We're doing a series on prayer at church right now. Pastor Rod is using the Lord's Prayer from Matthew to give us a pattern to pray. This week was the third week of the series, and he focused on the part of the passage that says, "Give us this day our daily bread." You would think there isn't much to say about that. Seems pretty self-explanatory. Boy, are you wrong! I learned more about that one sentence yesterday than I have in my 29 years of life (yes, I'm getting old!). And, I learned something I never really paid attention to before. Pastor Rod broke it down into even shorter parts, teaching about what each word or two meant and how it was useful in praying. But the part that really spoke to me was daily bread. He used the illustration of fresh-baked bread. If you've ever had it, you know that the day it is baked it is delicious. However, if you wait a day to eat it, it is hard and stale, nothing like it was the day before. God does not promise us tomorrow. However, He does promise us that He will meet our needs today. That is the whole point of daily bread. For God to meet our needs just for today. To give us enough strength, peace, hope, food, money, or whatever to make it through today. God knows what our day will hold, and if we can actually rely on Him, He will give us what we need to get through it. I'm sure most of you have heard the scripture that says to let tomorrow worry about itself. That's what we have to do...pray for enough for today, and then tomorrow do the same thing. It's day by day.
This lesson came at the perfect time. Our little family is in probably the roughest financial time of our lives together. I'm being very open and honest because I feel that some of you are right there with me (or have been) and need to hear this. When you have to tell people you can't do things (on a daily basis) because you don't have the money, it gets old. When you have to tell your child they have to wait to have something very simple until pay day, it makes you sad. But, God does not promise us that He will give us enough to go out to eat with our friends every week or to buy things for our children. What He promises is to meet our NEEDS. I have spent a great deal of time over these last weeks really focusing on what my needs are and what my wants are. I'm praying for God to meet our needs - food for today, gas for today, a roof over our heads for today. Do you see a pattern? I'm not praying for tomorrow. I need to focus on today.
Give us this day our daily bread.....
Will Update
Posted by
Mom to Will & Cate
on Friday, July 22, 2011
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Comments: (0)
I want to start by apologizing to anyone expecting an inspirational post. This will not be that. I just don't have it in me this morning. I will, however, update you guys on what's going on with Will and where we are in all of this.
First, a quick recap for those who didn't read my last post about Will. He saw his neurologist on June 3 and we had some very unexpected things happen. We knew his EEG was abnormal, but this seemed to concern the neurologist more than I thought it would. I guess it's because he is on such a high dose of Keppra that she expected it to normalize. He also had several abnormalities on his neurological exam that were new and concerning. So, long story short, we were referred to three more specialists: epileptology, neurosurgery, and genetics.
We have seen genetics. That appointment was on July 5. Will has had an extensive genetic work-up in the past, but given that his diagnosis is clinical at this point and all the changes, his doctor thought we should re-investigate. So, the geneticist said he would think about disorders or neurotransmitters or mitchondrial disorders. The first is only testable by a lumbar puncture (spinal tap). The second is a blood test. Jeremiah and I decided to think about it for a few days before making a decision, but ultimately we decided to pursue both. The reason for this is that some of these are treatable. Not that Will would be a "normal" kid, but treating could help stop the progression of what's going on and perhaps make that better.
We saw epileptology on Tuesday (July 19). He thinks Will probably needs a second seizure medicine but wants to do a 24 hour video EEG before adding it. This way if they are able to capture a spell they may be able to tailor which medicine they chose to his specific type of seizures. This will require an inpatient overnight hospital stay and Will to leave the EEG leads attached to his head for 24 hours. I am not looking forward to that. We had planned on having the blood drawn for the mitochondrial disorders after that appointment but we waited for over an hour in the exam room for the doctor, and by the time we finished with the appointment, the lab was closed. So, we're going to have to take him back up to the hospital to get the blood drawn.
