I knew yesterday was going to be a long day, full of emotion and I was right!
In the morning I headed to the hospital and gave Emma a bath. The nurse helped me a bit, but I did it mostly myself - and she really enjoyed it!! I was so proud and feel a lot more confident about bathing her.
For lunch I went out with everyone from my office. I was very nervous about that. You see I had to tell my boss (and good friend) that I would not be coming back to work after my maternity leave.
I’m sure that’s a stressful proposition for anyone, however after being with my company for over 9 years many of my colleagues are more like family. And if it wasn't for great people like my boss, Sharice, Jerry and Steve I might never have even had the opportunity to come to America (and subsequently meet my husband!!).
It was not an easy decision to make. When Emma was first diagnosed with Gastroschisis we had no idea how much care she would need, but after research it seemed like she would not need special care for long. My boss (and good friend) was awesome. I was able to arrange to go back to work part-time so that I could also spend time with Emma.
However, when we found out about Moebius syndrome all expectations were changed! It has been a waiting process to find out what impact this will have on Emma's needs when she comes home. We now have a better idea and know that she will need round the clock care.
While I did not hesitate to change my plans, it is still tough to give up that part of my life. Not only the fulfillment that working brings, but also the security of having two incomes. I will be learning to trust God in new ways for his provision!
I will miss being part of the team, but hopefully we can keep in touch.
After lunch (as if that wasn’t enough for one day) we met with Emma’s doctors to find out what the plan is. I will share what they told us with you – but I must caution that this is not set in stone! Things can change at any time.
Emma is having surgery next Friday 2/8 (not Feb 2 as I mistakenly wrote before!), and no changes will be made until then. She has continued to have minimal episodes, but we do have to keep on top of suctioning her!
Following surgery they will start to feed her using the g-tube and no difficulties are expected there. It will take a little while to get her into a schedule of feeding that will be manageable for us.
Once she is extubated, we will know what she needs for her airway. The docs are optimistic that it will be minimal support. If she does come home with external support, such as a canula, then we should qualify for at home nursing, maybe as much as 8 hours a day, which would allow me to sleep at night!
IF things go accordingly, then Emma could be home by the end of the month! (A long time – maybe, but I’m sure it will go fast and we have to make sure the home is equipment ready!)
It is our hope that as soon as Emma comes home we will be able to have a dedication ceremony for her at the church and you are all invited! We will also be inviting the nurses and doctors that have been so wonderful. Once we have details we’ll let you know.
And through it all, Emma is blissfully unaware of all going on around her! She just wants someone to keep her mobile running and her pacifier in!!