Friday, March 1, 2013
flaws...we all got em
I love, love, love the simply , innocent, nonjudgemental minds/thoughts/and words of kids.They just ask as if they want to know and there's no reason why they wouldn't ask. I kinda got a kick out of it really.
What I learned today is this: We need to accept others flaws and admit to our own!
Friday, February 1, 2013
2012 in review
In January he got his Baclofen Pump. This pump is placed under the skin on his lower torso. A catheter delivers medicine in to his spinal fluid. This medicine helps "loosen" his muscles. Instead of his legs being rigid and hard to move they are loose due to the continual release of medicine. I'm so glad that we did this. It has been so great for him in many ways...easier to dress and change him, less muscle spasms, helped him gain weight because muscles aren't always contracted, and improved walking. However at first he could not stand because he was used to using his tone. So...
In february we went to Kenny Rogers Child Center in Sikeston for our 3 week intensive. We purposefully planned this after the pump..knowing he would need intense work to get back to standing and walking. You can look back in the blog to read about that visit. Overall he got back to where he needed to be physically by doing this intense therapy.
March and April was spent continuing to work on strengthening his legs and upping the dosage of medicine released. However we did find out that he had large kidney stones (too large to pass) which are a side effect of the ketogenic diet. On that note....the diet is controlling his seizures wonderfully. He has 1-4 a month and they are small..lasting about 10 secs to 1 minute.
May, June, July
The summer was spent traveling to St Louis Children's Hospital to treat his stones. Basically we were going every 2 weeks. They were treating both kidneys. On our last treatment he did not react well. The next day he had a one and half hour long seizure that landed us in the icu 2 days and peds floor 4 days. A lingering temp was the mystery...
We did enjoy swimming and Silver Dollar City as much as possible in between trips to St. Louis
August
Baby Sydney Nicole was born 8-10-12. This was the highlight of our year!!! She was our little baby of the family at 7,14...My mom stayed on and off for 5 weeks due to the fact i couldn't lift Christian. We are so grateful. That was hard for me to not be able to work with Christian.
September-December
Christian started Kindergarten..hard to believe. His teachers are fabulous. He attends 3 hours a day. School can be tiring for him but he loves it. Always smiling when we mention it. We continued to up his dosage of baclofen and he is doing great with his pump. His transitional walking (walk to and from chairs or stander..10-15 steps) is improving. We are trying to get him to walk more so that we are not carrying him.
He has mastered signing for "more" and "drink". We are working on signing "yes" and "all done". He also has 2 buttons that say Hi and Bye and he has almost mastered that skill.
Christian continues to go to physical, occupational, and speech therapy outside of school and in school. We are waiting to be scheduled for our next intensive in Sikeston.
Overall 2012 was great... some medical highs and lows..and of course our newest addition Sydney. Can't wait to see what 2013 holds.
Wednesday, November 21, 2012
They dodged and made a difference
Thank you to all of the businesses who donated-Lambers, Express Care Valvoline, Taco Bell, Rib Crib, Sonic, Shoneys, Yogurtini, Family Video, Godfathers, Dominoes, Papa Johns, Caseys, Barnett-Davis Dental, Ozark Therapy Institute, Mandy Evans Photography, Stacey's Sweets, Primas Mexican Grill, Chesterfield Family Center, Famous Daves, Image Pro Group (tshirts), We could not do this without all of the generous people and businesses!
I would also like to thank my family and friends who volunteer every year to help make this successful. You are all amazing! Thanks to the parents and players who got your kids to the tournament, sponsored teams, purchased shirts and cheered everyone on.
It's really not about who wins but the fact that you are having fun and making a difference in one boy's life..our sweet Christian. We raised what we had hoped to raise to take Christian to physical therapy at the Kenny Rogers Child Center in Sikeston, MO. He will work in a 3 week, 3 hrs a day physical therapy program. The intensitity of it is what makes it so successful in helping Christian make more progress in his walking and standing. We were also raising money for speech therapy. Our insurance does not pay for speech therapy.
Saturday, September 15, 2012
DODGEBALL TOURNAMENT NOV.3RD
Dodgeball!!!!!!!!
The 5th Annual "Dodging to make a Difference" Tournament is SATURDAY NOV. 3rd!
More information to come!!!
Like us on facebook at dodging to make a difference.
Tuesday, August 21, 2012
Summer of swimming, stones, and St. Louis
Then we went back and they did lithotripsy on his left kidney and that went well and those stones were broken up and passed. Then we went for trip 3 to put a stint in his right ureter to dialate it so that they could put a scope up there to break up the stones in the left kidney and pull them out. This was more invasive than what they did on the left kideny. So we did that and went home. Then trip 4 was to do the procedure. That took about 3 hours and we went home that day. This is where things took a turn for the worse.
