Lots of PT last week, each day a little better than the last.
Thursday, she was cleared to stand AND clear to start working on walking AND cleared to start making plans to go home! As long as nothing major happens before our appointment this Thursday, we'll be headed out first thing Saturday morning!!! The incision from her first surgery hasn't fully closed yet so we are still keeping an eye on that but it had made a lot of progress and Dr. F was happy with where it was at.
So of course, at Friday's appointment we got busy with standing! She was a little nervous at first but absolutely rocked it...and then wanted to practice standing on Saturday and Sunday also 🥳
Today, things just kept getting better and better: SHE TOOK STEPS!
Here's looking forward to 4 more days of hard work and then HOME! This Thursday we'll do some final imaging to make sure everything looks ok, her legs are even and there are no other concerns. I'm sure we'll have some follow up appointments to come back for but we're looking forward to getting back home for awhile.
Not much to update on this week since we didn't do much after Thursday, but since I didn't post the update here after our appointment:
We had some good news and some disappointing news. Her second leg is healing beautifully! She handled the bandage and stitches removal like a champ...and there were a lot of stitches! She wouldn't let me count them after I showed her the picture 😂
But - her first leg still isn't healing as much as they'd like so he isn't ready to even consider clearing her for weight bearing yet. They've adjusted the wound care protocol and will re-evaluate next week and then we'll make a plan from there. So another Thursday appointment to look forward to and hopefully get some answers from to make a moving forward / coming home plan.
She has been working on increasing the length of time she is in her new braces each day so I made a deal with her on Saturday that we would go to Chuck E Cheese and stay as long as she kept her boots on. I underestimated her dedication to that mouse; it was a costly deal for mom but one I would do over again in a heart beat for 3 hours in her braces!
Other than that, nothing else to report on - see you next week 💙
Yep, Medical Monday didn't happen because we were too busy having fun with Nanny and Grandpa! They made it in Monday afternoon just in time to come see the therapy dog agility demonstration, hangout and play some games before you were worn out and ready to rest. We took them on a tour of the Quantum House, showed them around some of the places we've established as our regulars, and took a walk where we saw 28 lizards because they are EVERYWHERE!
Helping with the agility demonstration
Showing Grandpa around Quantum House.
So here's the update you would have gotten on Monday:
Last week went really well. Lexi had PT every day Tuesday-Friday and tolerated the stretching as well as could be expected. She had a follow up on her leg surgery along with the Pre-op appointment for her other leg on Thursday. She lucked out because Dr. Feldman told her she could keep the bandages from round 1 on until she was in the OR and they would take them off while she was under anesthesia so she wouldn't have to feel anything. Anything sticky on her skin is a huge no-go so for her, bandage changes as just as bad as the surgery itself 😧
Other than PT, we didn't have much going on. We had a slow weekend of resting and getting ready for this week. Tuesday was an off day for everyone - no therapy, no work for Mom; we went exploring with Nanny and Grandpa, found some Mexican food for lunch, a pretty waterside park and an iguana on the walking path that gave Nanny a heart attack when it ran in front of her.
Today, we were back at the hospital at 5:00 am, checked in and ready to go for round two! She did much better with pre-op, took the relaxing medicine as a nose spray and went back with no problems. Intubation went smoothly, surgery went well; they were able to match the first leg length and got the left side down to zero degrees also. From this point, it is Lexi's turn to do the hard work and commit to PT in order for the surgeries to be effective.
Thank you all for your continued prayers and support - she loves the cards she continues to get and we are thankful for all the wellwishes!
We had a pretty rough night. As usual, your metabolism was running at full speed so you were burning through the pain meds way more quickly that they were able to give them so for the last 20-30 minutes of each dose period you were pretty uncomfortable. We also found out that oxycontin has absolutely NO impact on you, but the morphine kicked in suuuuper quick! Most of today is going to be spent working on pain management and resting. Mama got a solid 3.5 hours of sleep (not all at once) in between bouts of pain, repositioning, wound dressing checks and breathing treatments. Crossing all the fingers we both have a better night!
Dr. Feldman and his team came by and are super happy with how the surgery went. We did talk some about working on getting your leg off of the pillows they were propped up on and flat on the bed so that gravity can help your hip open up some. But he also recognized that we are fighting 9 years of that joint being bent to some degree and that it is pretty tender right now. We will start PT on Monday working on laying flat and getting the hip joint stretched out.
