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This is my father, Joe Sabatine, doing what he loves best – preparing to fish!

First diagnosed 20 years ago. WLE on back, no further treatments suggested. January 2001 diagnosed Stage IV with met to adrenal gland, which was removed. June 2001 mets to both lungs and bone. January 2002 diagnosed with multiple micromets to brain. Passed into eternal life on Thursday, February 7th, 2002.He was 58 years old.

Joe was a loving husband to his wife Sharon for 38 years. He was loved by many, but especially by his children and grandchildren.He returned this love threefold. His laughter was distinct and would bring a smile to everyone’s face. He was the type of man who would do anything for anyone, and often did. Even in his darkest days he did not hesitate to talk with others about their cancer, and give encouragement. He had such a passion for living life to the fullest, and was quite the outdoorsman. He loved to fish, duck hunt, deer hunt, sail, camp, snowmobile, and even raced motorcross when he was younger.

My father will be missed so very much by so many people, but we all know he is in a much better place and no longer suffering. His body may be gone, but his spirit will live on in all who knew and loved him.

 
 
 


Jon Michael Warrington was born on July 10, 1973 in Minden, Nebraska to James and Candice Warrington. The second of four sons, Jon grew up in Gibbon, Nebraska, graduating from Gibbon High School in May of 1992.

As a young boy, Jon enjoyed camping with his family, swimming, playing baseball, and wrestling with his brothers. In high school, Jon excelled in football, cross-country and wrestling, competing at the state level. He played the drums in the school band. He also acquired a love for horses where he trained and competed with his mare, "Missed Flight".

He grew up in the Baptist faith, and at the age of seven accepted Jesus Christ as his personal savior and was baptized. He continued his walk with the Lord the remainder of his life.

As a very young boy, Jon was influenced by his grandfather, MSgt Charles Warrington. As a result of his grandfather's example and love of the Marine Corps, Jon enlisted in the Marines in May 1991 in the delayed enlistment program, at the age of 17.

On May 26, 1992 he left for MCRD in San Diego. After basic training, re reported for duty at Camp LeJeune in North Carolina. There he met and fell in love with Sheri Loper. They were married on May 14, 1994. In August 1995 he was stationed in Yuma, Arizona at LAV test directorate where he spent four years.

On September 16, 1995 triplet sons, Calder, Cullen, and Cody were born to Jon and Sheri in Phoenix, Arizona. After just a short time on earth, these three precious babies went to heaven. They have since been in the hearts and memories of the Warrington family. On December 31, 1996, Jon and Sheri gave birth to their fourth son, Colter Wyatt. He was the light of his father's life.

In 1999 Jon was transferred to SOI at San Onifrey, California where he was an instructor until his retirement.

In June of 1998, Jon was diagnosed with malignant melanoma. This started his four year battle with this dreadful disease. Through his continual struggle with surgeries, treatment, and hospitalizations, Jon continued serving his country as a Marine, attaining the rank of Staff Sergeant. Because of the limitations of his disease, Jon was medically retired in March of 2001.

Jon, Sheri and Colter moved back to Gibbon to be close to family and friends. Jon continued to valiantly fight his battle with cancer. He took pleasure in the times spent with family and friends.

Jon passed into heaven on Saturday, May 18, 2002 at his parent's home in Gibbon, surrounded by his family.

He leaves to mourn his passing: his wife and son, his parents, brothers, Kris and wife Pam of Gibbon, Brion of Omaha, Dan of Kearney, two nieces and one nephew, Grandparents, Charles Warrington of Gibbon and Virgil and Ruth Lusk of Minden, several aunts, uncles, and cousins, a host of friends, and Marine Corps comrades.

 
 
 

This is my dad, Sam Westmoreland, who was diagnosed with metastatic melanoma in January 2001. They found 7 brain tumors and 1 lung tumor. This is the result of melanoma on his face about 4 years ago. He was told there is no cure and that it was only a matter of time before he dies. Shortly after he was diagnosed he decided to try and fight this terrible disease. He went through a lot of chemo and radiation. After none of this worked, he was told at the end of August or beginning of September that it could be a few weeks or a few months. He was very courageous throughout his battle with cancer. He passed away on September 24, 2001. Even though we all miss him, I know he is in a better place where he will suffer no more. I pray a cure will be found soon.
 
 
 

This is a picture of my wife Brenda, 38 years old, who was diagnosed with Stage 3 Melanoma in 1996, small mole lower back. Had it removed and was told they believed it was all removed. Well four years later it returned and she was getting headaches. We both knew what it was and she had a MRI and it showed eighteen brain tumors. Brenda was a trooper all through this nightmare. She told all her friends that she was worried about me -- how I would handle all of this after she was gone. She was not worried about herself. She asked the oncologist what was going to happen, how she would die. He told her and she turned to me and said let's get out of here and she never said another word about it. We were married for 12 years they were the best years of my life and I miss her so much. I hope and pray for a cure to this insidious disease and all the misery it causes so many people. I know Brenda is with God and she suffers no more. Till I see you again my darling.
All my love,
Bob
 
 
 


