are functioning great and his bladder is filling like it is supposed to.  Right now, his bladder is just not working well enough and making him urinate like he is supposed to.  We are waiting for the surgeon to come assess him and he may tell them to give Michael a dieretic medicine that will hopefully help him be able to go to the bathroom on his own again.  Worst case scenario, if something doesn't start working right soon, he may have to get the real catheter put back in.  We pray that does not have to happen.  Michael is really frustrated and upset by that and for him the catheter causes a lot of pain.  So as silly as this sounds, pray that the boy can pee on his own!!  :-)

After a rough night dealing with the catheter issue, Michael is feeling really weak and nauseated.  They took his temperature this morning and it is at 100.2 degrees.  The cardiologist came in and he believes that the fever is not caused by an infection (which is great) but rather caused by the fact that his lungs may be trying to collapse (obviously, not so great).  He has a breathing thing that he is supposed to be doing 10 breath things every 2 hours.  We decided his lungs are not going to collapse and he is going to fight off his fever so we are making him do the breath thing 3 times every 15 minutes.  We really want him to make his heart and lungs work so that it makes them both stronger. (PS: I don't remember the medical term for "the breathing thing" I am referring to.  Basically he blows air in to this tube, holds his breath for 5 seconds, and then releases the air. This causes him to take really deep breaths, forcing his lungs to work and expand like they are supposed to.  The reason for this is because during the surgery, they collapse his lungs in order to work on his heart.)

Today they were supposed to make Michael get out of bed and walk around the unit but due to the low blood pressure they aren't going to.  We really need his blood pressure up.  If it doesn't come up, he can't get up and walk around, which in turn won't make his heart work and get stronger like we want.

 I feel like I'm being needy, but any more spare dust and prayers you have lying around are still appreciated!

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TTC #1 since February 2011
BFP #1 1/14/12 EDD 9/24/12 m/c at 8w4d on 2/20/12
March 2012- Dx with PCOS, started metformin
July 2012- SA completely normal

Re: Another update

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