What we thought was going to be a very low key relaxing Sunday, was in every way different. Our child! I swear, at the age of 27 I should not have this many gray hairs on my head! I think she adds more weekly! Let me explain.
On Saturday Lynlee was going to stay at her Mommaw and Poppaws (Ryan's parents) while Ryan and I went to dinner and a movie and out with some friends! Dinner was amazing, the movie was hilarious, and even though I'm over the whole bar scene we did enjoy ourselves. We got home about 1:30am, which is the longest we've stayed out in a VERY long time.
Around 6am I got a phone call from Ryan's mom. Lynlee had fell out of bed and was acting like she was hurt. We rushed over and Lynlee was acting okay but she wouldn't look up. We decided to take her to the ER and have them look at her. When I say we I mean Ryan and I plus my call to my soon to be sister in law at 6:30am to see what she thought. She told me if I ever needed anything to call, but I'm expecting for her to change her number any day because I take her up on it all the time! Anyways, we get to the local ER they took Xrays. They weren't happy with what they saw so they wanted us to go to Ruby Memorial for a CAT scan. After some discussion they let us go by car.
We get to Ruby and they rushed us back in. They had listed Lynlee has a trauma patient so when we get to the room we had at least 20 people surround us, and I'm not even exaggerating when I say that. One doctor was doing an evaluation on Lynlee and she moved her head up, down, all around. They decided to downgrade her and when they said those words the room cleared as fast as they came! They done some more Xrays on Lynlee. Everything turned out okay and we were released within 20 minutes.
So other than a stiff/sore neck she is fine! It probably took more years off my life than anything.
*Note to self: Make hair appt for color this week!
Monday, June 6, 2011
Thursday, June 2, 2011
Summer Days
I hope I'm not jinxing us when I say. I think summer is upon is. You will not hear me complaining about it. We (meaning Lynlee and I) take advantage of every pretty day we have. Lynlee loves it outside. I usually try to take care of any chores or errands of a morning so after her nap we can spend the rest of the afternoon and evening outside. Some days I give in like today for example. The other morning at 8am Lynlee brings me her shoes, and points outside. Since she was still in her pajamas I thought it might be just a little too early.
I think there is something about the sun that makes everyone happier. I know it does me. I'm in a much better mood and just more pleasant to be around. Lynlee seems to be the same way. We spend hours in the water table and just walking around the yard exploring.
It's been a while since I've given an update so here goes. In January we sat down with birth to three and made goals for the year. In regards to her physical therapy she has almost met every single goal we set. How awesome is that? On the flip side of that starting this month we have upped Lynlee's speech therapy to weekly. She is still signing (around 15 words) but hasn't replaced any signs with words yet. We just want to get a head of things if there is going to be a serious problem with speech.
There is never a dull moment in this house anymore. Most days I'm running around here cleaning up mess after mess. Chasing Lynlee because if she is quiet for more than 2 minutes you'd better go find her. So my blogs are few and far between. But no news is good news from us! I find it easier to write about the bad things, scary things, biggest worries..
We did have an amazing Memorial Day weekend! We spent Saturday in Valley Head for the big Valley Head Homecoming. In consist of all my favorite things. Pancakes, parades and dinners.. Yes, that was dinners! Sunday we spent the afternoon at Ryan's parents and put Lynlee in the baby pool. I'm sure you've seen the pictures from yesterday! Monday we took Lynlee to Kingwood to the Hovatter Zoo. It was nice. Lots of different animals, not a long drive, and Lynlee loved the Monkeys! Then we finished up with another cook out with friends. What a prefect kickoff to summer!
Speaking of summer, going to enjoy some sun :)
I think there is something about the sun that makes everyone happier. I know it does me. I'm in a much better mood and just more pleasant to be around. Lynlee seems to be the same way. We spend hours in the water table and just walking around the yard exploring.
It's been a while since I've given an update so here goes. In January we sat down with birth to three and made goals for the year. In regards to her physical therapy she has almost met every single goal we set. How awesome is that? On the flip side of that starting this month we have upped Lynlee's speech therapy to weekly. She is still signing (around 15 words) but hasn't replaced any signs with words yet. We just want to get a head of things if there is going to be a serious problem with speech.
There is never a dull moment in this house anymore. Most days I'm running around here cleaning up mess after mess. Chasing Lynlee because if she is quiet for more than 2 minutes you'd better go find her. So my blogs are few and far between. But no news is good news from us! I find it easier to write about the bad things, scary things, biggest worries..
We did have an amazing Memorial Day weekend! We spent Saturday in Valley Head for the big Valley Head Homecoming. In consist of all my favorite things. Pancakes, parades and dinners.. Yes, that was dinners! Sunday we spent the afternoon at Ryan's parents and put Lynlee in the baby pool. I'm sure you've seen the pictures from yesterday! Monday we took Lynlee to Kingwood to the Hovatter Zoo. It was nice. Lots of different animals, not a long drive, and Lynlee loved the Monkeys! Then we finished up with another cook out with friends. What a prefect kickoff to summer!
