Tuesday, April 23, 2013
The Canadian National Transplant Research Program
Today our thoughts are on Organ donation, if it wasn't for a family's decision to donate a heart, Sara wouldn't be with us right now. It's because of the thoughtfulness of another family, in the midst of grief and pain, that a heart was given to our child. We are forever grateful.
Improving organ donation is just one of the projects the Canadian National transplant Research Program hope to improve. A grant for this program was announced yesterday, and it's lead by one of the U of A's own researcher Dr. Lori West. It was something our family wanted to be a part of when they invited us to speak to CBC news and CTV news.
CTV News Edmonton "National Transplant Program Led by Local Researcher" VIDEO
CBC News "Organ Transplant program expected to boost success rate" Article
CBC news The National - April 22, 2013 VIDEO
*You can skip ahead to 33:40 to see Sara, after all the commercials the segment with Sara will play.
We know a few families also waiting for transplants and we pray that the wait will not be too long, as we already know, some can't last the wait. Signing your health card, or signing up in your province's site and donating blood is all a step in the right direction. Hopefully soon a new way to match donors with recipients will be available across Canada. Like the poster above, you can check out the Projects and Core Platforms from The Canadian National Transplant Research Program website.
Hope you enjoy reading through the links and watching the videos!
Here is Sara's page from the Children's Miracle Network that the Stollery Children's Hospital put together back in March 2013.
Friday, April 12, 2013
Funny girl.
Our posts are less & less frequent, as we're spending more & more time outdoors! Even if this spring is bringing us snow, we're still loving it, and really enjoying the warm sunny days. We've even had some fun family times lately. So I'll be posting pictures soon, but here's an update anyway:
Joel & I were happy to have an evening together, it was so nice to get out! Thank you Uncle John & Auntie Dawn for taking us out! We had a great time at the fundraiser dinner & concert for Ross Haven Bible Camp.
Hailey and I are working on school when we can. Hopefully we'll get through the book work faster now that she's getting into it a little more. We were working on maps today, I wouldn't be surprised if one day she decides to travel! She loved learning about different places, and sometimes I have to convince her that what I'm telling her is true, as she questions everything!
Sara has been doing so well. Our biggest struggle has not been so bad, she's been needing a higher and higher does of Tacrolimus. They say this drug will plateau and she'll stabilize at a dose at some point here, but so far we've just been increasing slowly. Now this week's blood work showed that her Tac was over 20, and they want her tac level between 10-12! We were worried she was getting the flu, and here it was probably her tac level being too high. It can cause headaches, vomiting and diarrhea and Tuesday and today she was feeling sick. Please pray that her level will come down and that we can manage her tac level with blood work just once a week. That she'd start holding down food, and not flush it out! Sara is also back on the Anti-viral drug because her last blood test showed signs of the virus CMV, the treatment dose is double what the maintenance does was. So please pray that this CMV count will lower or be back to zero signs of it, an therefore not developing any infection.
Part of what made our evening was not worrying about my girls, they were in good hands! Thanks to the Quist family, they had so much fun! Sara hasn't been feeling well, but we were hopeful that she'd still be up for being babysat by the Quist's. While at a their place, she had a messy diaper, and a bath to clean her up. She was telling us all about it on the way home and we laughed and laughed! Her words were: "Then I saw carrots! I didn't know they got in my diaper! They crashed in my diaper, I ever, ever (never) seen carrots in my diaper, I didn't even know that!"
Funny girl.
Our time in the hospital picking up meds or going to transplant Clinic often ends up being visiting time with friends who are there. It's so good to catch up, we really miss our friends there and try to visit as often as possible. We're so thankful to keep in touch with many of these families, when they're in the hospital and when they're not! Some are not sure what decisions will be made as it is unclear how to help they're little ones and some are headed down the transplant road, whatever the outcome will be we trust that God will help them through. Please keep praying for Hope, Joel, Grayson (who received a new heart!!!), Caleb, Rylan, Precious, Alexis, Cohen, Muskaan, Racquena, Melissa, Hilda, Jace, Sheldon, Makenna, Connor, Colton, Kolby, Hannah, Kaiya, Harrison, Austin, and please include the families who lost these loved ones: Jack, Addison, Isabelle, Drayton and those who gave life back to my girl and others, through organ donation. God Bless you.
