Back from Iowa - cast-free (for now)

We're back!  It's amazing how quickly the trip to and from Iowa goes by.  It used to seem to take forever, but now that the kids are bigger, it's a much easier drive.

Sunday we headed out a little later than we normally do - around 7:30 am.  We made our normal stop for gas, and only had to stop once for a potty break in Illinois.  The kids were troopers.  There was no complaining (of course, DVDs on the laptop, coloring, and snacks helped quite a bit!).

We made it to the Ronald McDonald House at 2:30 CST (that's only eight hours total!).  This was a record for us!  The house is the same as last year, but they instituted a couple changes.

1. When we arrived, the kids were each given a business card for their toy store.  A traveling motorcycle group (I believe it was the Golden Wings) donated a roomful of toys, clothes, books, and other items for the kids.  Little Lou chose a giant stuffed bunny. She has taken very good care of the bunny, he is lucky to be so well-loved! X-Man was having a hard time deciding what to choose until he saw a 96 pack of crayons.  He said "Ninety six crayons?! That's so many!" - then, his decision was an obvious one!  Everywhere we go, he tells people that he has a box of ninety six crayons.  He loves them!  So many thanks to the wonderful people who donated these items to put a smile on a child's face!
2. They now give you a parking pass. You can use the pass to park in the lots adjacent to the house (before, you could only park there on weekends and before 7:30 am, then, move your car to a far off lot).  You can also use the pass in the parking garage at the hospital.  I'm not sure if it gives you a discount or if it makes your parking free (we were there for less than an hour and had free parking), but it's going o be a big help for many families.

We also were able to go to the Children's Museum of Iowa (it's free for RMH residents).   They added a couple new exhibits and the kids had a wonderful time.

The next day, we had our appointment at 8:15am CST.  We got there a few minutes early because they have you fill out a survey before you go back. 

When Dr. Morcuende came back, X-Man was being very shy.  He told us on Sunday night that he was afraid to go because he hadn't seen the staff in a year but that "it felt like five years ago".  Right away, Dr. M started goofing around with him, and within a couple minutes, X-Man was excited to be there.  Dr. M checked X-Man's feet and had him walk a few times up and down the halls.  I told him about our concerns, and he talked with us about some long term case studies by Dr. Ponseti.  One thing that I really like is that Dr. M gives us a lot of information so that we can make an educated decision about X-Man's treatment.

He agreed that X-Man's right foot was pretty stiff.  He said it could be the result of a growth spurt, which would mean that it may loosen up in the next month or so.  He said they like for the kids to have dorsiflexion of around five degrees or better.  X-Man's left foot is five to six, so that one is good.  His right is at zero.  So, he told us that if we wanted to have him casted (right foot only), that we could do that, but, if he has a growth spurt in the next couple months, it may not be very effective.  Or, we could wait until April (he said that he doesn't want to wait until summer because he doesn't want him to have a cast in the summer) and come back.  He'll recheck him, and if he's still at zero or less, then we'll have one or two casts put on his right foot to get some extra flexibility.  Luckily, this time around, he would only need one cast and it could be a short leg cast. 

He told us that if we keep on stretching (we currently stretch for around 15-20 minutes each night), that we may be able to gain some flexion.  We told him that X-Man is still wearing his magic shoes at bedtime.  He told us that he only has three other patients that still wear the shoes at his age, and that it's wonderful that he is still tolerating them!  He did suggest that if X-Man is still having pain in his right foot, that we may want to remove the stops from his shoes.

Our favorite nurse, Maria, also came in to the room to talk with us.  We joked about the Iowa vs. OSU game, and asked X-Man how he was doing.  I love that even though they must see hundreds or thousands of patients, that they still remember us when we come.

They both thanked us for coming back - which cracks me up!  They're so appreciative of us coming, but we're the ones that are benefiting from them!  And, of course, we're so appreciative and thankful for them. Ben and I talk often about how going to Iowa was the best decision we could have made regarding X-Man's treatment. 

We had a great visit with great news (we also got to visit with my sister in Indy for a little while, and my mother-in-law who graciously agreed to watch our dog).  Thank you all for your prayers, well-wishes, calls, and text messages.  We're so blessed!

And we're back (and leaving in the morning)...

We're back from the Wonderful World of Disney.  We had a most wonderful time, and I can't wait to share some of our favorite memories and tips with you.  I'm still in denial about our trip being over (which is why we still have suitcases in our bedroom).  I'm just not ready to be back - we spent so much time getting ready, and then it's gone in the blink of an eye.  So, in the next week or two, I'm going to post a ton of photos and info - be prepared!

Until then, I wanted to ask a quick favor of our readers.  Please pray for us.  Tomorrow morning we're driving to Iowa.  X-Man has a check up on Monday morning.  Before nearly every appointment, I get a little nervous.  One of the things that I LOVE about X's medical team is their honesty.  They let us know that while his feet look good, there is always a possibility that he will need a tendon transfer surgery.  Of course, we're hoping that he won't need it, but it's always a possibility.

Lately, X-Man has been complaining of some pain in his right foot.  Unfortunately, this is his less-flexible foot.  We still do nightly stretching, and he still wears his boots and bar (with stops), but we've noticed that his right foot has significantly less mobility and flexibility than his left foot.  I'm concerned that once we get there, we may be discussing a possible relapse.  This could mean surgery (worst case) or recasting.  In the grand scheme of things, this really isn't so bad.  It's still helping him.  As a mom, I just worry.  I know the medical team in Iowa is the best in the world, and I have full confidence in God that he will grant them the discernment to know what is going to be best for X-Man's feet. I just need to keep my mind from wandering into worry and pessimism. And, I need to keep in mind that God's got this.

Once we get back, hopefully we'll have no news.  But regardless, we'll let you know how things went.  So please, pray for us, the medical team, and most importantly, for our sweet boy. 

Thanks for reading, and for the constant support, it means the world to us.

Almost a year?!

So I have not blogged since March 8, 2011. How ridiculous is that? I've decided I'm not going to wait this long anymore. That's my commitment to you and the two other people that still read this blog :)

So here's the past year in a nutshell:

• The kids are good - I now have a three year old and five year old, how did that happen?! X goes to preschool fours days a week and absolutely LOVES it.
• We took the kids to Disneyworld and they absolutely loved it. In the six days we were there, I fell in love and learned lots of tips on how to save time, money, and sanity there. Maybe I'll do a blog on it.
• We went back to Iowa last month. X-Man had a great visit. Every time we go the doctor is surprised at how good his feet are looking. I credit it to Dr. M fully correcting his feet, nightly stretching, nightly bracing, and daily prayer by those who love us. Thank you so much if you're one of them!
• We made a very exciting decision in the past two weeks. We're going to home school X-Man (kindergarten) next year! Over the next few months I envision this blog becoming a place that I can record and store lesson plans including the ones that are greatly successful and the ones that are less than perfect. I hope you stick around - I see many adventures in the next few months!