Dr. Asadi also came by to check in on you and test some of the feeling in your feet and legs to make sure all of the nerves are still working.
Overall, good progress. Everyone that has come by says today will be the hardest day but then things will start leveling out pain-wise. We'll start your feeds back at a very slow rate to make sure your system tolerates it before moving back to full feeds tonight.
Last week's post was short and simple: here we go!
This week, we have some catching up to do!
We took our time getting from Texas to Florida - 5 days of driving, swimming, playing in the sand and a few other things along the way, like feeding giraffes and visiting the Kennedy Space Center! I highly recommend the Jacksonville Zoo if you're ever in that area. We were there for almost 5 hours and barely got to see everything!
We got to our final stopping place Friday evening around 6:00, unloaded the car and crashed! Most of Saturday was spent unpacking, settling in, making the rounds between Target, WalMart and the grocery store to get everything we needed/forgot and just trying to figure out what is what at Quantum House. Things have been amazing so far and I am so thankful that we were able to get a spot for our stay here! After a shy first couple of days, Lexi has found herself a group to hang out with and they were all bouncing between the rooms this afternoon! They have a craft/activity of some sort almost everyday, and therapy dogs come visit several times a week. Today, the fire department came by and showed the kids the engine.
We had her Pre-Op appointment for surgery #1 this morning; everything went well, just standard medical history review, met the anesthesiologist, talked to the surgical team one more time, etc. They are going to end up doing a small release of her hip muscles after looking at the MRIs just to make sure that her legs have all the room they need for stretching down. They will call tomorrow once the surgical schedule is finalized to let us know what time we are up!
About an hour after her appointment, the office called back and said the spine specialist wants us to come back in tomorrow for a consult after reviewing her MRIs. Not sure what he saw, but would appreciate some extra thoughts/prayers/well wishes tomorrow morning for that appointment.
I'll post an update tomorrow once we find out the surgery time and will keep you all updated on Wednesday!
Pack - clothes, books, games, and all of the "necessities" for our stay
Laundry - should probably be listed first but there is a lot to get done so I'm procrastinating
Clean refrigerator - we've been eating a lot of random things this week
Car checkup - oil change, tire check, brake check... probably important to get done
Party prep - we're having a Surgery Send Off party on Saturday. If you're local and want to attend let me know and I'll send you the details.
We're in a weird holding pattern where it's too soon to really be doing all of the final packing, but there isn't anything left to do until then so we're just waiting for Thursday and Friday to knock out the final items.
And then we drive. and drive. and drive. and drive some more.
Thank you for all of the gift and thoughts and prayers that you have all have sent our way. We appreciate all of the support and continued encouragement!
We got a call last week that the first surgery was moved from Tuesday to Wednesday, but other than that we are good to go - all of the specialists have given their clearance and we are ready to rock!
Well today’s post almost didn’t as we had a busier day than I thought it would be! Today’s focus is on prepping and packing, which is tedious enough for a normal trip, but trying to plan for 8 weeks and a 5 day drive has been…fun? For my Type A, over planning brain it has been a little stressful knowing that about 90% of the packing can’t actually happen until 3 or 4 days before we leave because we still need clothes, and medicines, and equipment and all that jazz. So that leaves us here:
These tubs have been on my dining room table for about 2 weeks and I have been slowly collecting items that we don’t use daily and putting them in the assigned tub…
Because of course each tub has an associated, detailed packing list 🤷♀️
So the plan is that these four tubs will go in the back of the car and hold everything that we don’t need on the drive to Florida. We’ll have one suitcase with travel clothes, and of course beach stuff, for the trip. So all that leaves is feeding pump and supplies, percussive vest, nebulizer and supplies, and a wheelchair to fit…somewhere. I think I have a plan but we’ll find out the day before when we load up how good my spatial skills are 😳.
Other updates:
We’ve finished appointments with GI, Pulmonology, and her pediatrician. Added some extra breathing treatments to make sure her lungs are as strong as possible before surgery (thanks to all the Central Texas allergens and constant storms blowing through we’ve had some struggles this month.) We picked up her new manual chair last Thursday (that’s the one going with us) so she’s been building up her arm strength and endurance as much as we can. This week we check ENT off the list and get her ears fitted for new hearing aid molds that will be waiting for us when we get back!