2 John 1:3 " Grace, mercy, and peace be with us, from God the Father and from Jesus Christ the Father's Son, in truth and love." ESV
Joel & I were happy to have an evening together, it was so nice to get out! Thank you Uncle John & Auntie Dawn for taking us out! We had a great time at the fundraiser dinner & concert for Ross Haven Bible Camp.
Hailey and I are working on school when we can. Hopefully we'll get through the book work faster now that she's getting into it a little more. We were working on maps today, I wouldn't be surprised if one day she decides to travel! She loved learning about different places, and sometimes I have to convince her that what I'm telling her is true, as she questions everything!
Sara has been doing so well. Our biggest struggle has not been so bad, she's been needing a higher and higher does of Tacrolimus. They say this drug will plateau and she'll stabilize at a dose at some point here, but so far we've just been increasing slowly. Now this week's blood work showed that her Tac was over 20, and they want her tac level between 10-12! We were worried she was getting the flu, and here it was probably her tac level being too high. It can cause headaches, vomiting and diarrhea and Tuesday and today she was feeling sick. Please pray that her level will come down and that we can manage her tac level with blood work just once a week. That she'd start holding down food, and not flush it out! Sara is also back on the Anti-viral drug because her last blood test showed signs of the virus CMV, the treatment dose is double what the maintenance does was. So please pray that this CMV count will lower or be back to zero signs of it, an therefore not developing any infection.
Part of what made our evening was not worrying about my girls, they were in good hands! Thanks to the Quist family, they had so much fun! Sara hasn't been feeling well, but we were hopeful that she'd still be up for being babysat by the Quist's. While at a their place, she had a messy diaper, and a bath to clean her up. She was telling us all about it on the way home and we laughed and laughed! Her words were: "Then I saw carrots! I didn't know they got in my diaper! They crashed in my diaper, I ever, ever (never) seen carrots in my diaper, I didn't even know that!"
Funny girl.
Our time in the hospital picking up meds or going to transplant Clinic often ends up being visiting time with friends who are there. It's so good to catch up, we really miss our friends there and try to visit as often as possible. We're so thankful to keep in touch with many of these families, when they're in the hospital and when they're not! Some are not sure what decisions will be made as it is unclear how to help they're little ones and some are headed down the transplant road, whatever the outcome will be we trust that God will help them through. Please keep praying for Hope, Joel, Grayson (who received a new heart!!!), Caleb, Rylan, Precious, Alexis, Cohen, Muskaan, Racquena, Melissa, Hilda, Jace, Sheldon, Makenna, Connor, Colton, Kolby, Hannah, Kaiya, Harrison, Austin, and please include the families who lost these loved ones: Jack, Addison, Isabelle, Drayton and those who gave life back to my girl and others, through organ donation. God Bless you.
2 John 1:3 " Grace, mercy, and peace be with us, from God the Father and from Jesus Christ the Father's Son, in truth and love." ESV
Wednesday, March 27, 2013
Beautiful sunshine
While out on a sunny winter's day with our horses, we found pussy willows! Now we're anxiously waiting for winter to end, but still enjoying the snow and warm weather like +14C! Even Sara's doing well, getting out a lot, and keeping up to her sister Hailey! Sara's med levels are doing much better, and she's also down to 11 meds! Now it's getting easier to cover the cost of her meds and thankfully as she improves she'll be on less & less medications. Now that we're out of the hospital it seems like there's more costs, like trips to the city, and parking, and meds. So we're glad Joel's back to work, and hope that his job brings him closer to home! Please pray that Sara will stay healthy, continue to grow and that her weight will come up! She also needs to be drinking more to keep up with fluids.
Here's an interview the Joel did in January on the Radio! Listen to the Radio INTERVIEW on CISN! It was great to be part of a fundraiser that raised 1.25 million for the Stollery Children's Hospital! Thank you!
