If you ask any parent in the world, they’ll probably tell you that they would do anything for their child. Our lives transform in the most profound ways the day we become parents. We acknowledge that we will take care of, treasure, and worry about the new life we have brought into the world for the remainder of our days here on Earth.
However, regrettably, there are some things that parents are powerless to stop. Each year, far too many children suffer from circumstances and illnesses that are completely beyond their control. Accidents and disease are as much a part of human life as happiness and celebration.
The day Alina and Aaron Edwards found out that their nine-year-old daughter, Emma, had been diagnosed with acute lymphoblastic leukaemia, altered their entire world. They were dealt a heartbreaking blow when physicians informed them after a few months that there was nothing more they could do to save Emma’s life, despite their obvious anguish and desperation to hold onto the hope that she could overcome cancer.
With the limited time they had left, Emma’s anguished parents resolved to do everything in their power to grant their daughter’s desires. Of course, it goes without saying that the great majority of kids would relish the opportunity to meet a famous hero in such a situation, maybe go to Disneyland or watch their idol compete on the pitch.
Emma, however, had completely different wishes. She requested permission to wed DJ, her ten-year-old boyfriend. After Sunday, I will have so much more to say and so many people to thank, but for now, my brain is simply not working properly, and I
Emma’s campaign quickly gained a lot of support from her neighbourhood. The group of supporters and volunteers took on the moniker “Emma’s Army” and decided to fulfil this young girl’s aspirations before it was too late. Emma’s family eventually received assistance in raising money from the Make-A-Wish Foundation. “Most kids want to go to Disneyland, but Emma wanted to get married, be a wife, and have three kids,” Emma’s mother Alina clarified.
Reports state that Emma and DJ had attempted to get married before their “wedding.” When they were eight years old, the two kids attempted to tie the knot in school, choosing their own groomsmen and bridesmaids from among their peers. Sadly for Emma and DJ, though, their teacher would not allow the wedding to take place, no matter how informal.
But this time, their second attempt at marriage had the support of many wonderful people who wanted Emma to have the day of her dreams, as well as the approval of their parents. In less than two days, we put it together, and everything was donated in the end. It came together so beautifully and was so wonderful, Alina disclosed.
When the big day finally arrived, it was recorded on tape featuring interviews with a few guests, including the DJ and the groom. She struck me as the most gorgeous person I have ever laid eyes on. I’ve adored her ever since,” DJ remarked. Alina, on the other hand, was gushing about her daughter’s charming young partner. She sent a tearful message on Facebook that said
Since third grade, DJ has been Emma’s “Boo bear.” I promise that watching these two adorable together will make your heart melt. Her heart leaps when DJ helps and shields her. She adores him. I also know that he adores her! He has supported her through all of her highs and lows, never letting her smile. DJ and his family will always remain connected.
Emma’s big day finally arrived on June 29 when she arrived at the location pushed by her parents in a wheelchair. For the event, she dressed elegantly in purple, and she grinned as her father led her down the aisle. After exchanging vows and rings, Emma and DJ finished the ceremony with a kiss from DJ to his bride.
Emma went back to her bed to recuperate after the wedding, but everyone could see how happy she was to have experienced her special day. After her battle, young Emma passed away a few weeks later on July 11, 2023.
Emma’s obituary stated: “On July 11, 2023, Emma Brooks Edwards passed away and was embraced by her closest loved ones as she entered paradise in the tender arms of her great-grandma Frannie Annie. Emma, then ten years old, fought leukaemia, dubbed “The imposter,” for sixteen months.
The Edwards family was completed with the birth of Emma, our little unicorn, on April 22, 2013, to devoted parents and three elder siblings. She cherished DIY projects, clever jokes, her loved ones, Jesus, and her brand-new “husband,” DJ. To everyone she encountered and to those who loved her, Emma was an inspiration. She was the most wonderful friend, cousin, aunt, “wife,” haha, sister, grandchild, and cousin. Her legacy is one of humour, fortitude, and unending love for everyone.
Emma, rest in peace. A young girl of such beauty, taken far too soon. Please join us in extending our condol
Nurse believed that the young girl’s family was not aware of what she did daily
One of the worse things is cancer, even more so when it’s concerning children.
Jonathan and Shelby thought that their daughter, Sophie, who is two years old, was suffering from allergies. She was finding it hard to breathe and her doctor thought it might be asthma. Unfortunately, it was soon going to be evident that it was much worse!
The little girl, Sophie was set to have an allergy test a few day later, but she didn’t get to take that test.
One night she stopped breathing…
For every parent it’s a worse case scenario, Her parents ran to call an ambulance and within minutes they were on their way to the hospital.
It was just at that moment that doctors finally confirmed that Sophie had a condition that was much worse than just asthma or allergies. She had developed cancer, a T-cell lymphoma.
Sophie has since then spent many months in hospital having chemotherapy, even though fighting it hard the cancer spread.
The treatment affected her ability to talk, walk, use her hands to eat, her tiny body is going through the preparations for a stem cell operation.
Shelby is keeping a constant watch over her daughter and is by her side constantly. So many times Shelby forgets to take care of herself, it’s just the only thought she has, to get Sophie better!
Jonathan and Shelby have created a Facebook page to record Sophie’s fight against the disease, they want friends and family alike to have an easy method to see updates on how Sophie is getting along. The page is called Sophie The Brave.
It’s not just family that follows the page, there are over 12,000 people following Sophie’s fight.
There is one post on the page that has especially been welcomed. Moms with sick children will also relate, very likely, to what Shelby’s said.
Shelby wrote:
“I see you. I sit on this couch all day long and, I see you. You try so hard to be unnoticed by me and my child. I see your face drop a little when she sees you and cries. You try so many ways to ease her fears and win her over. I see you hesitate to stick her or pull bandaids off. You say ‘No owies’ and ‘I’m sorry’ more times in one day than most people say ‘thank you’..”
“I see all of those rubber bracelets on your arms and wrapped around your stethoscope, each one for a child that you’ve cared for and loved. I see you stroke her little bald head and tuck her covers around her tightly. I see you holding the crying mom that got bad news.I see you trying to chart on the computer while holding the baby whose mom can’t-or won’t be at the hospital with her.”
“You put aside what’s happening in your life for 12 hours straight to care for very sick and something’s dying children. You go into each room with a smile no matter what’s happening in there. You see Sophie’s name on the schedule and come to check on us even when she isn’t your patient. You call the doctor, blood bank, and pharmacy as many times as necessary to get my child what she needs in a timely manner. You check on me as often as you check on her. You sit and listen to me ramble for 10 minutes even though your phone is buzzing and your to do list is a mile long.
“I see you. We all see you. No amount of snack baskets or cards can fully express how appreciated you are. You are Jesus to us every single day. Our children wouldn’t get what they need without you. Moms like me wouldn’t feel sane or heard without you. You save our babies and we couldn’t do this without you.”
Shelby got 26,000 likes on her post, its easy to see and understand why, all the amazing people at the hospital, the nurses, all deserve to be thanked and recognized for their great work.
Let’s all hope and pray that Sophie makes a fast recovery, and as it happens the family got some really great news, Sophie’s cancer is almost all gone!
Let’s also share Shelby’s words about the nursery and hospital staff so that more and more people can hear about the amazing work they do.
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