I think that’s all for now. If you didn’t get an invite for her surgery send off party and are interested please let me know. If you would like to mail a card for me to add to her box of well wishes (hoping to get one card for each day) let me know also and I’ll send you our address. And if you’d like to send her some goodies to keep her busy during recovery, I think there are still a few things on her Amazon list ❤️
I feel like nothing has really happened since my last post in January - which is definitely a good thing medically speaking!
You were out of casts and back at school walking three days a week and using your chair two days a week by the end of January. After you learned about patterns, you were continually finding them in our everyday routines and your favorite to say is "chair walker chair walker chair". We are working on next year's pattern becoming "crutches chair crutches chair crutches!"
In February you started playing T-Ball, which you absolutely LOVED! We will definitely be doing that again next year! Unfortunately, your braces did not hold up so well and I had to do several repair jobs on them throughout the season... can't wait to hear what your doctors say about that at the next appointment :)
In March we had some fun at Spring Break with Grandpa and Nanny. Got to go swimming, fishing, took a road trip to see Pops and Gigi.
You continue to amaze me with how fearless you are. You have started walking up and down the stair by yourself instead of scooting on your bottom one step at a time. You have no issue with wiggling your way up onto or down out of a chair, the couch, beds, etc. It doesn't surprise me anymore to walk in on situations like this:
Your class went on their field trip to the park across the street from the school in April and you thought it was the coolest thing ever to get to play with your friends. They blew bubbles and wrote with sidewalk chalk then had a snack on the play ground. So. much. fun.
School wrapped up more quickly than any of us were ready for and now here we are! It's summer time! You got to spend some time with Nanny last week while Mama was at work and came home with all sorts of new accessories -
Yesterday, we took a trip to Sea World with Daddy's side of the family and you were absolutely fascinated with watching the trainers swim with the animals. You kept asking when it was our turn to swim with them and didn't quite understand what I meant when I said they had been practicing for a long time to learn how to swim with the whales and dolphins. Apparently, you know how to swim and that should be enough! You favorites were definitely the dolphins and sharks.
Today, we went to the dentist and had an appointment with GI doctor. Dentist took some quick x-rays and said everything looks good. He also said that your roots aren't quite as long as they should be, which isn't unusual for kiddos with medical issues since the "stuff" needed for growing teeth before they pop out usually go towards other, more pressing needs in the body. He said not to be surprised if you lose you teeth earlier than your friends and have to wait longer for your adult teeth to come in since they weren't growing under the gum line yet.
GI was thrilled to hear that you have only had two tube feeds since school let out and are eating all. day. long. Unfortunately, your weight is down from our last visit so he wants us to try to find something to boost your calories. If we can't get it on the upward trend again in six weeks when we go for a weight check, we will need to start doing at least one tube meal per day to make sure you're getting those extras in. It is a negligible amount, we only need to increase your intake by 10% of the calories to make a difference; but he doesn't want the downward trend to continue. The tricky part is: you like low calorie foods. You would eat broccoli and carrots all day long, but would need to eat about 1000 times as much as you normally do in order to see the calorie difference! We'll play around with some of the cooking methods and see where we can boost some of the fats in your diet and hopefully that will make a difference because the drink they sent home to sample tastes disgusting!!!
That's all for now - we'll check in at the end of the summer after we see ENT, Ortho, and GI again!
We wrapped up June at EYL Camp and you had such a great time playing with your "new friend Lane" (as you still call him). We also used that week leading up to AMC Awareness Day as a challenge week - each day we had different staff and volunteers participate in a challeneg related to your limitations with AMC. Once again, our EYL Family stepped up to the plate and were SO supportive of helping us out. Mr. Brent even made the camp shirts blue this year so that the group photo on June 30 could also serve as a #BlueforAMC photo!
Challenge #1: Say "Arthrogryposis Multiplex Congenita" three times as fast as you can
Challenge #2: Write "Arthrogryposis" without using your hands
Challenge #3: Go up and down the stairs without using your legs
Thank you to everyone who sent us a picture of your blue shirts / outfits to support AMC Awareness Day on June 30!
We had a little down time at the beginning of July so we stepped up our timetable and got our living room floor taken care of! It has been a huge plus to have smoother floors now that you're double casted and can't use your scooter - makes it easier for you to stay on the move!
Grandpa had a little pry bar for you to help!
Not a huge fan of the noise from the saw :)
We went to watch fireworks with Aunt C and the boys - you were NOT a fan of how loud they were...but eventually decided they were too pretty to not watch them.
