A blog about the dynamic journey the Buck family (Julie, Brian, Aubrey and Malakai), is now facing. Please be praying diligently for us as we seek constant guidance from the Lord, healing from his hands, and strength in his promises.
Tuesday, March 29, 2011
The Waiting Game
Two weeks. We close on our new home in two weeks. It is hard to keep the two kids occupied each day here. I have been planning outings and activities for the kids and I to do each day. We have spent lots of time catching up with old friends. We have been to the library, zoo, playland, indoor playground three times, one mall, and community rec center kindergym time twice. I signed Aubrey up for a gymnastics class and have plans to go to the indoor waterpark, and a church moms play group this week! Aubrey and I do a little homeschool preschool each day--usually when Malakai naps. Brian and I have been meticulously planning our garden, and the fence around it to keep moose out, and the compost bin! We are anxious to be homeowners again! We will have a large yard in our new home (over half acre) so we have been planning what we want to do with it! This place is very nice and I am thankful we could be in a place like this in this meantime. It is comfortable and fairly quiet. We are on the 4th (top) floor with views of the mountains. We have shopping carts in the garage to bring groceries and sleeping kids up from the car in the elevator. Brian works really close, too. Malakai has grown a lot since we got here over a month ago. He now crawls everywhere on his knees and pulls up and cruises all around the furniture. He is such a happy kid most of the time. I thought he had crawled down the hall to the kids room where Aubrey was but she came back not knowing where he was. . . we heard a "splash, splash" and ran to find him laughing and splashing his hands in the toilet! Aaaah!
Friday, March 4, 2011
Alaska Update
We have been in Anchorage for a little over a week. We have been looking for houses and are currently waiting to hear from one we put an offer on. (the third house we have offered on.) We are renting a furnished 2 bedroom appartment downtown. It is cozy and fine, but we are anxious to get into a home. We have nice views of the mountains and were able to see some dogsled racers from the kids's bedroom window last weekend. Aubrey likes the snow, but thinks it is too cold here. She has already had several play dates and loves her friends here. It hasn't been the easiest transition for the kids. Malakai arrived in AK with double ear infections and Aubrey seems to have caught a new cold just as her last one was almost gone. Neither kid is sleeping very well, so far--consequently, neither am I. It will be nice to get settled somewhere in our own beds again. I'll try and keep you posted. . . We are excited for the Iditerod start this weekend. Brian likes his job, and the challenge of doing something a little different. It has been fun catching up with old friends.
Monday, February 14, 2011
Tuesday, February 8, 2011
Moving Day!
The big truck is pulling up any minute! We are off on another adventure. Feb 21st we will be flying to Alaska to once again make Anchorage home. We are excited--though it is always bitter-sweet to move. We will greatly miss living near family, our church home, our neighbors, and the friends we have made--not to mention the pool and the sunshiny weather! Aubrey, at 3 years old, is SO excited and keeps telling us how much she loves snow and all the things that go with that. Malakai will hopefully become a little more flexible through this transition! They're here--gotta go!
Saturday, October 23, 2010
October 2010
I realize I have not touched the blog in some time. Thank you so much for checking it and continuing to pray for our family. I think I have wanted so much to feel "normal" again that things like writing in the blog got put on the back burner. It always forces me to reflect on all that has happened in our life--and sometimes I just don't want to do that.
Brian returned to work full time just three weeks after being released from the hospital. He feels as good as new. Brian expected the doctor to say he could go back to work after two weeks but he encouraged him to take one more week off--so we took a mini-vacation to a resort in Austin. It was good to get away. We are still trying to work out what the best activity level for him will be. A stress echo revealed that his heart isn't handling exercise as well as it should--so for now, the orders are to try and keep his heart below 120 bpm. We have been able to hike and play some tennis and do yard work at that level. Contact sports are off limits for now. I have been amazed at Brian's ability to focus on what he can do and not on what he can't.
Brian and I have very different ways of dealing with all that has happened. I do a lot of internal processing and occasional conversations with good friends--but I want distance from the pain and fears of that week and the implications for our future. I want to focus on the day to day and try and not worry about the future. Brian on the other hand takes a much more proactive approach. He has immersed himself with information and connected with people who have walked a similar road. He joined some organizations made up of people who have HCM or have children with the disease. These communities provide support and advice for families as well as advocate for heart healthy legislation. The Sudden Cardiac Arrest Coalition recently flew Brian to Washington DC to share his story with lawmakers. They are hoping to save lives through awareness and training. Brian sees his arrest as a platform God has given him to share Christ with others. And wants to be able to make the best decisions for himself and our children to keep everyone healthy.
This summer, besides adjusting to having a new baby and recovering from a cardiac arrest in the family. . . My parents came out for a nice long visit. My dad built us a beautiful window-seat in the living room. My mom and I made the cushion. We took a last minute trip in September to Nashville to spend time with Brian's sister Lori and her family. That was a great time. Aubrey started preschool at our church two days/week. She loves it. It took her a few weeks to talk to her teachers, but she is settling in well now. At home she is as spunky as ever--and never stops talking! She definitely has a mind of her own and a strong will for such a sweet little girl. We went camping with Brian's folks one weekend and I cut Aubrey's hair for the first time. Aubrey's birthday was Oct. 7th and we had a lot of fun celebrating it. She brought cupcakes to school on the 6th, we celebrated as a family on the 7th and then the next Saturday we had a costume party!
