Friday, January 1, 2016
Happy New Year 2016!
Posted by Jennie at 12:00 AM 1 comments
Saturday, October 10, 2015
The New Piece of Brennan's Sight Journey
Brennan's vision has been a challenge since he was born; his prematurity and underdeveloped eyes, then compounded by needing so much oxygen for so long did quite a bit of damage. It's been quite a journey trying to understand what he sees and what he needs to see best. Each stage brought different pieces of information, levels of understanding and ways of trying...
When he was a baby, we relied on the doctors and tests to tell us what he could see and when he needed more surgery to help reconstruct his eyes from his retina detachment and strabisimus but we kinda needed to wait til he grew up more and his eyes developed more to learn more.
When he was a toddler, a lot of other issues came into play that clouded the picture - as he started walking, we learned he had a balance disorder, but that also looked like it was because of his trouble seeing. He loved to bounce and we learned he had sensory processing disorder and needs high input, but it sure looked like he was trying to move his head & body to keep up with his racing eyes. We also started noticing that there might be problem with his vision field (not just the strength of his glasses prescription). He started talking (a bit delayed) then we could FINALLY ask him what he sees! He had some cognitive delays that impacted his comprehension of our questions & his answers, speech delays and mumbling that made it hard for us and frustrating for him. We did learn that he could make out some images from a distance, but to focus, he needed to see the object from the bottom left part of his left eye.
When he was a preschooler, the schools and therapists got involved, along with daily learning at home. There was a lot of focus on new learning that challenged him which (good & bad) really brought out the deficits and the need to figure out how to help him communicate. He worked on learning academically and relaying what he was learning. We kept trying to sort out sensory, balance, vision, possible cognitive delay, emotions and behaviors as he faced new experiences, expectations and challenges. Some things are easy to sort out, some crossed issues and others we're still not sure... School introduced several new techniques, large print and even a large touch screen computer! He was so eager to learn, willing to try new things, excited, but also got frustrated and wanted to do more at times. He mastered recognizing his letters, numbers and colors! His brain grew so much but couldn't get it out fast enough! He really made so much progress during preschool!
Now, he's a Kindergartner! We're continuing to sort things out, determine the best strategies to help him learn, navigate the world - and he really is doing great! He can walk down steps, put on shoes, find things he's looking for by himself. This year in school he's focusing on reading print and writing which are really hard for him. He can use the computer well, but we tried large print, writing with dark markers and haven't been successful to his standards yet. He can't read what he's written, or tell what he's drawn afterward and gets disappointed. The books are blown up so large, the papers are clumsy to use for him and he's gotten frustrated. Don't get me wrong, he's such a happy kid still and it's hard to see him get frustrated! The newest thing this year we've tried...Braille! He was getting pretty frustrated and he is so smart, we needed to try something else. We talked with the National Federation of the Blind representative and the school vision specialist introduced it this week and he embraced it!
I'm not going to lie, I was excited about him trying Braille when we were first talking about it, but now that it's a reality, it took a bit of acceptance. I'm so thrilled for him to have a great method to read and write! I'm also a bit overwhelmed at needing to learn another language and the thought of another adjustment for our family. The day he learned about Braille, we talked about it at dinner and Hailey was so excited. She had just learned about Helen Keller and how important Braille is for people to communicate! She asked Brennan what class he learned it in so she could join him one day to learn too...precious girl! I've said it before, but she is the perfect sister for these kids. :) After he get's a good handle on it (or probably while he's learning too!) we're going to all learn together so he can read to us! Of course, he'll continuing using his vision too, but knowing Braille will make communicating less frustrating for him - he'll have another tool and not have to work so hard at it. It's another adjustment, but we've been through quite a bit of adjustments already and are starting to know the drill. Don't get too comfortable with status quo - there's always something else in store!