Excuse the blue teeth - sugar cookie frosting :)
And then we had the big event of July: your first foot surgery! They had originally told us it would be a 2(ish) hour surgery; just when we were getting to the two hour mark and I was getting stuff ready to wait for the "all done" call, they called and said they needed another 1.5-2 hours!! Yikes!! But when Dr. B came in afterward he was very excited about the positioning he was able to get with your bones and the end result so I guess the extra time was worth it :)
Pre-Op meds made you super silly and sleepy!
Finally got to get out of bed... that's what you chose for breakfast (Fritos)
We were in the hospital overnight, went home the next day, spent some time with sisters, and have just been hanging out...NOT standing up... at least trying to remind you not to stand on it. If too much weight is put on the foot it can cause the pins to slip and the bones to shift enough that he woukd have to re-do the surgery. You've spent a lot of time reading books, playing babies and watching movies; especially the first few days when you were getting used to having two casts on!
Tuesday (Aug 1) we went back for your first cast change in the left foot and he said everything looked good for both feet. Second surgery will be sometime in the later part of September, which is later than we thought but glad it's not the first week of school!
Wednesday (Aug 2) you had your developmental check-up. He wants to continue following you (still) just so we have someone we can call on when it's time to start kindergarten if we get any push back about you being in regular ed classes instead of special ed (not that we're anticipating any) and to help write letters for any accommodations you might need - we're still not sure what adaptive / assistive technology or modifications you might need. He wants to see you back in February instead of another 12 months because they will be able to do an official cognitive exam - those are tailored for 4 years and above and even though you are still testing a 4+ year old level they can't administer the test yet.
April was a pretty calm month - not a lot to report on! You had a fun time going with Patches to his training classes and got pretty good at telling him to sit. So good in fact, that your teach told us you started telling the other students "No. Sit." very forcefully and commanding-ly (??) when they would try to stand up during circle time. Proud parenting moments. In particular, you have enjoyed the fact that the classes take place in the park where there are slides and swings!
We did have an appointment with the Pulminologist and while she isn't ready to discharge you quite yet, she did move you to an every 12-month appointment. Between 5 and 6 years old she wants to do some lung function tests and continue monitoring those results to give us a better idea of what to expect as you continue growing.
May has been a whirlwind; I can hardly believe we're already at the end of the school year! Your speech therapy has been decreased to once a week because your feeding issues have significantly improved! Now their primary focus is clearing up some articulation issues and working on conversational speaking.
Biggest news from May is that we scheduled your first foot surgery - we will start casting on June 5 and have your surgery on July 19. While I am not looking forward to you having to be off your feet for 12 weeks, and in a cast all summer when you are just starting to fall in love with the water, I am excited for this procedure to be taken care of. It should be the last major procedure until you are between 7 and 10. I am also thankful that our PT encouraged us to go ahead and get the power chair process taken care of so that you are already used to driving your chair around. It will be interesting to start transporting that with us all summer long!
We are working on reducing your tube feeds - your oral intake has shot up in the last few months and you started telling me "no green food" more often because your tummy was too full for anything else. I've been playing around with your blend and have figured out a few options (one for on the road and one for at home) to get the same amount of calories into you, but at a lower volume so you can still eat. There are days when I feel like that's all you do - your food list has expanded greatly: cheerios, fruit loops, pretzels, crackers, chips, chicken, french fries, broccoli, carrots, corn, apples and peanut butter, bananas, potatoes, sweet potatoes and (most importantly) SOMEGHETTI! You will eat and eat and eat if we have spaghetti.
We had some fun last week with a photo shoot we've been wanting to do since Christmas but just now made the time for - you and your babies in your Frozen outfits and matching boots! I am so so so thrilled with the way the shots turned out, and to start working with your Loftstrand Crutches! I don't know that we'll get them figured out before casting starts and you're off your feet for three months but you've had fun trying the last few days!
I think that's all for now - my brain is a little fried with end-of-school activities and appointments and schedules so I'm sure I forgot something! June and July will be busy, exciting, different and anxiety-inducing (at least for me) so I'm sure there will be a lot to report on then!
So since it's a third of the way through April and I'm just now getting around to the March updates, we're just going to pretend like the February one already happened... don't worry there weren't any major updates, which is why I never felt the need to write it. March however had some big things!
In February, we had to switch speech therapists. The ST that has been with us since you came home (the first time!) switched agencies and weren't able to move over with her. Your new ST has been amazing though and after a couple sessions of testing the waters with her, you spent most of March showing off everything that you know! Unfortunately, that means you are racing through all your goals and she has already started warning me that our sessions will probably get cut at the end of the month.