Thankfully, because of the Stollery Children's hospital and the Ronald McDonald House, our stay there is a memory, and not todays reality. They made us comfortable in a very uncomfortable time. By supporting them you're supporting families like ours, and others like ours.
Please continue to pray for our friends in & out of the hospital - Joel, Muskaan, Rylan, Makenna, Grayson, Caleb, Alexis, Precious, Hope, Austin, Harrison, Sheldon, Kaiya, Cohen, Kolby, Hannah, Hilda, Melissa, Connor, and Colton. Also the families of Isabelle, Jack, Drayton and Addison who are grieving their precious little ones. May God keep you in His care.
Stollery Children's Hospital Foundation
Ronald McDonald House Northern Alberta
Here's an interview the Joel did in January on the Radio! Listen to the Radio INTERVIEW on CISN! It was great to be part of a fundraiser that raised 1.25 million for the Stollery Children's Hospital! Thank you!
Thankfully, because of the Stollery Children's hospital and the Ronald McDonald House, our stay there is a memory, and not todays reality. They made us comfortable in a very uncomfortable time. By supporting them you're supporting families like ours, and others like ours.
Please continue to pray for our friends in & out of the hospital - Joel, Muskaan, Rylan, Makenna, Grayson, Caleb, Alexis, Precious, Hope, Austin, Harrison, Sheldon, Kaiya, Cohen, Kolby, Hannah, Hilda, Melissa, Connor, and Colton. Also the families of Isabelle, Jack, Drayton and Addison who are grieving their precious little ones. May God keep you in His care.
Stollery Children's Hospital Foundation
Ronald McDonald House Northern Alberta
Tuesday, March 26, 2013
Our trip to Salmon Arm
We went to Salmon Arm to visit family last week for the funeral of my Uncle Larry Dyck, and to visit with the extended family that came. I was so glad to see many cousins, Aunts & Uncles. It's too bad it was such a sad and shocking death that brought us together, I hope it's a reunion or wedding that brings us together next time. I'm so thankful for the ministry my Uncle was a part of, as a pastor for 47 years, he touched may lives with the Gospel of Christ, and the hope that it brings in Jesus. He will be greatly missed by all that knew him. We love you Auntie Marilyn, Jeff, Jessica, Amelia, Simon, Paul, Janine, Josiah, Kailey, and Hunter, we're praying for you all.
It was so good to spend time in Grandma & Grandpa's new house! It was so fun for the kids to play hide-and-seek and roller blade in the basement with their cousins! Thanks for having us Mom & Dad!
Monday, March 11, 2013
Please pray for Isabelle's family
This post was supposed to be for Isabelle and her fight for her life while waiting for a heart transplant. Instead it is a post for prayer for her family, sadly she passed away last night. Izzy and her Mom & sister were a huge part of our lives while at the Stollery hospital, they visited, laughed, cried, and shared so many times together with us. My girls Hailey & Sara are so sad they won't have their friend to visit or play with at the beach anymore. Many times when we were gone for supper, Sara & Izzy & Muskaan would be out in the hallway with the nurses, eating their supper together or watching TV. All of them would be laughing, and smiling and being goofy. Izzy was a spunky, silly, fun, and a loveable 6 year old girl. She was sure of what she wanted, and wasn't afraid to tell you! She stole all of our hearts, we miss you already Isabelle and you will be remembered always.
Please pray for Becky & Mady, they will need so much comfort & love right now. Pray that they will find relief in knowing Izzy is not suffering anymore, and hope that they will be with her again one day in Heaven.
"Yes, my soul finds rest in God;
my hope comes from Him...
Trust in Him at all times,
you people; pour out your hearts to Him,
for God is our refuge."
Psalm 62:5, 8 NIV
God knows our pain and sorrow, and he will never leave us. He is there for us in good times and in hard times. Lean on him and he will carry you through anything this life brings your way. His love for us is so great.
Please pray for Becky & Mady, they will need so much comfort & love right now. Pray that they will find relief in knowing Izzy is not suffering anymore, and hope that they will be with her again one day in Heaven.
