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Saturday, January 16, 2010

Justice's Story R.I.P. little angel


Justice Christopher Calvin Myers-Cannon was born August 16th 2006 . He came into this world at 2:31pm 7lbs 12.5 oz and 20.5 inches long. Justice is the Son of Ashley N. Myers & Christopher A. Cannon both of Hagerstown, MD. He came out fighting giving his Mommie a hard labor and a few scares. After his cord was cut the doctor noticed that in Justice's cord there was a knot that could of been deadly but he was our miracle baby. He Had his Daddy's Crystal Blue Eyes that would just melt your heart when he looked at you & Light Hair and was a combintion of us both in his looks. Justice brought Joy, Happiness and Love to everyones life. He had a smile that could light up a room and turn anyones bad day into a good one. He had a laugh that you couldnt help but to smile at. He loved his bath time (after a few trys) and Loved to play peek-a-boo with his Grammy, And boy did Justice love to eat(many of times he thought he could do it himself, that did get kinda messy, but soo cute at the same time) He loved to sit in his car, and in his boppy chair he was everyones little biggie boy. And Justice knew how to watch tv starting from the day we brought him home. He loved for you and him to just lay on the floor and he would just stare at the tv. Then we got into the barney and elmo and all the fun stuff that I still to this day find myself watchin on tv. Justice loved many toys anything really that played music or made any noise or he could put into his mouth. But most of all he LOVED his Mr. Bear, which was a lil baby blue blanket that had a teddy head and arms. Mr.Bear went everywhere with Justice. He loved his magic little turtle that played music in his crib, it put him to sleep everynight. Unless I had to rock him. He was a Momma's boy 100%. He was my pride and joy, my life, my EVERYTHING. He was my Tater as I called him. Everyone always said if they were watching Justice and he was cranky all it took was for him to hear his Momma's voice and see me and he lit up with smiles and laughter. He was a very Happy & Loving Baby Boy! Justice loved his grammy as she loved her Justice Christopher as she called him. My mom was very proud of her biggie boy. She could never get anything done when me and Justice was home because she could never walk away from him. She could NEVER go shopping with out bringing him something home. He was a very spoiled lil man. He had my room and his own room filled with toys and clothes. And he was Pop-Pops 'Lil Man, they had big plans together of raceing cars and doing alot of his first. He was Pappys Bubbie (as my father called him) they were going to go to cowboy games together and I am sure my daddy was going to teach him to bowl. He was loved very much by his Aunt Vicki she hardly ever left my side when I was coming close to my due date. She was there the night I went into labor and days after she stayed with me . She is such a proud Aunt and he loved her very much. Justice loved spending his days with his Ma-Ma and Pap as they watched him while I worked. Justice was very close to his Aunt Holly and Uncle Aaron (His God Parents), Uncle Morgan and Danny & Jen.

On Jan 6, 2007 @ 1:20pm Justice passed away from Shaken Baby Syndrome and Child Abuse @ the hands of Floyd Edward Bingaman III (Bing), Justice was only 4 1/2 months old. In those few months Justice changed SOOOO many lives and brought joy to so many. I still remember taking him to the doctors and they always made over Justice and said how beautiful he was. There was always Something SOO Special about him, I just don't know how to explain it. Justice was an Organ Donor. His right and left kidney went to a 60 year old woman, his liver went to a 11 month old lil girl and his heart went to a 1 month old baby boy. At last notice, the Kidney recepient and Liver recepient was doing very well. Unfortunatly we received a letter in November 2007 that the little boy who received Justice's Heart passed away, it was very heartbreaking to us, but we try to look at it as Justice gave him and his family more time together. We sent letters and pictures to the Donor Recepients, but to date we have heard no response, we hope that will change one day.

Parents: Ashley N. Myers & Christopher A. Cannon
Grandparents: Dorothea (Dee) Myers, Paul A. Spickler, Richard (Nink) Myers, Leslie Myers & Michelle L. Cannon-Spessard

We Love & Miss You Beyond Words Justice...

