24 December 2014

Merry Christmas!

Liam wants to wish you all a very merry Christmas! And tell you he's lost another tooth! He's looking very snaggly with only one permanent replacing the 5 he's lost so far this year.

We bucked tradition this year and instead of presents we gifted each other our presence. 

We took off with the kids to our favorite destination, the mountains, to experience some firsts: tubing, skiing, and snowboarding!

The kids have enjoyed it so much and wish we had done this years ago. 

Even  though Liam hates to travel (we laid him across Mimi's lap for half the car trip) and dislikes change, he's done really well. 

We got to cut down our very first real Christmas tree!

We are ridiculously grateful for the blessings we have been given this year.  It is not easy traveling with a significantly disabled young one: sleep is minimal, diaper rashes from long car trips, vomiting when he's nervous, afraid he feels left out when we take off to do the things he can't...but no matter the trouble, Liam's worth the trouble and we are grateful for every family moment when our kids are always headed in different directions these days. It's tough to find time to get us all together in one place and with Rylie transferring colleges to one quite some distance from us this next year we are cherishing and enjoying this Christmas. Much love from our family to yours.  ❤️

Merry Christmas!

Liam wants to wish you all a very merry Christmas! And tell you he's lost another tooth! He's looking very snaggly with only one permanent replacing the 5 he's lost so far this year.

We bucked tradition this year and instead of presents we gifted each other our presence. 

We took off with the kids to our favorite destination, the mountains, to experience some firsts: tubing, skiing, and snowboarding!

The kids have enjoyed it so much and wish we had done this years ago. 

Even  though Liam hates to travel (we laid him across Mimi's lap for half the car trip) and dislikes change, he's done really well. 

We got to cut down our very first real Christmas tree!

We are ridiculously grateful for the blessings we have been given this year.  It is not easy traveling with a significantly disabled young one: sleep is minimal, diaper rashes from long car trips, vomiting when he's nervous, afraid he feels left out when we take off to do the things he can't...but no matter the trouble, Liam's worth the trouble and we are grateful for every family moment when our kids are always headed in different directions these days. It's tough to find time to get us all together in one place and with Rylie transferring colleges to one quite some distance from us this next year we are cherishing and enjoying this Christmas. Much love from our family to yours.  ❤️

04 December 2014

Our Favorite Days

Liam's #fromwhereistand on Instagram
We've had a very beautiful fall in this area of NC this year. The colors have been gorgeous and long lasting due to extended amounts of rain. My Bradford Pear in my front yard just finished dropping its bright yellow leaves today.

I try to take advantage of the weather this time of year to get Liam outdoors. Liam does not handle heat well so it's too hot here in the summer to take him out for very long. We pretty much spend all July and August in the air conditioning which means when fall rolls around we are antsy to get out and enjoy our favorite season.
The only really good nature trail I've found around here that's wheelchair accessible.
 We have a nice short trail that ends at the river nearby that makes a really great place to take Liam on a hike. It's perfectly shaded all the way to the river landing. It's "wheelchair" friendly meaning it's flat and wide. The trail is not paved, it's gravel, and there are a few bumps in the off shoot trails but if you have a jogging stroller it's perfectly accessible.

I wish there were more places to be outdoors with Liam while he is in his chair. We all love being outside and hiking/walking but can't enjoy that much anymore with wee man confined to a wheelchair. You don't know what you've got 'til it's gone and we sure do miss the days of being able to explore and hike. You don't realize how hard life is in a wheelchair in the great outdoors until you're limited by where your wheels can take you.

My boys.
We came across this beautiful spot recently and was able to take Liam in his jogger for a short time through the trails along the river but the terrain became very rough and we had to abandon our journey and hang out at the river bank. Ian's such a great big brother and took Liam down to the river to dip his toes in.

No joke, I walked out to put Liam's stuff in the truck to take him to school the other day and this pile of leaves was in a heart shape on his wheelchair ramp. I was sure one of the kids did it but since it was very early in the morning and they all said they hadn't, I am taking this as a sweet message from the Lord. :) He loves Liam.

