Sunday, August 22, 2010
Happy Birthday Ava
Ava Rosemeyer was only 3 years old when she went to Heaven. One very hot day in Australia, Ava went inside the car that was parked in the driveway looking for lollies. She had locked the door of the car so no one knew she was in there. After about 30 minutes, Ava's mother noticed that she still wasnt back. Ava's mum thought she was with Grandad and Grandad thought she was with mum. Ava couldnt find her way out of the car... By the time rescue came, Ava was still breathing but not conscious. Ava was taken to the local hospital where they put her on life support and cooled her body right down in an attempt to limit brain damage. After fighting 2 days for her life, Ava was put out of suffering and called back home to Heaven. In the blink of an eye, Ava Rosemeyer was gone. Today is Ava's 7th birthday. She celebrates with the angels and blows her candles out in Heaven. Happy Birthday precious Ava. Its been so long...
August 22, 2003 - February 05, 2007
Fly High, SuperPrincess. You will always be loved!
www.AvasRule.com
www.sheyerosemeyerphotography.com
Friday, August 20, 2010
I Trust God...
Dear Mr. God, I’m writin’ you today- Because it seems like lately, I’ve forgotten how to pray.
A few months ago, before school was let out, my teacher had called me out of the classroom to talk. There was a girl that said some hurtful words about people with cancer and it broke me down. Some of my friends knew about it and a couple even confronted her. Before I was pulled out of the classroom, I heard screaming, yelling and swearing in the class next to mine. Everyone ran out to see what had happened and I walked out last with my 2 other friends. There was a big crowd of students surrounding the girl that had said the mean things. The students were yelling at her, and some were even crying. The teachers were trying to get everyone calmed down and that was when I really saw how upset and hurt people were. I asked one of the girls what had happened and she said that everyone found out about what the girl said about cancer patients. I was in shock. How did that get out so fast? How did everyone find out? I looked around my classroom and that was the moment I knew Cancer had, indeed, touched all of their lives somehow.
Cancer has become a part of everyones lives in one way or another. It has become a huge deal. This disease causes so muvh pain to everyone and when I found out how much people it was affecting, I stepped up. I decided I needed to do more. When I went out to talk to my teacher, she had told me how upset everyone was. She told me to "drop it" when I didnt spread it in the first place. She even told me that cancer took some of her family. I had one question for her when she was done talking- Why are you so okay with this situation? I didnt understand how she wasnt the least bit upset. I set my goal at that moment. I let God take my hand and lead me.
I trust God. I believe that he will put me on my path and guide me wherever I need to go. I wasnt as close to God before I was set on this "end cancer" journey. I pray more now. I believe in miracles. I have found hope. Once again- I trust God.
'Cause I need you, but it’s hard to see- Why anyone as big as You, needs anything from me. I know You’re there, so how ya been? I’m alright but I can’t lie, sometimes I feel like givin’ in, you’re all I’ve got..
-Melly
(This will also be posted on lifestormystyle.blogspot.com)
A few months ago, before school was let out, my teacher had called me out of the classroom to talk. There was a girl that said some hurtful words about people with cancer and it broke me down. Some of my friends knew about it and a couple even confronted her. Before I was pulled out of the classroom, I heard screaming, yelling and swearing in the class next to mine. Everyone ran out to see what had happened and I walked out last with my 2 other friends. There was a big crowd of students surrounding the girl that had said the mean things. The students were yelling at her, and some were even crying. The teachers were trying to get everyone calmed down and that was when I really saw how upset and hurt people were. I asked one of the girls what had happened and she said that everyone found out about what the girl said about cancer patients. I was in shock. How did that get out so fast? How did everyone find out? I looked around my classroom and that was the moment I knew Cancer had, indeed, touched all of their lives somehow.
Cancer has become a part of everyones lives in one way or another. It has become a huge deal. This disease causes so muvh pain to everyone and when I found out how much people it was affecting, I stepped up. I decided I needed to do more. When I went out to talk to my teacher, she had told me how upset everyone was. She told me to "drop it" when I didnt spread it in the first place. She even told me that cancer took some of her family. I had one question for her when she was done talking- Why are you so okay with this situation? I didnt understand how she wasnt the least bit upset. I set my goal at that moment. I let God take my hand and lead me.
