Roberta again---Sam didn't stay asleep too long after I left last night and was awake by 11pm. Erin was home long enough to turn around and head back to the hospital. He was awake on and off every hour or so and then the three of them slept in the tiny hospital bed! Cozy lil' family.
The Care Conference happened at 10am this morning. Erin, Jeff, and John were involved with Sam's doctors, RN's and Social Workers from Children's Care Hospital. They were supposed to come and get Sam for surgery to put tubes in his ears at 10:45ish and while waiting Sam was back to his old self at times with Grandmas Joyce and Donna and I. We read stories and walked the halls with the iPod. He wasn't able to eat or drink this morning and so when the surgery got pushed back, we were worried. He was a trooper and went to surgery about 1pm.
During the conference it was decided they would put in a PIC(sp?) line for the antibiotic and he would be transferred to Children's Care Hospital and be in their medically complex unit for a couple of weeks while he kicks the sinus and ear problems. Long term plans are yet to be determined for sure. They will also put in a feeding tube, but that will be a couple of weeks yet.
John, Donna, Jeff, Joyce and I toured CCHS this afternoon to see where he'll be for a while.
Again, I am sure I have forgotten details, and I haven't seen him since he's been out of surgery. I am on my way back to the hospital shortly.
thanks again for the support and prayers, keep them coming...change is difficult and we will continue to lean on our faith, family and friends.
Hi friends and family. We have had requests that we put info from Sammy's services online to read. Thanks so much for continuing to pray for Jeff, myself and our families as we move forward hour by hour, one day at a time with our special boy in heaven. Your prayers and support are a wonderful blessing to us! Phil 4:13~I can do all things through Christ who gives me strength.
Thursday, January 24, 2008
Wednesday, January 23, 2008
Update
Roberta is writing this update, so I am sure some details have been forgotten.
Sam slept pretty well last night and had to be woken up this morning. Erin went home last night about midnight and got some rest and Jeff stayed with Sam overnight. Sounds like that is the plan tonight too. He had a better morning, though still clearly uncomfortable and just not content. Sam had a swallow study and esophagram this morning and it showed he had significant reflux, which Erin thinks could be seeping into his sinuses and causing pain. Erin is practically a doctor, she doesn't have the letters behind her name, but dang she knows her son.
This evening Grandpa John and Grandma Joyce walked him and tried to calm him down to fall asleep and eventually he did fall asleep in his mommy's arms and was asleep when I left the hospital about 9:45pm
Tomorrow is a big day, Erin and Jeff will have a care conference with many of Sam's doctors and other representatives from support services. Sam will also have tubes put in his ears at 11:30am.
Erin and Jeff are truly amazing parents...Joyce, John, Donna, Kelsey, Brenda, myself and others are also taking their turns with Sam. It does take a village to care for our precious boy.
PLEASE keep us all in your prayers, we need them!
More to come after tomorrow or if Erin reads this and adds what I have forgotten!
Sam slept pretty well last night and had to be woken up this morning. Erin went home last night about midnight and got some rest and Jeff stayed with Sam overnight. Sounds like that is the plan tonight too. He had a better morning, though still clearly uncomfortable and just not content. Sam had a swallow study and esophagram this morning and it showed he had significant reflux, which Erin thinks could be seeping into his sinuses and causing pain. Erin is practically a doctor, she doesn't have the letters behind her name, but dang she knows her son.
This evening Grandpa John and Grandma Joyce walked him and tried to calm him down to fall asleep and eventually he did fall asleep in his mommy's arms and was asleep when I left the hospital about 9:45pm
Tomorrow is a big day, Erin and Jeff will have a care conference with many of Sam's doctors and other representatives from support services. Sam will also have tubes put in his ears at 11:30am.
Erin and Jeff are truly amazing parents...Joyce, John, Donna, Kelsey, Brenda, myself and others are also taking their turns with Sam. It does take a village to care for our precious boy.
PLEASE keep us all in your prayers, we need them!
More to come after tomorrow or if Erin reads this and adds what I have forgotten!
Sunday, January 20, 2008
Sam's at Avera Mckennan
We admitted Sam this afternoon because we were no longer able to control his pain at home. His blood tests are normal, so tomorrow he will have a head and stomach CT to try and find the source of his discomfort. He is on Morphine and that seems to be helping. More to come...
Saturday, January 19, 2008
Please pray for our boy!
We are in need of prayers for our Sammy! He has not been feeling well for the last 10 days. His neurologist, GI and pediatrician have not been able to figure out the source of his discomfort. As a result, he is on a lot of pain meds and Valium all day to try and control his pain. The doctors are planning on admitting Sam on Monday to the hospital. Please pray that they figure this out for our boy!