Posted by Jennie at 3:48 PM 3 comments
Labels: medical update, pictures
Tuesday, October 6, 2015
Welcome to Our Family
We had a sign that needed some repurposing love and Pinterest inspired idea that we totally made our own! We sat around the table and Brennan, Hailey & Brooke came up with the words that describe our family then voted on which would make the sign. We also came up with: accident-prone, kind, messy, energetic, fun, loving, happy and curious. It was so interesting to learn how the kids would describe our family!
Lately, we've had a good share of good times and rough times; I keep reminding myself that's part of parenting and raising kids to be adults with sound values and good adjectives that describe them too, right?! My New Year's resolution was to get to know each of the kids better and deeper, focus on building the firm foundation. It hasn't all been perfect, but we've intentionally worked through emotions, attitudes, tiredness, to try to create relationships and a home of feeling safe, understood and supported. This project gave me encouragement that we're on the right track! We've had it on the porch for a few days and the kids have said something or smiled about it when they come in from school. It turned out well, but the process of making it was awesome!
Posted by Jennie at 10:38 PM 0 comments
Saturday, August 29, 2015
Lesson on reliance and dependence thanks to a spica cast
We knew in advance Landon was going to have major surgery. The news was sprung on us pretty quickly but we had time to adjust, research and ask questions about recovery but no amount of planning can totally prepare you. Sure, the organizer in me wanted to know the surgical plans, how to diaper him after, what equipment I needed, his care schedule for recovery, along with about 200 other things...just ask Nich! :) But, planning only took me so far. There was a world of emotions, unexpected parts of this hospital stay, small complications, a bunch of things out of my control - just waiting outside my plans...waiting for my emotional breaking point. I've realized today, and appreciate the perspective of a journey of preparation versus shorter term planning.
Posted by Jennie at 3:16 PM 1 comments
Thursday, August 13, 2015
Hip Reconstruction Pre-Op
About 6 weeks ago we learned Landon needs a bilateral hip reconstruction surgery. At that point, his right hip was only 20% in socket and the structure of the socket is not fully developed to hold the femur. The tendons in his hip and groin area are really tight, so they'll cut and loosen them to add more flexibility. It'll be about a 4 hour surgery, in the hospital for a few days and then recovery in a 6 week spica body cast. I know recovery will be difficult, painful and long but we hope it'll be so helpful long term!
Posted by Jennie at 10:38 PM 0 comments
Labels: medical update
Tuesday, June 9, 2015
Progress in His time
Next, the trial run at home, his first 2 years. He was still frail, we were still young but armed with the knowledge, confidence, tools and continued support. He spent a lot of time still in the hospital, the other kids and rest of our family adapted, learned how to accept and ask for help when we needed it. We tried to fit in developmental activities, therapy, etc between clinic appointments and hospital stays as best we could. We practiced our advocacy, negotiating and flexibility skills working with professionals for Landon's best interest. I grew as a parent, Christian and person. I think we were still focused on survival, trusting our instincts and getting to know Landon.
Posted by Jennie at 11:58 PM 1 comments
Labels: video
Sunday, March 29, 2015
Reaching Contentment
This has been going round and round in my head and my life for the last 5 years, and I'm so thankful God's put all the pieces together and I can honestly say I've reached a point of contentment in my life, and man is it freeing! The - It Is Well With My Soul type of contentment! This post is largely for me to mark this stage in my faith, personal and parenting journey, but also maybe to provide hope for somebody that's on the doorstep of being content. When I think of being content, I thought of Paul's words in Philippians 4:12, when he wrote of having lived in plenty and and in need, hungry and full, but it's taken on a new meaning for me. Not just in material things, but in concepts. The secret of being content is in Jesus and only through Him, and for me was through a journey of other big words and seasons - Regret, Struggle, Acceptance, Peace and Joy.