I trust God. I believe that he will put me on my path and guide me wherever I need to go. I wasnt as close to God before I was set on this "end cancer" journey. I pray more now. I believe in miracles. I have found hope. Once again- I trust God.
'Cause I need you, but it’s hard to see- Why anyone as big as You, needs anything from me. I know You’re there, so how ya been? I’m alright but I can’t lie, sometimes I feel like givin’ in, you’re all I’ve got..
-Melly
(This will also be posted on lifestormystyle.blogspot.com)
Tuesday, August 17, 2010
Acute Lymphoblastic Leukemia (ALL) - Alijah's Story
"We know we'll be able to handle whatever comes."
Alijah's Mom
Meet Alijah:
Watching your child grow and move forward through developmental milestones – learning to sit, to crawl, to take the first tottering step – what a joyful process for a parent! How frightening, then, to watch your child suddenly seem to “grow backwards.” That is what Kyle and Jamekka experienced when in 2005, shortly before Thanksgiving, their two year old son Alijah stopped walking.
Going Backwards from Milestones
“He just started crawling again,” recalls Jamekka. “He would go for four or five days crawling with his foot up in the air like it was hurting. Then he’d walk for a few days, then go back to crawling. Sometimes his right ankle hurt, sometimes his left, sometimes it was his wrist. We thought something might have happened at daycare . . .” but that turned out not to be so.
Soon, Alijah started running a high fever at night and Jamekka took her son to the family’s regular pediatrician. After repeated visits, with tests and x-rays coming back negative, the pediatrician referred Alijah to a rheumatologist, suspecting his mysterious pains might be a sign of rheumatoid arthritis. Once again scans and tests showed no problems. Alijah definitely did not have RA. However, the rheumatologist thought Alijah should be seen by a hematologist. She was concerned that a blood disorder might be causing his symptoms. She referred the family to Dr. Joseph Neglia, section chief of pediatric hematology-oncology at the University of Minnesota Medical Center, Fairview. The next day, January 20, 2006, Dr. Neglia diagnosed Alijah with acute lymphocytic leukemia (ALL) after performing a bone marrow biopsy and finding leukemia cells in his marrow.
A Cancer Diagnosis With A Good Prognosis
Coincidentally, Alijah’s cousin was in University hospital at the same time, being treated for a heart problem; so, many of Alijah’s relatives were present when Alijah was diagnosed. Dr. Neglia broke the news to a crowd of parents, siblings, aunts, uncles, and grandparents, who have been Alijah’s support group and cheering section since that day. He told them that Alijah was lucky to this extent: though it was once almost always fatal, ALL is now a very treatable disease. Thanks to research like that sponsored by Children's Cancer Research Fund, today more than 80 percent of children with ALL are cured.
Dr. Neglia started Alijah’s treatment immediately. The medical team inserted a “port” in his chest through which he would receive chemotherapy drugs. A physical therapist coached Kyle and Jamekka about ways to get Alijah walking again. The family began the long journey, marked by terrors and triumphs, that is cancer treatment.
Life After Cancer Should be Pretty Simple
Today, Alijah is still being treated for leukemia. He has about a year of therapy to go. The little boy who once seemed to be growing backwards is now quite an advanced four-year-old. For Alijah, infusions and transfusions are facts of life. The steroid medication he takes five days a month can make him irritable and emotional but on most days you can’t tell he’s not completely healthy boy – a high-spirited one with a precocious interest in golf! “If there’s a good thing in all of this,” says Jamekka, “it’s watching Alijah grow up. He is a brave kid and we admire him so much. He’s only four-years- old, yet he knows how to put his own medicine in his port! We figure the rest of our life is pretty simple. When we look at what Alijah has done and how he has stood up to this we know that we’ll be able to handle whatever comes.”
-http://www.childrenscancer.org/stories-of-hope/kids-stories/alijah.html
GO Alijah!
Alijah's Mom
Meet Alijah:
Watching your child grow and move forward through developmental milestones – learning to sit, to crawl, to take the first tottering step – what a joyful process for a parent! How frightening, then, to watch your child suddenly seem to “grow backwards.” That is what Kyle and Jamekka experienced when in 2005, shortly before Thanksgiving, their two year old son Alijah stopped walking.
