Survivor Stories
Below are the amazing survivor stories of just a few of SHADE’s friends. Are you a survivor or have you been affected by skin cancer? Send us your stories to info@shadefoundation.org.
Read John’s Story · Read Meghan’s Story · Read Rachel’s Story
John
My story starts with an adventurous, blonde, boy next door, who grew up in the Midwest but spent all his summers in South Florida. He was drawn to the beach, loved the water, and praised the sun. As a result, he spent many nights suffering from excessive UV radiation. Yeah, that’s right — a sunburn! Little did he know, he was damaging my DNA and setting the stage for future drama.
I was just a kid in the 1970s and most people were in the dark when it came to realizing the dangers of prolonged sun exposure. I now pay the price with regular biopsies, surgeries, and cancer diagnoses. I am a malignant Melanoma survivor.
Fast forward to the present. About one million Americans now develop skin cancer each year and every hour one will die from melanoma. What sounds like an insidious epidemic from a science fiction movie is, indeed, a jaw-dropping reality in modern America. Bottom line, when kids blister or burn from being in the sun, trouble may loom in their future.
If I could send a message in a bottle through time to that blonde kid on the beach it would say: “Respect the Sun’s power. Get healthy doses, but don’t get burned. Protect yourself and your children! Wear sunscreen and protective clothing! Get real and spread the word!”
Your natural skin color is beautiful, so only tan from a can if you must. Examine your skin regularly and see a dermatologist if you notice anything suspicious. Examine your kids. Examine your friends! Heed this advice and control you own destiny. Don’t quote me on this, but I believe the Surgeon General determined that sunburn is the direct result of stupidity. Live smart, live strong and live long.
Thanks,
John
Meghan
- Age: 23
- Diagnosis: Stage 2 Melanoma
- Date of Diagnosis: January 2004
In January of 2004 my life was turned upside down when I was diagnosed with Melanoma at the age of 20. Since I was 18 I had been visiting tanning booths in an effort to hide my pale complexion and erase all indication of my Irish heritage, so I could “look like everyone else.” Three years later I have come to realize that looking and acting like everyone else is far from what I want to do.
Rachel D.
My name is Rachel D. In March 2008, I was diagnosed with Melanoma, the deadliest form of skin cancer. I am only 11. This is my story.
I live in a beach community in Narragansett, Rhode Island. I have always grown up on the water. My parents have a boat and all summer we water ski, kneeboard and tube. We also have a pool where I swim all day, even at night too. I always wear sunscreen 30+ because I have light skin and red hair, putting me at risk for skin cancer. I was always told that the sun could cause skin cancer because of harmful ultraviolet rays of the sun. But, until now, I never truly understood exactly what that meant.
I remember my Mom always checking my skin for freckles or spots called moles. My Mom has blonde hair, blue eyes and very light skin. She has been having spots removed from her body for a long time, all due to the sun. So I guess that’s why she always checks me even though it is very annoying.
My mom noticed this spot on my back that she said seemed to be “changing”. She told my Dad when I went to the doctors to have them measure it. The doctor said it appeared to be fine but gave us the name of a Pediatric Dermatologist. A Dermatologist is a doctor of the skin. An appointment was made and off we went.
I have to tell you, I was very nervous going to the Dermatologist. I didn’t want someone to check my skin from head to toe the way my Mother does. It was kind of embarrassing. The doctor began at my scalp. Did you know you could get skin cancer up there too? She looked at my face, neck, ears, body, arms, legs even fingers and toes. When she checked my spot on my back, she said, “my gut feeling says it’s fine, I am 99.9% sure it is nothing to worry about.” “We can monitor it.” But, my Mom wanted it gone and I am glad she did. Although, at the time, I was not happy with her.
They brought in a tray of all sorts of things including needles, which I hate the most! The needles were used to numb the skin so they could cut out the spot and stitch the skin back together. Once they give you the needle, you really don’t feel a thing. They send the skin to another doctor who looks at the tissue under a microscope. They are looking for typical (normal) cells, atypical (changing cells) or cancer.
My Dad got the phone call on a Wednesday night a week and a half later. The doctor said I was diagnosed with Melanoma In-situ, which means the cancer was on the epidermis, the upper layer of my skin. She also said I had to go in for surgery to remove more tissue to make sure they got all the cancer.
My surgery was scheduled for Good Friday at 8:30 in the morning. The surgery was done by a Plastic Surgeon because of the large cuts and amount of tissue they have to take. These doctors are trained in making the best scars. Although, my Mom, Dad and I told him we didn’t care about how big or large the scar was because all we cared about was that the cancer was gone.
This surgery was different because now I had five needles poking me in the back to numb the area. And it took longer. But, it wasn’t too bad. My Mom and Dad told me they cut a lot and deep. They also said there were so many stitches they couldn’t count and that they would eventually dissolve. They sent this tissue back to Boston where they could biopsy it. A few days later, we got the phone call again. This time the tissue was cancer free!
Now I’m just waiting for the stitches to dissolve. I also have to go to the doctors every three months, but that is OK compared to how it could have been. If my Melanoma was not caught in time it could have spread to the rest of my body. I might have had to get chemotherapy or radiation; instead I am cancer free. My Mom pretty much saved my life! My new saying is, “Make a positive out of a negative by teaching others.”
Rachel also creates and sells her own jewelry. A portion of her sales are donated to the SHADE Foundation. Support Rachel and SHADE by visiting Rachel’s Sun Safety Website.