5 years ago our lives were turned upside down....5 years, 6 months and 5 days to be exact. Brennan, Landon, Katelyn and Brooklyn were born 17 weeks, 6 days early and we had no idea what was in store! Three days later Katelyn died, many times in the weeks shortly after, Brennan, Landon and Brooklyn were very critical and Landon many times still in the last several years. I've cycled through different periods of grief. Grief over death, over changed dreams for my kids, over seeing my kids live a of special needs and everything that comes with it, over changed relationships. I had so many real struggles with what-ifs, wanting to change the past or situations, regret over not doing enough therapy with them, anger toward my prenatal doc, comparison with healthy preemies - you get the picture...regret and real struggle. Most of my kids beat the odds - 3 were alive and making progress and I desperately wanted to believe the cliche, "I wouldn't change a thing." I was/am thankful for the experiences we've had, people we've met, perspectives I've been opened to, but I couldn't buy in. Who would willingly choose to loose their daughter, see their kids live such difficult lives? Real struggle here. Apart from my own internal struggle; parenting in general is hard - parenting kids with sensory issues, cognitive impairments, physical disabilities, explaining these to Hailey and each other and encouraging each of them to see each other for the beautiful person God made them but being free to work through their own thoughts, feelings and questions and grief - sometimes we did well, sometimes not so well and need to ask the kids for forgiveness and help!
I tried to do this on my own and change my attitude when needed, but I'd get knocked off center, just the normal challenges of the day (of course, in retrospect, right?!). Dog gone it Jennie - Trust in the Lord, with ALL your heart, lean not on your own understanding. Not part of it, not the easy parts, not the parts I think I need work on. Give myself to Him and see the plans and paths He has for me. Now, the human side of me still struggles with why me and why the kids, but - why not us? Things happen, there's evil and bad situations in the world. But I HAVE FAITH that He has a plan for me and for us for His plan, not just for my life. Throughout the situations that come up, He will comfort us. He will give us peace that passes all understanding. He will take care of me and my family. I love this quote from CS Lewis: "God, who foresaw your tribulation, has specially armed you to go through it; not without pain, but without stain." We're not meant to live an easy life because we're Christian's, but when we experience God taking care of us, that's a show stopper. When I was in the middle of the regret and struggles and sought Him, I never felt such peace. I certainly am thankful I haven't had a life of daily battles, but the depths have magnified the joys.
This picture of Brennan and Landon is a snapshot of that - their relationship means SO MUCH, especially because of the life they've already lived and all that's impacting the life they're living!
Now the next big word, Acceptance. I accepted diagnoses (though difficult too!), the modifications we needed to make at home, changes in how we parent and talk to each kid but also convey expectations for what they can do, changes in relationships, different lifestyle, many of the outside stuff; and my heart accepted my new life. This stuff is hard, but I've accepted it's necessary. That's the part of the cliche I would buy into, for as different as my life is now than I had planned, I wouldn't trade these kids. Brennan, Landon and Brooke had a 15% chance of survival and I am blessed to have them, I remember that everyday. I think Contentment is beyond Acceptance though. Once I feel content, I can truly look forward, not just backward or in the day-to-day. Maybe it's just semantics, but for me, it was a difference and has been in lots of areas.
I just love the joy, love and laughter on their faces! There's so much going on bigger than they know, but they don't worry. It is what it is! :)
I think true Peace and Joy for me has come after I've become content with my life. "The secret of being content in every situation..." is from God. He's prepared my heart and changed my heart. Situations aren't necessarily going to get easier, but how I navigate through them is. I'm not fighting them (or the overall picture of my life) - I'm going with the flow, because I trust the Creator. When I'm going with His flow, I'm aware of the teachable moments for myself or with my kids, I have energy, peace and patience for the challenges - I'm not leaning on myself. I've seen parallels as I've had different seasons in my life - pretty sure that's God at work, getting me ready for the next thing in store, understanding Him better, understanding my kids better, understanding how He made me better; and I'm really excited!
Never in a million years would I have expected to be living this life, but I'm thankful I serve a God that's bigger than my expectations and carries me through, no matter the specific situation or season!
Posted by Jennie at 5:18 PM 2 comments