So for now I'll keep it short and sweet. More to follow. I promise.

December Iowa Trip

We went to Iowa during the first week of December. I love traveling around Christmas time. It's so hard to believe that last year during the same time, we were flying every week to Iowa. I do miss seeing the airports decked out in their holiday cheer, and I miss that time that I got to spend with X-Man (or Little Lou when the husband took X-Man). This trip, all four of us drove to Iowa.

We made really good time - I was a little nervous for this trip because 1 - it was our first trip with a potty-trained kid, and 2 - it was December. We got to see a lot of snow. I believe snow in the country is so much more beautiful than our city snow. The drifts on the side of the road were beautiful.

'Icebergs' on the Mississippi

Once we made it to Iowa, we checked in at the Ronald McDonald House - it looked so beautiful with all the Christmas trees! We got to meet some wonderful people who helped put our lives in perspective. There were a couple clubfoot babies there, it was nice to be able to talk to a mom who was in my situation last year. I was excited for her on the changes that were going to happen to her baby! We also met a woman who had a child with several heart issues. She said her child had to be revived almost daily - whenever she gets upset there's a chance her child will lose consciousness. I can't even imagine how scary that must be for her. It helps me keep my life in perspective and want to help others whose children were born with defects.

Also, in the house I read this poem. I remember reading it before, but kind of forgot about it. I love it so much and it really does voice how I have felt and has helped me make the most of our situation:

Welcome to Holland

I am often asked to describe the experience of raising a child with a disability – to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this…

When you're going to have a baby, it's like planning a fabulous vacation trip – to Italy. You buy a bunch of guidebooks and make your wonderful plans. The Coliseum, the Michelangelo David, the gondolas in Venice. You may learn some handy phrases in Italian. It's all very exciting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland."

"Holland?!" you say. "What do you mean, Holland?" I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy.

But there's been a change in the flight plan. They've landed in Holland and there you must stay.

The important thing is that they haven't taken you to some horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.

So you must go out and buy a new guidebook. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It's just a different place. It's slower paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around, and you begin to notice that Holland has windmills, Holland has tulips, Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy, and they're all bragging about what a wonderful time they had there. And for the rest of your life you will say, "Yes, that's where I was supposed to go. That's what I had planned."

The pain of that will never, ever, go away, because the loss of that dream is a very significant loss.

But if you spend your life mourning the fact that you didn't get to Italy, you may never be free to enjoy the very special, the very lovely things about Holland.

Written by Emily Perl Kingsley

Love it. Every time I read it I get a little teary.

Okay, back to our Iowa visit. The morning of X-Man's visit, we had breakfast while the hubby loaded the car and warmed it up for us (since, Iowa is arctic-like in December!). Well, our car wouldn't start. Luckily, there's a free bus that goes between the parking lot across the street and the hospital. The kids actually LOVED the bus!

We arrived at the hospital and got in to see Dr. Morcuende very quickly. Unfortunately, X-Man decided that he needed to throw a huge tantrum. We were still able to get him to cooperate - Dr. Morcuende was very impressed by how good his feet look. He said we'll need to get at least one more set of Mitchell's with the plantarflexion stop, then we'll be able to get a 'normal' pair of Mitchell's.

After our appointment - we took a bus back to the RMH. We arrived just as AAA was finishing up with our car - luckily, it was just a dead car battery. I don't really remember our drive home, so it must have gone well!

I cannot tell you how incredibly thankful I am of all that Dr. Morcuende, and all the staff has done for my X-Man. I am so thankful for Dr. Ponseti who first implemented a non-surgical method of treatment and for all those that have followed in his footsteps.

Lou is two and X has flexible feet!

So, this time I'm not going to apologize for taking months (again) to post an entry. I'm a slacker. If you've been following, this is nothing new. Well, let me re-phrase... I'm a slacking-blogger. I'm a busy girl, for real. I've been busy taking care of my amazing kids, planning a two-year party for my darling Little Lou (she chose an insect themed party, which was AWESOME!), taking X-Man to weekly PT appointments and AWANA (more on that later), working more hours from home than ever (job-security yo!), all while trying to keep a clean home and sleeping eight hours a night. So, blog posts have been pretty low on the priority list - understandably so, right?!

As I mentioned, Little Lou is now two. It's so hard to believe. I remember when that sweet girl was born. Perhaps the most prominent memory is that of the first night in the hospital. In the middle of the night, I hear the LOUDEST baby coming down the hall. The baby was getting closer, and closer, and I think I may have said "That better not be my kid!" - guess who it was...

This girl:


Now, two years later, she is a confident, spunky, beautiful little girl. She loves animals (in fact, she has to kiss them when she sees them in books or in real life), baby dolls (she tries to sleep with five of them each night and names them all 'Kitty Cat' or 'Turtle'), and insects. If she sees a bug, she'll immediately try to hold it, and, if for some reason she's not allowed to hold the bug (because of pinchers on ickiness), she will stomp it until it no longer moves. She's passionate.

So, X-Man has started AWANA - he is a first year Cubbie and LOVES it! He is so good at memorizing scripture and enjoys earning things for his efforts. Tonight he earned his first patch for his vest, I am one proud Mama!

As I mentioned above, X-Man has been going to physical therapy each week. Three weeks ago, his physical therapist, measured his dorsiflexion, and it measured at... ready for this? Twelve-fifteen degrees. If you have a child with clubfoot, you know this is amazing, especially for my guy who was at zero less than a year ago! So, the following week, Lindsay (his PT) measured again, and both feet were again, between twelve-fifteen degrees. So, we are now going to PT every other week - we're very excited about this! We still stretch every evening, and I can tell there's a huge difference between now and even two months ago.

I can't believe that tomorrow is the last day of September. It's even harder to believe that a year ago I felt unsure and scared of X-Man's future with clubfoot. We thought for sure that he would have to have an ATTT and even that didn't have guaranteed results. Luckily, we were able to avoid that surgery and he is doing better than ever. He has a very confident walk - most people call it a strut, and he runs as quick as children his age without clubfoot. So, life has been good here. There's been a lot of craziness and keeping bust, but the big things are all in place, I feel incredibly blessed.