Speaking of summer, going to enjoy some sun :)
Wednesday, June 1, 2011
Wednesday, May 25, 2011
Wordless Wednesday
Wednesday, May 18, 2011
Emotional Rollercoaster
If I had blogged this time last week I would have been sure by today Lynlee would be on the transplant list. We would be waiting for the perfect liver. I would be writing about me feeling scared but confident with the decisions we made. However, this blog is nothing like that.. Let me back up for you.
Last week was busy, long, and very overwhelming. We had appointments every day starting at 8am and lasting until at least 2pm. Some appointments were classes about the surgery, how much it would cost us, how to handle it, and some were Lynlee getting her EKG, ex rays, etc. Other than Lynlee falling in the hallway, biting her lip, and us ending up in the ER the week went off great (no stitches need, just lots of blood.) Ryan and I had left there on Thursday with the decision that we were going to list Lynlee. We felt and still feel that she will one day need to be transplanted. It's better to transplant early for a majority of reasons. One, she won't remember it. Two, she is healthy now, and healthier babies come out of transplants better, and three, she doesn't need a liver now, so they can wait for the perfect liver for her.
We were told that "they" meaning all the teams we met with would get together and decide what was best for Lynlee and they would call us Monday to give us the answer. If they said transplant, and we agreed she would be listed on Monday. I was shocked on Friday night when they called to tell us that they felt Lynlee didn't need to be listed yet. We would evaluate again in three months. She won't have to go through all of that again, just meet with the transplant team.
Are you confused with this yet? Yep, me too!!
I finally talked to them again today. I wanted to know why we were turned down after they pushed for this, and I wanted to know what has to change in 3 months for them to list her. Here's the answer I got: That they feel she is stable enough now to wait. They don't feel like transplanting her right now is needed. They want to watch her levels over the next 3 months and go from there.
I know I should be jumping up and down with this news. It's great news to be told we can wait. I should be sighing with relief, but I'm not. I'm not sure if it's just because I finally had my mind set with transplanting, I was finally okay with that decision. Now in three months I'll have to go back to that place and find comfort in that decision again? Or I guess we could be told to wait longer. I just feel like we've been on an emotional roller coaster, and I'm ready to get off of it.
We are back to waiting. I should be good at it by now, right?
Last week was busy, long, and very overwhelming. We had appointments every day starting at 8am and lasting until at least 2pm. Some appointments were classes about the surgery, how much it would cost us, how to handle it, and some were Lynlee getting her EKG, ex rays, etc. Other than Lynlee falling in the hallway, biting her lip, and us ending up in the ER the week went off great (no stitches need, just lots of blood.) Ryan and I had left there on Thursday with the decision that we were going to list Lynlee. We felt and still feel that she will one day need to be transplanted. It's better to transplant early for a majority of reasons. One, she won't remember it. Two, she is healthy now, and healthier babies come out of transplants better, and three, she doesn't need a liver now, so they can wait for the perfect liver for her.
We were told that "they" meaning all the teams we met with would get together and decide what was best for Lynlee and they would call us Monday to give us the answer. If they said transplant, and we agreed she would be listed on Monday. I was shocked on Friday night when they called to tell us that they felt Lynlee didn't need to be listed yet. We would evaluate again in three months. She won't have to go through all of that again, just meet with the transplant team.
Are you confused with this yet? Yep, me too!!
I finally talked to them again today. I wanted to know why we were turned down after they pushed for this, and I wanted to know what has to change in 3 months for them to list her. Here's the answer I got: That they feel she is stable enough now to wait. They don't feel like transplanting her right now is needed. They want to watch her levels over the next 3 months and go from there.
I know I should be jumping up and down with this news. It's great news to be told we can wait. I should be sighing with relief, but I'm not. I'm not sure if it's just because I finally had my mind set with transplanting, I was finally okay with that decision. Now in three months I'll have to go back to that place and find comfort in that decision again? Or I guess we could be told to wait longer. I just feel like we've been on an emotional roller coaster, and I'm ready to get off of it.
We are back to waiting. I should be good at it by now, right?
Monday, May 9, 2011
Bitter Sweet
As most of you know we are in Pittsburgh this week for Lynlee's liver evaluation. We came up this afternoon because our schedule starts at 8am in the morning. When I talked to the lady last week she wasn't sure exactly where we would be staying, but we were hoping it was the Ronald McDonald House. I was so relieved when they called me this morning to let me know they did get us in at RMH! The room is connected to the Childrens Hospital so all we have to do is go down the elevator and we are connected. It's a really a one bedroom apartment. I hated the thought of having to drive anywhere and share a kitchen/bathroom etc like we might if they could only get us in the family housing.
When we pulled into the parking lot today it was pretty much bitter sweet! I was hoping this would be a place we might never see again. Wishful thinking I know! But in a weird way I find comfort here besides the fact it's most convenient for us. When we walked into the door it wasn't that exciting feeling (maybe I'm the only ones that gets excited to check out a new place?) but it was just like we left it. Yes, we are in a different room, and a different floor from when we were here 16 months ago, but it was just like yesterday. The elevator has the same smell it had when we left, and the helicopters are still flying over which always makes me cringe!