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27 October 2014

My other rant from the DR trip

When it was time to head home from the Dominican Republic and after checking in with Delta, we headed through to security. When we stepped up to security, I took our bags, shoes, and food and put them on the conveyer belt. I wheeled Liam to the metal detector and waited our turn. Security started speaking to me in Spanish. I spoke back in English and motioned that Liam couldn't come out of his wheelchair. They motioned me to take him out and continued talking in Spanish. I motioned that he doesn't come out of his chair and they just continued to stare at me.

Here's where stupidity really comes into play.

I am speaking English. I don't expect them to speak my language but since I just came from a counter where everyone spoke English and I was obviously trying to convey something about my obviously handicapped son, I assumed they would get someone who spoke English. I was not removing him from his wheelchair. Man, was I wrong.

They continued to look at me.

Finally a woman came across the detector to my side and asked me if he was a nino or nina. I said nino. She then motioned for me to take him out.

I might have started to get teary eyed at this point.

I shook my head no at her.

Rylie is standing to the side and telling me that they aren't going to let us through that I should just take him out of his wheelchair. I, however, was adamant that I not remove him from his "legs" and that it was a violation of all things sensical and humane for disabled persons to be treated in such a way. I knew Liam, who can not stand changes or transitions, was going to get upset, cry, and try to throw up on me right there in security at the airport all because they were too inept at how to handle a person with a disability who is in a WHEELCHAIR!

Rylie just looked at me like I was nuts.

The security lady just looked at me like I was nuts.

I wasn't getting anywhere.

Which meant I wasn't going anywhere.

I went against every fiber of my being and started taking Liam out of his wheelchair. And he started to cry.

Rylie took the chair apart and put it through the conveyor.

I stepped up to the metal detector carrying Liam who is now trying to throw up on me. Deep down I am thinking this is one of the most humiliating things I have ever experienced in my life and they kinda deserve to get puked on. At the same time I'm thinking that I don't really want to travel all day with puke on.

I walked through the detector when motioned through and by this time Liam was so upset and awkward to hold that I had to kneel down. I am now sitting on the floor just past the detectors waiting for them to come pat down Liam. The dude honestly did a tiny swipe of his left and right side and that was it. He couldn't really get to Liam with the way he was curling into me all agitated.

I was furious by the time it was over. I really was. Did they expect a 10 yr old, 15 yr old (insert an age), etc... to be taken from their wheelchairs and carried through a metal detector? The idea was preposterous and yet I was expected to do that with my 7 yr old. What happened to common sense? It apparently isn't very common these days, eh?

Coming into the US and going through security here was a breeze. When I got to the metal detector in Atlanta I looked at the man and I said "Please don't make me take him out of his wheelchair."  This sweet angel of a man said he wouldn't ask me to do that. I was able to go through the gates with Liam in his chair. After getting through we both got bomb residue tested (like Liam could make a bomb when he can't even hold a toy) and we both got patted down.

It would be great to have my grievance heard by the powers that be at the Santo Domingo Airport. I would just like them to understand a few things. I did email customer service after a few days of being home but I've never received a response back.

I want to be clear that I don't think they were doing anything malicious or intentionally humiliating. I believe they didn't think anything of what they were asking and didn't pay close enough attention to notice that Liam wasn't just another little kid in a stroller. If they had taken the time to look, and for sure they noticed afterword, my wee man is not your typical kid. He isn't even your typical special needs kid. But he is different and that was obvious.

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20 October 2014

Getting back to normal.

I've been wanting to give an update to our stem cell trip but some parts of the trip have really angered me and I needed a break before posting lest I look like I'm a ranting lunatic. But I probably will anyway so here goes...