No news is...

Good news. Right? Things have been going very well here. I realize how much I complain, I am much better about posting when I'm complaining or worrying - luckily there hasn't been much of either lately!

So here's a recap of the last three months (yes, three months, I am a slacker).

In March - X-Man's foot did heal. In only a week or two he was back to being himself, running and jumping. Now, because of daily stretching and weekly PT, he can even stand on his toes and squat for a few seconds (YAY!).

In April his flexibility continued to improve. He gained a few degrees of dorsiflexion on each foot. In April we also found out that my husband was offered a new job. Unfortunately, that meant that beginning on May 1, we no longer had health insurance for a month (unless we chose to have Cobra which cost more than our mortgage payment!). I talked to his therapist and she was kind enough to let us come every other week and shorten the sessions so that our self-pay bill (which, BTW costs $231/hour) would be greatly reduced.

In May we went to Iowa for a follow up appointment. Because of Ben's new job, he wasn't able to come; however, my sister S stepped up in a big way and traveled with the kids and I. Dr. Morcuende seemed very happy with X-Man's flexibility. Since our last visit, X-Man had gained about 5 degrees of flexibility in each foot. He said the main thing is to continue stretching and going to PT. Nurse Maria was on maternity leave (in February she didn't even look pregnant - lucky lady!), we missed her but still had a good visit.

Aunt S with Little Lou and X-Man

X-Man at THE Ponseti Clubfoot Clinic (we are so blessed!)


In June we took a much needed vacation. Little Lou and X-Man fell in love with the ocean. Our church also had VBS which was a lot of fun. On June 1, our new insurance benefits kicked in so we went back to weekly PT visits. His therapist also gave me some information on the local University's physical therapy department. Because of his clubfoot, the students would like to study him and learn more about how to treat other children with similar conditions. I'm thinking about going, I just have to figure out childcare for Little Lou.

We've been having a pretty great summer so far. Near our home is a pretty large reservoir with many steps and a ramp right next to the steps. About once a week we go and walk up the ramp two or three times to stretch his feet. By the way, in case you were curious, there are 123 steps - in the photo below, X-Man and Ben are about halfway down (or up).


I know this post was short and sweet, I'm hoping to post more throughout the summer, but no promises! At any rate, I continue to see how incredibly blessed we are and am so thankful to have the life that I do.

Some notes I should have included in my last post...

Okay, so I tend to get a little overwhelmed by this whole blog thing. I wait forever to post and then forget to say what I wanted to say. Here's a few notes that I either forgot to list or just felt to lazy to type:

1 - If physical therapy doesn't help with flexibility, Dr. Morcuende suggests that we look into getting an AFO for X-Man to wear during the day, then bracing at night and bedtime. He would prefer not to go this route because X-Man already has severe atrophy of his calf muscles and the AFO could cause this to get worse. So for now, we spend an hour at PT each week and then do exercises daily and stretching twice a day. We go back at the end of May, so we're hoping and praying that we good get results! Of course, he's already had AFOs and it really wouldn't be a huge deal - I'm just as happy as can be that we're not even discussing surgery at this point. It's amazing how much different the treatment is from a true Ponseti doctor compared to one who just claims to be.

2 - So, X-Man somehow broke his foot. We noticed after his initial Physical Therapy consultation that he was turning his left foot out and hyperextending his knee when he walked. He would also scream whenever we tried to move his foot or put them in shoes. I emailed Dr. Morcuende on a Sunday afternoon and he had emailed back by that evening (how amazing is that?!). We emailed back and forth and he recommended that we either come out to Iowa or see a doctor here in town. We took him to our pediatrician and they wrote an order for an X-ray. The X-ray showed that he had a reaction to an occult fracture in the shaft of the third metatarsal. I emailed the report to Dr. Morcuende and he said that it was likely a hairline fracture that would heal on it's own in 7-14 days. Luckily, that was the case and X-Man is walking great again with no pain (thank you, God!).

X-Man just finished week 4 of PT (week 3 with his "physical parakeet Windsey" (PT Lindsay)). He loves PT, not a big fan of stretching, but normally I can bribe him with some sugarless gum. His ankles are already feeling looser. They're still very stiff, but it's progress, and we'll take it!

A month later...

So, obviously I am not the most consistent of people, at least in terms of blogging. X-Man had a follow up visit on February 15, so a month later, I figured I'd update you all on how the appointment went as well as other happenings.

Mini-Vacation

So, we heard that it was supposed to snow on Sunday, the 14th, and maybe a little bit on the 15th (although our local meteorologist said the snow should miss us on Monday). We decided to head out to Iowa on Saturday evening and then spend Sunday in Coralville enjoying Valentine's Day together. The drive to Iowa went well. We ate in the car and changed diapers at gas stations. Outside of gas-stops, we only stopped at one rest stop. We made it to Iowa in a little over 9 hours, which is excellent time.
The kids as usual had a lot of fun at the Ronald McDonald house. We ran around and played games. A local church made us some delicious dinner and dessert. X-Man and Little Lou played in the playroom and we checked out the new library (they got brand new furniture and it looks amazing). Ben and I stayed up for hours playing chess. Ben and I have been together for over seven years, and I never knew he played chess (quite well!).
Sunday was Valentine's day. We headed into Coralville and spent a few hours at the mall. The babies LOVED watching the ice skaters (we're going to try to get X-Man into speed skating soon). We also went to the Iowa Children's Museum.

X-Man showing Little Lou how to get to the museum
The kids loved the exibits, and it was wonderful to get out of the house and do something different as a family. I think we'll have to do this more often during our Iowa trips. We came back to the house and played and then went out five to seven games and only won two times.

The appointment

We arrived for X-Man's appointment on time. Nurse Maria saw us in the waiting room and said "Hi X-Man (only she said his real name :))!", I think it is amazing that she remembers us by name. It just goes to show how much they really do care. When we went back to the room, X-Man didn't cry or fuss at all, that is, until I tried to get him to sit on the table! He wanted to sit on my lap the whole time, and luckily they were able to examine him on my lap.
X-Man was a little shy with Dr. Morcuende. This time, he had a physical therapist from Australia with him. I just love the education and awareness that is spreading about the Ponseti method.
Dr. Morcuende said that his feet were looking pretty good. Unfortunately, X-Man has complex clubfeet, so many of the rules of bracing don't really apply to him. His magic shoes were at 40 degrees (typical clubfoot is normally set around 60 degrees). but due to some sores, they decreased the angle to 30 degrees. Luckily, we have moved down to only 16 hours of bracing each day.
Dr. M wanted to see X-Man walk. I bragged about the fact that this is the best X-Man has ever walked. He doesn't limp or hyper-extend, he walks like a little boy with normal feet.
His dorsiflexion still isn't very good. He's got seven degrees in one foot and zero in the other (on one of my earlier posts, I mistakenly noted he had 15 degrees of dorsiflexion). The stiffness is likely because of the tendon lengthening surgery he had at 18 months of age. Unfortunately, at that time, we didn't realize that this surgery was not part of the Ponseti Method. Also, because of this surgery, a second tenotomy will not be possible. Dr. M does think that Physical Therapy could help with flexibility and strengthening.
Dr. M recommended that we find a Physical Therapist in our hometown to help with flexibility and strengthening.

