I’m doing a happy dance over the moon because our anthology of short stories, Kissed by an Angel is here at last! This is a dream come true for a very worthy cause.
All proceeds will benefit the Sturge-Weber Foundation. Sturge-Weber Syndrome is a rare genetic condition that can cause seizures, blood clots, stroke, glaucoma, blindness, paralysis, and more.
“The Kissed by an Angel anthology includes 10 stories and one poem featuring children who are gifted or have special powers. Some are ordinary people, others are extraordinary, and several aren’t what they seem to be. Read on and be enchanted.
“Wander with us onto a magical island ship, uncover an amazing secret, and solve a very fishy mystery. Discover a World War II codebreaker, captivating garden, time machine, undercover agents, bug master, plus more. And meet a special boy who was kissed by an angel.
“This anthology benefits the Sturge-Weber Foundation. Children who have Sturge-Weber are born with a port wine birthmark, which varies in color and size, and stays with them their whole lives. “You were kissed by an angel” is how author Robyn Campbell explained to her son Christopher, who suffers from Sturge-Weber syndrome, about his tell-tale birthmark. He is the creative genius who helped choose some of the names of the characters, and he is our inspiration.”
In the words of one of our authors, 13-year-old Erik Weibel (This Kid Reviews Books blog):
“This anthology is dedicated to my buddy, Christopher Campbell, every other person who has been kissed by an angel, and the people who work to find treatments to help those with Sturge-Weber Syndrome.
“These stories are dedicated to every kid with different abilities and the people who advocate for them. I want to grow up in a world of inclusion, opportunity, and equality for everyone.”
Very well said, Erik!
Our anthology begins with this beautiful poem:
Don’t overthink it
Learn to be patient
In this moment
And all the moments that God gives me
I will cherish this life
~ Catherine Johnson
Robyn Campbell, Christopher’s mother, wrote the Foreword:
“When my son Christopher came into the world, he looked different. A dark red birthmark covered most of his body. The doctor thought the birthmark would go away in a few days. That was not to be. It was a port wine birthmark and was a sign of a devastating genetic condition—Sturge-Weber Syndrome.
When he was two weeks old, he turned blue and was unresponsive. We called the pediatrician and rushed him to the hospital. The doctor met us there and explained about Christopher’s seizure. He said he’d only seen one case of this disorder. And that was in medical school forty years previous.
The next day I went to the library, and I found a medical book that had one definition for Sturge-Weber. The brain will waste away. Armed with this knowledge, I made life great for Christopher while his father and I waited for his brain to dissolve. It was then that a neurologist told us that Christopher would die before he was two years old. Not great news for a momma and daddy to hear.
Fast forward to thousands of seizures later, an excellent pediatric neurologist, Dr. D’Cruz, family love, and much prayer, Christopher is still with us. His brain is still intact.
Sure, the seizures hurt him in more ways than one, but he loves life, and he loves the authors of this anthology. He can talk, think, count money, and he does a lot of chores around the farm. Christopher graduated from high school and works for his dad and me. He can take care of himself (for the most part).”
Robyn’s foreword is compelling and so is her anthology story, which is told from Christopher’s point of view. Writing it was extremely difficult for this mother of seven. All the emotions of the close calls they’ve lived through came flooding back, but the story is beautiful. It’s about a very special and brave little boy.
As you can imagine, it hasn’t been an easy road for the Campbell family or other Sturge-Weber families.
A few months ago Christopher was diagnosed with a brain aneurysm after going through a battery of tests. Imagine the despair this family suffered, only to find out it was a mistake. Sheesh! This will be an extra-special Christmas, knowing he’s not dealing with such a life-threatening condition.
While the port wine birthmark is a common sign of people with Sturge-Weber Syndrome, Christopher’s is unusual in that it covers about 90% of his body. It gets thick and becomes brittle and painful, so he has to have laser treatments on the birthmark every two to three months. The procedure itself is painful, but it’s necessary.
What a trooper he is. I’m amazed that he endures so much and still remains such a gentle, loving soul.
The gene that causes Sturge-Weber was discovered in 2013. It’s GNAQ. We’re all hoping this discovery will lead to a cure.
If you’d like to help raise money for the Sturge-Weber Foundation, plus be entertained by some wonderful short stories:
You can purchase Kissed by an Angel
Available in both print and digital formats.
The Campbell family and the other Sturge-Weber families thank you for purchasing this anthology and supporting them.
“Face” – A beautiful piece by Bianca Wood. This is her first single.
Robyn says, “Bianca is from South Africa and has Sturge-Weber Syndrome. Clearly, she doesn’t have a lot of the problems that most have. But that’s why she did this song. To speak for the ones who can’t talk for themselves. To teach people that this is diverse too. Don’t stare. It hurts.”
Kissed by an Angel – Contributing Authors:
Robyn Campbell – Kissed by an Angel Short Story
Yvette Carol – Grandpa and Loor
Catherine Johnson – Kissed by an Angel Poem
Lynn Kelley – Invisible
Vivian Kirkfield – Travis and Talia – Time Traveling Twins
Ellen Leventhal – Codebreaker
Suzy Levinson – Lucky Huck
Hope Lim – Master of Bugs
Theresa Milstein – The Captain’s Call
Cheryl Secomb – The Flying Fish Mystery
Erik Weibel – The Accidental Agents
Special thanks to Mikey Brooks for taking over the formatting when I got stuck and couldn’t go any further. He’s also a professional illustrator and children’s author. You can find him at http://www.insidemikeysworld.com.