Going Backwards from Milestones
“He just started crawling again,” recalls Jamekka. “He would go for four or five days crawling with his foot up in the air like it was hurting. Then he’d walk for a few days, then go back to crawling. Sometimes his right ankle hurt, sometimes his left, sometimes it was his wrist. We thought something might have happened at daycare . . .” but that turned out not to be so.
Soon, Alijah started running a high fever at night and Jamekka took her son to the family’s regular pediatrician. After repeated visits, with tests and x-rays coming back negative, the pediatrician referred Alijah to a rheumatologist, suspecting his mysterious pains might be a sign of rheumatoid arthritis. Once again scans and tests showed no problems. Alijah definitely did not have RA. However, the rheumatologist thought Alijah should be seen by a hematologist. She was concerned that a blood disorder might be causing his symptoms. She referred the family to Dr. Joseph Neglia, section chief of pediatric hematology-oncology at the University of Minnesota Medical Center, Fairview. The next day, January 20, 2006, Dr. Neglia diagnosed Alijah with acute lymphocytic leukemia (ALL) after performing a bone marrow biopsy and finding leukemia cells in his marrow.
A Cancer Diagnosis With A Good Prognosis
Coincidentally, Alijah’s cousin was in University hospital at the same time, being treated for a heart problem; so, many of Alijah’s relatives were present when Alijah was diagnosed. Dr. Neglia broke the news to a crowd of parents, siblings, aunts, uncles, and grandparents, who have been Alijah’s support group and cheering section since that day. He told them that Alijah was lucky to this extent: though it was once almost always fatal, ALL is now a very treatable disease. Thanks to research like that sponsored by Children's Cancer Research Fund, today more than 80 percent of children with ALL are cured.
Dr. Neglia started Alijah’s treatment immediately. The medical team inserted a “port” in his chest through which he would receive chemotherapy drugs. A physical therapist coached Kyle and Jamekka about ways to get Alijah walking again. The family began the long journey, marked by terrors and triumphs, that is cancer treatment.
Life After Cancer Should be Pretty Simple
Today, Alijah is still being treated for leukemia. He has about a year of therapy to go. The little boy who once seemed to be growing backwards is now quite an advanced four-year-old. For Alijah, infusions and transfusions are facts of life. The steroid medication he takes five days a month can make him irritable and emotional but on most days you can’t tell he’s not completely healthy boy – a high-spirited one with a precocious interest in golf! “If there’s a good thing in all of this,” says Jamekka, “it’s watching Alijah grow up. He is a brave kid and we admire him so much. He’s only four-years- old, yet he knows how to put his own medicine in his port! We figure the rest of our life is pretty simple. When we look at what Alijah has done and how he has stood up to this we know that we’ll be able to handle whatever comes.”
-http://www.childrenscancer.org/stories-of-hope/kids-stories/alijah.html
GO Alijah!
Sunday, August 15, 2010
neuroblastoma - Bradens Story
HOPE...
Meet Braden:
Braden was admitted to Children's Mercy on Friday, December 28, 2007 after a visit to the ER for abdominal pain. After countless tests and scans Braden was diagnosed with stage 4 neuroblastoma. Braden didnt give up. He fought long and hard! Those cancer cells had nothing against the superhero that was fighting them off! Even though Braden was in the hospital for long stays fighting for his life, that smile never left his face. The Hofen family had complete faith that Braden would be healed. There was a huge battle going on- and Braden was winning.
I know there is no known cure for neuroblastoma. It is rare and agressive. Braden was given the chance to be a kid again when he went into Remission! There was no evidence of disease in Bradens body! The family, of course, must have been ecstatic! Their baby boy was done with the treatments. Done with all the pain. In the back of their mind they knew that NB had a great relapse rate. Even after Braden beat the odds of NB (which has a 30% survival rate) it would of been stronger, and extremly harder to beat a neuroblastoma relapse.
On August 11, 2009 the Hofen family learned that Braden's cancer relapsed and there is no known cure for relapsing neuroblastoma. They were given a choice of either quitting and allowing him to die or continuing with treatment in the hopes of prolonging his life a bit longer. They chose to fight. Braden has had two MIBG treatments in Philadelphia as there are only 5 hospitals in the US equipped to do MIBG treatments. It is an IV injection of a radioactive isotope that attaches to neuroblastoma cells and can kill them. Braden's response was favorable but cancer remained. He is currently going through chemo rounds of Irinotecan and Temodar in the hopes of killing the remaining cancer. We all battle and join in BRADEN'S MIGHTY FIGHT!
