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E - Nevus Notes

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012.

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E - Nevus Notes | e-nevusnotes.blogspot.com Reviews
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A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012.
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E - Nevus Notes | e-nevusnotes.blogspot.com Reviews

https://e-nevusnotes.blogspot.com

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012.

INTERNAL PAGES

e-nevusnotes.blogspot.com e-nevusnotes.blogspot.com
1

E - Nevus Notes: May 2012

http://e-nevusnotes.blogspot.com/2012_05_01_archive.html

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012. Thursday, May 24, 2012. Time has never been on Evan’s side, and it seems that this adage remains true. But we would ask you to consider this reality: If time marches relentlessly toward a future, a future Evan wishes to embrace; should we not engage the time we have with the living of life rather than the avoidance of death?

2

E - Nevus Notes: Obituary

http://e-nevusnotes.blogspot.com/2012/08/obituary.html

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012. Monday, August 20, 2012. Evan MacGilvary Jenkins Coleman, age 13 of Raleigh NC was called home to heaven at 5:45 am Saturday August 18, 2012. After a five year battle with malignant melanoma, Evan was held in his mother’s arms as he came to eternal rest. Evan is survived by his parents, Paul and Lizy, his sister Morgan, Grand Father Re...

3

E - Nevus Notes: Hey Dad . . . When am I gonna get better?

http://e-nevusnotes.blogspot.com/2012/07/hey-dad-when-am-i-gonna-get-better.html

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012. Monday, July 9, 2012. Hey Dad . . . When am I gonna get better? So began one of the most profound conversations in the life of Evan’s family. And more important than how the question is to be answered; should or could that question be answered with any truth or integrity? 8221;, “Mercy! 8221; or “Oh Golly! All the while Evan looked out...

4

E - Nevus Notes: July 2010

http://e-nevusnotes.blogspot.com/2010_07_01_archive.html

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012. Saturday, July 31, 2010. First an apology; this news should have been shared as soon as we heard it as proof of the power of prayer; positive thinking, caring and compassion. Evan’s tumors are smaller. Let us repeat that: Evan’s tumors are smaller. And now for the rest of the story . . . . Excited voice, “Their smaller! Thanks be to yo...

5

E - Nevus Notes: July 2015

http://e-nevusnotes.blogspot.com/2015_07_01_archive.html

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012. Tuesday, July 7, 2015. The death of a child wrings you out like a chamois at a high school carwash on a Saturday morning in July. You are left damp, wrinkled, dirty and without a semblance of love discarded on a line to be dried crispier than a tortilla chip in Texas. But before I continue, perhaps a little Donald Trump humor would lig...

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everybodylovesaustin.blogspot.com everybodylovesaustin.blogspot.com

Everybody Loves Austin: Garage and Bake Sale benefiting Nevus Outreach

http://everybodylovesaustin.blogspot.com/2012/09/garage-and-bake-sale-benefiting-nevus.html

Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Sunday, September 23, 2012. Garage and Bake Sale benefiting Nevus Outreach. Please join us if you are in the area this weekend. We so appreciate all the support. Subscribe to: Post Comments (Atom). My son Austi...

e-observations.blogspot.com e-observations.blogspot.com

Observations: December 2012

http://e-observations.blogspot.com/2012_12_01_archive.html

Monday, December 24, 2012. Morgan’s Monday Message. 18 years ago today, at about noon, our beautiful daughter, Morgan Elizabeth Jenkins Coleman, was delivered by C-Section after 22 hours of labor. Today she has become an adult as she takes her first steps as an 18 year old. Today is like many of the other milestones in her life, they mark not only amazing growth for her, but also changes in the lives of her parents. Saturday, December 22, 2012. Music, Madness, and Passion. That fact should not minimize t...

everybodylovesaustin.blogspot.com everybodylovesaustin.blogspot.com

Everybody Loves Austin: July 2009

http://everybodylovesaustin.blogspot.com/2009_07_01_archive.html

Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Friday, July 17, 2009. Subscribe to: Posts (Atom). E - Nevus Notes. Checking Back with Zac. Journey to Our lil Angel in China. The Wonderful World of Vance. The Sweet Life of Sophie. News from the Nagel's.

everybodylovesaustin.blogspot.com everybodylovesaustin.blogspot.com

Everybody Loves Austin: August 2009

http://everybodylovesaustin.blogspot.com/2009_08_01_archive.html

Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Friday, August 7, 2009. I can't believe that my baby is turning 2 on August 24! We are so happy and thankful that we have made it this far! Subscribe to: Posts (Atom). E - Nevus Notes. Checking Back with Zac.

everybodylovesaustin.blogspot.com everybodylovesaustin.blogspot.com

Everybody Loves Austin: January 2009

http://everybodylovesaustin.blogspot.com/2009_01_01_archive.html

Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Thursday, January 22, 2009. Subscribe to: Posts (Atom). E - Nevus Notes. Checking Back with Zac. Journey to Our lil Angel in China. The Wonderful World of Vance. The Sweet Life of Sophie. News from the Nagel's.

everybodylovesaustin.blogspot.com everybodylovesaustin.blogspot.com

Everybody Loves Austin: September

http://everybodylovesaustin.blogspot.com/2011/09/september.html

Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Monday, September 26, 2011. Home after first shunt. In the hospital in critical condition. Subscribe to: Post Comments (Atom). E - Nevus Notes. Checking Back with Zac. Journey to Our lil Angel in China. If you ...

everybodylovesaustin.blogspot.com everybodylovesaustin.blogspot.com

Everybody Loves Austin: America's Giving Challenge

http://everybodylovesaustin.blogspot.com/2009/10/americas-giving-challenge.html

Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Tuesday, October 13, 2009. Our cause just entered in America's Giving Challenge, which gives us a chance to win $50,000! Please donate today: http:/ www.causes.com/donations/select donation method? Journey to O...

everybodylovesaustin.blogspot.com everybodylovesaustin.blogspot.com

Everybody Loves Austin: Amazing 3 year old

http://everybodylovesaustin.blogspot.com/2010/09/amazing-3-year-old.html

Austin is a preschooler with a condition called neurocutaneous melanocytosis (NCM). He has a shunt in his brain due to hydrocephalus. He is a smart, adorable little boy and this is his story. Welcome to all of Austin's friends, family and supporters! We hope you enjoy reading about his adventures. Monday, September 6, 2010. Amazing 3 year old. It's hard to believe but Austin just turned 3! There was an overwhelming feeling that day that a lot of earth shaking (at least to those in our world) information ...

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E - Nevus Notes

A journal of events surrounding the life and passing of Evan Coleman, a boy diagnosed with malignant melanoma in November 2007. He succumbed to the disease in August 2012. Tuesday, February 16, 2016. And Thanks for the Inspiration. The Giant Congenital Melanocytic Nevus that was a birthmark of biblical proportions cover his back from his neck to the cleft of his glutes, and wrapped around both sides of his body to almost meet and join over his belly button. The colors and textures were a physical rep...

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