We were finally called about his MRI yesterday. It is going to be on August 11 at 1:00 in the afternoon. He has to be put to sleep for his MRIs because he can't be still enough when he's awake. (I'm sure that surprises all of you!) What this means is that he won't be able to eat all day before the MRI. He can have clear liquids and jello (which he doesn't like) until around 10:00 but then nothing until he wakes up from the anesthesia. That morning is going to be a nightmare! We are attempting to coordinate the lumbar puncture with the MRI so that he won't have to be sedated on two separate occasions. I've been told that this should be possible, so I have my fingers crossed. We will see neurosurgery after the MRI is done, but we don't have an appointment scheduled yet. I emailed the specialty nurse this morning to let her know when the MRI was in hopes that she can get us in with the neurosurgeon the next day.
Both kids start school on August 15, and I would be thrilled if we could complete this work-up prior to school starting. I am doubtful we'll get the EEG done before then, but hopefully we can get the rest done.
Please continue to pray for us as we journey down this road of figuring out what's going on with Will. Any of you who know me well know that I am the type of person who needs answers. I'd rather have a not-so-good answer than not know anything at all. My prayer is that whatever is causing all of this is easily fixable, whether that means surgery or medicine. Regardless, I definitely need wisdom about how to go forward with future medical decisions, peace about the situation, hope that things will be okay, and strength to deal with this on top of the other stressors in my life. I appreciate you all and will keep you posted as the work-up progresses.
First, a quick recap for those who didn't read my last post about Will. He saw his neurologist on June 3 and we had some very unexpected things happen. We knew his EEG was abnormal, but this seemed to concern the neurologist more than I thought it would. I guess it's because he is on such a high dose of Keppra that she expected it to normalize. He also had several abnormalities on his neurological exam that were new and concerning. So, long story short, we were referred to three more specialists: epileptology, neurosurgery, and genetics.
We have seen genetics. That appointment was on July 5. Will has had an extensive genetic work-up in the past, but given that his diagnosis is clinical at this point and all the changes, his doctor thought we should re-investigate. So, the geneticist said he would think about disorders or neurotransmitters or mitchondrial disorders. The first is only testable by a lumbar puncture (spinal tap). The second is a blood test. Jeremiah and I decided to think about it for a few days before making a decision, but ultimately we decided to pursue both. The reason for this is that some of these are treatable. Not that Will would be a "normal" kid, but treating could help stop the progression of what's going on and perhaps make that better.
We saw epileptology on Tuesday (July 19). He thinks Will probably needs a second seizure medicine but wants to do a 24 hour video EEG before adding it. This way if they are able to capture a spell they may be able to tailor which medicine they chose to his specific type of seizures. This will require an inpatient overnight hospital stay and Will to leave the EEG leads attached to his head for 24 hours. I am not looking forward to that. We had planned on having the blood drawn for the mitochondrial disorders after that appointment but we waited for over an hour in the exam room for the doctor, and by the time we finished with the appointment, the lab was closed. So, we're going to have to take him back up to the hospital to get the blood drawn.
We were finally called about his MRI yesterday. It is going to be on August 11 at 1:00 in the afternoon. He has to be put to sleep for his MRIs because he can't be still enough when he's awake. (I'm sure that surprises all of you!) What this means is that he won't be able to eat all day before the MRI. He can have clear liquids and jello (which he doesn't like) until around 10:00 but then nothing until he wakes up from the anesthesia. That morning is going to be a nightmare! We are attempting to coordinate the lumbar puncture with the MRI so that he won't have to be sedated on two separate occasions. I've been told that this should be possible, so I have my fingers crossed. We will see neurosurgery after the MRI is done, but we don't have an appointment scheduled yet. I emailed the specialty nurse this morning to let her know when the MRI was in hopes that she can get us in with the neurosurgeon the next day.
Both kids start school on August 15, and I would be thrilled if we could complete this work-up prior to school starting. I am doubtful we'll get the EEG done before then, but hopefully we can get the rest done.