Coming Home

We headed home after the appointment. The drive was going very smoothly until we got about three hours outside of our hometown. Then the snow started falling. We drove for about two hours (and traveled the same distance we normally travel in an hour and a half) and stopped at my favorite pizza place. It was nice to sit and relax. There was only two other people eating in the restaurant. As we ate, we realized that the snow was accumulating at a very rapid rate. We decided to pack up and have the babies eat their pizza in the car.
The rest of the drive was traveled at no faster than 40 MPH (in a 65 MPH zone). It was very scary, the snow was so heavy that you couldn't see where the road started and the shoulder began. We prayed quite a bit and made it home in about two to three hours. We saw many cars that had wrecked and even saw some that had flipped over (including a semi-truck). I was so happy to have made it home.

All in all, it was a wonderful trip. We got to spend some time together as a family, had wonderful new at X-Man's appointment, and stayed safe. What could be better than that?

Snow!

So, here in Ohio, we have tons of snow. Not as much as the East Coast, but still, quite a bit. On Friday, we had no snow on the ground, by noon on Saturday, we had 15 inches. And I welcomed all 15 inches. It's beautiful, and the kids love it.

X-Man and Little Lou all bundled up

Fast forward to Tuesday. We got 4 more inches of snow. Once again, I welcomed all 4 inches, although my welcome wasn't nearly as warm.

Fast forward to today. I see that we're supposed to either get snow showers or 2-4 inches of snow on Monday. Snow has overstayed its welcome. Enough already. Don't get me wrong, I love the way it looks. It's gorgeous. It feels magical to watch it fall all day. However, we are headed to Iowa on Saturday for a 4 week follow up appointment on Monday. The weather is supposed to be decent on Saturday and Monday from Ohio to Iowa (minus Monday's snow showers), not so nice on Sunday... This is part of the reason that we'll be headed out early. We also thought it would be nice to take Little Lou and X-Man to the museum and maybe ice skating for Valentine's Day.

I'm hoping the appointment goes well. X-Man's feet are looking better and better. His left foot has almost completely dropped, his right foot still has maybe 5 mm until it drops all the way down into his shoe. Each day, we've been doing stretches for half an hour two times a day, and I can tell that they are helping. His feet don't feel nearly as stiff as they used to. And, X-Man is walking better than ever. Tonight he was running, and I was amazed at how fast he runs now! I am a little concerned about his right foot as it just doesn't seem 100% corrected yet. Dr. M said that there was a chance he would have to have a tenotomy on the right foot... I'm hoping we won't have to do this (as it would mean driving 10+ hours with a child who just had surgery, followed by 4 weeks of casting and relearning to walk... again), but, I have peace that Dr. M knows what he's doing. We're hoping and praying that we have safe travels and that X-Man's feet continue to progress.

Support charity by searching online

Hi everyone! We haven't blogged in a while; I could blame it on cleaning, or planning a birthday party, or just laziness. At any rate, I wanted to let you know about a very cool search engine.

If you use www.goodsearch.com, they will donate $.01 for every search to your favorite charity. If you don't have a favorite charity, consider using mine - the Ponseti International Association. http://www.goodsearch.com/nonprofit/ponseti-international-association.aspx
Please consider making this your homepage.

Thanks for reading!

Before and after

Before - photo from October, 2009


After casting - they look so much better. It really is amazing.


This is his "difficult" foot, but it still looks so much better than it did a few months ago!




It amazes me how much different this foot looks now


X-Man and his magic shoes - he really likes them



We're very pleased with the results from his casting. We're hoping everything is corrected and that he won't need to get a second tenotomy. We won't worry about it right now because that won't solve anything.

We will keep bracing and praying and we'll leave the rest to God.

Cast free is the way to be!

So, X-Man is cast free! We are so excited. He's been in casts since the middle of October, so we're so happy to have made it to this point.

We were able to get an Orthopedic office to take his casts off. I was so proud of X-Man, he didn't cry at all when he had his casts taken off; even the cast tech was impressed! He really did a great job. At one point, he did start to panic a little bit and started counting super-fast. The tech stopped for a minute and said, "it's alright, I'll give you a minute". I was really impressed with the tech, he was really good with X-Man and wanted to learn more about why we went to Iowa and X-Man's treatment (I love when I get the chance to educate people about the Ponseti method!). He even helped me figure out how to get X-Man's "magic shoes" on.

I can't wait to post photos of his new shoes - unfortunately, we seem to have miss-placed our camera. I have a feeling that a certain little girl hid it somewhere... She's lucky she's cute.

When we got home from his doctor appointment, he was so excited to take a bath in the bathroom (we've been doing waterless baths and sponge baths in the living room). His skin is so dry and his legs and feet are really sensitive. I can tell that his knees are sensitive to extension too (probably from being bent for so long!). He tried to stand up, but his legs were unable to hold him up. I'm sure this is temporary, but I think it scared him. Luckily, he has figured out how to crawl with his brace.

His feet look so much better than they did in October; when our camera is found, we'll post comparison photos - you'll be amazed.

Three years ago

X-Man on his birthday - pre-casts

Pre-casts, he was one or two days old

X-Man and his first set of casts, three days old

So sitting here, I just realized that exactly three years ago, X-Man got his first set of casts. I remember him being so tough. He was only three days old and was already the love of my life. I remember trying so hard not to cry while they put his casts on, but I couldn't hold back tears. I remember putting his clothes back on, trying to be careful with his new casts. I remember feeling the warmth of his casts and panicking, thinking that they were burning his legs. I remember calling my mom from the car, I was sitting in the backseat, to X-Man's right, I remember exactly where on interstate 71 that we were. And I remember sobbing, telling her that my sweet tiny boy had huge heavy casts all the way up his legs. I remember just wanting my mom and dad. I never felt more like a child in that moment. But also in that moment, I realized that ready or not, I was an adult and was responsible with the most beautiful child I had ever seen.

