Wednesday, August 15, 2012

Good Times in Utah...

 We took our annual trip to Utah this summer and had a fun time with both sides of the family.  We first spent some time in Bountiful with the Oldroyds.

At the Clark Planetarium in Salt Lake City

 
Molly had fun with her cousins playing at City Creek in downtown SLC.
 


I enjoyed having a morning and evening to get some pictures of the Bountiful LDS Temple.
To see more pictures I took of the temple, visit my photography website.

The LDS Salt Lake City Temple--workers had already started putting up Christmas lights on the trees!

The Mormon Conference Center in SLC.

We swam at Grandma and Grandpa's pool nearly every day.  Annie even loved it!  It was so fun to hold her in the water.







Molly has really started becoming more comfortable swimming on her own this year.

Hanging out at the pool

After several days in Bountiful with my family, we drove to Draper to spend time with Justin's parents.  

Annie wasn't too sure about feeding the geese at Wheeler Farm.

But Lexie LOVED chasing all the pigeons and geese!








One day we drove to Oakley, Utah to see Tolmans' new cabin being built.  We stopped for a picnic in the mountains and ate quickly since a bear was sighted less than 100 yds from where we were!  But it was wonderful to be back in the Utah mountains!
 







We went to Provo and walked around BYU to remember our college days. 
This classroom is where we first met in 1999 in Math 113H--Honors Calculus.

BYU Campus


My primary position on the 14 hour drive to and from Utah.

Annie was SO grumpy on the drive home and just wanted to sleep, but couldn't until we tied her head back to her headrest!
We always love our trips to Utah, but they seem to go by so fast!  We sure wish we were closer and could visit family (and the mountains) more often!  :)

Saturday, July 28, 2012

2012 Aicardi Syndrome Family Conference!

We just got home from a fabulous week in St. Louis to attend the Aicardi Syndrome Family Conference!  We look forward to these conferences with more anticipation than we have at Christmas time!  For several days we get to be surrounded by dear friends who live in our world of Aicardi Syndrome.  For several days, monitors and pumps beep without anyone thinking about it, and seizures happen without any strange looks. Nobody stares at us, because we are all the same there. We are surrounded by wheelchairs and friends who give complete love and acceptance.  It truly feels like going home when we are surrounded by all our dear Aicardi friends.  This conference was wonderful--every part of it--except for the fact that it had to eventually end.

We started our trip by going to the St. Louis Zoo with several of our Aicardi friends on Thursday.  We are usually aware of people staring at us in public when they see Annie, but walking through a zoo surrounded by 20 or more girls in wheelchairs just felt perfectly normal and we forgot about all the stares we must have received!

At the sea lion tank--Molly and Lexie traced their fingers along the glass and the sea lion followed their every move!


After being out in 105 degree weather, we cooled off in the 40 degree penguin building!  It was pretty neat to get right up close to them.

 
Justin crashed after being at the zoo all day, and Molly quickly grew tired of waiting for him to go swimming!


Our conference officially began on Friday.  It's a wonderful feeling to be in a conference hall surrounded by Aicardi families!



Group photo of nearly all the girls with Aicardi Syndrome in attendance--about 80!  Click on photo to make it bigger.


My dear friends Carrie and Debi with their daughters Macey and Azaria.  We joined the "Aicardi Club" all around the same time and it's been wonderful having such close friends with girls the same age as Annie.

Dr. Justin Tolman presenting a lecture at the conference on seizure drugs.  His session is always well attended and he does a fabulous job!

This 2012 conference was a bit different for me from conferences in the past.  For this conference I served on the conference planning committee, working for two years to help organize this conference.  It was such a wonderful opportunity to serve on the committee and give back a little to this organization that has changed our lives.  It was wonderful being in such close contact with other members of the committee, oftentimes on the phone with conference calls for hours, or emailing each other several times a day.  I loved this close contact with Aicardi friends and the chance I had to help contribute to the conference.  We had an amazing committee this year and I loved working with them all!  It was great to be in a position to more easily meet all the newly diagnosed families, and help lead some discussions for some breakout sessions, although when I had to fill in for the orthopedist that ended up cancelling last minute, I felt far less than adequate to lead such a session.  Fortunately there were wonderful parents in there who have more experience with orthopedic surgeries than I do that helped me with that class.