Please continue to pray for us as we journey down this road of figuring out what's going on with Will. Any of you who know me well know that I am the type of person who needs answers. I'd rather have a not-so-good answer than not know anything at all. My prayer is that whatever is causing all of this is easily fixable, whether that means surgery or medicine. Regardless, I definitely need wisdom about how to go forward with future medical decisions, peace about the situation, hope that things will be okay, and strength to deal with this on top of the other stressors in my life. I appreciate you all and will keep you posted as the work-up progresses.
Unanswered Prayers
Posted by
Mom to Will & Cate
on Tuesday, July 5, 2011
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Comments: (2)
This is something I feel should be addressed. So many people believe that their prayers go unanswered. In fact, there is even a country song about it..."Sometimes I thank God for unanswered prayers, remember when you're talking to the man upstairs, that just because he may not answer doesn't mean he doesn't care, some of God's greatest gifts are unanswered prayers." Thank you Garth Brooks (and now you will all be singing this song all day long!). I think this is wrong, but so many people believe it's true. If God doesn't answer your prayer, exactly how you want it answered, in exactly the time you want it answered, then He doesn't care, wasn't listening, isn't going to answer, or whatever. Forgive my bluntness, but that's a bunch of crap! It has taken me several years to learn this, but God ALWAYS answers prayers. I know it's hard to see that when you're staring down the barrel of a loaded gun, per se, but it's true. It may not seem like it when your world is crumbling down around you. If God answers prayers, why did I lose my job? Why did my spouse/child/parent/best friend get sick? Why did my spouse cheat on me? Why aren't my kids following the Lord? Why is there so much war and sadness going on all around the world? Why? Why? Why? I have asked these exact questions. Why is my son disabled? Why can't we figure out what's wrong with him? But over time, God has shown his greatness over and over. Will can say more words than any other child I've met with his condition. He is a sweet boy who loves his family. He brings joy to every room he enters and blesses others beyond belief. God always answers prayers, but it may not be in the manner or timing we desire. We must remember that God's will and His timing are perfect. I know that's easier said than done, but it's true. Spend time with Him in His word and in prayer and you'll see it. I have several friends and family members going through some pretty serious trials right now, and I hope if you're reading this that you'll remember that in His perfect timing, God WILL answer your prayer with His perfect answer. I pray that we have the peace and understanding to accept God's will and answer to our prayers. So don't think you're prayers are going up into the big empty sky and that no one is listening. He is there. He is always listening. And, He will always answer.
Parenting 101 (By Pastor Rod)
Posted by
Mom to Will & Cate
on Monday, June 27, 2011
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I want to be sure everyone is aware, this information is not from me. These awesome words of wisdom come from my pastor, Rod Loy, who is a very Godly man and a much more experienced parent than I am. He has two sons, one who is around age 20 or 21 and the other is 18. He shared this with us last night at church, and it's too good to keep to myself. So, here goes...
Principles for effective, Godly parenting:
1. Be physically affectionate with your children.
Don't let a day go by without telling them that you love them and hugging/kissing them.
2. Model sacrifice.
Sacrifice should not be unusual. It is a part of following Jesus. Let your kids see that.
3. Teach your children an outward focus.
Be open with your giving. Let them know it is a habit and a lifestyle. Open your home to people who need you and your family. There is joy in giving to others.
4. Don't interfere with your children's peer problems and conflicts.
They have to learn to manage conflict at some point. Let them do it while they still have a safety net.
5. Encourage other healthy voices in their lives.
Kids need other spiritual leaders in their lives they can talk to and with. It needs to be the right people. It doesn't take a village to raise a child, it takes a church (that's one of my favorites!).
6. Worship and pray in front of your children.
Your kids need to see you visibly love God.
7. Apologize when you make parenting mistakes.
Your kids already know you made the mistake. You will gain respect from them when you do this.