I teared up a little bit thinking back to that moment. But I wouldn't change it for the world. It was one of the most difficult, yet most wonderful moments of my life. And the past three years have been (hands down) the best years of my life. My X-Man continues to bless me everyday, he really is a tough, amazing guy. I don't know that many other children would do as well as he has with everything.

We really do have an easy life compared to so many people; we feel incredibly blessed to have two smart, kind, healthy children. Clubfoot has become a normal thing to our X-Man. He's not embarrassed, and neither are we. When people come to our house, he loves to show them his "cool, blue casts" and his new "magic shoes". On Wednesday, X-Man gets his last set of casts removed here in town. We've been telling him each day how many days until his casts are removed. Last night, as we were getting ready for bed, we told him "three more days until you get your casts off!" and he said "no, we leave my casts on!". He actually likes his casts!

When his casts are removed, he'll start wearing the Mitchell/Ponseti boots and bar 18 hours a day. It seems daunting and I was a little worried about his mobility. Then, I remembered that's what I was worried about when we started casting. Luckily, his casts haven't held him back, and I wouldn't be surprised in the least if his braces met the same fate.

The past three years have been filled with so much love and amazement. I'm looking forward to the next three years; but for now, we'll enjoy one day at a time.

Lucky number seven

So last Monday (December 21) was week seven of our Iowa visits. Before we got to Iowa, we spent over thirteen hours in airports. Before I tell you about the good news we received, I'd like to tell you about our crazy travels.

So, Sunday morning, around 8:30 am, Ben dropped X-Man and I off at the airport, about two hours before our flight was to leave. As usual, TSA screenings went well - we had to sit in the clear box so they could test X-Man's casts, but it was no big deal. By the way, since we've done so much traveling (X has been on 21 flights in the past two months) we can now go through the expert traveler line! We did our Starbucks run so he could get his chocolate milk (he LOVES the organic chocolate milk and enjoys drinking it while watching the planes go by). We waited at our gate for a good hour and a half before the gate attendant announced that our plane would be delayed. The lady at the desk was very helpful and got us on a plane from Detroit to Cedar Rapids later in the day in case we missed our flight (due to our first flight being delayed).

Chocolate milk time!


Once our plane arrived, we had a smooth flight into Detroit. The flight attendant asked that everyone wait on the plane and let the people with short connections get off first (I thought this was wonderful - I've never had an attendant do this before). We got off the plane and walked very quickly to the gate for our next flight; unfortunately, we did miss our flight (it was 12:20 and our flight left at 12:10). Since we had seats on the next flight, X-Man and I walked around and had some lunch. We played and read books until about an hour before our next flight was scheduled to leave. Normally we don't go to the gate until right before the flight leaves, but for whatever reason, got there early this time. When we got there , the gate attendant announced that our flight (3:50) had been cancelled due to the weather. She was very helpful and got us onto a flight to Minneapolis (around 5:00) and then a flight to Cedar Rapids (we would arrive around 7 or 8).

Can I just tell you that the Detroit airport is beautiful? It was built in 2002 and is absolutely gorgeous. There's this crazy-long hall that connects the two terminals - it looks like you're under water and they play calming music with lights that change colors in rhythm to the music - very impressive. They also had a bunch of people dancing and doing karaoke (some girls were dancing to a song about "dropping a booty" or something - X-Man felt the need to sing this song for the next ten minutes), and they also have a tram and a bunch of really nice stores, it was like going to a mall.

While waiting for our flight, lots of people stared at us and asked what happened to X-Man. I also met a girl named Sarah who was really nice. She was getting irritated that so many people kept asking about X-Man. I told her how it used to bother me too, but now I consider it an educational opportunity. Our flight to Minneapolis was short and sweet, everything went well.

We didn't have a lot of time to spend in Minneapolis, so we grabbed some dinner and walked very quickly to our gate, which, naturally was on the complete opposite end of the airport. If you've ever flown into Minneapolis, you were probably taken aback by how huge the place is. I was sweating and out of breath by the time we got to our gate (we must have walked a mile to get there - no joke). When we arrived, we were told that our flight would be delayed, so we decided to eat. X-Man was so restless. By this point, we had already been traveling for 11 hours. So, we decided to walk on the moving sidewalks. Hey, anything to make the screaming two-year old happy! Our flight kept getting pushed back farther and farther, about two hours later.

Finally, around 9:30 central (two and a half hours after our flight was to depart) they decided to delay our flight until 7:15 am. Luckily, they gave us a hotel voucher for a very nice hotel suite and meal vouchers. When we got to our hotel, everyone in the lobby (there were probably 10 people in line ahead of us) let us go ahead of them. I was so touched.

We grabbed a snack and settled in around 10:30 central time. I called Ben and told him about all the craziness - God was certainly working overtime on me because I didn't lose my cool at all. Our hotel was so beautiful, some place that we never would stay in, so really, it was kind of a blessing. X-Man and I fell asleep around 12 central time. Can I just say that I love my little guy, but it is no fun to share a bed with a kicking two-year old in casts?! I woke up around 2 am and couldn't get back to sleep. I had to wake X-Man around 4:15 so we could get dressed, check out, and catch the shuttle to be back at the airport by 5 am. Oh, did I mention that the hotel room had a view of the Mall of America?! Man, I wish we could have gone! Oh well, casting is much more important!

The gorgeous bathroom in our hotel


The view from our hotel


When we arrived at the airport, X was very fussy. Luckily, those vouchers covered our breakfast. Our plane got us to Cedar Rapids without any issues. And the shuttle company was kind enough to waive our fees (we normally aren't charged because we normally go straight to the RMH) and take us to the University of Iowa. Ben had emailed Maria and Dr. Morcuende and told them that we would miss our 8am appointment due to our traveling issues. They said not to worry as they would be there all day.

X did better than ever when he got his casts off. Al, from Russia (who we met the week before) was getting his casts off at the same time. Once X-Man realized that Al wasn't crying, he also stopped crying. I was very impressed! Once they took his casts off, we waited in the waiting room. WW (X-Man's friend at the RMH) was coming in for her appointment at the same time, it was great to see them!

We didn't have to wait long. X-Man started crying as soon as we put him on the bed. We sang songs and I told Maria and Dr. M about how well he did in the casting room. Dr. M said "X-Man, Al is here, do you hear him crying?" X-Man stopped crying when he realized Al wasn't crying. Man, I wish we would've thought of this weeks ago!