Atlanta on the way down.
Can't you just see him asking if we're there yet.
The flights down there went pretty great. On our first Delta flight into the Dominican, a gentleman from business class immediately got out of his seat when he saw me get on the plane carrying Liam in that seat and he grabbed one side and helped me carry him all the way to the back of the plane. Not that I was going to refuse, but there was no way he was going to let me carry him alone. :)

On our return flight home I texted Shawn and told him I was never.ever flying with Liam again. It was the heat of the moment and I was done. Liam was over done. And I never want to do it again. Liam was a trooper. He really was. But sitting confined in a seat all day long when your body wants to move is painful.

On our first flight coming home from out of the Dominican he did pretty good. I got him situated well but he still isn't 'properly' seated so it can be a problem with his head control.

And that makes him cough.

So that's what he did.

The entire flight.

And the gentle(cough cough)man in the seat in front of Rylie rubber necked the ENTIRE flight to look at Liam. He even put his sunglasses on so he could stare with out looking so obvious. Like that wasn't obvious! I put Liam's iPad right in front of his face so the lookey loo couldn't see him.  Now, I understand, Liam is coughing. A LOT. But COME ON! Where did manners go? You look once or twice, can see the child has issues, then turn your face back around and keep to your own seat. Or, if you have a heart, ask if there's anything you can do. But don't ogle my son as if he has the freaking plague. He's obviously healthy, not crying, and I am attending to his needs. Leave us alone and get your staring fix by watching a movie. Rylie got a chance to stare him down when we switched seats and when he realized what she was doing he never looked back again. asdfghjkl...

After landing, a REAL gentleman in front of my seat, who never once turned around to look and stare, asked us if he could get our bags for us. That's what an empathetic, considerate person should do. I was so proud of him for being so kind. I wanted to tell him that but thought it would be too weird.

Trying to wake from the propofol after the extraction. This time they extracted stem cells from both hips.
When we got to Atlanta we had a three hour layover. I was happy about that because it allowed us time to get Liam out, eat, and just relax before another plane ride. Well, Liam was at his over done point. He was crying and crying and while Rylie and I tried to eat he wouldn't calm down. I had to get up and walk with him and let Rylie finish and then we'd switch off. Each time I walked him back to the tables where we were eating he would freak out and cry even harder. We switched off and I finished my now ice cold dinner and kept an eye on Rylie as she walked with Liam. Whenever she'd get close to my table he would cry again. I grabbed Liam and took off for the bathroom so he could lay out on the counter and relax and when I picked him up I lifted his shirt and saw a dark black and blue depression on his spine. His stroller straps had gotten twisted and had knotted right on the middle of his back and even though there was a thin cushion over it it was still digging into his spine.

After the cath, he wasn't complaining & for that I was shocked & happy.
I felt horrible. My poor wee man had been trying to tell me he hurt and I thought he was just bothered by all the traveling. Mom fail.

With the bruising on his thighs from the procedure and now the bruising on his back, he was not a happy guy. He cried for the rest of the layover. I felt so bad for the people in our tiny little terminal. They were probably only 20 seats and there was no escaping Liam's irritability.  None of them stared at us though. ;)

Once we were home Liam ran a low grade fever off and on for days. It would only last a couple of hours at the most.  He wasn't miserable, but he wasn't his happy self either and with not being able to give any medicines due to the stem cells, we relied heavily on homeopathic treatments to treat his discomfort. We did onions on the feet, egg whites on the feet, essential oils on the chest and feet, colloidal silver, and extra vitamins. It was the first time I've ever had one of my kids go medicine free for pain from a fever and Liam ended up doing really well.

He had to miss several days of school out of pure exhaustion and crankiness though and it took a full week following the procedure before he was back to his old self.

People ask when we will see improvements. It's a valid question. When will we see improvements? I want to see them now too. I'm praying we will see them now. But we might not see improvements for a while. It could be up to a year. And that's a long time to wait looking for signs of answered prayers and hopes and dreams.

This is the moment, after 20 min of a flipping, curving catheter, the Dr finally got it through and up into his carotid. You can't hear them in the room but they all shouted and whooped and were giving thumbs up in relief for finally getting it.