Aidan's Story


February 26, 2006 began like any other day. It was a Saturday and Kate’s scheduled weekend to work as a nursing assistant in a large acute care and rehabilitation hospital. She woke at 6 a.m., dressed, and before leaving the house, kissed her three month old son, Aidan, who lay sleeping in his crib. She told her husband that she was leaving for work and closed the door behind her. What she did not know was that in that split second, her life would be forever changed.

Kate drove to work to begin her day. On her first break, at approximately 9:00am, she called her husband to check on her son, Aidan. Her husband said that Aidan was fine and that their step-daughter, four years old at the time, was playing in the living room. Kate said goodbye to her husband and that she would talk to him later. About an hour later, around 10:30am, the nursing supervisor came into the room where she was helping a patient and told Kate that she had a phone call from her husband. The nursing supervisor told her that her husband sounded scared and that she should take the phone call right away. Her husband would tell her that he had left Aidan and their step-daughter alone in the living room together for a few minutes. When he returned to the living room, he said that Aidan was in a different position and crying. He told her that when he picked up Aidan, Aidan went limp and seemed to stop breathing for a minute. She could hear Aidan in the background. His scream was shrill and high pitched and Kate knew that something was immediately wrong. She told her husband to get Aidan and their step-daughter ready and that she would be home within half an hour.

Kate left work immediately and proceeded home. She called the pediatrician on the way and explained the story that her husband had told me: that he had left the baby on the floor alone with our four year old step-daughter for a few minutes and had left the room, and that when he returned, the baby was in a different position and was screaming. Once at the pediatrician, the doctor came into the room and examined Aidan. Aidan was no longer crying, but the top of his head was beginning to swell. The pediatrician told Kate and her husband that it appeared Aidan was having a cerebral hemmorrhage, or bleeding of his brain, and that the couple needed to get to the hospital as quickly as possible. The doctor also ordered stat x-rays and CAT scans. Once they arrived at the hospital, there was a flurry of activity. Aidan had a CAT scan of his brain and several x-rays and the family was sent to the emergency room, where Aidan had an IV inserted into his arm. The attending physician came into the room and began to explain that Aidan’s brain was bleeding and that his injuries were too severe to be treated in their community hospital. Aidan needed to be transported to a children’s hospital for evaluation. A pediatric trauma team was assembled from the Children’s Hospital at the Milton S. Hershey Medical Center in Hershey, Pennsylvania and within two hours, Aidan was on his way to the Children’s Hospital.

Kate and her husband returned home to their house and packed for the trip. They arrived at the medical center later that evening. Aidan was laying in a small cradle in the Pediatric Intensive Care Unit. The physician had fitted him with a neck brace until further radiologic tests could be performed to rule out fracture in his neck or spine. They were not allowed to talk to Aidan because the doctors said that he would recognize their voices and would want to be held. Aidan was also taken off nutrition by mouth, due to the fact that his brain was bleeding and his body was beginning to shut down. Her baby who had been taking over 8 ounces of milk from the bottle that morning now could not even eat on his own. Over the course of the evening, the physicians and interns in the PICU interviewed Kate and her husband and were asked how Aidan has been injured over and over again. A caseworker from the Dauphin County Protective Services unit came to the hospital later that evening to interview the couple. Kate’s husband grew angry at the questioning and she assured him that as long as he stayed calm, everything would be fine. Her worst fears would soon unfold before her eyes.

Between 7p.m. and 11p.m. the couple was told several times by the medical resident that the neurosurgeon wanted to speak to them. The neurosurgeon was still in surgery, however, and her husband was becoming increasingly agitated. He told her that he was hungry and wanted to find a hotel where they could stay for the night. They left for the night and returned back to the hospital in the morning. When the couple returned to the intensive care unit, a nurse ushered them to a computer and explained the radiographs of Aidan’s bones. Aidan had seven fractured ribs and a fractured wrist that were in varying stages of healing. The radiologist later determined that the fractures were seven to ten days old. The nurse stated, “Now we’re really looking at this as a case of abuse.” Once this statement was made, her husband grew immediately tense. He told Kate that he was not going to stay at a hospital if he was going to be accused of abuse and he told her to drive him back to the hotel. After taking him to the hotel, they would make the hour and a half trip back to their hometown and Kate would return to the hospital alone. She begged him to stay with her and tried to convince him not to leave. He cared only that he was being accused of abuse. Kate told the charge nurse in the intensive care unit that they would return later, knowing full well that it was a lie and that she would be returning to the Children’s Hospital by herself.