Dr. M showed me how to put on X-Man's new braces. They are really, really nice. They're much softer than his old braces, and seem like they would be much more comfortable. Like I said last week, his left foot is 100% corrected, but even this week, his right foot still isn't 100%. Both feet are now at 15 degrees when dorsiflexed (normal feet are 25 degrees), so we're getting there. Unfortunately, Dr. M said he may just have stiff feet. It could be from unnecessary surgery, or it could just be how his feet are. He did have to get re-casted this week. Before we went to the appointment, I prayed "God, I don't want him to have to be re-casted, but if his feet aren't corrected, please let the doctor see that," so, even though I was hoping he would be out of casts for Christmas, I know that it's an answered prayer that he was re-casted.

His casting went well (after we reminded him that Al wasn't crying) and we scheduled our next appointment (for mid FEBRUARY!!!). We then waited in the lobby (while watching the piano) for our ride to come. Our ride had to pick up a couple of people on the way to the airport (one of which was an, um, interesting guy who informed us of the role that El Nino plays and how the meterologists have no idea what they're talking about). X-Man serenaded us with Sunday school songs. Oh, to have faith like a child!

When we got to Cedar Rapids, we tried to get on an earlier flight home (since ours was to arrive home at 10:20 pm) to no avail. We were stuck in the airport for at least four hours, so X and I used some more of our meal vouchers and had a nice sit-down lunch at a diner in the airport. We also bought some entertainment materials to keep us busy. The TSA employees recognized us right away as "regulars", I told them we wouldn't see them for a few months, they seemed genuinely happy for us.

After playing for a while, WW and her mom came in. X and WW got to play together for an hour or so, it was really nice. They scooted around the airport together (they're not allowed to walk on their casts for the first 24 hours) and we read books, and colored in X-Man's new coloring book. I love that X has had the opportunity to meet other kids in casts. It's truly been a rich time in our lives.

X-Man and WW (please ignore that my child is trying to play with an electrical outlet) - check out their awesome casts!


Our flights (THANK GOD) left and arrived on time. We got home around 10:30 or so... I have never been so tired in my life.

The good news is that X-Man is on his last set of casts. He'll wear these for three weeks, and then will have the casts removed in our hometown. Once the casts are removed, he'll wear his new braces (with a bar between them) for 18 hours a day. Fourteen of these hours will be while he's asleep, we'll just have to figure out when to do the other four hours... Any ideas or advice on this would be great. I'm worried that he's going to absolutely hate them since they will restrict his walking (although, I thought this about his casts and we see that they haven't held him back!). My wonderful sister Sam said that she's willing to help me make a padded cover for the bar. Maybe if we let him pick out the fabric, he'll like it a little more.

I'm thinking we'll postpone his party until after he gets his casts off so that we don't have to worry about him injuring anyone during his party (I got a black eye last week from his casts).

Iowa - week 6

I have a feeling this is going to be a pretty long post - so, unless you have five or ten minutes to read my ramblings, you may want to come back later :)

This week, we were thinking about driving to Iowa. Special thanks to my sister Kris who was willing to drive out with me. Luckily, on Thursday, Ben found some tickets for a very low rate as long as we flew out on Saturday instead of our typical Sunday.

So, our flight was around 4pm which gave us time to spend with the family before leaving. This week, X-Man and I went to Iowa, and Little Lou and Ben stayed home. The flights went well - as usual, X-Man was very well behaved. From the Cedar Rapids airport, we took a shuttle, the driver was VERY nice. He took us to the RMH - it was strange to be there on a Saturday, almost everyone of the 30+ rooms were booked.

Our home away from home


Since we would be in Iowa all day on Sunday with nothing to do, we decided to head into Coralville and visit the Iowa Children's Museum (it's free for RMH residents). A couple volunteers from the house drove us over to the museum. The museum is located in Coralville mall - we were quite impressed as there is a HUGE ice rink when you walk in. The museum was very nice too - there were lots of pretend stations (a grocery store, doctor's office, ambulance, dentist office, pizza parlor, post office, bank, house, farm and barn), a motion exhibit (you can build cars and tracks and send golf balls down the tracks, there was also a rock climbing wall), a puppet kingdom, and a new flight exhibit (with an actual cesna, hot air balloon, HUGE 2+ story slide, air rockets, air guns, pretend planes, flight simulators, control tower, etc). We had a lot of fun there, and spent 2-3 hours there. We took a break and got some lunch at Panera (their new macaroni and cheese is quite impressive) and walked the mall.

After lunch, we came back to the museum and met Dr. Dobbs' sister-in-law (he's an excellent Ponseti doctor in St. Louis). One thing that I love about being in Iowa City, is that I don't get the dirty looks that I do here; people don't stare at X-Man. People recognize X-Man's casts as clubfoot-treatment. Almost everyone I've run into in Iowa has been very non-judgemental and kind. People seem genuinely interested in him and how treatment is going. It's a great place to be.

Here are a few photos from the museum:

Dr. X-Man, DDS

X-Man the pizza-maker


Buying groceries
He LOVED this walker, in fact, he tried to steal one from a child at the RMH
X-Man the medic

Huge Slide - yes, I did get to carry him up the steps too many times to count!

When we were done at the museum, we called the RMH and asked if someone would be able to pick us up. Unfortunately, there weren't enough volunteers to give us a ride, so they suggested that we call a taxi company (the free bus doesn't run on Sundays). When I called the taxi company, they said they couldn't pick us up because I didn't have a carseat for X-Man. So, I went to the information desk at the mall and explained our situation. The girl I talked to gave us a number to another taxi company. I called them and asked if they could give us a ride. Since we didn't have a carseat, the dispatcher said that it would be up to the driver. Luckily, the driver was willing to give us a ride. It was my first time ever riding in a taxi, so I didn't know what to expect. The driver was super nice - he told me that he spent a lot of time in the RMH as a child for a genetic disorder that he has. I told him all about X-Man. He took us to the RMH and said, I'm not going to charge you. I said "Please, let me at least give you a tip" - he said that he wouldn't accept any money from us. How amazing is that? He could have made at least $15 off of us, but instead did a good deed. There are still good people in this world. Please, if you ever go to Iowa City, use the Yellow Cab Company.