8. Don't try to be fair and equal if you have more than one child.
Kids need to learn that life is not fair and equal all of the time. You don't have to treat your children the same because they aren't the same. (Bet that stings for a lot of you!)
The other thing he shared is what I consider to be the most important thing of all, what he and his wife wish they'd done differently. Here it is:
Don't raise your children based on your expectations or what other people may think. Raise them to please God first, not you or other people. The only thing that should truly matter is that your children become life-long followers of Jesus Christ. Consider what matters to you most - it shouldn't be all the little details or making you or someone else happy; it should be that your children become life-long followers of Christ (noticing a theme here?). Make that decision now, and parent toward that one goal. There will be a lot less stress in your life and your home if you put aside your expectations for your child and concern for what others think. What is the absolute best place for your child? (My Daddy has told me this every day) In the center of God's will.
So, I hope this helps some of you. I know it was eye-opening and helpful to me. I plan to put every one of those principles into action and to focus on what really matters - raising kids who know and love the Lord and seek to follow Him daily. The rest is just details.
Principles for effective, Godly parenting:
1. Be physically affectionate with your children.
Don't let a day go by without telling them that you love them and hugging/kissing them.
2. Model sacrifice.
Sacrifice should not be unusual. It is a part of following Jesus. Let your kids see that.
3. Teach your children an outward focus.
Be open with your giving. Let them know it is a habit and a lifestyle. Open your home to people who need you and your family. There is joy in giving to others.
4. Don't interfere with your children's peer problems and conflicts.
They have to learn to manage conflict at some point. Let them do it while they still have a safety net.
5. Encourage other healthy voices in their lives.
Kids need other spiritual leaders in their lives they can talk to and with. It needs to be the right people. It doesn't take a village to raise a child, it takes a church (that's one of my favorites!).
6. Worship and pray in front of your children.
Your kids need to see you visibly love God.
7. Apologize when you make parenting mistakes.
Your kids already know you made the mistake. You will gain respect from them when you do this.
8. Don't try to be fair and equal if you have more than one child.
Kids need to learn that life is not fair and equal all of the time. You don't have to treat your children the same because they aren't the same. (Bet that stings for a lot of you!)
The other thing he shared is what I consider to be the most important thing of all, what he and his wife wish they'd done differently. Here it is:
Don't raise your children based on your expectations or what other people may think. Raise them to please God first, not you or other people. The only thing that should truly matter is that your children become life-long followers of Jesus Christ. Consider what matters to you most - it shouldn't be all the little details or making you or someone else happy; it should be that your children become life-long followers of Christ (noticing a theme here?). Make that decision now, and parent toward that one goal. There will be a lot less stress in your life and your home if you put aside your expectations for your child and concern for what others think. What is the absolute best place for your child? (My Daddy has told me this every day) In the center of God's will.
So, I hope this helps some of you. I know it was eye-opening and helpful to me. I plan to put every one of those principles into action and to focus on what really matters - raising kids who know and love the Lord and seek to follow Him daily. The rest is just details.
What's Really Important
Posted by
Mom to Will & Cate
on Friday, June 17, 2011
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As many of you may have read on my Facebook page yesterday, I got called pathetic by a coworker for couponing. Well, this set off a flurry of comments and excitement that I totally didn't expect. And, after reading them all, I started thinking. What's really the big deal about this? All I could keep coming back to is, taking care of my family is important to me. Right now, that requires more (financial) sacrifice than it hopefully will in the future, and I'm willing to make that sacrifice. If you don't know, I'm the sole bread winner for my family right now. While pediatric fellows do make more than pediatric residents, we still don't make much money. Especially when you compare it to "real doctors" who are in practice and done with training. On top of the not-so-great salary, I have a husband and two children, one of whom has special needs. We have student loan bills, credit card bills (unfortunately), and medical bills just to name a few. I know you've all felt this way, but it seems like just as we start to make a dent in one of them, or maybe even get one paid off, here comes another one, bigger and badder than the one before. Anyway, back to the point of this post. I felt like it was important to reflect back on what's really important in my life, my priorities. So, here they are, in order:
1. God. He is and always will be the most important thing in my life. Yes, more important than my children or my husband. More important than my family or my job. To be a true follower of Christ, He has to be the most important thing in your life. Without Him, I am nothing, I can do nothing, and I have nothing.