That night we got home Christian started running 103 temps on and off thru the night. I rotated tylenol and motrin and kept in contact with his urologist that night and the next day. He suggested we go see our pedicatirican to check out his lungs and urine for an infection. My pedicatrician was off that day but her sister is also a doctor there and so we got in to see her. Once we got there it turned out that our pedicatrician was there to see a couple of patients. So we get there and Christian is geting warmer because he is about 20 minutes overdue for his next round of tylenol. As the doctor is asking questions Christian starts having a seizure. I tell the doctor "he's having a seizure...take note of the time". I can tell by his more agressive jerking movements that this one will probably last 5 mins and I will need to give his emergency medicine that we always carry. At 4:25 it had been 5 mins and I gave the diastat. At this time my pediactrician had already been called in since she is familiar with Christian. After 1 minute the medicine did not work and I told them to call 911. This has only happened one other time to Christian. His temp was up to 105 by now. They put oxygen on him and waited for the ambulance. The good thing is that the hospital is 2 mins down the road from the office. Eric was already on his way to the office to help with Christian but did not know what was happening. Poor guy was greeted by the nurse to be informed before he walked in to a room with his son seizing and oxygen mask on. I just watched and waited. In my mind i watched the time tick by each 5 minutes passing and knowing this was not good for is body and brain. At one point I asked if it should be taking so long.
The ambulance arrived and we relayed info..seizure started at 4:20...10 mg diastat given at 4:25...uteroscopy done yesterday...stint in...do not give dextrose...
I rode in the front seat and repeated do not cry ,, do not cry....knowing when we got to the e.r i would need to give them vital info about Christian's complicated history and the diet he's on. I just wanted the ambulance to go..to get to the hospital. They took a couple minutes to start an i.v but gosh i just wanted them to go! So I just sat there and waited for what seemed like forever.
It's now been 20 mins of seizure...the paramedics run the gurney to the blue pod of E.R. I try to keep up at 8 mths pregnant but i'm a tad slow and figure I will get there eventually. I can't believe this is happening. About 10 people proceed to work on him. One doctor giving orders. It was like a well running machine..each person with their job. I dictated everything they needed to know to one nurse who stood behind a computer...typing away everything I said and asking questions as needed. I stood in the corner and watched and answered questions. The clock just kept ticking by. Just breathe Robyn. All the while I kept praying that God would stop the seizure! They had also put ice bags and a fan on him to get his temp down. Eventually we hit 45 minutes of seizure activity! I just stood there after I had given all of the information...i just stood there and watched and waited. There was nothing else for me to do.
They called his neurologist and followed protocol of giving a certain drug and certain amount at intervals..hoping that it would stop. After an hour he was still seizing! I felt like I was in a movie. How could this be happening. His heart rate stayed in the 200's. After an hour and 10 mins, the doctor warned us that they would have no choice but to give him something to shut him down which would likely include intubation if this last drug didn't work. Sometimes kids can't keep breathing on their own once they are given such powerful drugs. And we had agreed that if that happened we would fly him to st louis childrens. Then of course I start thinking oh no if that happens I can't fly with him because I'm 8 mths prego! Thank God the last drug worked. The jerking stopped and his heart rate came down.Oh thank you God!!! I hate to admit it but at one point as we just waited I wondered how this day would end. Is this what happens? Will I be one of those parents? God intervened and the seizure stopped.
Christian slept for the next 2 days due to the exhaustion from the seizure and powerful medicine given to stop the seizure...we stayed in the hospital for the next 7 days while they tried to figure out why his temp kept going up. That was the mystery. Nothing was ever found that gave us an answer as to why he kept running a fever. We all figured it may of just been his bodies reaction to the kidney procedure. Christian did regress in areas of his motor skills but has since bounced back.
During this time we were so grateful for all prayers, meals, and well wishes.
Tuesday, May 15, 2012
stones
Thursday, February 23, 2012
last day
Well we are almost done here in Sikeston. I have to say this has been one of the more stressful intensives we've done due to the fact that we were "starting over" with Christian's body as far as standing and walking and I have a 1 year old and 14 wks pregnant...needless to say that adds a little more to the plate. I would also say this has been one of the more umm rewarding (i guess that's the word) visits. I saw Christian go from the first week of barely standing to this last week of totally pushing up and standing and walking. He and Brandy have worked so hard. I am very proud of him! He still has a ways to go but at least now I'm not worried that he may never get it figured out.
I don't know what I would do without the opportunity to come here and have Christian participate in this intense physical therapy. It makes a world of difference. The pt is able to get a real look at him over the 3 hours a day/3 week session. It also gives her time to see what needs to be worked on and try out different equipment, braces, and techniques to get him doing what he needs to do. I am glad that we got the baclofin pump and are on our way back to better walking.
VIDEOS -these are from these last couple of days work.
THANK YOU- to my mom,dad, granny for all of your help with Bryant, laundry, meals, your house and much more!!!! To everyone who participated in the Dodging to make a Difference Tournament! This fundraiser makes it possible for us to come to this!! My husband who has to miss us for 3 weeks except for visits on the weekends! All who have been praying for Christians' health and progress!!