2012 Aicardi Conference Planning Committee

On Sunday we were able to walk across the street from our hotel to visit the St. Louis Gateway Arch with a large group of our Aicardi friends.  Unfortunately, the older girls, including Annie couldn't comfortably ride up in the pods to the top of the arch without their wheelchairs--it's definitely not ADA compliant.  But I took Molly and Lexie and rode up in a 5 seat pod with 2 other Aicardi friends and each of their 4 year old girls.  When we got out of the pod at the top, one man watched us filing out of the pod like clowns in a little car and asked, "How many?!"  It was a fun experience, but Molly and Lexie weren't quite sure about being crammed in the tiny pod and riding up so high!

Brooke and Nicole with their Aicardi daughters Madeline and Cece, riding in the pod.


At the top of the St. Louis Gateway Arch.  Molly wasn't thrilled with being up so high!
Lexie looking out the window at the top of the St. Louis Arch

View from the Gateway Arch

St. Louis Gateway Arch
  We had a fabulous trip to see our Aicardi family and we're so grateful for my mom who helped me drive the kids to St. Louis while Justin was away.  She helped us a lot at the conference too, giving us the opportunity to stay up extra late laughing and having fun with our friends in the hotel lobby each night.  We had a great time and already miss all our friends.  July 2014 won't come soon enough!

To see more pictures from the conference, click here to see my Facebook Album.




Annie's 10th Birthday

Annie turned 10 in May and we had a fantastic time celebrating this huge milestone!  We held an ice cream social fundraiser to support the Aicardi Syndrome Foundation which we belong to and love dearly.  We are so grateful for all the generosity of friends and family who helped contribute to the Aicardi Syndrome Foundation.  We were so touched to learn of how many people made donations in honor of Annie, from neighbors, co-workers, and extended family and friends from all across the country!  Thank you so much!  Your donations are much appreciated! 

 


At Annie's party we displayed pictures of some of our dearest friends from our Aicardi Syndrome Family.  Donations to the Foundation help support family conferences where we can unite with other families and support and lift each other up.  These conferences have become absolutely priceless to us.



We also displayed lots of pictures of Annie from the past 10 years.  They remind us just how precious life is.  Annie is an inspiration to us, that she has found so much joy, and brings so much happiness to others, despite all her challenges.  She is definitely a happy girl!





I wish I had gotten some pictures of all the kind people who attended our social, but we just got too busy celebrating! 

Also for Annie's 10th birthday, her Grandma Tolman made her a gorgeous quilt to go with her new bed that Justin and I built.  It is absolutely beautiful and we know Annie loves it!


And, so we don't neglect the other kiddos... Lexie's corneas have been healing nicely over the past 9 months, so it's getting much easier to get pictures of her now!  She's able to go outside now and enjoy the sun!


And Molly lost more teeth!  All four front teeth have fallen out and a new one on the bottom is growing in.  She's excited about it all, but unfortunately, she hasn't been able to enjoy corn on the cob this summer!


Kansas City

A brand new Mormon temple was recently built in Kansas City, so our family drove down to see it at the end of April.  Entry into Mormon temples is reserved only for church members living certain standards of righteousness, ages 12 and older.  However, after a new temple is built, before the building is dedicated, anyone is welcome to attend the temple open house and take a tour through the temple.  This was a special opportunity for us to take our children to see the inside of the temple.  It is a beautiful place and we felt the Spirit of the Lord in this holy house.



We then stopped at Liberty, Missouri, to see the Liberty Jail where the prophet Joseph Smith was imprisoned.


We also stopped at Independence to see the visitor center there.  The kids loved the pioneer play room.


We also went to the Hallmark Visitor Center and Kaleidoscope craft place, which the kids loved, but we quickly ran out of time.  We finally calmed Molly's and Lexie's tears by promising to make another trip back to Kansas City soon!






Monday, June 25, 2012

Building a Bed for Annie

Several years ago Justin and I discovered that our backs were getting sore due to leaning over Annie's bed to change her and trying to lift her off a low surface.  So we decided it was time to raise her bed higher to prevent injuries to us.  We used the common bed risers--little black "cones" that the wheels of the bed frame sat in.  After a while we realized her bed needed to be even higher for us to prevent strain on our backs, so about 3 years ago Justin built this support to raise her bed to be at our waist level.