"Yes, my soul finds rest in God;
my hope comes from Him...
Trust in Him at all times,
you people; pour out your hearts to Him,
for God is our refuge."
Psalm 62:5, 8 NIV
God knows our pain and sorrow, and he will never leave us. He is there for us in good times and in hard times. Lean on him and he will carry you through anything this life brings your way. His love for us is so great.
Sunday, February 17, 2013
Family DAY!
We're so blessed by our community and really wanted thank them!
We are in Evansburg tomorrow with our Mechanical Bull for Family Day!
More pictures to come!
Tuesday, January 29, 2013
January Fun
January has be full of birthday parties, sledding, sleigh rides, fun with friends, the birth of a new cousin, hospital check-ups, visits with friends from the hospital, and mostly enjoying time out in the snow! Thankfully we are all well. Joel's busy working and the girls & I are actually keeping up around the house! Getting back into a routine, finally!
______________________________________________
January has also has brought sorrow for many who knew Margaret Bayne, of Camp Homewood on Quadra Island, BC. Marg was 96 and still on fire for Jesus. She was such an inspiration to anyone who had the priveledge of meeting her. Her determination to share the gospel of Jesus and the power of God's word was incredible! We loved her, and pray for her husband Alf and all of Homewood's staff. It won't be long until we meet again, thank you for the blessing you've been to us Marg!
Friday, January 25, 2013
"She Had a transplant, She's fixed right?" by Linsey
My thoughts exactly! Here's a heart transplant Mom sharing details that I have yet to explain:
Thank you Linsey from crazybeautifulrippys.blogspot.ca
Thank you Linsey from crazybeautifulrippys.blogspot.ca
"She had a transplant, she's fixed, right?"
It's a common misconception that when someone gets a heart transplant they are "fixed." I can definitely see how people would think that, but it's simply not true. Yes, a heart transplant can allow a person to have a much better life. It can make it so that they finally feel better, can climb stairs, run & play, or just live. Heart transplants save lives. But it's not an easy road, that's for sure. Here, I'd like to shed some light on what it's like to live in the transplant world. It's my hope that I can help others understand why there are some areas in my girls' lives that are very very different than their childrens' lives. And also why it's so important to really adhere to what some may call my "paranoia" about the things we can and cannot do.
First things first: a heart transplant (or any other organ transplant) is trading one disease state for another. Any organ transplanted into a body is perceived as a foreign object by the recipient's immune system. In order to (hopefully) prevent rejection, there must be immuno-suppressive medications on board at all times. These drugs, while they help so that the organ doesn't reject, do a lot of damage to the body's other organ systems, and also set the recipient up for any type of infection that is around them. They become very susceptible to germs, cannot have live vaccinations, and are at an extremely high risk for developing cancer. In the case of my children, these medications also cause their white blood cell counts to be off, blood pressure to be high, kidney function to be diminished (most heart transplant patients will end up needing a kidney someday), appetite suppressed, and hemoglobin to be low. They cause excessive hair growth, skin issues, gum overgrowth, and a myriad of other scary side effects that I won't even go into right now. So there are other medications added to their drug regimen to combat all the issues that the immuno-suppressant drugs cause. Being on these meds is just another situation of "the lesser of two evils".. the alternative, of course, being that the person is no longer alive.
Another common myth: once you are transplanted, that organ will last forever. False. Most heart transplants last around 10-ish years. Now this is just an average. Plenty of people live 20 years without needing a new heart, and others will need another one two years out. For some reason, transplanted hearts very easily succumb to Coronary Artery Disease, and must then be re-transplanted. Of course, they are working on getting to the bottom of this mystery, and I so hope that my children won't face a re-transplant, but chances are they will. And I don't even want to think about the possibility of having to do a kidney transplant, too, like I mentioned above. So I don't.
