Meet Brogan, Mairin, and Keira

Images Captured By Trevor Allen Photography

Meet Brogan. 


This sweet four-year-old was diagnosed with childhood epilepsy last year. His first seizure was just over a year ago, when he was only three, and it was sudden and completely unexpected. After a month, Brogan suffered another seizure. Within a few weeks he was having multiple seizures a day. 


Within a few months of the first seizure, the diagnosis of childhood epilepsy was made. His parents felt a sense of relief at knowing. Still, this was a terrifying time. The seizures scared Brogan, often causing tears. He has been strong and now has a better understanding of what is happening. He is cautious on bad days, which his parents stress is so important for his safety. And to other parents in her shoes, his mother says: “Epilepsy is terrifying, it’s hard, and it’s frustrating. Getting control over the seizures is difficult but you will you get there.” 


Despite these interruptions, Brogan is a boy who loves trains, cars, and trucks — his favorite movie being Cars! He is excellent at doing puzzles. He is a big help with his little sisters, who he loves so much. 


His parents hope that he will outgrow epilepsy, though it is unlikely. While there was a time his seizures were out of control, medications have helped this. He is now in control and as he gets older he understands what to do while having a seizure to avoid falling or hurting himself. “We try not to think too much about the ‘what ifs’ and take each day one step at a time.”



Meet Tiny Lights Mairin and Keira. 


These sweet twin girls recently celebrated their first birthday! While they share their journey, they each have their own distinct personality. Mairin loves dancing and making faces that make people laugh. Keira is always on the move, and she adds words to her amazing vocabulary daily!


At 20 weeks gestation, it was discovered that there were two babies and that they had TTTS (Twin to Twin Transfusion). Without medical intervention, there was almost no chance of survival for the twins, so their mother underwent surgery that saved their lives. The girls were born at 31 weeks.


The TTTS has come with many other problems for the girls. Both girls have some brain abnormalities, and it still is not certain what this will mean for their futures.  Mairin also had a cloudy, almost white left eye, which has required two surgeries.  She has no vision in this eye, and her parents are hopeful she will not lose the eye.  Because Keira was the donor TTTS twin, she was much smaller and at higher risk for brain damage in utero. She is doing great now, with only slightly delayed motor skills. Mairin, however, is significantly behind in her motor skills.


The twins’ parents worry for their girls, as there are concerns around their brain abnormalities. Still, “there are worse things than limitations.” They find that the girls compensate for their limitations in other aspects. They are happy girls with a loving family. While there have been such big worries for these sweet girls, they have proved to everyone just how strong they are.


Stories by Angela Stephen-Dewhurst

Connor's Story

Images Captured by Kimberly Rashed Photography

This is Tiny Light Connor. He has a very easygoing and has a happy disposition. He loves riding bikes, acting, and video games.


Connor was born three months premature. He weighed only 1 lb 3 oz. He was fed by feeding tube at birth and was on oxygen, which he would not have survived without. Connor was in the hospital for six months before he finally got to go home.


Connor has had struggles due to premature birth. He has chronic lung disease as well as hearing loss for which he still wears a hearing aid. He has three learning disabilities: dysgraphia, global delay, and a non-verbal diagnosis. This has made school a major struggle for Connor.


Though things have been tough, Connor maintains an amazing attitude. He is a charming and very likeable boy. He has applied for mechanics at high school, as he wants to follow in the footsteps of his dad and grandfathers. His mother’s wish is for Connor to be the very best he can be. She also hopes that he will be socially accepted and takes comfort in knowing that he has nice peers that are understanding of him.  


Story by Angela Stephen-Dewhurst

Meet Camryn

Images Captured by Cindy Moleski Photography Studio

Meet Camryn. She is only two, but holds a pencil like an artist (or so her mom thinks!). She loves music and dancing. She makes people laugh and is always hugging. “She is just an inspiration of her own!”


At 17 months old Camryn was diagnosed with severe sleep apnea as well as overly large tonsils and adenoids. There have been several other diagnoses along Camryn’s journey that have gradually gone away. Because of the severe sleep apnea, Camryn has developmental delays. Her parents felt relief at the diagnosis because Camryn had been ill for so long and had already gone through so much testing. They finally had answers and could move forward.