Aidan was a patient in the Children’s Hospital for twelve days. He had been diagnosed with two brain hemmorhages, in addition to the broken bones that had been found. One brain hemmorhage most likely occurred on the day of the initial visit to the hospital and a previous brain hemmorhage had taken place one to three weeks prior. The neurosurgeon, Dr. Mark Dias, was able to determine this because they had cultured the blood collecting around the brain; some blood was new from the current bleeding and some blood was old, from the previous hemmorhage. Due to the fact that there was so much bleeding in the brain, however, it was difficult to pinpoint the exact date when the first hemmorhage occurred. It was also revealed later that Aidan had two fractures in his lower spine. He has two scars on his spine where those fractures occurred.

In addition, the blood vessels in his retinas had been hemmorhaged, a clinical sign that Aidan had been shaken. Scar tissue had formed on the retina in his right eye, leading to blindness, and the pediatric opthamaologist stated that the disability was permanent. Each morning, the pediatric neurosurgeon would come to the bedside and evaluate Aidan with his team of nurses, medical residents, and specialists. Most days, they would return to drain the blood that was building on his brain with a large catheter needle, sometimes returning to the bedside multiple times throughout the day to repeat the procedure. Dr. Dias could give Kate no guarantees of Aidan’s prognosis. He stated that besides evacuating the blood that was collecting on the brain, there was nothing that he could do to stop the bleeding. He also was unable to tell what damage would be permanent. Dr. Dias told Kate that Aidan could be stable in the hospital, and after returning home, his brain could shrink and he might become permanently disabled. The doctor also was considering placing a shunt in Aidan’s brain to help with the blood that was collecting around his brain. Thankfully, around the tenth day of Aidan’s hospital stay, the bleeding began to subside and it was decided that Aidan could return home.

Aidan and Kate moved out of the house and moved home with her parents. Kate filed for divorce three months later. The next six months were filled with visits to the Children’s Hospital, with follow-up appointments for x-rays, cat scans, bone scans, and meetings with the pediatric neurosurgeon and pediatric opthamologist. Aidan’s head was very swollen, even months after returning home. He also had a deep furrow in his head from where the blood had been evacuated during his hospitalization.
Aidan cried and screamed often, the same high pitched cry that Kate had heard over the phone the day he was injured. Dr. Dias later would tell the family that this cry is a hallmark of brain injury. Aidan did things very slowly and was watched cautiously for signs of any recovery, but also for signs of any delay. Aidan took his first steps at eleven months, on Halloween, one month before his birthday. The blindness in his right eye has since resolved. Kate’s family personally believes in the power of prayer and is grateful for the many friends and family who prayed for Aidan’s life and for his recovery.

Today, Aidan is a healthy and happy child, with some delays. In the first three years following his injuries, Aidan received occupational and speech therapy, worked with an educational therapist on social skills, and was followed by wraparound therapists to address his anger and aggression, controlled by the areas of his brain that had been damaged. The therapists taught Aidan to learn to hold utensils, drink from an open cup, develop social skills, and sit with his classmates. Aidan now only receives speech and educational therapy; he spends four hours three times a week with a special education pre-school classroom.

Kate has used this a traumatic experience as a way to help others. In the months following Aidan’s initial injuries, Kate received support from social workers and therapists who helped her confront the situation and the impact that it had on the family physicially, emotionally, and spiritually. With their assistance, she was able to turn a personal tradegy into a healing experience that allowed her to increase the awareness of shaken baby syndrome in Berks County. She speaks to young parents on ways to avoid losing their temper with a newborn. Kate is pursuing her Master’s Degree in Social Work at Temple University and hopes to continue to give back to families with interventions for difficult children and parenting instruction.