There were so many tears shed in this building, so many prayers said, and so much hope was found here. It was really only a place to sleep and shower. I cant really think of any real moments we just relaxed here. We usually left very early of a morning and usually only came back late at night. But this trip is different!! Of course it's mostly because Lynlee is here with us and not in the hospital, butIt's been a trip of laughter and happiness! Lynlee loves it here. She has so many new places to explore and everything is empty so she can open and close the cabinets 1000 times if she wants.
I'm not saying that tears won't be shed or prayers won't be said because I will probably do a little or a lot of both! However, it's nice to have better memories of a place.
When we pulled into the parking lot today it was pretty much bitter sweet! I was hoping this would be a place we might never see again. Wishful thinking I know! But in a weird way I find comfort here besides the fact it's most convenient for us. When we walked into the door it wasn't that exciting feeling (maybe I'm the only ones that gets excited to check out a new place?) but it was just like we left it. Yes, we are in a different room, and a different floor from when we were here 16 months ago, but it was just like yesterday. The elevator has the same smell it had when we left, and the helicopters are still flying over which always makes me cringe!
There were so many tears shed in this building, so many prayers said, and so much hope was found here. It was really only a place to sleep and shower. I cant really think of any real moments we just relaxed here. We usually left very early of a morning and usually only came back late at night. But this trip is different!! Of course it's mostly because Lynlee is here with us and not in the hospital, butIt's been a trip of laughter and happiness! Lynlee loves it here. She has so many new places to explore and everything is empty so she can open and close the cabinets 1000 times if she wants.
I'm not saying that tears won't be shed or prayers won't be said because I will probably do a little or a lot of both! However, it's nice to have better memories of a place.
Monday, May 2, 2011
Punishment? No, a Blessing!!
I was watching a TV show last night when the last lines of the show was: Every child comes with a message that God is not yet discouraged at us. It made me sit and think.
It's really easy for us to blame God and a lot easier for us to question him. But how often do we thank him when things don't go our way??
Oh probably about a month ago it was brought to my attention that there was a healing preacher coming to West Virginia. They thought we might want to take Lynlee to see if the preacher would heal her. I didn't. My belief is that God made Lynlee this way for a reason, and he will heal her when he is ready.
Not to long after that I was talking to my little brother about this. Tyler knows more about the bible then almost anyone I know! I told him my belief, and when I said that God made Lynlee this way, he was like you are correct! A lot of people would say that God done this to Lynlee, meaning to punish her.
I've never EVER thought that God is punishing Lynlee or us! Don't get me wrong, I've questioned Why, but don't we all? I've thought why Lynlee? Why pick me as the mother of a child with this disorder! But all I have to do is take a second look at Lynlee and know that God has blessed us! He has given me my prefect child.
Next week we go to Pittsburgh for Lynlee's liver evaluation. I received the packet of info and our schedule last week. When I opened the fed ex packet to a folder saying Pediatric Transplantation Services, I got sick. I went numb. Transplanting Lynlee scares me to death. As bad as this disorder is I know all about it, I know what to expect every day. Transplant could be so wonderful for us, but there is that chance that it couldn't.
But going back to God, he will get us through this also. I'm still asking for prayers for Lynlee, and for our family. Prayers that God continues to watch over her and us, and that he leads us down the right path that is best for Lynlee.
It's really easy for us to blame God and a lot easier for us to question him. But how often do we thank him when things don't go our way??
Oh probably about a month ago it was brought to my attention that there was a healing preacher coming to West Virginia. They thought we might want to take Lynlee to see if the preacher would heal her. I didn't. My belief is that God made Lynlee this way for a reason, and he will heal her when he is ready.
Not to long after that I was talking to my little brother about this. Tyler knows more about the bible then almost anyone I know! I told him my belief, and when I said that God made Lynlee this way, he was like you are correct! A lot of people would say that God done this to Lynlee, meaning to punish her.
I've never EVER thought that God is punishing Lynlee or us! Don't get me wrong, I've questioned Why, but don't we all? I've thought why Lynlee? Why pick me as the mother of a child with this disorder! But all I have to do is take a second look at Lynlee and know that God has blessed us! He has given me my prefect child.
Next week we go to Pittsburgh for Lynlee's liver evaluation. I received the packet of info and our schedule last week. When I opened the fed ex packet to a folder saying Pediatric Transplantation Services, I got sick. I went numb. Transplanting Lynlee scares me to death. As bad as this disorder is I know all about it, I know what to expect every day. Transplant could be so wonderful for us, but there is that chance that it couldn't.
But going back to God, he will get us through this also. I'm still asking for prayers for Lynlee, and for our family. Prayers that God continues to watch over her and us, and that he leads us down the right path that is best for Lynlee.
Subscribe to:
Posts (Atom)