Wednesday, September 22, 2010

Hemophagocytic Lymphohistiocytosis - Levi's Story


"Now I see a rainbow, but what a storm it was..."
Levi's Mom


Meet Levi:

Levi is the fourth child of Roseanne and Mark so trips to the doctor for a fever or sore throat were not uncommon for this family. With 3-month-old Levi fighting a higher than usual fever, his parents decided to bring him to Urgent Care for what they expected to be an ear infection. Doctors were immediately concerned and admitted young Levi to the hospital for additional tests.

After a sleepless night, doctors decided that Levi's condition required a higher level of care than the local hospital could offer. Upon hearing the news, Levi's mom felt numb. Before she knew it, she and her precious child were rushed to a waiting helicopter and being air-lifted to a Minneapolis Children's Hospital. After landing on the hospital roof, they were quickly escorted through the halls while nurses yelled "sick baby move." Roseanne vividly remembers everyone stopping and staring as they went running by. Within minutes Levi was on a ventilator and in a drug-induced coma. For four days Levi's parents sat in wonder and did nothing but pray and cry. No one had any answers to what was wrong.


A Rare and Frightening Diagnosis
After a multitude of tests, Levi was finally diagnosed with hemophagocytic lymphohistiocytosis (HLH). HLH is a rare disorder usually affecting infants and young children. While the exact cause is unknown, it is thought to be caused by a disorder of immune system regulation, which leads to the activation of infection fighting cells called histiocytes and lymphocytes. These cells normally travel throughout the body and destroy foreign material and fight infections. However, patients with HLH have too many of these activated histiocytes and they begin to accumulate in normal tissue and cause inflammation and damage to a variety of organs. The only known cure for HLH is a blood or marrow transplant.


Preparations began for Levi's umbilical cord blood transplant. In order to give this procedure the best chance to cure Levi's HLH, they needed to get the disease into remission. For the next four months Levi fought infections and endured surgeries and chemotherapy. Finally, the HLH went into remission and he was ready for his transplant at just seven-months-old.

Treatment at a World-Leading Hospital
The transplant alone is a relatively quick procedure and takes only 20 minutes to complete - Levi and his mother smiled the whole time; although, Roseanne's smiles were accompanied by tears of joy and relief. Levi received his umbilical cord blood transplant at the University of Minnesota Children's Hospital, Fairview. Physicians at this hospital are world renowned for their innovation in the field of blood and marrow transplants. They conducted the first successful pediatric bone marrow transplant in 1968 and the first successful double umbilical cord blood transplant in 2000.

Doctors and researchers at the U of M have paved the way in development of new standards of care using this procedure. In fact, the University of Minnesota recently completed their 5,000th blood and marrow transplant. Although thousands of transplants have been performed, the after-effects can be dangerous and sometimes deadly. Researchers are investigating different therapies and preparative regimens that may mitigate these after-effects and ultimately improve cure rates for diseases like cancer and Levi's HLH.

Hoping and Praying for their Healthy Baby to Return
Unfortunately, Levi experienced complications after his umbilical cord blood transplant. For weeks after the procedure he battled high blood pressure, vomiting, breathing issues and fevers, sometimes needing his bed stuffed with ice packs to help bring down the fevers. He was also diagnosed with veno-occlusive disease, a complication caused by the high doses of chemotherapy, which can cause the liver to shut down and result in death. His tiny body was invaded by tubes and lines, ventilators and dialysis machines, all necessary to mend this baby back to good health. Doctors worked diligently to maintain the delicate balance required to help Levi survive.

During the most trying of times, Roseanne would often look at pictures of Levi before he was hospitalized and think, "how can this be, where is my Levi?" Even though she spent nearly every waking hour with him, she missed him and yearned for the day when she could once again hold him, play with him and love him outside of the hospital walls, free of tubes and medication. That day came, a little more than two months after Levi's transplant; he was able to leave the hospital. Although not yet free of all tubes and medications, Roseanne and Levi moved into a tiny, temporary apartment near the hospital.


100 Days Later and a New Beginning
100 days after a blood or marrow transplant is often considered an important day. Typically, a spinal tap is done to measure whether or not the healthy, donated marrow has engrafted and become part of the transplanted patient’s body. Day 100 brought joy to Levi and his family. After receiving the test results, Roseanne wrote in her journal, "Levi is truly a miracle! The results from his spinal tap said NO disease at all --- ANYWHERE --- GONE!!"
One year after that dreadful diagnosis, Levi is home and thriving. The family recently returned from a restful trip to Florida where Levi thoroughly enjoyed watching the ocean and playing in the sand. Life is returning to normal and his family will never forget the journey they have been on, as Roseanne said, "It has been one year since my world changed. Now I see a rainbow, but what a storm it was..."

Story from: http://www.childrenscancer.org/stories-of-hope/kids-stories/levi.html

Thursday, September 9, 2010

6 months...

"Spread Your Wings and Fly, Layla!"


It has been 6 months today since precious Layla Grace Marsh left the troubles of this Earth to be with God. To say that I miss her would be an understatement... Layla changed my life. Now, its been half a year since she left us and it hurts like hell. Please continue to pray for her family as they cope with the loss of their angel. Fly High, Layla. I love you forever and always. Rest In Peace.

<3

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)

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!

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

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