After surgery, Camryn’s improvements were amazing. Knowing what they were dealing with meant knowing how to help her developmentally. Camryn’s journey has been hardest on her wonderful big sister Jordyn, who was only four when Camryn was born. Because Camryn was ill, this meant a lot of attention on her and not a lot left for Jordyn, who ended up with separation anxiety.


Camryn’s parents learned a valuable lesson and encourage other parents with multiple children to not push other children aside to focus on one child’s illness. They also recommend building a support system of family, friends, and others going through similar situations. From here they see Camryn’s developmental journey only going uphill! While her mother worries that she will be behind in school, she hopes that what Camryn has been through will make her a stronger person. “She is a strong-willed girl who is ready for the world!”


Story by Angela Stephen-Dewhurst

Meet Adam

Images captured by End Of The Road Photography

Meet Adam. In only two short years this Tiny Light has already taught his parents so many things. They’ve learned to trust in God, to ask for and accept help, and that no matter how hard things get, the world keeps on turning.

When Adam was born seven weeks early, they knew right away something wasn’t right. Five days later they were given the diagnosis and they struggled to deal with the news and the many emotions attached to it. Their baby had Down Syndrome and they were in a fog of confusion for the next few weeks as Adam started his life in the NICU. 


Looking back his mom wishes things could have been different. That acceptance could have come faster. "I feel a bit sad that Adam’s first two years are over. Sad that I didn't enjoy his babyhood as much as I should have. Sad that I wasted way too many tears, and hours and weeks of worry... when I could have replaced those tears and worry with love. Simple PURE and beautiful LOVE. “

Adam gives the best smiles. He loves to wave and wave and wave. He also loves to clean up. Anything and everything goes in the garbage:  his Daddy’s wallet, Mommy’s keys or his big sister’s camera! 


“We know that our little man came to complete our family. We love him with all that we have. We look forward to teaching him... and even more importantly learning from him."

Today they are looking forward to all the excitement and challenges that their future holds. Their greatest hope for ALL their children is their happiness. Their greatest goal is to do right by them.

 Story by Sue Renaud

Say hello to Cash

Images Captured by Indi Claire Photography


Spunky, sweet and goofy.  Three words that describe this Tiny Light with the effervescent smile, and charming personality.



You'd never guess it, but at only 6 months old, this happy-go-lucky little man, Cash, has been through more than most people 10 times his age.  You see, Cash was born with Port Wine Stain, a condition that creates a reddish birthmark to cover the skin that can turn into nodules, cause seizures and even mental disabilities.  Cash also struggles with Congenital Glaucoma in his left eye, that has left him with a tube in his eye, in an effort to stave off blindness.  He endures regular MRI's, Doctors visits and laser treatments, as a part of his daily life.  But you'd never guess it, by looking at him.



Jami and Darcy, Cash's parents, describe their little man as the love of their lives, saying that Cash has always been a happy, bouncing little boy.  One look at this little family, and that statement can clearly be seen.  Cash loves snuggling into his mommy, and uses his terrific sense of humour to get a laugh out of his daddy.   Wherever Cash is, smiles are sure to follow.   His presence lights up the hearts of those around him, which truly makes him a Tiny Light.   Cash hasn't had the easiest life, and will, most certainly, have many more bumps in the road.  But, with the fierce, and palpable love of his parents, support from his wonderful family, and his sweet personality; one can plainly see that he will handle those bumps with the heart, strength and courage that only a Tiny Light can. 

Story written by Samaria Kapcsos

Nicolas' Story

Images Captured By Studio 9 Photographics

This is Nicholas.  He loves playing with the computer, reading books, and he loves cars.  He is an inspiration to his family and those who know him.He has taught them that “hope is everywhere every day.”

Nicholas has been diagnosed with Developmental Delay, Seizures and Hypotonic (meaning that he has very low muscle tone, and is not strong enough to participate in regular activities).  It was discovered that he has low muscle tone after he was born, but at that time, the enormous affects were not known.  The full diagnosis came at six months old.  His parents were in disbelief that there was something wrong with their sweet baby.

Nicolas spent so much time in the hospitals that close relationships
with many doctors and nurses were made.  At seven years old, the family was able to be home for Christmas for the first time.  Now, with the help of specialized professionals, their lives are functioning normally.  Nicholas is a happy boy who is always smiling.  His seizures are under control with two medications that he is taking for this condition.