2. Jeremiah. Yes, my husband and my marriage is the #2 priority in my life, more important than my children. I may not always act like it, and it hurts me to say that. This is something I'm actually working on right now, to make my wonderful husband know how much I love him and that he is the #2 (#1 earthly) man in my life. Those of you who think it's crazy to have your marriage and husband above your children in your list of priorities need to read your Bible. This is a biblical thing!
3. Will and Cate. The cutest kids on the planet. Most of the time the sweetest kids too! Being a mother is one of the greatest gifts a woman can be given, and I cherish my children greatly. I will do whatever I have to (as long as it is ethically and morally sound and legal) to take care of them and provide for them. And yes, if this means couponing, well then show me the inserts and hand me a pair of scissors!
4. My family and friends. I mean my parents, siblings, nephew, etc. They are the world to me. Any of you who know me well, know this is true. I love my family. I talk to them daily, alright, multiple times a day, on the phone. I go home to my sweet home Alabama whenever it's possible. I crave the time I have with them and wish I had more. They are my support system, the walls that hold me up when all the crazy storms in my life start brewing. Love you guys!
5. My job. I love my job, and I feel it is God's calling for my life. But, that does not make it more important than my relationship with Him, my marriage, my children, my family, or my friends. I think the world has this one totally wrong, and it makes me sad. Yes, I do on occasion have to sacrifice time with my family for my job, but this is temporary, and I make every effort to never miss the big stuff. And, it goes back to my desire to provide for them. The long hours of residency are over (hooray!!!!!). And fellowship too will end (although the hours are awesome compared to residency!). My point is, a job is nice and necessary, but it does not provide what is truly important in life. A good job cannot provide you with eternal life, and that is what really matters. This life is temporary, but well, eternity is forever (duh).
I could go on and on down the list from here, but I think you catch my drift. I hope you'll take time to look at your priorities and make sure they're in the proper order. Just remember what's truly important in life. Let the nay-sayers be just that.
1. God. He is and always will be the most important thing in my life. Yes, more important than my children or my husband. More important than my family or my job. To be a true follower of Christ, He has to be the most important thing in your life. Without Him, I am nothing, I can do nothing, and I have nothing.
2. Jeremiah. Yes, my husband and my marriage is the #2 priority in my life, more important than my children. I may not always act like it, and it hurts me to say that. This is something I'm actually working on right now, to make my wonderful husband know how much I love him and that he is the #2 (#1 earthly) man in my life. Those of you who think it's crazy to have your marriage and husband above your children in your list of priorities need to read your Bible. This is a biblical thing!
3. Will and Cate. The cutest kids on the planet. Most of the time the sweetest kids too! Being a mother is one of the greatest gifts a woman can be given, and I cherish my children greatly. I will do whatever I have to (as long as it is ethically and morally sound and legal) to take care of them and provide for them. And yes, if this means couponing, well then show me the inserts and hand me a pair of scissors!
4. My family and friends. I mean my parents, siblings, nephew, etc. They are the world to me. Any of you who know me well, know this is true. I love my family. I talk to them daily, alright, multiple times a day, on the phone. I go home to my sweet home Alabama whenever it's possible. I crave the time I have with them and wish I had more. They are my support system, the walls that hold me up when all the crazy storms in my life start brewing. Love you guys!