Kate’s ex-husband, Aidan’s father, was tried in the Berks County court system in spring of 2008 on counts of aggravated assault, simple assault, endangering the welfare of a child and endangering the welfare of another person. Because the investigation had been focused solely on him without interviewing any of the other people who had babysat for Aidan, there was not enough evidence to convict him beyond a reasonable doubt and he served less than six months in county prison. He has always maintained that he did not hurt Aidan, and has stated it was either his four year old daughter or one of our caregivers that caused the injuries. The district attorney provided evidence in court that it would have required extreme force to cause the kind of injuries that Aidan had suffered, and that a four year old child would have been unable to cause those kinds of injuries, even if she had picked him up and dropped him.

Aidan is now four years old. When he arrived in the intensive care unit at Hershey Medical Center, the neurosurgery team did not know if he would live. They said that if he did live, they could not guarantee what kind of quality of life he would have. Kate was often told that Aidan could grow to live in a vegetative state and that the future was largely unknown. Kate is grateful that God provided a second chance at life. Aidan is a bright boy, who has a keen interest in the way that things work. Most of all, he loves his friends and family. Kate is thankful for the second chance that Aidan has been given, and count their blessings every day.

Friday, January 8, 2010

Mirandas Story R.I.P sweet angel

My family tragedy began on October 2nd it was my husband's birthday and I worked all day. My husband and my two daughters walked to my work to walk me home. It was suppose to be a normal day; we were going out to dinner that evening to celebrate my husband's birthday. As we walked home, we were talking; my 17 month old daughter (Emily) was happy as could be, and it looked as if my 4 month daughter (Miranda) was sleeping. For some reason, I felt the need to pick up my 4 month old. As soon as I did I knew something was terribly wrong. Her body was limp, she was unresponsive, and her breathing was shallow. Of course, like any other mother, I was quite frightened and got home with her as quickly as possible. Fortunately for me, my own mother only lives two houses away. Still not being able to get any response, I whisked her over to my mom's house along with the rest of my family. My mom took one look at her we knew we had to call 911. So I called 911, and within minutes they were there. They took Miranda in the ambulance to the hospital and I went along, still having no clue what could be wrong with her. When I left her at 7:15 that morning, she was sitting in her swing cooing and happy. We arrived at the hospital and they worked on Miranda. All the time, I was standing there with my husband, crying and trying to understand what could possibly be wrong with my beautiful baby girl. I kept asking my husband if anything happened; was she okay all day? He said she was fine that day and that nothing had happened. I was trying desperately to help the medical field with any questions they may have had to help them discover what was wrong with my once healthy baby girl. Approximately one hour later, they decided they were going to fly her to Hershey Medical Center. My husband and I raced to meet them there, along with the rest of my family. Hours later, when the doctors came in to talk with the family, I was told my baby was bleeding from the brain. Well I was in disbelief; I was told her chances of pulling through this were very slim. The doctors left for a period of time, and I was waiting to be able to see Miranda. Some time later the doctor's came back to talk with my husband and I. They told us that this looked like a case of Shaken Baby Syndrome. I was in shock, because the only people who ever cared for our children were family members, including ourselves. I spent the next several hours with Miranda, trying to find some other reason for her injury. The next day, a social worker and police came to talk to me and my husband. They questioned me and my husband together, then talked to each of us separately. Four hours later, my husband confessed to shaking our baby girl. From that point on, my life took a whole new turn. I spent everyday and almost every hour by Miranda's side, praying for God to work a miracle. On Tuesday, October 5 th, we met with the doctors and were told our daughter's injuries were so severe that she would definitely die. I was told that the part of Miranda's brain that was destroyed controlled her thinking, sense of touch, eyesight, & hearing; everything that would make her quality of life whole was flushed away. And of course, with the brain dying there is no such thing as a replacement. So I was told that we had two choices; we could let her the way she was not knowing how long she would live, breathing only by machines and in a coma state; or we could take her off life support and give her to God. They said she would not make it more than 48 hours off life support, probably less. So on Wednesday, October 6 th, I made the decision that the best thing for my once healthy, beautiful, baby girl was to take her off the life support and give her to God. So on Wednesday evening, we took her off life support. I was able to hold my baby girl then, and had somewhat of a comfort; if that is possible when you know your child is going to die, and there is not a thing you can do to stop it but put it in God's hands. Miranda, to everyone's disbelief, lasted off life support for almost 7 days. She died in my arms on Wednesday, October 13 th, 2004 at 8 am. So I am now faced with trying to cope with the loss of Miranda, and my family being ripped apart. My husband, of course, can no longer be with us; nor do I choose to have him with us. He is not allowed to have any physical contact with my other children, and is now living with his parents awaiting charges that will be brought against him pending a thorough investigation. So I am faced with taking care of my family on my own now. I returned to work on Friday, November 12 th, 2004 - one day before the one month mark of Mirandas death (much too early). I had to return to work to be able to support my other children. I have had no help whatsoever from his family, financial or otherwise. They have not even tried to call or drop a note to see how their other granddaughter is doing. I will never understand the judicial system. It is unbelievable to me that someone can confess to a crime as heinous as killing their own child, and walk free for 5 months before charges are brought against them. My husband has since been arrested for the death of Miranda. He was arrested on March 2 nd, 2005 exactly 5 months from the day Miranda's life was snipped away from her. I have had almost nine months before writing this part of the story. I have now, through God and the great support of my family, been able to go on with life the best I can. Yes, I have good days and bad days, but just months ago I thought I would never have even a half good day. I still miss Miranda so much everyday. My whole family has been torn inside in some way or another by this. It is as if they have lost a child too. After all, Miranda was a daughter, grandchild, a niece, a sister, and most of all she was a precious child who was not given a choice as to how her life was so suddenly shortened. The only peace I have is knowing that she is an angel now with God, and I know she knows how much her mother loves her and will never stop loving her or remembering her. So now, almost 9 months later, with my brother's strong will to get this foundation off the ground, we are starting the Miranda Joy Foundation to enable us to help with and educate about domestic violence and Shaken Baby Syndrome; to keep Miranda's name alive and to bring some sort of sanity to what has happened in our lives. I want to thank you for visiting our website, and if you choose to help support us in our efforts, I thank you for that from the bottom of my heart. No family should have to go through the death of a child and especially the deliberate death of a child. May peace and prayers be with you. Just so you are aware that it has been 5 years since this happened but I carry the hurt with me every dayThank you,Amy Raymond