Sunday, December 23, 2007
Crazy Horstmeyers!
Celebrating Grandpa John's Birthday


We celebrated my dad's birthday last Sunday night, so we had him pick up Applebees on his way over! Cooking is not our specialty at the Horstmeyer house, but we are really good with take-out menus! On his actual big day, he braved dinner and Christmas shopping with his girls. As you can tell from the pictures, Sam had lost of hugs and kisses to share.
Sam is 6 years old!
Hy-Vee Field Trip
Monday, December 10, 2007
Halloween 2007
Monday, October 08, 2007
Zoo Fun




Today Sam and I joined Roberta and friend Adam for an afternoon at the zoo. Sam had a great time listening to the very noisy monkeys and feeding the horses in the petting zoo. He almost made it through the whole zoo without listening to his IPOD! He was a very good boy this past weekend too. He especially enjoyed dancing up a storm at Jeff's aunt Sue's surprise birthday party on Sunday evening. Our boy has quite the dance moves! He had three seizures this weekend and we have come to see a pattern of multiple seizures every 7-10 days. Please continue to pray for complete seizure control and for our boy to stay healthy and happy!
Friday, September 28, 2007
Grandma Hoddy
This past week has been filled with mixed emotions as we say goodbye to a very special lady. My grandma Harriet Bennett passed away Tuesday night after a very uncomfortable week and several years of memory loss. She was a wonderful grandmother, mother and friend. She always put others before herself and took care of those around her. She blessed many lives through her 35 years of teaching. She was my inspiration for becoming an educator, and I enjoyed many stories of her experiences teaching in a one room school house. She spent hours playing with us and always had a fun craft or activity to entertain us. Her jars of brown sugar cookies and white sugar cookies were always full and she made many Sunday roast beef dinners for us. My memories are great and I feel so blessed to have had the opportunity to grow up with my grandparents in town. They were such a wonderful part of my childhood. She will be greatly missed, but I know that she is receiving her rewards in Heaven and watching over us each day!
Visit Roberta's noise from the zoo (link on the left) for another special note about my grandmother and a link to her obituary.
Visit Roberta's noise from the zoo (link on the left) for another special note about my grandmother and a link to her obituary.
Vacation on wheels!



Jeff recently surprised me with a new toy! He thought it would be fun for me to drive something other than our "handivan" and also something for us to enjoy together. Since our little man doesn't allow us very much time together or an opportunity to vacation, we will be enjoying short respites in our Audi TT!
*Maggie is ready for a ride!
Wednesday, August 22, 2007
First Day of Kindergarten 2007





Sam had a wonderful first day of Kindergarten! He was very happy and such a good boy at school! They are short staffed in his room, so I have been helping out and staying all day at school too. We are working on getting him a one-on-one aide that is not his mother! With the help of his own EA, I think he will do great at school! Here are some pictures of the big day.
Thursday, August 09, 2007
Updates, finally!
Well, it is official! Jeff and I broke the mold with little Sammy! We received our results from Rochester regarding the genetic testing and everything was negative. We are back to the original diagnosis of autosomal recessive microcephaly. Although we are disappointed with the lack of information we received from our Mayo trip, we are glad that we went. Sam has been having fewer seizures in the last two months, however, he continues to have 3-4 every week to ten days. He has a type of seizure disorder that is hard to control with medication. Also, he can have days without seizures and then have a cluster of them on the same day.
We started Sam on a new sleep med on July 4th which is helping a great deal! Of course, it is causing problems with other parts of his delicate system. Finding the right balance of meds is always a challenge. We also have a night nurse which has been a huge blessing for us! She comes from 10pm to 6am Sunday through Thursday nights. Jeff and I are finally sleeping again in the same room!
We are looking forward to the transition to Kindergarten. Sam has his first day on August 20th. Hopefully, Sam will do well and enjoy a longer day of school. We are so happy to report that he has started to do a little standing again! I think the combination of sleep and seizure control has given him the strength to take steps again! We are so thankful for the return of some of his lost motor skills! We were afraid that we would not see him standing and walking again.
Thank you for the continued prayers and support for our family! We are so grateful for the positive changes that we have seen in the last two months with Sam! Please add Jeff's aunt Sue and her family to your prayers. She was diagnosed with a brain tumor last weekend. She has a CaringBridge page which can be accessed through the link Carson Corner on our site.
We started Sam on a new sleep med on July 4th which is helping a great deal! Of course, it is causing problems with other parts of his delicate system. Finding the right balance of meds is always a challenge. We also have a night nurse which has been a huge blessing for us! She comes from 10pm to 6am Sunday through Thursday nights. Jeff and I are finally sleeping again in the same room!
