Thursday, June 12, 2014

Socks



Our sweet heart has learned how to put shoes on.... however not her shoes! The other day I noticed she had went and put on Haven's socks and shoes and was prancing around the house in them. May I add that she didn't fall once.... and it's hard to walk in shoes twice as big as your feet when you don't have an issue with your gait. I ran to get the camera so I could catch a few shots of her....


Each day she accomplishes something new, I'm so lucky to be this little ones' Momma!!!!


Sunday, June 1, 2014

Baseball Games and WaterParks


 Everyday Hadley experiences something new, something she's never seen or done. New people, and new places. It's awesome watching her! Makes me see things so differently. Without blinders on. Hadley has inspired so many people, and she's not even been home 6 months yet. What a testimony our girl has already! In exactly 6 days we will be home 6 months with our girl. In these short 6 months I have learned so much more than I ever thought I would. As I type this now, she  is sitting contently under my feet looking at a book. How boring was our life before December 7th 2013? Very, and we didn't even know it.
  Sharing our adoption story is a passion for me, and I think now even so for Brian. It's not us we want people to know about, it's her, it's Christ and what he's done for us. He is the reason we get to share our life with this sweet little one.
Updates:  
School
Hadley is doing so good, school has been such a great experience for her. She is soaking everything up like a sponge. She will return to Memorial this fall and hopefully will be joined by her own ASL interpreter all year. We just met with her school faculty in hope they will be able to provide one for her. Hadley will be staying home this summer with the other little ones. Can't wait to see what they teach her. Maybe if we're lucky we can work on potty training.

Medical
Hadley goes back to UC on 6/18 for hearing aids and follow-ups with lots and lots of special doctors. We know that hearing aids might not help her enough but we will try them first. She is a cochlear implant candidate, however we know God can and still does perform miracles so anything is possible (just ask the blind man, he's seen miracles and if you don't buy his story talk to the deaf man he heard all about them too). "Our God is so big, so strong and so mighty there's nothing my God can't do for you."  there's that song too.
In July we go back to see Dr.T at U.K. for our 6 month check-up, I can't wait for her to see just how great our girl is doing. The last time she saw us Hadley couldn't even walk, now she's running.

Advocating
I don't want to get to in depth here about advocating, most all parents advocate for their children at one time or another. But, we are learning that having a child with different needs then the majority is challenging. However, not impossible. The love we share for our children is a common bond between all of us, what doesn't kill us only makes us stronger. Keep advocating, even when you don't feel it makes a difference, it does.....

Home life
The kids are all still doing great with our newest addition. None of them have had behavioral changes, at least not in a negative aspect. Rather a change for the better..... they are learning patience and love without boundaries. They don't seem to even notice that they're more of us. We have happy kids, that's all I can say. They enjoy watching her change as much as Brian and I do. They feel apart of something bigger than all of us, and that's living a life serving others and sharing God's true love for us all.
We took her to the water park yesterday, and she LOVED it!!!! Hadley is such a water baby.....

We couldn't be more happy with our decision to follow God's perfect plan for our family through adoption. It's not cookie-cutter perfect, there are some times when it's crazy, hectic, chaos, and you wonder if you'll survive another minute. But then the minute is over, and you think "oh, that wasn't so bad." If you are interested in adoption, sponsoring a child, or even advocating for orphans there are so many things you can do to help. If you have any questions you can call or email me anytime. I'm no expert, but I do know where to get answers/information.

"Whoever welcomes one of these little children in my name welcomes me; and whoever welcomes me does not welcome me but the one who sent me." - Mark 9:37


Friday, May 2, 2014

The Good, the bad, and the ugly....