We got back to the house and played in the playroom and had some dinner. A local sorority made us some very yummy cheese tortellini, salad and garlic bread. The girls were so nice, we walked into the kitchen and they immediately started talking to my little guy. We also met a few other children with clubfoot (I counted four other children there!) - there was someone from Russia (this was the 4th country that she's taken her son to for treatment) and someone from Colorado. It was really neat, I met one of the ladies that belongs to the Yahoo nosurgery4clubfoot group and her daughter WW!

Playing at the RMH

The rest of the evening, we played and read books. I gave X-Man a bath and we prayed for a good appointment on Monday morning (I stayed up late reading The Shack - so far, it's really good!).

On Monday morning we ate breakfast (donated by Panera - YUM!) and walked to the hospital. Oh - did I mention, last week, they had the worst blizzard in 20+ years? There was snow all over the place, but the sidewalks were clean. The weather wasn't too bad.

X-Man did much better than normal. He still cried, but not nearly as much as usual. We sang songs and looked at books. Dr. Morcuende said his left foot is 100% corrected (take that ATTT surgery!) but his right foot is still a little stiff. He's hoping that the right foot will be corrected after this cast. They took impressions of his feet for new braces - which should be in by our next appointment on Monday. His braces will need some special inserts because of the stiffness of his feet (likely because of his second surgery).

After his new casts were applied, Maria told me that they will give us his braces free of cost (they are over $500). How amazing is that? They are so good to us. I gave her a big hug and cried a little. I really feel like God has favor on us and takes care of us. I feel so silly when I worry about these things and they're solved in ways that I never would have thought of.

We walked back to the house and ran into Susann and her daughter WW. They were on their way to get casts with Dr. M.

We cleaned our room and did our chores and had some lunch before checking out. Then our shuttle came to pick us up (BTW - if you're ever in Cedar Rapids or Iowa City, please contact the Airport Shuttle Service - they give free rides to residents of the RMH). Susann and WW rode with us to the airport - it was so nice for X to have a friend with casts, and I loved talking to Susann about her experiences.

Our driver from Saturday night is also a TSA agent, we saw him and he recognized us right away. A lot of the other agents recognized us as well (one said - "I see you came with Mommy this week!") It's such a small airport, that they remember you after being there a couple times.

Our flight to Chicago went well. We had a two hour layover, so we did some Christmas shopping and ate dinner (we of course had to buy some more of their delicious popcorn!). The flight home went well, X-Man actually fell asleep.

Flight to Chicago


After our plane "taxied in", X-Man woke up and started coughing. Right as I asked him to please cover his mouth, he got sick. All over the place. He continued to get sick for the next five minutes. I think everything that was in his stomach came out. Everyone was so nice, people were grabbing bags, and giving us paper towels, someone even gave us all her baby wipes. After all the passengers left, I changed his clothes. The attendants (United Airlines) were so nice, they asked if we needed anything and patiently waited for us to get off the plane. The pilot walked us off and asked if we needed a ride. He also wished us luck in X-Man's treatment.

All in all, it was a great trip, minus the puke.

BTW - side note, if you need to get odors out of casts, make a paste of water and baking soda and apply it to the stinky parts. The baking soda will harden, but it won't smell bad!

Iowa - Week 5

Week 5 = festive casts!
This morning, X-Man got his 5th set of casts. As usual, he cried when they removed his casts, and when the doctors came in to apply his new ones. Ben was told that X-Man's left foot is progressing as expected (YAY!), but his right foot isn't as loose as they thought it would be. It sounds like he may need another cast on his left foot, but probably two or three more on his right. He may also need a tenotomy on his right foot (he had a tenotomy on both feet at seven or eight weeks of age).

I'm kind of bummed, but I know things will be alright. We were hoping to only go out one or two more times, but now it sounds like it may be closer to four times. His next appointment is on Monday, so we're hoping to get airline tickets for Sunday/Monday. Also, Nurse Joyce (she was Dr. Ponseti's nurse for years) gave us some information on Angel Flights. It's a charity that gives free private flights to children (and their families) for medical treatment. I think we may look into this option.

At any rate, please keep praying for us. Everyone has been so generous and kind, and we are forever thankful for that.

Awesome article!

This is definitely a feel-good article. I am so thankful for them. Because of people like this family, our son is able to go to Iowa and receive treatment.

Thank you Mr. and Mrs. Whitmore!

http://wcco.com/health/minnesota.couple.donation.2.1350296.html

Dec 4, 2009 5:18 pm US/Central

MN Couple Donation Intended To Continue Doc's Work

IOWA CITY, Iowa (AP) ― The gift from Bob and Molly Whitmore of Eden Prairie to the Ponseti International Association is intended to let more children around the world benefit from the work of famed orthopedic surgeon Ignacio Ponseti.

A Minnesota couple has given $1 million to an association that trains doctors and nurses to treat clubfoot with a method developed by former University of Iowa surgeon Ignacio Ponseti.

Ponseti developed a low-cost, non-surgical alternative to treat clubfoot, a genetic defect that leaves children unable to walk normally. He died Oct. 18 at age 95.

"Right now, we are not at a point where we can be self-sustaining, so this gift will allow us to achieve our fundamental goals of worldwide education of the Ponseti method," said Dr. Stuart Weinstein, an orthopedic surgeon who trained and worked with Ponseti from the early 1970s until Ponseti's death. "Even though we have a foundation, we don't have any funds."

The money will allow the Ponseti International Association to hire a full-time staff for fundraising and pay part of the cost of sending physicians to teach the method in dozens of countries. The association also hopes nurses, midwives and physical therapists can learn the method and take it back to places with limited access to doctors.

Bob and Molly Whitmore's donation is the largest the association has received since it was started in 2006.

The Whitmores, of Eden Prairie, Minn., have close ties to Ponseti. Bob Whitmore's father, Bill, was a longtime orthopedic surgeon in Davenport, who studied under Ponseti and helped train African doctors in the method. Molly Whitmore's brother, Matthew Osterhaus, suffered from clubfoot and was treated as a child using the Ponseti method.

Osterhaus went on to run for the University of Iowa's cross-country team.

Ponseti developed his method in the mid-1940s, and in the following decades saw or advised in the treatment of 60,000 patients, most of them young children. His method involves gentle manipulation of the foot, plus the use of plaster casts to hold the foot in a new position while tendons and muscles stretch.

Dr. Jose Morcuende, a University of Iowa physician who worked with Ponseti for 18 years, said the low-cost treatment is ideal for developing countries.

"You are not using the time for the (operating room) that they really need for traumas and infection," Morcuende said. "The impact is tremendous in developing countries."

