I/we decided to start a blog to keep everyone updated on all the "stuff" going on in our lives--since there is a lot of "stuff" going on!!! I can not promise to update daily, but it is my goal to update often--it is our hopes that when we move we will be able to keep family and friends in the know! There is kind of a lot to start with, so I am going to organize this first post by topic!
House: We went from 3-5 showings a week, to having two offers submitted to the bank to NOTHING. We lost both buyers and have not had a showing in over a week. My realtor said they have SLOWED down since the tax credit ended... so, we are still hoping and praying for an offer that sticks.
Jon:
The interview at Vanderbilt last week went very well. He felt like it was more of a recruiting session versus a regular interview. He was supposed to come home and talk to me about moving to TN and then get back to Dr. Conn. On Friday, Dr. Conn emailed and made a formal offer to Jon about working in his lab at Vandy Medical Center. The "official" paper work is on its way, but the email included information about salary and benefits. Jon will be accepting the offer!. Its kind of crazy to think that it is official--Nashville here we come (in July!)
Kati/Baby:
Finally, my blood pressure is under control. Thursday at the hospital, my bp was 130/66...the best its been. I am still off work, and have been for a couple weeks now. I was sad to stop work early because I miss my friends and family at FHS, however, the baby and I are doing so much better. I think being on my feet all day and the stresses that come with teaching was just a little too much on the little girl/guy. The baby is doing great now. I go for an ultrasound/biophysical profile every Monday and a Non-Stress test at the hospital every Thursday. Last week--all appointments went very well and it seems I will stay pregnant for at least a couple more weeks :) I can not wait to see our little girl/guy when he/she finally gets here!
Emma:
She is definitely the joy of our lives--and she has developed a new attitude called "two." She is becoming a little sass, and if you ask her whats wrong with her, she says: "two." She keeps us hopping, and is for the most part quite a happy little girl.
We recently had to have some testing done because of a couple of minor cuts that bled for long periods of time. Her bleeding time tested long--so a panel was run to test her for Von Willebrands Disease. As of right now, she has been diagnosed with type 1 Von Willebrands Disease--which essentially means that she does not clot well after she is injured and she bleeds for a long time. Day to day life is not really affected; she basically can not take aspirin or Ibuprofen and we will have to make sure everyone who is watching her knows how to respond to her cuts and bleeding. We will be having a DDAVP challenge test to see if she responds to the treatment. Essentially, she will only need DDAVP in the case of surgeries/major injuries.
At first, I was pretty stressed about the idea that something could be wrong with Emma--she is my perfect girl! However, now that I am more informed about whats going on with her, I am grateful that VWD is not a more serious disease. I am also grateful that we know in advance that she has this bleeding disorder and did not have to discover it through some serious injury. Essentially, she had to get it from Jon or I and we have both been fine. So, while I can say I am a little disappointed that she has this disease, I am grateful that it is not life threatening.
If you made it this far--thanks for reading :) Being Jon's wife and being a mom has been the most fulfilling and satisfying job I could have ever imagined. Though we have a lot going on right now, I would not trade it for the world---I love our life and can not wait to see what our future will bring!
Monday, May 10, 2010
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I love this idea for the blog. I think that it is one of the easiest ways for everyone to touch base with you guys, too. Glad to hear it appears you have found a home in Nashville (soon at least). I will keep you guys in my thoughts.
ReplyDeleteOur end is still looking good. It's hard to believe our little ones are two already! I'm sure Emma is running around all over the place like Owen. Maye this week, we could make a play date? I'm actually off Friday with a personal day. I had to take it because Tracie requested that day off back in October. What are you guys doing then? We could come out and visit you.
About Emma: I have Hemophilia-A. The symptoms/treatment is nearly identical. The root cause is slightly different. Whereas I do not make enough activated Factor8, she would have a protein that "scrubs out" activated Factor8. I found out about my blood problems when I was ~16. My maternal grandfather was in the hospital and was having some bleeding issues. He had so many transfusions at that point that they could not test him for Hemophilia or VonWilibrons, so they tested his grandkids.
ReplyDeleteThe only issues I have ever really had are my knees are going bad slightly faster than most people, and I cannot take aspirin or ibuprofen (or any NSAIDs). When I had my wisdom teeth out, I had a 3 day stay in a hospital for Factor8 replacement transfusions.
One thing to keep in mind when/if you need to go to a hospital: There are 2 Factor8 replacements out there right now. HumateP and Recombinate. HumateP is human blood derived and Recombinate is "manufactured". If you worry about the blood supply safety, go for the Recombinate if possible.
If you have ANY questions about this, call me.
Love the blog! It's so great to hear about your family, Kati. :)
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