You got to have your first capitol day in March also! We met up with a bunch of other families to meet with legislators about the cuts in therapy funding and the switch from Medicaid to STARKids, which has been fairly disastrous across the state. It was quite the experience - much different than other advocacy days that I've taken part in...mostly because I've never had to navigate the building with a stroller before! More details about that day can be found here.
We had a great time over Spring Break! We spent the first few days with Nanny and Grandpa fishing, driving the tractor, playing hide and seek through unfinished walls and burning marshmallows every evening.
The next week we had an appointment with your ENT and you were discharged!!! She said unless we started having any issues, that there was no reason for her to see you anymore! Dr. B has been absolutely amazing and I am so glad she was on your team, and although it's weird to think we won't be seeing her anymore, it's a phenomenal feeling to know that you are doing so well that we get to start dropping specialists! Maybe we'll have similar news with your pulmonary appointment later this month.
You had an absolute last at Cousin L5's birthday party and have already started talking about when we go back to Chuck E. Cheese "in December for Lexi's birthday"... I love watching you and L5 play together - you got to spend a couple hours at their house one Saturday when I had to take Patches to his obedience class and spent the next several days telling me stories about it and how it was "so much fun!"
Last big update: you had an appointment at Shriners at the end of the month and they were so thrilled with your progress that we are ready to move forward with your vertical talus surgery! It's quite a process so we don't have dates yet - they said they are estimating 2-2.5 hours for surgery on each foot so they want to do them one at a time. Each foot has to be cast for 6 weeks before (changing the cast every 2 weeks) so we're looking at a 12 week process. During that time you are not allowed ANY weight bearing so I am especially thankful we have the power chair now!
If you want more medical details about the surgery here's a good site; simply put, both of your talus bones are not laying the way they should be. The casting will help make the foot as flexible as possible by pulling your foot down (think of a ballerina pointing her toes down) which is why you will be recast every two weeks - a little more stretch each time. They will then go in and put the bones in place. After the surgery you will actually have less mobility and flexibility in your foot, but the structure and stability will be what it needs to be for walking.
What we're waiting on now is for them to look at the surgery schedule for the second foot, back up six weeks for casting and make sure that aligns with the first surgery and then back up six more weeks for casting. Should know more specifics in the next 2-3 weeks (they told me to give them 4-6 weeks; but if I haven't heard after 4 weeks to call and check in...) but once the process starts we'll have a total of 8 trips to Houston and back, with 4-5 days there for each surgery...should be fun to try to schedule
We wrapped up the month with the PTA carnival at school where you had a blast. Unfortunately, you have decided now that you are "a big girl now because I played with the big kids at my school."
Those are the major updates - now for the cute stuff:
Ignore the hair - we've been working on the books of the Bible. This was actually in mid-February; now you can make it all the way to Ecclesiastes without any prompting!
Another big highlight in March - you VERY QUICKLY picked up on riding your bike!
Last bit of adorable: we've been working on training with Patches and you are determined to not be left out in having someone to boss around!
AMC Awareness day is June 30 of each year. This year I had the unique opportunity to tell your story and share about AMC while we were at EYL Camp. In addition, the group took up a collection that we were able to take to the AMCSI Conference the very next week - what great timing!
You're probably asking, what does all of that stuff that happened in June / July have to do with a post in September? I've had several people ask me about the presentation I gave at camp and I FINALLY got it made into a video to be able to share with everyone! Building the presentation took quite a bit of mental (and emotional) effort - it was both amazing to look back at how far you've come and heart-breaking to look at how close we came to losing you a couple of times!
So here is that video:
Now for the fun part: you have made SO MUCH progress since June!!! Going back to the presentation just two short months later, it amazes me how out of date it already is!
We got your trach stoma closed in early August so we are completely through with that. Just yesterday we had a follow up with the ENT and she cleared you for aqua therapy - which is great because you LOVE the water!
She was pretty sad though because she is out of reasons to keep seeing you! She went ahead and scheduled one more check up in 6 months "just to make sure", but after that we are down one specialist! It's a bitter sweet thought because Dr. B has seen us through so much and has always been open and honest and direct with me about what's going on!