Also, thank you, Kathy Halsey, for blogging about our book, Thanksgiving?Writers Giving! You Giving? and for your patience and support while hanging out in our FaceBook group. We had to wing it (pun intended), but our lovely angels guided us through the process, slowly but surely.
Did this year go by as fast for you as it did for me? What are your plans for the holidays? We haven’t put up any decorations yet. Do you think the grandkids will believe me if I tell them reindeers stole our Christmas tree? Ha-ha!
Merry Merry to you and your family!
Congrats, Lynn, and all the authors. It sounds like a wonderful project, and a great way to raise awareness of a rare condition.
Thanks so much, Lindsey. Awesome to have you stop by!
Wow, what a wonderfully interesting way you’ve put this post together. I love it, Lynn. Someone should pipe up here, I feel, on behalf of our group and say, you deserve a medal for how incredibly hard you worked on the formatting for this book. You selflessly slaved away for weeks behind the scenes. Despite the fact you have demands in your own busy life, you kept putting the needs of the anthology first. The fact the book is out in time for Christmas is because of your sweat and tears. Thank you on behalf of all of us!!! Bless.
And yes, I know what you mean re the pace of the year and Christmas speeding up. It’s the 22nd here, so Xmas is even closer for us!! 🙂
Aw, bless you, Yvette. I couldn’t have done it without your help. And your beautiful artwork inspired me to keep plugging along. I had a lot of fun with your lovely angel!
Ditto and congratulations, Lynn! I wish you all the best with this project. It is such a great idea. I have no doubt that many children will enjoy the stories. Adults as well! 😉
Thanks a million, Karen! Wonderful to have you stop in!
I LOVE YOU!!!!!!!!! What an excellent post. THANK YOU, BUDDY! We’re all jumping up and down here on the farm. SMOOCHESSSSSSSS and SQUEEZESSSSSSSSS too.
Merry, Merry bestie. You forgot to mention ALL the work you put in. So I will.
I’m there in spirit jumping up and down with all of you! Happy dance! WE DID IT! Can you believe it? Cheers, Bestie!
I am standing up and applauding you all for this! What a beautiful gesture Lynn. I know how hard you’ve worked to make this happen! This subject is one that is close to my heart. One of our dearest friends in the world (he was in our wedding 40 yrs ago), and his wife gave birth to a daughter with Sturge-Weber syndrome. A gorgeous daughter was born, Autumn, who just got married this year, almost bleed out and died as an infant. I cannot tell you the trauma our dear friends went through. They were so close to losing her. Thankfully they were able to save her. But I am so glad to hear that Christopher is still with us! My brother suffers from grand mal seizures, so can only imagine what this family has lived through. I’m sending lots of love and hugs!! 🙂
Karen, thanks for sharing this story of your good friends’ close call with their daughter, Autumn. I can’t tell you how happy I was when I read that she survived and just got married this year.
The families with Sturge-Weber loved ones are all in touch through the SW Foundation, and when one of the members is lost, it affects every family. Just before going to publication, one of the girls passed away, Ava Duchene. We added her to the dedication page: “To Ava Duchene and all those Kissed by an Angel, who have gone before us. You will never be forgotten.” *sigh*
I’m sorry your brother suffers from grand mal seizures. I hope he’s on a good medication that controls them.
Thank you for your awesome support, always and in every circumstance. You’re an amazing friend.
Ooo, my magical island ship!
Lynn, this is such a thorough and well-done post. Can I cut and paste it into my blog?
I am really proud to be part of this anthology. I know how hard you worked on it. You should be very proud.
Yes, I’m so proud of our anthology. It feels amazing to have reached this point. Sure, Theresa, feel free to copy this post. Glad to be able to help. Thanks for stopping by!
I’m going to add this post now! 🙂
Wow – that’s some heavy stuff. Thanks for tackling this project and enlightening us about how some people must live every single day.
I hope your book and the foundation do very, very well.
w/a Jansen Schmidt
Thank you, Patricia. Yes, it’s heavy stuff, and I admire these families who live with these conditions every day. They’re amazing and yet they need support to keep on keeping on. Thanks for stopping by and leaving this comment. I know all these families appreciate you taking the time to recognize them.
I am waaaaay behind on my blog reading, but wanted to say congrats on the anthology release! I had not heard of Sturge-Weber syndrome, so I learned something too. Hope you sell tons of copies for this great cause.
I didn’t put my Christmas tree up until the 16th, LOL. So you weren’t alone there!
Wonderful post, Lynn…I don’t know how I missed it…but I am so happy I discovered it tonight. 😉 And we’ve actually left our Christmas tree up because hubby loves to see it…just took off the ornaments and garlands for the summer. 😉
Thank you, Vivian! What a treat to have you stop in. I think that’s wonderful that your hubby loves the Christmas tree so much that you left it up!