Malachi's Part 2

Malachi's vision is very damaged he can see but he has to be at least 6 times closer than a normal child of his age. At the aged 18months malachi has only just starting to walk. Malachi has shown that he's a fighter by doing thing they said he might not be able to do. Malachi has check up's every 3-6months for the eyes and 3-6 with the consulten.Troy will be realsed from prison over the next 4wks after doing the sentance for his crime.No jugdest is it really. x

Malachi's Story

This is to tell you my son's story. My sons name is MALACHI KEEN (KAYE) he was born a happy baby back in july 2008, but when malachi was just 8 wks old malachi was shaken quite voilently, malachi injuries were 2 bleeds to his brain , one 9mm and the other12mm he also had bleeds behind both eyes. Malachi has been left with long term damage to his eyes and his brain, but to what extent we dont know yet until he gets older. So it's just a waiting game. That on its own is quite bad but the person who caused all his injuries was his dad TROY KAYE. It took troy 3 days to own up to what he did to malachi but during this time malachi was in alot of pain and was having tests that he didnt need, if only troy had said what happened he would have saved alot of discomfort for malachi . At the time i was unaware that troy would have done the injuries.From the 5TH SEPTEMBER 2008 my life changed, malachi was no longer the same normal baby i gave birth to, but he is my special little boy i have now.From the 6th september troy owned up to what he had done but not be4 he put me through hell, because they were unsure on who had done it, both of us was cautioned and released on bail, i wasnt allowed to b with my two amazing boys or other kids under16 on my own. I couldnt take my oldest boy jack to the toilet with out being watched, it was so heart breaking to not be able to every day things with my boys. On the 6th september troy was charged with all malachi's injuries but a few weeks after troy changed his mind and said he didnt hurt malachi and then my life and the kids changed so much (social service where involed from the 3thseptember when malachi went to hospital) . Social service throught the best thing for my boys was to be taken out of my care and given to my mum because troy had said he didnt do it ,so that ment it could have been me, (i was allowed to see them 8hours a day), since that day i was fighting to get them back and prove to theto everyone i had nothing to do with malachi's injuries and on the 3rd april 2009 i won, i got then back and they are still in my care. As for troy he was sentanced to 2 year but to do only 1 in prison that was back in Febuary 09. SO I ASK ONE THING of everyonePLEASE HELP ME IN GETTING SBS (SHAKEN BABY SYNDROM) OUT THERE AND EVERYONE TO BE AWARE , IT SHOULD NEVER HAPPEN BUT IT HAPPENS MORE THAN YOU THINK. So for more information try googling it because theres alot of info about it.Before it happened to malachi i had never heard of sbs before, i think they say only 1 in5 children survive it and if they do its not with out its long term damage, it leaves them with brain damage,blindness or vision problems, behavour problems the list goes on, SO PLEASE HELP ME stop this happen to another child please just pass this on to all your friends and thier friends. thank you very much in taking the time to read malachi's story xxxx You will see when i put the pics of malachi on why i named this group ( never jugde a book by its cover) as Malachi looks like any normal little boy but he still has a mountain to climb, how big the mountain is we have still yet to find out. This is the case for alot of SBS children. xxxx