The gorgeous sunset view from our room. Ocean on the left & mountains on the right.
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03 October 2014

Glad thats over

Our driver picked us up at 12:45 yesterday to take us to the hospital and Liam was already sedated and getting his stem cells extracted by 2:00.  We were in a different area of the hospital than when we were here last time and it felt much more like a typical US hospital set up. Last year our room had a thick bed comforter and a wooden armoire and couch so this set up started out feeling like much more sanitary.

The extraction was done literally on the other side of a glass partition from our room. It was clouded so I couldn't completely see but it was comforting knowing he was within reach.

Last time when they did the extraction I didn't see Liam again until it was time for the infusion. This time Liam was brought back to me, pleasantly sedated on propofol, and he slept for most of the next two hours while they processed his stem cells. Again, it was nice to have him with me right there while we waited.

Once the cells were ready they took Liam right next door through another clouded door where they got him all set up in the cardiac cath lab. Once they had threaded the cath through his femoral artery in his left leg and had it up in his carotid, they called me back so I could watch the procedure. While the procedure is done Liam is continually under an xray and I am in the room with the monitors so I get to watch the stem cells pulse through his brain. It is still such a really cool thing to witness.

I watched them infuse on the right side of his neck, then they did something different from last time in that he went up some vessel on the back of the neck with another vial that sent an infusion right to Liam's cerebellum and parietal lobe.

Next they went to the left side but the cardiac interventionist couldn't get the cath threaded. I stood there watching and getting really nervous because he kept shooting it up his torso and then it would just bend and reroute. I didn't want to watch but at the same time I was rooted to my spot and couldn't move. The CI threaded that catheter out and switched it out a few times and after 20 min he finally got it threaded up to his neck. The whole lab fave out whoops and hollers and started giving thumbs ups to me. It was a huge relief to see that catheter up where it needed to go.

When they finished with that infusion I was asked to leave while they finished up with Liam. When the CI was done they asked me back to the room and we all gathered around and prayed over Liam.

It is a full two hours in the recovery room before we can be released and Liam did such a great job. I was dreading his recovery because last time he screamed for the entire time. And if you've ever heard Liam cry, you know he cries very quietly. But not after the last procedure. He wailed like a mortally wounded animal. This time he was so calm and only fussed a couple of times.

We were given the green light to go back to the hotel and 8 hours after leaving we were back. I was a bit concerned that Liam was running a low grade fever and sure enough in the middle of the night he woke up hot and dry and uncomfortable. I spent two hours awake with him trying to make him comfy with no meds. Dr. Anthony didn't want me to give anything if it wasn't necessary in order to allow the stem cells to proceed with out interruption. I used some essential oils tried to get him back to sleep.

This morning he still felt a bit warm so we took him to the pool for a couple of hours and it really cooled him off. I gave him a cool bath back in our room and I am praising God that he has been fever free the rest of the day.  But I'm still keeping essential oils on him for now.

Dr. Anthony called to check on him and will do so again his evening. We just feel so blessed and are thankful that things are going well.  There is a lot of bruising from the cath and they took extractions from both hips this year but he is healing very nicely. I really think the worst was having to take off the tape. Liam and tape are not friends.

Thank you for all the sweet texts and messages!The comfort felt knowing others have your back is indescribable. We are excited to head home tomorrow.  We have a long day with 12 hours of travel but after a week of isolation and this trip, I am looking forward to getting back to normal and moving Liam forward.

02 October 2014

Today is the day

post signatureWith a very early wake up call of 4 am, I had a pretty grumpy, coughing Liam for the first leg of our flight to Atlanta. I was pretty absorbed with taking care of Liam and really didn't notice anyone else on the plane. Apparently a lady kept giving me and and Liam the stink eye and Rylie got her to stop by giving her one back.😳 I understand his coughing fits will have people looking at us, concerned to see if he is sick (I might do the same), but there is no reason to stare us down. As always, the attendants on the flight were wonderful and the pilot even helped me get Liam through the door.