Though Ponseti perfected the method decades ago, Morcuende said it received little acceptance in the U.S. and the rest of the world until this decade. It has been endorsed by the American Academy of Orthopedic Surgeons, and the National Institutes of Health and the Centers for Disease Control support initiatives to promote the practice.

Some of the money will likely be used to send Ponseti International Association doctors to conferences in Guatemala and Russia next year, Morcuende said, though a final decision hasn't been made.

"Right now, most people are interested to learn the method," Morcuende said. "And that's why this money is going to be extremely important for us. It will allow us to go much faster than before."

Delays

So, today Little Lou and I dropped X-Man off at the Airport around 10:45; their flight was supposed to leave at 12:30. Ben calls me at 1:30, the plane is still on the ground. Apparently, there was some sort of mechanical malfunction (thank God they noticed this on the ground!) so they had to wait for a mechanic to work on the plane.

At around 2, the mechanic shows up, then they find out that something else is wrong with the plane, so they have to wait. Finally around 2:45 or 3, they let everyone off the plane because there is something else wrong with the plane. They re-board and finally leave at 4:00pm. I can just imagine how crazy that must've been to have a two year old on a plane for over two hours, not going anywhere.

Now, here's the good news. Their connecting flight in MN was supposed to leave at 3:45. Luckily, this flight was delayed until 7pm, so they were able to catch their flight (totally a God-thing). Then, Ben called the RMH to tell them what was going on (I talked to them earlier in the day and was told that they wouldn't be able to stay there tonight because they would be arriving after check in hours; they did find some hotel accommodations for a reasonable rate) one of the employees volunteered to stay late to check Ben and X-Man in.

Without a doubt, the people at the RMH are amazing. Because of this employee, we saved so much money. The shuttle company from the airport charges $70 round-trip; however, as a RMH resident, we get a free ride each trip (we just have to tip the driver) also, volunteers bring dinner to the RMH most Sundays (so if they stayed in a hotel, they would have needed to purchase dinner) Panera brings breakfast on Monday morning (so they would have had to buy breakfast too). How amazing. I am so thankful for the Ronald McDonald House. They really are amazing.

Ben had a rough day today, but he said X-Man was a trooper. I am so proud of my little guy; I can't wait to see him tomorrow! He said he's going to get one green cast and one red cast, what a spirited little guy! This may be his last week of casts if everything is still progressing. Looking back, it's hard to believe how quickly the past couple months have gone by. I'm so thankful for this chapter in our lives; it has made us stronger as a family and has made us re-evaluate our values. Thank you God.

Iowa week four recap

Week 4 = yellow casts
So, last Sunday and Monday, X-Man and I were in Iowa. I've been meaning to update you all but have been so busy. Here's a recap:

Sunday morning Ben and Little Lou dropped X-Man and I off at the airport. We got there about two hours before our flight took off. When we arrived, TSA had us wait in a glass box so that they could test X-Man's casts for explosives, drugs, whatever. They wanted him to sit in a seat by himself, but he completely lost it. One of the TSA agents said I could hold him in my lap - so I chose to listen to him. They were very nice, I'm glad that they do all that testing even if it is a little inconvenient. After all the security stuff we had about an hour and a half to wait for our plane. We treated ourselves to some Starbucks and watched planes.
Our first plane

X-Man loved looking at books during our flights

Our first flight was to Chicago O'Hare. I cannot believe how big that place is, seriously, I think it's bigger than my hometown. HUGE. We had a three hour layover. We got some popcorn and ate lunch (Ben packed our lunches for us). Then, we spent about an hour watching planes and reading books (one of the families at our church gave us boxes of books last week, so those were life-savers!). Unfortunately, the layover was during his normal naptime so he was very restless. We walked up and down our terminal for a half hour or so to burn energy. People stared - it still bothers me. Some people asked "what happened?!", that used to bother me a lot, but now I see it as an educational opportunity.
Watching planes in Chicago

Our second flight was to Cedar Rapids; when we arrived, we took a shuttle to the Ronald McDonald House. Our driver was nice.

We played for a while at the RMH and then ordered dinner. I didn't meet anyone new this week, there didn't seem to be a lot of people in the house. We spent a lot of time in their extensive library reading books, so maybe we were to sequestered to meet new people.

On Monday morning, we walked to the hospital. It was pretty cold, but the hospital is only maybe a half mile away so it wasn't too bad. Once we arrived, we played for a few minutes in the waiting room (it will be a miracle if we don't end up with H1N1 by the time we're done with all his visits!) and then went back to the cast room. He immediately started crying and saying that he wanted to keep his purple casts. We sang to him and talked to him - he still cried. Once they were done taking off his casts, he was fine. The skin under his casts was so dry - he scratched his legs and they began bleeding. Poor guy, we need to remember to bring his eczema cream next time.

Next they took us back to the examination room. We read books and he continued to scratch his legs. As soon as Dr. Morcuende and his team entered the room, he began crying again, so they left for a few minutes. When it was time to get new casts, X-Man was very upset. We tried toys, books, bubbles, etc. Finally, we discovered that the alphabet song kept him from crying so we sang that twenty times. One of Dr. M's med students/residents is from China and one is from Japan, nurse Maria jokes that the residents could learn their ABC's in English from X-Man.

Dr. M said that he thinks only one more round of casting should be necessary, maybe two on his right foot (YAY!). It's so nice to have an end in sight. I'm so glad that we were able to avoid surgery.

After our appointment, we watched the self-playing piano in the lobby and then headed back to the RMH to play and get our daily chores done.

The shuttle service took us to the airport and we headed home. X-Man did very well on all four flights (two each day). He loved singing and looking at books.
Waiting for the shuttle at the RMH

All in all, we had a great visit - better news than I imagined. I feel so blessed; just all that is going on makes me so thankful.

Heading to Iowa in the morning!

Tomorrow, X-Man and I will be flying to Iowa. I'm a little nervous because I get a little bit of motion sickness in planes; I also get scared with take-offs and landings. Luckily he's flown before, so hopefully he can help me to be brave!

I try my best not to complain, but I am disappointed in the airline industry. We're trying to find tickets for November 29 - 30 and December 13-14, but all the tickets are $200 more than other weeks (that's $400 more for two tickets). It's so frustrating! I'm trying to brainstorm what other options we have. We're thinking about maybe staying out there for a week so that he can get two sets of casts in one trip.

At any rate - we're still feeling incredibly blessed to get to see such a wonderful medical team. I have more things, people, etc, to be thankful for than ever.

When we return on Monday, I'll have an update on our visit. Hopefully they'll tell us that we only need to come out one more time - that would solve our traveling dilemma!