Malakai is really a delight and a blessing in our family. When I look back on that week Brian was in the hospital and Kai turned 8 weeks old, I am so thankful for him. He is such a sweet baby and he got a lot easier for me that week--in terms of eating and sleeping well. I think that sitting and nursing him every 2-3 hours was so good for me in so many ways. He is just now about 6 months old and I just adore him. He is so smiley and friendly. He loves attention. I am thankful for those two mornings a week when it's just him and me at home.
I think I'll stop there. Know that our family is doing well and so appreciative of all the prayers and love you all have shown us.
Saturday, July 3, 2010
Processing
I have been wanting to write on the blog, but it is hard to know what to say. Brian is doing great. We went in for follow-up appointments with the cardiologist and the electrophysiologist. Both appointments gave us a good news that he is healing well and will be able to resume an active lifestyle soon. We learned more about the devise (defibrillator) they installed in his chest. I liked the point the nurse made that the AICD is meant to help him get out there and live life not to keep him home.
On Tuesday, we went to Brian's work as a family. We wanted to thank the women who responded to the emergency and preformed CPR on Brian. We also just wanted people to be able to see Brian and how well he is doing. I know that was really important to Brian and I think it helped him a lot. He is still trying to piece together all that happened to him. It was pretty emotional to meet one of the girls that initially saved Brian's life. I know what I went through and I can imagine what Brian went through, but I realized that the event must have been pretty traumatic for those that were there in a whole different way.
Though I was so excited to have Brian home from the hospital and healing so well, I was unprepared for the tidal wave of emotions that hit me over the next week or so. There has been much to process. I avoided the thoughts and fears that were lying just below the surface for a few days. Brian asked me to share my heart with him--knowing that it must have been hard for me, but it took me a couple of days to be able to do that. Brian and I were on such opposite sides of this event that it is almost like we experienced two different events. Never before in our marriage have we not been able to be there together through the trials.
Still, God is faithful in all of this. He continues to teach me not to live in fear and to give my cares to him. Brian feels that God has given him a second chance at life and want to live for what is important. We see God's glory all around--in saving Brian's life, in walking with us through the trial, in providing sleep when sleep seemed impossible, in the support we've received from the community, in the new depth of love in our family, and in new perspectives. We are thankful for life–-not only this life here and now, but we can look ahead to eternity because of our Savior who bore our sins on the cross.
Tuesday, June 29, 2010
Brian's Perspective
It has been about two weeks since the incident. This whole ordeal was actually tougher on others than it was on me, though. I've been well taken care of – starting with CPR, getting shocked, getting accompanied in the ambulance, being visited in the Houston Medical Center by many, brought meals after coming home, etc. There are some strange discomforts still - like unusual muscle twitches and the tight skin around the defibrillator, but other than that I'm just moving slow and not allowed to lift my arm over my shoulder.
I wish I had something really profound to say, but instead I will right down a few of my thoughts:
As I was waking up, I kept thinking I was dreaming and just couldn't wake up. I remember all the details of the hospital room. I woke up in the same place about 5 or more times before I realized it was not a dream. That's when I started to realize something was wrong.
About half a day or more after I realized something was wrong, I started to understand that whatever I was going through was a fairly big deal. At that point I thought about Julie and the kids and thought I should really try to get better for them.
Every time I truly think about the thought process Julie has been through, it is very difficult. There were two days when she did not know if I would be OK, was given some information that I might not be OK, and I can't imagine the difficulty of that situation.
People have poured out support for me and my family. Here in town, we've had lots of visitors both before and after I was aware of their presence at the hospital. Family came in from out of town. It was pretty confusing waking up and seeing so many old friends and family at the hospital. I soon realized they were only there because my health was so poor, which is humbling.
I read through the blog that Julie wrote and the comments from people all over. It was emotional to see what people wrote and how people care.
God has protected us in a very real way. We are praying he uses this situation for a greater good…
I wish I had something really profound to say, but instead I will right down a few of my thoughts:
As I was waking up, I kept thinking I was dreaming and just couldn't wake up. I remember all the details of the hospital room. I woke up in the same place about 5 or more times before I realized it was not a dream. That's when I started to realize something was wrong.
About half a day or more after I realized something was wrong, I started to understand that whatever I was going through was a fairly big deal. At that point I thought about Julie and the kids and thought I should really try to get better for them.
Every time I truly think about the thought process Julie has been through, it is very difficult. There were two days when she did not know if I would be OK, was given some information that I might not be OK, and I can't imagine the difficulty of that situation.
People have poured out support for me and my family. Here in town, we've had lots of visitors both before and after I was aware of their presence at the hospital. Family came in from out of town. It was pretty confusing waking up and seeing so many old friends and family at the hospital. I soon realized they were only there because my health was so poor, which is humbling.
I read through the blog that Julie wrote and the comments from people all over. It was emotional to see what people wrote and how people care.
God has protected us in a very real way. We are praying he uses this situation for a greater good…
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