When we got to Atlanta we had a two hour layover where Liam got to stroll the airport and really relaxed and enjoyed himself. He was having such a good time that we actually missed our early boarding to Santo Domingo. When we got to our terminal, with 45 min to spare before takeoff, they were on zone 2. I was a little panicked about trying to get a forty lb boy sitting in his car seat, down the tiny aisles with people already in them. Thankfully a wonderful gentleman in first class offered to help me take Liam down to my aisle and I took him up on it. Liam did amazing on this flight. Probably due to me being able to get him out of his seat and into my lap. He relaxed, and hung out with me the entire flight. I had another lady who kept looking at us on this flight too. I looked at her and smiled. A little while later she looked back and smiled. I did the same. Then she started a conversation with me telling me how much she loves kids like Liam and that it's what she does for a living in the Murfreesboro school district. She was such a sweet lady and so fun to talk to. And she exhibited the perfect way to approach a special needs parent, smiling, gentle, and genuine in her approach.

When we landed in Santo Domingo the weather smacked us in the face. It's hot. Liam doesn't do heat. The last time we were here it was February and perfect. I didn't even think about it still being so hot here right now. Liam kept it together as long as he could and made the hour drive to the hotel (in an air conditioned van) before the heat got to be too much and he threw up. We were literally sitting in front of the hotel unloading and all I had left to get out was Liam when he had had enough.

I was happy that if he was going to throw up that he picked the end of the trip, right as we were getting our hotel room. Unfortunately, the hotel was not ready for us and we had to wait over half an hour for our room to get ready. Liam was crying and drenched in sweat so I took him to the lobby couch, stripped him down, and cooled him off with some wipes. It helped some, but he pretty much cried for the entire wait. He was done.

Once we got to the room he settled down and had a great night. We watched the sunset and all of us were asleep by 9:00.

 Our driver will be picking us up at 12:45 today to take us to the hospital and I suspect Liam's procedure will start about 2:00. I anticipate getting back to the hotel about 8 or 9 tonight.

 I can't believe the day has arrived already. It's almost surreal to be here again. Thank you so much for all your love and support and prayers. We are so thankful to not be doing this alone. 💚

15 September 2014

Two weeks to go! Eeeek!

Traveling with Liam isn't the easiest thing to do, let alone flying in an itty bitty plane. It's actually quite a feat to be sure. I have to call ahead to the airline and make sure they are aware that I will need extra time in order to board and help with his wheelchair/car seat/bags/etc. This is to our advantage as it means we actually get to board before everyone else. It's actually a huge relief to not have everyone's prying eyes watching you try to wrangle an almost 7 year old into a car seat when his body is fighting you every step of the way and in such a tiny spot as an airplane seat. I've received many fat lips and bruised eye sockets from his flailing fists and the less people watching that happen, the better my psyche will be. And since we exit last, no one is around except for the flight attendants and they are usually very helpful to me, asking me what they need to do to accommodate Liam and expedite our departure.

Liam is fed homemade food, not the commercially prepared cans of  formula that he used to get so this time our travel has a different set of requirements regarding transport. Since he's g-tube fed and entirely dependent on what I make for him, I will be making all of the food in advance, freezing it, and packing it in gel pack freezer packets for the duration of the trip. When I called ahead, I asked the airline if it will be a problem bringing his food on board and she said no, they can't keep me from bringing his medically necessary items.  She says that, but you watch, they are going to be eyeing me suspiciously when I try to get through security with four 32 oz containers full of liquidy goodness. Oh, you don't want to go through x-ray with the wheelchair? We get an automatic bomb residue check. Hooray.
Liam lost another tooth yesterday! That makes for 3 empty spaces in there!
We only have $782.40 to go! Liam has the best friends, truly. Thank you for all your prayers, questions about how this all works and our expectations from it, and for your continued belief that God is still in the miracle making business. This trip wouldn't be possible with out all of you.

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03 September 2014

We've almost done it.

I could use your help! I am beyond amazed in telling you that Liam's next stem cell trip is now 92% funded! I am blown away again by the beautiful generosity of God's people and have watched in awe as you love on us and Liam and give out of the overflow of your hearts.