So last week Hadley had an MRI and ARB performed at UC Children's. I was out of town on business for school, so Brian and Mom went together to be with our sweet girl. Brian called me to tell me that Hadley was doing great, I must say how thankful we are for the amazing staff that worked with her. They had everything done in a few hours and were back on their way home in no time. The audiologist did tell Brian that the ARB results showed severe hearing loss (as we had suspected), not exactly what we wanted to hear though. I guess deep inside I wanted the previous test obtained in China to be wrong. For a moment I allowed myself to cry, no one was watching, just me standing outside my classroom. I had to ask myself "why are you upset Jennifer? You know she can't hear, this isn't new information?" Still it hurts.....I just want her to hear!!!
    Flash back to last November, actually the week prior to our travel. I was standing in my room looking at the suitcases trying to come up with the best way to get everything packed, my phone rings and I see it's AWAA (our agency). They wanted to talk to Brian and I together about new information on Hadley. Praying she was okay first, and then worrying that they were going to stall our trip I didn't know whether to faint or puke. They told us that recent testing had revealed that she has a severe hearing loss, and they need us to reassess our feelings towards a child with a hearing impairment. Our assessment was short, we told them that the fact that she has a hearing impairment doesn't change the fact that she is our daughter, so let's get this show on the road and get our girl home. In this moment I questioned my ability to parent a child who is deaf, not my ability to love her or care for her. Down deep inside fear started to creep in and left me pondering if I would be the best parent for her because I don't know how to sign, would I fail her?
   After returning home, Hadley began to flourish in so many ways. God gave me the confidence that I needed in my ability to parent a child with hearing loss, I set my mind to learn ASL and provide Hadley with every resource available. My daughter will have her needs met, whatever it takes! Hadley's school has been diligent in meeting her needs, and I must say that they all love her so much! It makes me smile everyday when I see the little kids run over and greet her at the door, most of them signing "good morning Hadley!". Makes me wonder "are we teaching her or is she teaching us?" maybe it's both.
   On Wednesday, they called with Hadley's MRI results. I'm not going to give all the details about Hadley, we are protecting her privacy. I will share some of the bits and pieces because I want you all to know, and just maybe it will help another family or child in the future. Hadley's injury (brain bleed) was indeed caused by abuse. More than likely repeated abuse, and probably an injury of being forcefully shaken. Her hearing loss is indeed a result of the brain injury, and is permanent. I have grieved for my daughter's hearing loss since the first day I found out. Now, I'm just MAD!!!!!!! MAD is actually an understatement!!!!! I am furious!!!!!!!! I'm furious that my daughter can't hear because of another person's actions, that someone used force to shake my daughter so severely that she bleed in her brain..........With that being said, I also know that I will forgive that person, not now, but when I'm ready.... I will love Hadley so much that she will know that we will never let anyone else ever hurt her. We will teach her that we are forever!!!! She was born to be ours and nothing will ever change that.
      I am thankful that we didn't know about her hearing loss in her original file, because fear of raising a child with a hearing impairment would have scared me away.... I'm sad that I felt that way, but it's true. Sometimes fear scares us from meeting new people, going to new places, experiencing many different things, and living our life as God has planned for us to. I have learned in the past 5 months that I'm stronger than I thought, and living inside my comfort zone is really not living at all......



Friday, April 4, 2014

It's April.....

My I did a horrible job blogging through the month of March. Let's see here where should I start????
let's start with Hadley's medical updates shall we? We returned to UC Children's in the beginning of March to meet with Hadley's ENT team (and I mean TEAM) this is just one of the many things to love about UC it's a interdisciplinary team effort to treat each child with the best care available. We met with her ENT MD Dr.G (for short) and as soon as he walked into our room he asked "when was your gotcha day?" I quickly responded by stating how impressed I was that he spoke "adoption lingo" and he said "well I have 2 adopted children myself" coincidence? I think not... Just an example of how detailed God really is in orchestrating his plan for our girl.... he did shed insight on the next few steps we will be taking in getting Hadley to hear and talk as soon as possible. Next step MRI of head, ear and an ARB while she's asleep for the MRI. The earliest appointment not until 4/25 which just so happens to be the same time I will be at Frontier attending Clinical Bound. Not happy about that, but my mom said she would go with Brian, so it will be okay.
   Next update...... FOOD.... our girl is still eating like a bird, with very little things on her menu. I have researched this topic and it can take months to get children to eat better. It's hard to tell what's a normal 3 year old and what's just Hadley. But, our Chinese doll loves spaghetti..........



