Blogs from the Nevus Family

From Where I Sit

by Mark Beckwith
Blog for one of the largest, if not the largest, patient advocacy group(s) for those affected by large congenital melanocytic nevi and neurocutaneous melanocytosis, in the world.

The Baker's Sweets

by Nicole Baker
Blog about the Baker family and their adopted daughter, Ava, who has a giant congenital nevus.

The Low Down On Logan

by Stephanie Burmeister
My name is Stephanie Drought and im a mom to a wonderful little boy Named Logan. He is very special because he has a Giant Congenital Nevus.

The Little Burns Family

by Carrie Burns
I decided to start one of these things so some of our friends and family can see what we are up to all the time and so I have somewhere to put down all the joys and frustrations I face daily.

Help 4 Evan

by Debra Carr
We hope you enjoy reading about our family and our journey with our children.

Marshall Chalk

by Kate Chalk
James Marshall Chalk was born on November 14, 2008 with a rare skin condition called Giant Congenital Nevus.

Our China Angel

by Tracey Downey
Journey to Our lil Angel in China.

We Were Led to You

by Tracey Downey
By adopting a child and helping them reach their potential, they help us reach ours.

Haleigh's Story

by Crystal Greer
This is a story of struggle, of hope, of family & friends, of love, this is Haleigh's Story.

The Hase Posse

by Holly Hase
This story will be filled with joy, perseverance, and maybe a few (very few) moments of sadness.

Austin's Angels

by Jennifer King
Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). We hope you enjoy reading about his adventures.

Reid

by Maggie Mangold

Journeys with Joshua

by Christine Melton
My name is Joshua, and I was born with a rare and very special medical condition, and most people have never even heard of it.

Sweet Sophie

by Eric M.
This blog is a chronicle for family and friends to follow our adventures as Sophie grows and as we deal with her medical care related to treatment of her giant congenital scalp nevus.

Riley Anson Mitchell

by Jennifer Mitchell
Blog about the Mitchell family, and an account of their son Riley, who passed away on March 11th, 2010.

Checking Back with Zac

by Amie Moller
Zachary was born with Giant Congenital Melanocytic Nevus. This very rare condition affects only 1 in 500,000 so I guess you could say he's one in a half-million.

News From the Nagel's

by Beth Nagel
A step at a time… Our story of walking through life with God by our side.

Our Treasure in China

by Beth Nagel
Blog of Beth Nagel and her family's process to adopt a little girl from China.

Beautiful Claire

by Kelli Pavlish

Brayden's Journey

by Krystal Phillipson
Continue to follow Brayden's Journey and you will learn all about nevus.

Aiden's Amazing Life

by Melissa Rexroat
This is the journey of my son, Aiden, who was born on November 1, 2010 with Congenital Melanocytic Nevus.

The Sweet Life of Sophie

by Becky Rigby
This blog chronicles the events leading up to the adoption of our daughter Sophie and life after.

Sophie's Blog

by Amanda Travis
This blog, for my baby girl, is to keep everyone across the country who has been graciously praying for her informed about what is going on.

The Wonderful World of Vance

by Merilee Vance
We hope this blog will be a great way to inform you of what we're doing in our lives, as well as show off a few pictures of our family!

Waite Family Blog

by Amanda Waite
Blog of Amanda and Mason Waite, and their daughter Claire, who was born with a congenital melanocytic nevus on the back of her neck.

Addison's Leg

by Deb Whetstone
Blog set up to assist others that are making the same journey as the Whetstones.