The clips in the video presentation show you slowly moving in your walker, but in the last two weeks it has finally clicked that you can go on your own and now YOU ARE GONE! You started chasing puppies at our family reunion over Labor Day and every day since then (with the exception of one or two) you have spent at least 25-30 minutes walking. We've gone from spending 30-45 minutes in your HKFOs to almost 3-4 hours straight - which the doctors at Shriners should be thrilled about. At the last visit they said they wanted us to work up to 7-8 hours a day and we almost laughed because we thought we were doing good to get the 45 minutes!!
My favorite walking experience in the last couple of weeks would have to be you walking into the NICU yesterday and getting to see your doctor, a few nurses, AND your PT, OT and ST all happened to be right there when you walked in. There might have been a few tears.
It is so hard to believe that we have only been home for two years now; but at the same time, every time we go back to visit it feels like a lifetime ago!
Most of our walking has been done outside - you've now mastered walking in grass, on sidewalks, going uphill and downhill, on asphalt and on dirt paths. Our neighbors have been pretty patient with us as we take up the entire sidewalk...and walk down the middle of the street sometimes.
Having family close by has given us a walking goal as well - the first week we were walking outside and you got it in your head to walk to Mimi and Papa's house (at the other end of the block). We made it across the cul-de-sac and past one more driveway before you gave up - but have asked a couple of times since then to walk there again! You've also really enjoyed taking your walker to Bible class and walking around the church building.
Slowly but surely making it to Mimi and Papa's house!
I've been working on this post for a few days now and trying to het things finished enough to be posted, but in between EYL Camp in Kerrville and now, we went to Tulsa for the AMCSI Conference and then I flew to Texarkana for EYL Round 2 so it took a bit longer than I thought it would.
You were so much more comfortable at camp this year - you really opened up and talked to so many more people! You had a great time with Nanny and LOVED helping her drive her chair. You got pretty good at it by the end of the week, but still haven't grasped the concept of holding the controller down to keep it going. Nanny said you had some pretty jerky rides a few times!
You actually ate really well this year at camp - which is usually not the case when we're away from home! You had a blast going to the dining hall every day and helping Mama count as the participants came in, giving high fives and waving and clapping to everyone.
The biggest part of the week for us this year was June 30 - Arthrogryposis Awareness Day. We were given the chance to share our family's story and present some information about AMC and how it has effected our lives.
The participants were given the opportunity to donate money to AMCSI as part of the Big Give activity (in the past we've collected school supplies, sports equipment for an after school program, etc.) In less than three hours, they collected almost $500 for us to bring with us to the AMCSI Conference in Tulsa! We are so blessed that there are so many people who love and support our family, and this was an amazing out pouring of their love!
We took a big group camp picture this year and got some great shots with the students holding their blue bracelets up high in support of AMC Awareness Day!
It was a great week and you definitely have some more friends and fans after those few days!
Surgery went AMAZINGLY well! The ENT said it was almost a "normal" procedure...which is saying a lot for Lexi! It was a long two and half days at the hospital, but we made it. We watched Bunny (Zootopia), ElsaAnna (Frozen) and Horton (Horton Hears a Who) at least three or four times each. Read every book. Played with every toy. But overall, it was a much better stay than last time.
Smiling and Happy while we wait
Getting ready to head back - not as happy after this...
Time to head home!
This is what your incision looked like the week after surgery:
And here it is now:
Another suggestion the developmental specialist had was to start helping you learn how to type now because it will likely be a huge communication tool for you. I searched and searched for a couple of weeks but all kids toys have all of the letters in ABC order. I FINALLY found something at Walmart that looks like a little keyboard and you have been challenged to figure out where the letters are at when they aren't in order!
They made some changes to your HKFOs (hip knee foot orthotic) at Shriners so that they are much lighter and it made a HUGE difference! You've been walking really well in your reverse walker these last few weeks instead of just standing and crying!
Working on the video from AMC Awareness day didn't happen in the waiting room. Got the slides in video mode, just have to find a time when everything around me is quiet for about 30 minutes (HAHAHAHA!) to record the voice portion. I'm going to go ahead and post the EYL post because I don't know when I'll get the video finished and that post was started at the end of June and has just been sitting in drafts since then.
Singing has become one of your favorite things - lately you love singing the B-I-B-L-E, Days of Creation, Elsa Song (Let it Go), Olaf Song (Summer) Itsy Bitsy Spider and Twinkle Twinkle Little Star. You love singing with us during worship and usually start saying "More sing songs" after each one ends.