She's also doing so good at school and with all of her therapies.... Couldn't be any prouder of our girl!!!

Tuesday, February 25, 2014

Hadley's 3

The plan was to have a big birthday party for our sweet girl......
Our intentions were good......Our party planning not so much...... but God knows just how to intervene when I need him to.

 Our schedules didn't leave out room for a family get together, I know imagine that right?
So during our family sweetheart dinner at my parents house we had a little cake
and although Hadley wasn't into eating any, she was definitely into playing in it

and at this point Hadley is still not comfortable with lots of people coming into our house. So maybe this summer we can do another party for her.




Saturday, February 8, 2014

Look who's walking now


On Tuesday 2/4/2014, our sweet girl accomplished a major milestone. Our girl started walking unassisted. Brian called on his way home from picking her up at preschool, he was so excited. He said "Honey this can't wait until I get home, Hadley walked to the lunchroom today at school all by herself!" We were both so happy and proud. In just 2 months Hadley has learned to walk on her own, and before her 3rd birthday!!! Once they got home I waited in the kitchen and when he sat her down, she walked right into my arms. Tears of joy ran down my face, Thank you Lord for helping my girl walk!!!



I tired to upload the video, however I can't figure out how to rotate it. Oh well!!!

Sunday, January 12, 2014

A new year and a new beginning


I am so happy that we traveled to bring Hadley home late in the year, actually at the best time of the year. We finished out the year as a family of 7, and we got to celebrate our homecoming with friends and family the same time we we're celebrating the birth of our savior. How perfect! God does have perfect timing! Hadley has made great progress in the short 6 weeks she's been with us, especially in the month we've been home as a complete family. We've had some doctor's appointments, and have met with first steps, and some of her therapists and I will post about them shortly. But today our girl made a big step.... a step I thought wouldn't come for quite sometime..... See she is not as mobile as most children her age, her preferred route of transportation is scooting..... She can bare weight however walking isn't happening right now, she will walk one day (hopefully sooner than later). She amazes me everyday, just the way she gets up with a smile on her face, she is such a great inspiration to me!!! I'm not sure how she is as strong as she is, and where that strength comes from. But, she is a fighter, after all all orphans are fighters or they wouldn't survive. Hadley faces challenges sometimes fearless, others day not so much. I have learned when to push her, and when not too. I have learned that sometimes when I think she can't do something she shows me she can, and I have learned that I can't put limits on her, and I won't let anyone else either.... The other children have been so good for her. We were told by many people that bringing her into our home with other little kids would be so good for her. How very true that was..... They teach her new things everyday, and they enjoy doing it. She teaches them too.

They have learned that you can love anyone that may be different from them, they don't even acknowledge that she is adopted anymore. They introduce her as their sister, and they say "she was born in China though". They don't judge with colored glasses, unlike the crazy old lady at the YMCA pool the other day (I will leave that alone for now). They have learned to be more patient, by waiting on her, and us to get her ready. They have gone to her doctors appointments, and have waited hours to get tests, and evaluations done. They have watched her come out of her shell, and she is teaching them day by day to take on their own fears and never back down...

A few weeks ago this girl couldn't and wouldn't even acknowledge the staircase, then after watching day after day her siblings running up and down the stairs so effortlessly, she walked over and up she went. Haven and Hagan waited patiently for her at the top, while I followed within an arms reach behind her biting my nails.... She took her time, and they cheered her on each step of the way....
She saw her challenge, grabbed it by the horns and rode it all the way to her victory!!!!!! She is my daughter, so brave and strong and I have a feeling this is just one of many victories coming in the next year for this little one. To God be all the Glory, for without him we would be and do nothing.