Because we are so close, we have stepped out in hope and faith that the last amount needed, $1,082.40, will be supplied in God's perfect timing.

So, we have gone ahead and set the date and bought the tickets!!

Liam will be getting an infusion of his own stem cells on October 2nd!! 😱

 Please pray for the remaining money to be provided. We are so close!

Also pray for good weather (no hurricanes!), and for a safe procedure with miraculous results. I am never in doubt that we serve a big God and he is fully capable of answering big prayers. I am always amazed at how he works things out and trust that this will all go according to His plans. So please join me in praying for big, crazy, bold changes for Liam.

I never imagined God would provide most of the money for this trip with out us having to fund raise or even announce to everyone that we were even thinking of going again someday. And yet He boldly showed up and did just that.

I never thought Liam would go again, which just goes to show that God works in amazing ways. I assumed the last time was the only one Liam would get so this trip in and of itself is truly miraculous too!

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25 August 2014

First Day of First Grade

This was the beautiful smile that greeted me this morning when I told him that today was finally the first day of school. He was so excited.

We've been counting down the days for the last week. 

He started first grade today! 

 I always have much to be grateful for but this year I am especially grateful for the ability for Liam to go to school, to get to participate in activities with kids his age, to be educated in a setting where he is well cared for and loved, to receive therapies while in school...because I know there are many children who don't get the privilege that we are so accustomed to as being a right. 

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20 August 2014

A few thoughts: Belarus July 2014

I've been asked how my trip to Belarus went and it's been hard to render an explanation of my experiences in a concise yet comprehensive manner. Normally it's just easy to answer that it went wonderfully. And it did. But there is so much more to be said about my trip.
Visiting Khatyn, a memorial to the village burned by Hitler. Belarus is no stranger to tragedies.

I had heard of reverse culture shock and been told I might experience it after getting home to the US from spending two weeks in Belarus.  I didn't think too much of it until I got back. As I process and deconstruct my time over there I am left with many differing emotions. Thankfulness is the most prominent feeling. I'm thankful for getting a glimpse of what's important.

In a world where you wear the same clothes over and over and over because you don't waste soap and water on clothes that aren't really dirty, our walk in closets are filled with overpriced clothes and 87 pairs of shoes that we don't even need. It is a thought unfathomable over there to have such over abundance. I packed a suitcase full of clothes and only ended up wearing a few of the items because it's normal to look the same day after day there. It was a freely enjoyable experience of not caring about whether anyone had already seen me in that set of clothes that week. No one cares!

Dirt roads, clay houses, and outhouses are still common place outside the city and you use your yard to garden, not to grow grass. Every inch of the yard was used to grow food. And you use what you grow. You don't run down to the pizza place for dinner if you don't feel like cooking because there isn't a local pizza place. There are no fast food dives. You make what you eat, from scratch. No boxes of mac and cheese let alone 20 different varieties that our local market dizzyingly offers.

You see block upon block of socialist apartment housing.

Restrictions on free speech, free assembly, and religion remain high. Members of a religious organization don't even have the right to share their convictions or to carry out religious activity beyond the borders of the location where they are registered.

In the US where practically everyone here is familiar with Protestants and the Baptist faith and what we stand for, it's odd to be in a country where you are seen as being a member of a cult. Old superstitions are still spread around that you stay away from the Baptists because we might eat your children and we drink people's blood. In Belarus where there is strong restrictions on being able to start a new church, proselytize, and advertise, the way to change people's thoughts about what we believe about Jesus Christ is through direct one to one personal relationships. It was actually refreshing and a constant reminder about how Jesus lived and told people about the Kingdom. He did it one to one, person to person, by loving and reaching the people who society marginalized. He didn't use a tv station, a radio program, or an internet podcast. He used his life to tell people who he was. Joy and peace like that can not be suppressed no matter the governments control.