Nicholas’ parents have a wish for him; to continue to develop and
progress.  They worry about his future, and they worry about who will take care of him when they are gone.  For now they are taking things one day at a time, doing all they can to help Nicholas’ conditions.  Their excitement continues with every goal or improvement he attains, regardless of how big or small it is!  Progress is progress.

Story by Angela Stephen-Dewhurst


Meet Madison!


Images Captured by Stephanie Fieldberg Photography


This is Madison.  Madison loves Max and Ruby.  She loves to stack paper and spin shoes.  Madison also loves ice cream.  Madison has Down Syndrome and Autism Spectrum Disorder.  She has seizures, thyroid issues, and has had Atrial Septal Canal Defect with holes in her heart, which required corrective surgery when she was just three months old.


It was not until after she was born that Madison’s parents were hit with the news that their baby had Down Syndrome.  Before this news could even sink in, she was sent to another hospital to confirm her life-threatening heart condition.  “It was a rollercoaster of emotion.”


The diagnosis of Autism is a new one for Madison.  Eleven years later, her parents feel that this diagnosis helps them to understand why Madison does the things she does.  They have taken the Autism diagnosis and are now moving forward, making things work for Madison instead of against her.  Madison’s speech is limited, so there is hope that her communication skills will improve with the help of therapy.  She is a happy girl, and no matter what in life is thrown at her, she keeps laughing and finding the joy in the small things.  Who wouldn’t be inspired by this!?


Madison’s parents do worry that she will not move past the level she is at now.  “Part of learning about life is learning how to keep going…even when times get tough.”  And it has been tough for this family!  But there have been many positives, such as learning the joy and laughter that a child with Down Syndrome can bring into your life.  “There is nothing like a hug from Madison.  She puts all of her heart into it!”

Story by Angela Stephen-Dewhurst

Charlie's Story

Images Captured by O La La Photography

Tiny Light Charlie always has a smile on his face. He loves to play with his big brother and read stories with Mom and Dad. Charlie loves his toy kitchen and also toys that make music. 

Charlie has a very rare and complex condition known as Tetrology of Fallot. This condition is caused by four heart defects that do not allow his blood to carry a normal amount of oxygen. This causes the body to become cyanotic or “blue” because of the poorly oxygenated blood that flows through his veins. Charlie’s parents found out about this condition in the 19th week of the pregnancy. His parents were shocked by the diagnosis but decided to do everything they could for Charlie even before he was born. Unfortunately, Charlie was not able to be carried to full term and was born five weeks early.  It was at that point the severity of his condition became known. 

When Charlie was just over a month old, he had to have open heart surgery to repair his heart. He weighed less than six pounds at that time, and his heart was the size of a California strawberry. After the surgery, Charlie’s heart rate skyrocketed, and he had to recover with his chest open while on a cooling bed for several days. However, the support from the health care team, as well as family and friends, helped Charlie's family through those difficult days. 

Charlie’s heart condition will continue to be monitored, and he may need further surgeries as he gets older. His parents hope that he will be stronger every day, that he will be able to achieve every goal he sets for himself, and that he will see every dream he dreams come true. 

Story by Shauna Salmon 

Anson's Story

Images captured by Bobbi Carpino Photography


We would like to introduce you to Anson.  He is nothing short of a miracle.


At just eight weeks gestation it was believed that his mom was having a miscarriage but this determined little guy held on. Anson and his mom were admitted to the hospital at 23 weeks gestation with the news that the next 48 hours were crucial. Again, Anson held on. Just before 27 weeks gestation, Anson was born. He only weighed 971 grams and dropped down to 835 grams in the first month.


No one ever imagines that their pregnancy is going to end in preterm delivery, Anson’s mommy never got to experience the third trimester and his daddy never got to feel him move. But they were both very grateful that he was born alive and that he was so determined to live. Anson was so small but also so determined to do what he wanted. And he wanted to live.


Anson was nicknamed Mr. Wiggles while the family was in Vancouver as he would constantly wiggle his way almost out of the nest in his incubator. As of right now he is doing well at his corrected age of four months. Only time will tell if he has any lasting health issues to deal with but at the moment it just seemed like little Anson just needed more time.


His mommy’s advice to everyone in a similar situation: “Take each day as it comes and allow yourself to do things for you. Don’t consume yourself with the hospital as your baby needs you to take care of yourself.”