5. My job. I love my job, and I feel it is God's calling for my life. But, that does not make it more important than my relationship with Him, my marriage, my children, my family, or my friends. I think the world has this one totally wrong, and it makes me sad. Yes, I do on occasion have to sacrifice time with my family for my job, but this is temporary, and I make every effort to never miss the big stuff. And, it goes back to my desire to provide for them. The long hours of residency are over (hooray!!!!!). And fellowship too will end (although the hours are awesome compared to residency!). My point is, a job is nice and necessary, but it does not provide what is truly important in life. A good job cannot provide you with eternal life, and that is what really matters. This life is temporary, but well, eternity is forever (duh).
I could go on and on down the list from here, but I think you catch my drift. I hope you'll take time to look at your priorities and make sure they're in the proper order. Just remember what's truly important in life. Let the nay-sayers be just that.
Not What I Was Expecting
Posted by
Mom to Will & Cate
on Friday, June 3, 2011
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Comments: (1)
Will had a neurology appointment this afternoon. He had an 8 hour video EEG back in April because he was still having seizures despite a fairly high dose of Keppra and hadn't had an EEG since December 2007. So, we had one, and it was abnormal. His first one was as well. He is having subclinical seizures. For those of you who aren't familiar with medical terms, it means that even when we can't see physical symptoms of seizures, his brain is still having seizure activity. It's not constant, but it is frequent. Don't misunderstand, Will is also having clinical seizures (ones we can see), but since the last medication increase about 3 weeks ago, they have gotten better. But they have not stopped completely. Anyway, today at the doctor, she was pretty concerned that his EEG was still abnormal and that he is still having seizures on such a high dose of medicine. In fact, she said she probably wouldn't have even gone that high on this medicine, but her partner did. He doesn't seem to be having any ill-effects from it. So then she examined him, and it got worse. His reflexes in his legs are more brisk than they have been before. They're actually pretty brisk. For those of you in medicine, they're at least a 3+ if not a 4+. She also illicited clonus in both legs, more beats in one leg than the other, but I can't remember which.All of these are neurological changes that are abnormal. In and of themselves they are worrisome, but add that to the fact that there is a questionable cyst on his lower spine, and it's pretty scary. Will has been seen by neurosurgery a few times for the cyst and has had a few MRIs to watch it. The last MRI showed that it was stable and that it may actually just be that his spinal cord is wider at that point than normal and not actually a cyst. This was good news. We were supposed to have one more MRI in March and see the neurosurgeon again. If everything was stable or improved, we would be discharged. Well, the appointments got cancelled because the neurosurgeon was leaving...but not until the end of June. So why was his appointment for March cancelled you may ask? I have no idea. Well, today Will's neurologist said she wanted Will to get back in with this neurosurgeon before he leaves because this needs to be addressed. This, and the fact that Will is becoming tighter in his heel cords too. He's getting tighter in his feet, ankles, and lower leg. Also not good. His physical therapist at school was the first one to notice, and I'm glad she did. So, neurosurgery is referral number one. Now, onto a different neurologist. Because Will continues to have seizures and an abnormal EEG despite a good deal of medicine, his doctor wants him to see an epileptologist. This is a neurologist who specializes in epilepsy. She's hoping that this doctor will be able to recommend any further testing that needs to be done to figure out why he's still having so much trouble and any medication changes that might help. Referral number two. Finally, she says Will should see one of the geneticists here at Children's. He has had a genetics work-up before, but because his diagnosis of Angelman is clinical and he is having all these neurological issues, she wants a different doc to take a look at him and see if there is any other testing that needs to be done or any other diagnoses to consider. Now, this is referral number three. I'm sure you all realize this, but when you take your child to a specialist for an appointment, and she wants to send your child to three more specialists, that's not a good sign. I'm not sure when all of these appointments will occur. I'm assuming the neurosurgery appointment will be within the month since that doctor is supposed to be leaving at the end of the month. A perk of being a doctor is that I can get in a little quicker, well, sometimes. The neurologist spoke with the geneticist who said for me to email or call him and we'd set it up whenever was good for me. I don't know when the epileptologist appointment will be. I think within a few months (or at least I hope) because we usually have to increase his medicine every 3-5 months (at least we have over the last year or two). Anyway, that's what happened at the doctor today. I hope it's clear. If you have questions, feel free to ask, and I'll try to answer them. I do ask that anyone who is willing pray for Will. Pray that whatever is going on won't require any major interventions like surgery on the spine. But regardless of what happens, we know God has Will in his hands and that He has a plan for all of this. It's a little scary not to be in control, but it's pretty great that God is. So, to leave you with a smile on your face, here is a picture of the cutest little guy on the planet (with his beautiful little sister)!