This helped tremendously and we have been using it ever since, but it has become an eyesore as we've worked to get Annie's room decorated in our new house.  We looked into getting Annie a SleepSafe bed that is basically a hospital bed with motorized tilt functions, but with a cute "crib-like" appearance.  However, insurance would not approve it for her, so it was out of the question. 

http://www.sleepsafebed.com/Dealers/Images/SleepSafe_11.png
Sleep Safe Bed (image from SleepSafe.com)

So, Justin took it upon himself to build Annie a new bed.  We knew we wanted a captains bed style to make good use out of all the space beneath her raised bed, but none of the captains beds we saw in the stores were tall enough to get her mattress at waist height, and none of the beds in the stores would accommodate the use of bed rails that Annie requires.  So we designed a bed together to make sure it would be the right height and work with her bed rails without having the rails hit the drawers.

We worked for 2 1/2 months to finish it, working late into the evenings and all day on most Saturdays.  We were very grateful for a quick jump-start from Justin's parents who really helped us get the actual building started.  So here are some pictures of the process and the end product.  I am SO pleased with it.  We learned a lot and made lots of errors, and if we could do it again, it would probably be even better, but I'm very happy with how it turned out.  The beautiful quilt was made by Justin's mom for Annie's 10th birthday and it turned out so perfectly with the bed.


We built the base out of 3 separate components so we could move it into the house more easily.  There are 4 drawers and 1 cabinet on each side of the bed.



 One day we decided to take Annie's mattress out to the garage to check our measurements and it was a good thing we did because we discovered that we made it too tall!  And this picture doesn't even show her 2" thick memory foam topper that goes on top of this mattress.  We had originally planned to put a toe space down both sides of the bed to make it easier for us to get right up next to the bed to change her and transfer her without our feet hitting the drawers, but we had to eliminate the toe space.  Otherwise the bed would have been 3" taller than before which would have made it very difficult to lift Annie into.  We should have double checked our measurements way before this point!

Measuring it with her mattress.  Got the bead board cabinet doors built.

Finished the head board and foot board with bead board.  Got the top platform built to lay over the 3 compartments.  Nail holes are filled and it's ready to paint!

Painting...  (Eager to park the cars in the garage again!)

Sanding and more painting...

More painting and polyacrylic finish... almost done! 

Ready for assembly! We attached fabric pads to the bottom to prevent scratching the wood floor, and moved the compartments into Annie's room!

Getting the headboard attached.

Top slab attached.  It's done!

Both sides of the bed have one cabinet and 4 drawers.  This cabinet is slightly open because of cords we need to tidy up.  We used grommets to screw the bed rail ties into the top slab of the bed, so they won't wiggle or loosen.

Footboard

Annie's new bed and beautiful quilt!


 We built a shelf in this cabinet to keep Annie's suction machine and CPAP machine tucked away instead of taking up space on her chest of drawers.  We still need to drill a hole through the side of the cabinet and headboard to feed the cords through.  Then we can just grab the suction yankauer or her CPAP mask to use and still keep the machines tucked away.  It helps make her room look a little less hospital-y.  The storage this bed makes will be super for storing all of her diapers, chux pads, syringes, suction supplies, and all her other medical supplies.
 





Head board

So here's Annie's room with her new bed and quilt (and new lavender paint from a couple months ago).  Our next project is to use the leftover bead board from the head and foot boards to put on her dresser and nightstand to help them match even better.  We also plan to built an IV pole post onto the back of her dresser so we can get rid of the metal IV pole on wheels.  I need to still get curtains made and hung and put some pictures on the walls.  But I'm so glad this part is DONE!

Annie's room.

Monday, May 14, 2012

Help Us Celebrate Annie's 10th Birthday!


In honor of Annie on her 10th birthday, we are hoping to raise money to support the Aicardi Syndrome Foundation.  We will be collecting tax-deductible donations with checks made payable to the Aicardi Syndrome Foundation.  Donation information is also available online at the Aicardi Syndrome Foundation website to mail a check directly to the Foundation or to make a donation online with a credit card. 

The Aicardi Syndrome Foundation has been an incredible blessing in our lives--connecting us with other families dealing with our same challenges.  We find great strength and comfort by regularly connecting with Aicardi families who are now some of our dearest friends.  We also love attending all the Aicardi Family Conferences where we get to strengthen and support each other in the unique challenges our daughters face.  Donations to the Aicardi Syndrome Foundation help provide funding for these conferences as well as for medical equipment for affected children. Money donated to the Foundation also helps researchers at Baylor University and the University of California at San Francisco conduct medical research into the causes of Aicardi Syndrome and agenesis of the corpus collosum.  Thank you so much for considering a contribution to this Foundation that means so much to our family.