We are looking forward to the transition to Kindergarten. Sam has his first day on August 20th. Hopefully, Sam will do well and enjoy a longer day of school. We are so happy to report that he has started to do a little standing again! I think the combination of sleep and seizure control has given him the strength to take steps again! We are so thankful for the return of some of his lost motor skills! We were afraid that we would not see him standing and walking again.
Thank you for the continued prayers and support for our family! We are so grateful for the positive changes that we have seen in the last two months with Sam! Please add Jeff's aunt Sue and her family to your prayers. She was diagnosed with a brain tumor last weekend. She has a CaringBridge page which can be accessed through the link Carson Corner on our site.
Wednesday, June 06, 2007
Mayo Pics
Sunday, June 03, 2007
Mayo Trip #2
We survived our second trip to Rochester last week! It did not go as well as the previous trip. Sammy had a very difficult day on Thursday due to the tough eye exam he had first thing in the morning. Needless to say, we heard sounds out of our little man that we had never heard before and never want to hear again! He was so upset and we were sure that he was going to have a seizure during the appointment, but he waited until we made it back to the room. After he finally calmed down, he had a big seizure lasting about 6 minutes and we had to give him meds to stop it. Jeff and I decided that it is going to be a very long time before he has another eye exam! We didn't learn very much new in relation to his eyes, however, we did learn that the Mayo Dr's think his eyes are even worse than we had previously thought. His retinas are detached in addition to the previous six or so problems he has already had diagnosed. The visit with the geneticist went fine and Sam had blood drawn for further genetic testing. Unfortunately, we have to wait until the end of July before we will have results back. The doctor thought that Sam may have characteristics of a couple of different syndromes, so we will have to wait and see. We are happy to be back home and do not plan a return trip to Rochester until fall. The sleep study and behavioral psychologist appointments our 4-5 months out on the schedule. I guess since we have survived for 5 1/2 years without much sleep, another 4 or 5 months won't make much difference! We continue to thank the Lord for our humor and our ability to keep the glass half full!
Saturday, May 26, 2007
Mayo Trip #1
We successfully made our first trip to Rochester last week! Sam was a very good little boy and the trip went well. Sam had an EEG on Monday morning and a consultation with a pediatric neurologist who is doing a two year fellowship in epilepsy at Mayo, in the afternoon. He spent two hours with us and offered some new information. He was most concerned with diagnosing Sam. He feels that Sam has something other than an autosomal recessive form of microcephaly. He also feels that a diagnosis would help to treat Sam's seizures and give us more information regarding what we can expect for Sam's future. He recommended that we see a geneticist for more information which will send us back to Rochester on Wednesday the 30th. Sam will see an opthamologist on Thursday morning and the chair of the Mayo genetics department in the afternoon. I guess that if anyone could figure out our complex little boy, this should be the woman to do it! The neurologist informed us that Sam's sleep problems are not behavioral, but connected to the underdevelopment of his brain. This was reassuring to us since we have heard from doctor after doctor that they think it is a behavioral sleep problem, even though, Jeff and I continually try to keep a sleep routine in place with no success! We have always felt that there was more to the problem than behavior. We are also awaiting appointments for a sleep study and a behavioral psychologist at Mayo. Hopefully, the sleep study and psychologist will be able to determine the correct plan and medication for Sam. We are cautiously optimistic that we may sleep through the night at our house in the next year! Sam also had an MRI while we were there and was put under general anesthesia. We were very impressed with everyone at Mayo and how smoothly everything works together. Please pray for success with our second trip on Wednesday and for the doctors who are working with us. We appreciate all of the thoughts and prayers from everyone!
Sunday, April 15, 2007
Easter 2007
Sam's Surgery Update
Sam had surgery on Friday morning at Avera Mckennan. We arrived bright and early at 5:30ish am and he was taken into surgery at 7:00. That was quite a moment for us to watch our little boy being carried away from us into a room full of strangers. He had a couple of procedures done by two different doctors. He had his adenoids removed and some work done inside of his nose to allow him to have a clearer airway. His adenoids were over 50% enlarged and the ENT doctor was quite happy to report that he was certain that Sam would be breathing better soon! He also had an endoscopy to look at his esophagus and stomach. No tumors or ulcers! We will receive the results of the three areas biopsied this week. His reflux looks to be under control too! Sam was such a great patient and he came through the anesthesia like a champ. We were able to come home in the late afternoon on Friday. Our nights have been a bit challenging as he is draining a lot and kind of miserable, but nothing we can't handle. We were certainly blessed with tons of prayers and so thankful to have so many people praying for us! We were not able to have the feeding tube placed at this time because the surgeon was concerned with Sam having three procedure on one day. We will have to see what the future brings and decide if the g-tube is necessary after the test results are back.
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