Germs, germs everywhere. Did you know that there are fungi that live on rosebushes (and other plants) that could kill someone with a weakened immune system? Yeah, neither did I till I had two kid with transplants. Or how about birds and reptiles-full of salmonella and other unmentionable creepy-crawlies. Public pools? *Shudder* Not for my kids-I'd be better off letting them swim in the toilet. School, of course, is a necessary evil. But the thought of all those un-vaccinated kids with runny noses, chicken pox, whooping cough, etc. is enough to make me want to run for the hills and home-school my kids, Duggar style. But being as I have zero patience to teach a special-needs kindergartener, and I want my kids to have a meaningful education, I suck it up and send them to school. With hand sanitizer. And a bubble wrap suit. Just kidding. (Wouldn't that be cool, though?!?! Ha ha.)
Constant monitoring and doctor's visits. When was the last time you had to bring your 6-year-old to have a bone scan? What's your three-year-old's resting blood pressure? How's your daughter's fluid status today? Don't know? To all of the above, I say: been there, done that. Every single organ system is monitored in a transplant patient. Most heart transplant patients even have to have heart catheters done frequently, where they are put under anesthesia and a catheter is threaded through the groin up into the heart to study heart pressures, the state of the coronary arteries, heart function and the like. Sometimes they take biopsies. Many, many children who have heart problems and/or transplants are developmentally delayed or disabled, which brings speech clinicians, special education teachers, occupational and physical therapists to the table. My 6-year-old could direct you around the Mayo Clinic. It's just a fact of life for us.
Still think transplant's a permanent fix?
In no way do I mean to gripe and groan about transplantation. If not for transplants, and organ donors, neither of my children would be alive today. I am a tireless advocate for organ donation. I will never rest. We are absolutely and totally blessed with our two beautiful girls. They are miracles, and testaments to why organ donation is a wonderful, fantastic and magical thing. It's just that it's not an easy road to travel. Is it worth it? You bet. I'd choose the same road again and again if it meant that I can have my kids here to drive me crazy till I am an old, senile woman. They are both doing extraordinarily well. They live their lives as normally as possible, and that's what matters. They'll never be the same as their peers. We have basically fought for every single aspect of everyday living that most take for granted. That's ok, though, because it has made us open our eyes to the blessings that surround us. We really have stopped to smell the roses. We just don't touch them. Fungus on the rosebushes, ya know.
First things first: a heart transplant (or any other organ transplant) is trading one disease state for another. Any organ transplanted into a body is perceived as a foreign object by the recipient's immune system. In order to (hopefully) prevent rejection, there must be immuno-suppressive medications on board at all times. These drugs, while they help so that the organ doesn't reject, do a lot of damage to the body's other organ systems, and also set the recipient up for any type of infection that is around them. They become very susceptible to germs, cannot have live vaccinations, and are at an extremely high risk for developing cancer. In the case of my children, these medications also cause their white blood cell counts to be off, blood pressure to be high, kidney function to be diminished (most heart transplant patients will end up needing a kidney someday), appetite suppressed, and hemoglobin to be low. They cause excessive hair growth, skin issues, gum overgrowth, and a myriad of other scary side effects that I won't even go into right now. So there are other medications added to their drug regimen to combat all the issues that the immuno-suppressant drugs cause. Being on these meds is just another situation of "the lesser of two evils".. the alternative, of course, being that the person is no longer alive.
Another common myth: once you are transplanted, that organ will last forever. False. Most heart transplants last around 10-ish years. Now this is just an average. Plenty of people live 20 years without needing a new heart, and others will need another one two years out. For some reason, transplanted hearts very easily succumb to Coronary Artery Disease, and must then be re-transplanted. Of course, they are working on getting to the bottom of this mystery, and I so hope that my children won't face a re-transplant, but chances are they will. And I don't even want to think about the possibility of having to do a kidney transplant, too, like I mentioned above. So I don't.
Germs, germs everywhere. Did you know that there are fungi that live on rosebushes (and other plants) that could kill someone with a weakened immune system? Yeah, neither did I till I had two kid with transplants. Or how about birds and reptiles-full of salmonella and other unmentionable creepy-crawlies. Public pools? *Shudder* Not for my kids-I'd be better off letting them swim in the toilet. School, of course, is a necessary evil. But the thought of all those un-vaccinated kids with runny noses, chicken pox, whooping cough, etc. is enough to make me want to run for the hills and home-school my kids, Duggar style. But being as I have zero patience to teach a special-needs kindergartener, and I want my kids to have a meaningful education, I suck it up and send them to school. With hand sanitizer. And a bubble wrap suit. Just kidding. (Wouldn't that be cool, though?!?! Ha ha.)