I can't believe Annie is turning 10!  We are celebrating big this year--10 is a HUGE milestone for her!  Before Annie was born, we were told that she had some very serious brain malformations and we were told that if she survived birth, she might only live a few days or months.  We never thought that we would be so fortunate to now be celebrating her 10th birthday!  The past 10 years have brought many emotional and physical challenges, but all of those struggles pale in comparison to the wonderful blessings our family has experienced by having Annie in our family.  She brightens our days and helps us keep a proper perspective in our lives.  She has taught us more than we could have learned any other way.  We are so grateful for her and the sweet spirit she brings into our home.  Our lives would not be the same without her. We love you Annie, and hope you have a fantastic 10th birthday! 


To learn more about Annie and her diagnosis, please read Annie's Story, or her Frequently Asked Questions page.  To learn more about Aicardi Syndrome please visit the Aicardi Syndrome Foundation website.

Sunday, May 13, 2012

Lessons From My Daughter With Special Needs


I have been blessed to have many learning experiences in the past 10 years since I was told the baby I was carrying had severe brain anomalies and might not survive birth.  Miraculously, our sweet Annie not only survived birth, but has grown to be a beautiful 10 year old—a milestone doctors told us she would never reach.  

About 5 years ago, a friend asked me, “What have you learned from Annie?”  I paused before answering, a little surprised at her question.  I wasn’t sure what kind of response she was expecting, but I quickly told her about traits Annie has helped me develop and mentioned how much medical information I have learned from caring for Annie as well.  The conversation didn’t go on long, but since then I’ve often reflected on what Annie is continuing to teach me.

Annie teaches all those that come in contact with her greater lessons than could be taught anywhere else.  She has taught me about compassion, service, patience, enduring, unconditional love, humility…  A complete list of everything Annie has taught me could surely fill a book, but here are just 25 things I have learned from my 10 year old daughter who has Aicardi Syndrome.

1.    God doesn’t always give us what we want, but we know He will always give us what we need, even when it’s not what we think we need.  I need Annie.  I never would have asked to have a child with such severe disabilities, yet now I can’t imagine my life without her. 

2.    Christ suffered not only for our sins, but for all our heartaches, grief, and physical suffering.  I often think that Annie is able to handle so much pain and suffering because she knows how to turn all of that over to Heavenly Father and she knows He'll always take it from her and help her through it.

3.    Eternal families are real.  The uniting of families forever inside the holy temple is real and I know that our family will live with Annie forever.  She will be made whole through the resurrection and we will feel her hugs, be able to speak with her, and probably continue to learn even more from her in the eternities.

4.    The Holy Ghost brings real peace and comfort.  We won’t always know “why” in this life, but we have faith that God has a perfect plan for us and we can enjoy the journey and trust that he has only good things in store for us.

5.    The Lord continues to work miracles and show us His tender mercies.  We may not receive the miracles we pray for, but He gives us the miracles that He knows we need.

6.    Annie has taught me how to better serve others, especially to serve without having to ask “What can I do to help?”  Just go do it!

7.    I’m not alone.  Because of Annie, I have been able to meet amazing mothers who also have daughters with Aicardi Syndrome.  My life would not be as rich if I did not have those wonderful women in my life.  I have also learned about true friendship and have learned the power and strength that close friends and family can be. 

8.    The veil between heaven and earth is very thin.  I often get the sense from Annie that she sees angels and I don’t doubt that she does. I know Annie is close to the Spirit and has a close relationship with her Heavenly Father.  She is a celestial being here on earth and more perfect than any of us.

9.    I have definitely learned more biology, medical terms, acronyms, procedures, and insurance processes and lingo than I could have learned from any class in college.  I’ve learned how to deal with frequent seizures, put a chronically dislocated knee back in place, how to change a gastric feeding button, use suction, prepare and run pump feedings, etc. 

10.    I’ve learned that just because a person can’t talk doesn’t mean they don’t have anything to say--we just need to learn how to listen.  And a person who can’t talk may have the most to teach us about life. 

11.    Annie is a special spirit in a frail frame, yet she can be so much stronger than any of us.

12.    Most people have good intentions, and they don’t mean to be insensitive. On the flip side, I’ve learned how to better communicate with people facing their own trials and grieving their own losses.

13.    We shouldn’t compare our trials to anyone else’s.  We can’t relate to other’s trials because no matter what, we truly won’t understand unless we’ve walked in their shoes.  Everyone’s trials are custom-made just for them and everyone handles trials differently. 

