Showing posts with label Life Decisions. Show all posts
Showing posts with label Life Decisions. Show all posts

Wednesday, February 22, 2012

Just Another Hurdle to Jump

Over the past few weeks, we have been getting excited (and anxious) about starting infertility treatments. On Monday, I received a call with my liver results, which we were expecting to be good (due to my enzyme levels in Dec. and the ultrasound tech saying that my liver looked good).  My Dr. stated that my ultrasound, did indeed look great, but my new enzyme level draws (from 2-9) showed that my levels were once again elevated.  Because of this, she can not recommend us for fertility treatments or for me to carry a pregnancy because she is unsure what is going on in my liver (IVF drugs and pregnancy can throw a regular liver into overdrive, so a liver that is already damaged can have permanent damage).  She said that she wants to re-draw my liver enzyme levels in another month, and if they are still high at that point, she wants to do a biopsy to figure out what's wrong.  Hopefully, the blood draw will come back ok.

Basically, we've reached yet another hurdle that we have to jump over.  This time, however, I'm not able to see the finish line beyond the hurdle.  I realize this may be a bit dramatic, but honestly I'm just getting tired of hearing "just one more test," or "you need another approval letter."  I want to hear, "Ok, we're all set to go with this."  I just don't see it happening anytime soon.

Because of yet another hurdle (this one being more serious than ones we've encountered in the past), we are trying to prepare ourselves for the worst, but still hope for the best.  We are seriously considering, for the first time, that maybe our path isn't meant to include children that are genetically ours.  We are openly talking about adoption or fostering, and we are also trying to accept that it may just be the two of us forever.  Right now, we can barely afford to keep ourselves afloat, let alone be accepted for adoption or fostering (and this is before the CF consideration). Adoption and fostering may simply be out of the question. Yes, these are possibilities that may never occur, but they are real possibilities, and they have to be considered.

Needless to say, Monday night I sat and cried for hours, and my husband held me for hours.  He told me we'd face it all together, no matter what.  He told me that while it has always been his dream to have kids, he'd throw it all away if he could just have me in his arms forever.  As much as we both hate this infertility journey, we can't disagree with the fact that it is bringing us closer and closer with each new barrier we have to break down.

It's Wednesday now, and we're able to look at everything a bit more rationally and a bit less emotionally.  That said, we are (despite what the doctor stated) going to keep trying for a baby naturally. Although it may not be recommended, most of the CFers I know have slightly elevated liver enzymes, and they still are fine throughout a pregnancy.  I'm ok with not having fertility treatments for another few months, but I'm not ok, and will not be ok, with abandoning trying to conceive altogether. My doctor has done every test, short of a biopsy now, and it all looks ok, just with an elevated enzyme level (of 44 I might add which isn't much higher than normal). We will keep trying naturally.

So for now, our plan is to continue trying, continue praying, and continue trusting in God's plan. We firmly believe it will work out the way it's supposed to, and if we are meant to not have kids, then that's the way it goes and we will figure it out together

Thursday, September 1, 2011

Questioning...

Thoughts and Questions that keep running through my mind:

Will I be a good mommy?
What if we can't get pregnant?
Is my lung function ok to handle a pregnancy?
I know it will be hard to fit in all my treatments and a crying baby....
Am I throwing too much responsibility toward my husband when I get sick and he has to take care of both of us?
What if we can't get pregnant?
What if the baby has CF?
What if I take another few months to get healthier and then start trying?
What if we can't get pregnant?

My darling hubby and I have addressed these concerns and we are still wanting to start trying now..but the questions still run through my mind...

Tuesday, August 30, 2011

The biggest decision of our lives...

I remember when my now-husband and I first started dating.  I remember thinking that marriage was the biggest decision we were going to face and I remember it seemed terrifying at the time. My poor husband was more terrified of the actual engagement question and asking permission from my parents, I think, than a wedding.  In reality, marriage is a huge decision and it certainly should not be taken lightly, but compared to the decision we made a few months ago, it seems easy.

In fact, our engagement came and went and we were incredibly excited. Then, our wedding rolled around faster than I thought possible and we found ourselves staring at each other at 1:00 AM on our wedding night saying, "Wow. We just spent how much for one day?" Don't get me wrong, our wedding was beautiful and we were incredibly blessed with friends and family who traveled long distances to see us exchange our vows.  The actual day of the wedding, however, goes by so quickly that you feel like you blinked and it was done.  I wish there was a way to relive that day at any time. 

Going from being engaged to being married seemed hardly any different and we loved that. We enjoy being the type of couple that stays in on a Saturday evening to watch a movie together.  We enjoy laughing at each other's corny jokes and just sitting, doing nothing. We're boring and we love it! So now comes the twist: over the summer we officially decided we were ready to become parents. Throw boring, lazy, and doing nothing out the window! We just knew we were ready and the decision had ultimately been coming for a few months.  This decision is BIG for any couple to make, but I have cystic fibrosis which just adds another level of BIG.

More on my actual mutations and lung function later, but ultimately cystic fibrosis, or CF, is a challenging genetic disease which effects the lungs and digestive system.  Originally, I believed I would never be able to have children but (obviously) as far as my lungs go, my doctor is 100% on board with the idea.  From what I've read from other CFers (those with cystic fibrosis), getting pregnant with CF can be difficult..more so than for most women. With so little being written about this, I decided it may help someone else who is trying to come to this decision with her spouse and thus created the blog. Well, let the "difficulties" begin.  We are keeping our fingers, and toes, and hair crossed that it all goes smoothly and easily, but preparing ourselves for the alternative at the same time.  Here's wishing luck to all those going through the same process we are right now.  More to come soon...