The Greatest Day Ever!
Posted by
Mom to Will & Cate
on Thursday, May 26, 2011
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So, if you live under a rock, then you may not know that Monday, May 23, was the first annual Will Saunders Day at Wild River Country, a local water park. This was a gift from our church to Will (and us of course) so that he could enjoy the water park and we could enjoy him. You see, as part of Angelman Syndrome, Will has a fascination with and love for water. I mean it too! If he sees water, he's in it. You name it, and he's played in it - the sink, the bath tub, the toilet, the dog bowl, the water hose, a puddle, a cup with water in it, and even the deep end of a pool (that was scary!). So when our church said, we love you enough to give your son something he'll love, we were elated! Okay, maybe that's not exactly what they said, but that's what I heard. Anyway, I want to show you some pictures from our day. There was a "real" photographer there, and when I get his pictures, I'll share them too. But, for now you're stuck with our amateur photography.
To say the least, the day was amazing. I don't think I can really put into words what it meant to us to get this opportunity. But you know me, I'll try! We never thought we'd be able to take Will to Wild River Country. We knew he'd love it, but we would be way too stressed out trying to keep up with him and prevent him from getting lost, kidnapped, or drowning. This day allowed us to be "normal." We got to see our son do something he loves and something that "normal" kids get to do all the time. We've heard story after story from other families who felt the same way. We love our children, and wouldn't change them for the world, but I think deep down, every parent wants to get to do this type of thing with their child.
First Assembly North Little Rock is a church that, as my mom says, puts feet to their faith. Their motto is "Every soul matters to God" and when they do things like this, they prove that they mean it. To anyone who participated in organizing, setting up, working, or attending Will Saunders Day, thank you from the bottom of my heart. Thank you for loving our son, and my family, so much. Thank you for loving other families too so that they could enjoy this day. Thank you, thank you, thank you! I cannot wait for next year!
| Posing in front of the Will Saunders Day sign (I'm covering the "S" at the end of Saunders) |
| She was ready to swim! |
| His lips were blue and his teeth were chattering, but he was not getting out of the water. |
| I'm pretty sure he could have stood there all day and played in that little toy. |
| Her parents were in tears and said "Thank you. We never thought we'd be able to bring our daughter to a water park. This was amazing!" |
| Me and Will with Blythe and her mom, Donna. Blythe also has Angelman Syndrome, and her mother had never met another child with it. It was pretty neat getting to meet them. |
To say the least, the day was amazing. I don't think I can really put into words what it meant to us to get this opportunity. But you know me, I'll try! We never thought we'd be able to take Will to Wild River Country. We knew he'd love it, but we would be way too stressed out trying to keep up with him and prevent him from getting lost, kidnapped, or drowning. This day allowed us to be "normal." We got to see our son do something he loves and something that "normal" kids get to do all the time. We've heard story after story from other families who felt the same way. We love our children, and wouldn't change them for the world, but I think deep down, every parent wants to get to do this type of thing with their child.
First Assembly North Little Rock is a church that, as my mom says, puts feet to their faith. Their motto is "Every soul matters to God" and when they do things like this, they prove that they mean it. To anyone who participated in organizing, setting up, working, or attending Will Saunders Day, thank you from the bottom of my heart. Thank you for loving our son, and my family, so much. Thank you for loving other families too so that they could enjoy this day. Thank you, thank you, thank you! I cannot wait for next year!