14.    I have learned how to be assertive and how to be an advocate for my child.  I never thought that I would have it in me to challenge a doctor about a plan of care or to insist on certain things that I know Annie needed.

15.    I can do hard things.  I’ve signed a “Do Not Resuscitate” order for my daughter, enrolled her in hospice, watched her suffer through countless procedures and surgeries, learned daily medical treatments and therapies, and I face the inevitable premature death of my child.  I’m not able to do these things because I am strong, but because I receive strength from the Lord and from supportive family and friends.

16.    I knew this before Annie was born, but I’ve learned even more in the last 10 years that I married a truly kind and selfless husband.  I am continually grateful for Justin’s help in getting up in the night to help Annie, taking time off work to go to doctor appointments with me, encouraging me to develop my own talents and go out and get breaks, and providing a shoulder to cry on when I just can’t bear another wave of grief.

17.    Annie has helped me know how to teach my children about unconditional love and about how to treat and interact with those that are different from them.

18.    I’m not superwoman.  I need help and I’m continuing to learn how to ask for it.

19.    It’s important to celebrate the small things.  We celebrated when Annie finally learned to hold her head up, when she learned to reach for toys, or whenever she is discharged from the hospital, etc. 

20.    Often, the simplest things from others mean the most.  Like having someone sincerely ask how Annie or I am doing and stop to listen to the “real” answer.

21.    We truly love the people we serve, even if they will never reciprocate the service, or communicate gratitude or thanks, give a hug, or say “I love you”.

22.    I learned very early on to not compare my children to others.  Watching missed milestones pass us by only brings grief and heartache.  Every child has their own unique set of strengths.

23.    The power of the priesthood and sincere prayer is real and can comfort us, inspire us, and work miracles.

24.    Life is too short and our loved ones won’t always be on this earth with us.  It doesn’t matter if the dirty dishes are left out, the laundry piles up, or the bathrooms haven’t been cleaned.  We never know which day might be our last to hold our loved ones.

25.    True joy comes in small packages, like in that of Annie’s smile.  Her laugh can light up a room and helps us remember that life is good!  Because it really is.



Friday, April 13, 2012

Time is Going So Fast!

I'm realizing I've been rather neglectful at posting updates lately.  Life is just passing us by so quickly.  I wish I could slow down time.  So here's a quick update since it's been so long...

Annie had more surgery in February.  Although she had her sublingual salivary glands removed last fall, her ranula amazingly still managed to grow back.  In February she had the ranula drained and the surgeon did end up finding some residual gland tissue that he had missed last fall.  Hopefully now it is all out and her ranula will not return.  She seems to be doing well now (except for continued drooling despite only having 2 of her 6 glands intact) but we continue to monitor for another ranula.

Annie also had her semi-annual renal sonogram in January.  It is incredibly uncomfortable for her since she can't manage to lay on her side or tummy well due to her scoliosis.  But after a full hour scan, and many tears, we learned the mass in her kidney hasn't changed in the last 6 months, so we'll just continue to monitor it.

Recently, Lexie finally met all the goals in her IEP for her speech delay.  Her therapist now believes that Lexie is age-appropriate enough to be able to be discharged from special education!  She will continue through more extensive evaluations for 3 more weeks before a final decision is made, but her teachers expect her to pass her evaluations well and be discharged from special education in May!  Lexie has been in some sort of special therapy services since she was about 8 months old, so we are excited to have only one child in special education again soon and eliminate half of our IEP school meetings!

Molly has been reading everything in sight lately.  She has finished all the Junie B. Jones books, Magic Tree House books, and several other series and is now reading the Geronimo Stilton series and My Weird School series--finishing 2-3 books a day!  I love that she gets so excited about books! 


Justin hasn't been teaching any courses this semester, but he has managed to stay busy with writing grants, doing research, and getting manuscripts published--on such tight deadlines that some nights have only given him 2 hours of sleep.  He is a superhero.  He has several wood-working projects waiting for him in the garage that hopefully he'll have time to get to them soon.  He's hoping to build a new captain's bed for Annie by her 10th birthday next month!

As for me, I'm having fun with my photography business and things are going very well.  I was just assigned to be the organist for our church services each Sunday, so I've been spending a lot of time practicing the organ which has been fun.  I'm also getting VERY excited for our Aicardi Syndrome Family Conference coming up this summer.  We're getting down to crunch time on getting the last speakers and details all together. 

So there's the quick run-down on our family.  Things are going really well.  We are so blessed.  We survived winter and spring is finally here! Life is great!