Please keep Braden and his family in your prayers as Braden fights to beat this cancer once and for all! We love you so much Braden!
GO Braden!!!
Updates:
- www.caringbridge.org/visit/bradenh
- www.Twitter.com/BradensHope
Meet Braden:
Braden was admitted to Children's Mercy on Friday, December 28, 2007 after a visit to the ER for abdominal pain. After countless tests and scans Braden was diagnosed with stage 4 neuroblastoma. Braden didnt give up. He fought long and hard! Those cancer cells had nothing against the superhero that was fighting them off! Even though Braden was in the hospital for long stays fighting for his life, that smile never left his face. The Hofen family had complete faith that Braden would be healed. There was a huge battle going on- and Braden was winning.
I know there is no known cure for neuroblastoma. It is rare and agressive. Braden was given the chance to be a kid again when he went into Remission! There was no evidence of disease in Bradens body! The family, of course, must have been ecstatic! Their baby boy was done with the treatments. Done with all the pain. In the back of their mind they knew that NB had a great relapse rate. Even after Braden beat the odds of NB (which has a 30% survival rate) it would of been stronger, and extremly harder to beat a neuroblastoma relapse.
On August 11, 2009 the Hofen family learned that Braden's cancer relapsed and there is no known cure for relapsing neuroblastoma. They were given a choice of either quitting and allowing him to die or continuing with treatment in the hopes of prolonging his life a bit longer. They chose to fight. Braden has had two MIBG treatments in Philadelphia as there are only 5 hospitals in the US equipped to do MIBG treatments. It is an IV injection of a radioactive isotope that attaches to neuroblastoma cells and can kill them. Braden's response was favorable but cancer remained. He is currently going through chemo rounds of Irinotecan and Temodar in the hopes of killing the remaining cancer. We all battle and join in BRADEN'S MIGHTY FIGHT!
Please keep Braden and his family in your prayers as Braden fights to beat this cancer once and for all! We love you so much Braden!
GO Braden!!!
Updates:
- www.caringbridge.org/visit/bradenh
- www.Twitter.com/BradensHope
Saturday, August 14, 2010
Burkitt's Non-Hodgkins Lymphoma - Olivia's story
"I took my eyes off God for just a second and the enemy filled me with fear. Thanks to prayers and friends, I was quickly re-focused. We know that our God is an awesome God and we trust him and are not afraid."- Olivia's mom
Meet Olivia:
July 2010 wasn't what the Haveri family expected, at all. Their sweet 7-year-old daughter, Olivia, was just diagnosed with Stage 3 Burkitt's Non-Hodgkins Lymphoma. This was a hard diagnosis for, not only Olivia, but her family too. Olivia had cancer.
During Hospital stays Olivia suffers from depression. She is physically tired, and in pain. Her hair has started falling out which makes Livi even more sad. This current round of chemo has Olivia tired and throwing up. With everything that has been happening, The Haveri family trust in God. They trust that our healer will completly rid Livi's body of cancer.
Currently, Olivia has sores on and in her mouth from vomiting. Please pray with us that they go away and she can eat and keep it down. Her spirit is good though, we are very proud of her.
Mrs. Emmy and Mr. Chris have to take turns being with Olivia because they have 3 other kids at home. Even though Gage is 18 and Abby is 13 or 14, Natalie is only 4. It's hard on them being away from Livi. Its rough on Olivia, too. She's only 7 and shes in the hospital fighting cancer so she cant be with her siblings like she used too.
Please keep Olivia Haveri in your prayers. Also, please include Emmy, Chris, Gage, Abby and Natalie in your prayers.
Olivia is currently getting Chemotherapy.
GO Olivia!
-Follow how Olivia is doing here- www.Twitter.com/CancerKickers
Meet Olivia:
July 2010 wasn't what the Haveri family expected, at all. Their sweet 7-year-old daughter, Olivia, was just diagnosed with Stage 3 Burkitt's Non-Hodgkins Lymphoma. This was a hard diagnosis for, not only Olivia, but her family too. Olivia had cancer.