Constant monitoring and doctor's visits. When was the last time you had to bring your 6-year-old to have a bone scan? What's your three-year-old's resting blood pressure? How's your daughter's fluid status today? Don't know? To all of the above, I say: been there, done that. Every single organ system is monitored in a transplant patient. Most heart transplant patients even have to have heart catheters done frequently, where they are put under anesthesia and a catheter is threaded through the groin up into the heart to study heart pressures, the state of the coronary arteries, heart function and the like. Sometimes they take biopsies. Many, many children who have heart problems and/or transplants are developmentally delayed or disabled, which brings speech clinicians, special education teachers, occupational and physical therapists to the table. My 6-year-old could direct you around the Mayo Clinic. It's just a fact of life for us.
Still think transplant's a permanent fix?
In no way do I mean to gripe and groan about transplantation. If not for transplants, and organ donors, neither of my children would be alive today. I am a tireless advocate for organ donation. I will never rest. We are absolutely and totally blessed with our two beautiful girls. They are miracles, and testaments to why organ donation is a wonderful, fantastic and magical thing. It's just that it's not an easy road to travel. Is it worth it? You bet. I'd choose the same road again and again if it meant that I can have my kids here to drive me crazy till I am an old, senile woman. They are both doing extraordinarily well. They live their lives as normally as possible, and that's what matters. They'll never be the same as their peers. We have basically fought for every single aspect of everyday living that most take for granted. That's ok, though, because it has made us open our eyes to the blessings that surround us. We really have stopped to smell the roses. We just don't touch them. Fungus on the rosebushes, ya know.
Thursday, January 17, 2013
a touch of the flu.
Sara's been sick all day, thankfully she's able to hold liquids down now. Please pray that she'll be over this soon, she needs to get better and hold down her fluids & meds, or it will be in to emerge for an IV.
Keep washing your hands! Hand Sanitizer works for bacterial infections, but does not stop viruses. Simply using soap will get rid of both! Also, if you have been sick, you're usually contagious for a week to 10 days after you feel well. This is one of the worst years for the flu, so help stop the spread! With so many flus & colds going around it's hard to keep clear!
Please continue to pray for our friends - Hope, Caleb, Joel, Harrison, Morgan, Marwa, Safa, Makenna, Sheldon, Alexis, Precious, Muskaan, Lukas, Isabelle, Grayson, Austin, Melissa, Hilda, Isabel F, Kaiya and Cohen. Also pray for the families of Drayton, Addison & Jack, three precious lives that have left us and will be forever cherished. God Bless you.
Keep washing your hands! Hand Sanitizer works for bacterial infections, but does not stop viruses. Simply using soap will get rid of both! Also, if you have been sick, you're usually contagious for a week to 10 days after you feel well. This is one of the worst years for the flu, so help stop the spread! With so many flus & colds going around it's hard to keep clear!
Please continue to pray for our friends - Hope, Caleb, Joel, Harrison, Morgan, Marwa, Safa, Makenna, Sheldon, Alexis, Precious, Muskaan, Lukas, Isabelle, Grayson, Austin, Melissa, Hilda, Isabel F, Kaiya and Cohen. Also pray for the families of Drayton, Addison & Jack, three precious lives that have left us and will be forever cherished. God Bless you.
Wednesday, January 16, 2013
Happy 4th Birthday Sara!
Sara is so full of joy, it over flows! It's hard to believe what she's gone though in her life, starting out at 5lbs. 3oz! We're so happy to have her running around again! There's no stopping her now!
Your prayers have got us through the last 4 years, we are so grateful for what God has done in her life and in ours. Our hearts rejoice!
James 1:17a " Every good and perfect gift is from above, and comes down from the father of lights..."
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