Lauras Story

Laura has now been at a special needs school for 2 years. She is now at the level of a 3 1/2 year old. She lives life to the full and is such a happy carefree child.Laura was shaken a 6 weeks old on the 6th march 2002. She was shaken/slammed and thrown against the wall. She suffered from subdural haematoma, Acute subdural hematoma also retinal bleeding behind the eyes. She had 3 skull fractures and severe bruising to her arms. She was on a ventilator for 2 weeks and had severe epileptic fits. She still suffers epileptic fits today and is on anti convulsant medication. She had an operation to remove the fluid from her brain that was slowly killing her. Her recovery is very slow and there is no guarantees that she will be able to live a normal life. Her disabilities will stay with her forever. Life is tough for laura, my other children and myself. People do not understand when my 8 year old daughter starts to have a temper tantrum over a toy in a supermarket i said she could not have. They stand stare make comments like "that child needs a good hiding", but if only they knew how hard it is for her to undertstand her world and how lucky they are that they do not have to live in this terrible nightmare. So next time you see a child misbehaving in a supermarket, before you comment, just make sure that child is not special like mine. Today she is a little girl who amazes me, she is so full of life and mkes me so very proud every day.

Zachs story part 2

Zach amaze's us everyday we have been on this sbs journey for nearly 6 years,zach has started at a new school and he his enjoying the move,as zach is getting older is development is slowing down,and the widespread damage to his brain is starting to show more,but one thing i will say is zach lives his life to the full,and despite the wiespread damage,brain injury,epilepsy,lld,learning difficulties,visuiall impairment,and a list of other probs which would take ages to list,zach never let's them get to him and is a true starzavh is now 6 years old,we have had a few appoitments the last week,which hav'nt been that good,the eye clinic are unsure how zach sees with the sight he as left in his left eye,and are unsure how is sight will turn out but say they is chance it will most likely get worse,his physio wants him to use a splint 24 hrs now on his leg as she said we could lose the abilty,she also wants him to increase his exercise's .the sbs journey is very hard with all its twist and turns Zach is now 6 years old he is my world and amazes me so very much,we have more up coming appoitments,physio on thursday zach is getting more shaky with his movements and his lld is getting more noticable,i just hope they can do something for him before we have to consider surgery as this is the next step,but zach is very high risk.In septemper zach will be going back to school,zach is not moving class this year it is sad to think if is dad had not caused such injurys he would be going into year 2 then next year going up to juniour school,though i am sad i know zach is very happy in his school and loves the class he is in.10 oct 09 thought i best all update you on zach,he continues to amaze me and the people who work with him despite all his problems he his one little boy who lives life to the full and i am so very proud of him.Now since zach was shaken/slammed we have been trying to get some kind of justice the court applied to the cica in oct 2003 criminal compenstion,well after 5 years of fighting we are hopefully near the end,the money zach gets will never take away the pain we have suffrered as a family if some said to me tmorrow you have a choice of all the money in the world or this to never have happend to zach in a heartbeat i would choice the zach option,but it did happen and as much has i would like to turn the clock back i cant,i can not change the fact zach's dad tried to murder him but what i can do is make sure zach as a comfortable live.