During Hospital stays Olivia suffers from depression. She is physically tired, and in pain. Her hair has started falling out which makes Livi even more sad. This current round of chemo has Olivia tired and throwing up. With everything that has been happening, The Haveri family trust in God. They trust that our healer will completly rid Livi's body of cancer.
Currently, Olivia has sores on and in her mouth from vomiting. Please pray with us that they go away and she can eat and keep it down. Her spirit is good though, we are very proud of her.
Mrs. Emmy and Mr. Chris have to take turns being with Olivia because they have 3 other kids at home. Even though Gage is 18 and Abby is 13 or 14, Natalie is only 4. It's hard on them being away from Livi. Its rough on Olivia, too. She's only 7 and shes in the hospital fighting cancer so she cant be with her siblings like she used too.
Please keep Olivia Haveri in your prayers. Also, please include Emmy, Chris, Gage, Abby and Natalie in your prayers.
Olivia is currently getting Chemotherapy.
GO Olivia!
-Follow how Olivia is doing here- www.Twitter.com/CancerKickers
Monday, August 9, 2010
Time Flies....
5 months ago today on Tuesday March 9, 2010 precious Layla Grace Marsh went to play with the angels. She was
Only 2. As I sit here writing this with tears in my eyes I realize for the hundreth time that Layla is never returning. It has already been 5 months but it feels like yesterday. A broken heart keeps beating.
Please keep the Marsh family in your thoughts and prayers as they cope with 5 months without their baby. Pray for their strength and comfort in this devestating time.
I miss and love you so much baby Layla. Fly high precious angel!
"Time passes by so quickly. But I guess I thought you'd be here forever. I never even got the chance to- say goodbye"
Rest In Peace precious Layla Grace Marsh.
Save a place for me....
Only 2. As I sit here writing this with tears in my eyes I realize for the hundreth time that Layla is never returning. It has already been 5 months but it feels like yesterday. A broken heart keeps beating.
Please keep the Marsh family in your thoughts and prayers as they cope with 5 months without their baby. Pray for their strength and comfort in this devestating time.
I miss and love you so much baby Layla. Fly high precious angel!
"Time passes by so quickly. But I guess I thought you'd be here forever. I never even got the chance to- say goodbye"
Rest In Peace precious Layla Grace Marsh.
Save a place for me....
Friday, August 6, 2010
Burkitt's Lymphoma - Mathew's Story
"You never think these things are going to happen when you're bringing your baby home from the hospital."
Mathew's Mom
Meet Mathew:
The summer before he was set to start Kindergarten, Mathew, an active boy from central Minnesota, fell ill with what his family thought was the flu. Most of his symptoms were not out of the ordinary, his tummy hurt and he had the chills. But there were a few oddities. He was hungry and at one point was actually craving chili dogs. How odd, his parents thought, he has the flu, but is craving CHILLI DOGS? His stomach also felt hard and it was swollen.
Lives Changed with a Few Words
After a week without getting any better, Mathew’s parents took him to the emergency room. There the doctors found a large mass in his abdomen and he was later diagnosed with Burkitt’s Lymphoma. Mathew went through six months of intense treatment that was supposed to dissolve his tumor. Unfortunately he needed surgery to remove the reminder of the tumor and a stem cell transplant, which was performed by the University of Minnesota, Children’s Hospital Fairview, one of the best transplant programs in the country due to the support of Children’s Cancer Research Fund.
Attitude is Everything
Mathew maintained an incredibly positive outlook and did not even consider death as a possibility when he was going through his treatment, even though his cancer was not responding as they had hoped. Ever inquisitive, he always wanted to know everything that was going on when he was going through treatment. He wanted the doctors to talk to him, not just his parents.
Taking a Unique Path
Mathew took his own unique route to get to a cure. Mathew’s treatment was a success. Today, after having won his battle with cancer, he is pursuing acting, sports and at just age eleven, is considering a career in medicine. Again, Mathew demonstrates that he is wise beyond his years. Those who love him just want him to grow up to be happy and fulfilled.
Story: http://www.childrenscancer.org/stories-of-hope/kids-stories/matthew.html
GO MATHEW!
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