I was in Belarus to help a local church and to work with people who have special needs. And even our help is legally restricted. We can not teach with out a legal license or we could be arrested. And good luck getting one of those licenses.We helped run a camp for 'kids' of all ages (6-28 years of age) who were so excited to be able to come together and create crafts, sing songs, and learn about Jesus. Their joy was infectious. They would light up each day when they saw us and would yell our names across the room and come running to greet us.

Believers are few and far between there. Less than 1 in a 100 are Christians. The Russian Orthodox Church is the state promoted religion which is steeped in mysticism and paganism with Catholicism thrown in. But the joy in the hearts of the fellow believers is a beautiful thing to witness. They have so many obstacles to overcome in reference to the political climate, the history, and negative misconceptions and yet they have such peace and thankfulness in the midst of it all. They make no assumptions. It was something to be jealous of actually, because they have a deep respect for their faith, which America (as a whole) seems to take for granted. They are full of hope. Hope that the people on their street will come to know Jesus because of the joy and peace they have in their lives, even in the midst of the oppression of their people.

Belarus is a country that is not ready or able to be a democracy yet. That was something that was very hard for me to experience. Growing up in a country where we are given so many freedoms, it was hard to see the people there have so much less than we do. My close translator and guide summed it all up for me though. The people of Belarus are tired from all the wars, the fall of communism, Chernobyl, etc...  They just want peace. Even if that peace means they aren't as free as persons in the US, they are still ok with the old ways of the dictatorship because they are pretty much left alone, as long as they follow the rules.

It was a poignant response, one that filled me with an understanding of the bigger picture in Belarus. The people are oppressed and most don't even know it.

October Square, Independence Ave.,Minsk
Building built specifically for the circus.
October Square
Minsk is clean, beautiful, and safe.
I honestly can't wait to go back. I can't imagine not getting there again and living and working alongside such amazing people as we work with special needs families. I even came home and started learning Russian. I left there with a determination to try to make life easier for Belarusians in any way I can. The wheelchairs in Belarus are still wooden, education for the multiply disabled is either minimal or completely lacking, support for the special needs family is non existent, the suicide rate is high. I don't know why I have been given the life I lead here in the US, but now that I have been able to experience Belarus for special needs families and Christians, I can't not help. <3 p="">
Our VBS team, translators, and the pastor & his wife.

Thankful for new friends.

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21 June 2014

On to 1st

We are two full weeks out from the last day of kindergarten and Liam is already bored. He cried on the last day of school. It could have been the loop of Pharrel Williams "Happy" being blasted through the intercom system on continual loop, but I'm pretty sure he was sad that the year was coming to an end.

First & last day of school. Mostly just longer hair, and a crappy pic but otherwise looks the same.

We had an IEP meeting the last week of school and I learned a few things about how Liam's year and goals were going. I was surprised to hear that some goals were met and excited to hear that he was holding his head in prone for 5 seconds at a time. That is so very, very hard for him. The most important was his communication skills and seeing the progress he has made and how they are going to move forward this next year. He's got a good team on board working with the PODD communication system and will be implementing them at the beginning of the year. His aid will be wearing pictures in order to provide constant opportunities for Liam to see and use the pictures.

Liam's one to one aid was a fabulous fit for him and she worked very hard with him and for him.  She knows him really well, can read his cues, and makes sure he gets to participate and be an active member of his class. It's not a definite that she will be hired back this next year and if she's not I will be one irate momma. It's in Liam's IEP that he requires a one to one and she's perfect so we are praying she gets to come back. It doesn't make sense not to hire her back.
The dynamic duo- and look at that awesome t-shirt!

We are 82% funded for our stem cell trip!  If we keep on the path we are on it will be Sept before we will be able to go, but that's just fine. It's still early in the year and God's timing is always perfect. Please pray we continue to sell the remaining tees and if you'd like to donate anything at all, you can click on the link below. It goes right to Liam's account for his medical trip only.

Thanks for all your prayers, for following along, and the kind words of your support. Liam doesn't understand what all everyone has done to make his life better, but his family will never forget! :)

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