My son LeRoy Smith was diagnosed with mm in Nov. of 1996. Mole on lower left back removed and sent away to PA and was told all was clear. Was diagnosed as only .7. In July of 1998 noticed lumps under left arm. I'll always remember the surgeon's sad look when he came out of surgery and said it was melanoma. Still he fought hard. Owned his own trucking business, all from hard work, went on a full year of interferon, always positive, always a smile. I never knew till he was gone, he was told then that he had between 3 to 5 yrs. He was going to beat it and be a survivor. He regained his strength and weight and we thought he was doing great. Summer of 2000 we entered our Kenosha Cty Relay for Live Event. I raised the highest single donation of over $2000.00. Then September of 2000, just after getting home from work went into seizure and rushed to hospital. Found golf ball sized brain tumor, had surgery, radiation, made 2 trips to TX to Burzinski Clinic, once again went back to work until Jan. 2001 looked in mirror and like overnight a massive lump right above his heart. Biopsy and was melanoma. Through it all he remained so strong continuing to go up north snowmobling with his family between chemo treatments. Then more small brain tumors, did the gamma knife, went on massive chemos, all to no avail, sold his business, tumors progressed and lost some speech and major crisis when he could no longer drive. Driving had been his life. He loved his flag pole, it was a gift from one of his drivers, and he died at 4:30 p.m. beautiful sunny day on Flag Day, June 14, 2001. His wife went out and lowered the flag. His twin sons were 13 on January 12, 2002. Oh, how we all miss him.
His loving Mom and Family

Tribute from the company LeRoy hauled for:
His forever smile said it all
No one loved his family more,
No one loved his friends more,
No one loved his work more,
And no one but no one loved his truck more.

 
 
 

Here is my precious sister Anissa Chambers Spann, 30 years young, who died of melanoma on July 29th, 2001. She was a beloved sister, daughter, mother of three wonderful children, wife, and friend to anyone she came in contact with. Her smile and warm personality could brighten up any room. She never had much monetarily, but she was always content as long as her husband and her children: Tommy, Clint, Taylor, and Carly were taken care of. Her battle with melanoma was a short one, lasting only three months from diagnosis, but she fought courageously, maintaining her smile and sense of humor until the end. She is gone, but SHE WILL NEVER BE FORGOTTEN, and I'm sure that Heaven is a better place now that she is there. Your family and friends Love you Anissa, and we long for the day to see your warm smile throughout eternity!!!
 
 
 


This is my Mom, Donna Reith. She was finally diagnosed with Stage III MM in July '91 after she went through 5 biopsies over the period of a year. Her Primary appeared on her nose. All 5 were read incorrectly. By the time it was diagnosed, she was Stage III with one lymph node positive for MM. She went through a total of 17 surgeries as a Stage III, many were reconstructive as they removed 1/2 of her nose due to the primary Melanoma. She attempted interferon in '91, but the side effects were incredibly severe and treatment was terminated. She remained NED until March 4, 2000 when a large lump was buldging out of her back and growing at a rapid pace. The Core Needle Biopsy indicated it indeed was Metastatic Melanoma. As months would pass, she would develop metastases in both lungs and in her brain.

She tried EVERYTHING and then some to combat this beast. She participated in two different clinical trials after FDA Approved treatments failed her. She was involved in Phase I trials for Perillyl Alcohol as well as Endostatin. She was dropped from both studies due to progression. When the brain mets caused seizures and left her unable to communicate, she decided to try Gamma Knife, without success unfortunately. Two months before she died, she developed several very large blood clots in both lungs and in one of her legs. Meanwhile, the brain mets was progressing. Mom needed to make a choice between Hospice and continuing the battle. There was no choice in her mind.......she continued to fight. She began Temador just 12 hours before she died. She was an inspiration and a Godsend to all who had the pleasure of knowing her. She loved life so much and fought very hard, always........always with a positive attitude and a smile to share even during the worst of her battle. She passed away peacefully on April 14, 2001.

To those who love her, she will forever be the strongest, most amazing woman we'll ever know.

 
 
 

My sister Irene died of malignant melanoma on July 8, 1988. She was 29 years old. She had resigned her commission as a Captain in the U.S. Marine Corps to purse full-time training for the Hawaii Ironman competition. She was diagnosed with melanoma shortly after she began her training, and died without completing the event. I completed the Vineman Ironman in July 1999 as a tribute to everything she has taught me about life and the role of happiness in staying emotionally and physically healthy. I miss her!
 
 
 


This photo of Jerry Keeling was taken only months before he was diagnosed with nodular melanoma in April 1998. He was dressed in costume for a role in one of the many plays he performed at our community theater. I'm certain that he is still singing, blending his rich baritone with the other voices of the Angel Choir.

Jerry confronted melanoma with the same quiet determination as he did most things. He resolved to stay positive and not give up, and in the end he faced death with dignity, grace, and even humor.

He left a legacy whereas by example he taught those who knew him to not dwell on what might have been, but rather to embrace the possibilities, and to not fear death as an ending, but to anticipate it as a new journey.

Gerald M. Keeling
December 11, 1951 - October 20, 2000
Son, Brother, Husband, Father, Grandfather and child of God

 
 
 


Here's Joe Tuso, dancing with his sweet wife, Jean. Melanoma took his life, but not his spirit, on Feb. 4, 2001. He fought a long and hard battle, but never gave up hope--we know he wants you all to keep up your fight in the hopes of a cure for this terrible disease. He valued all of the friendships and words of encouragement he received on this MPIP board.

He was first diagnosed in August, 1998, became Stage III in July of 2000, Stage IV in December of 2000, and passed away Feb. 4, 2001. He was willing to try ANYTHING to be around longer, even if a treatment only had a 1% chance of helping his MM, he would have pursued it. His wife, five daughters, son-in-laws, 12 grandchildren and mother will miss him greatly, but are very thankful for the wonderful impact he's had on their lives.

In one of the books he translated, Beowulf was described as "...the mildest of men and the gentlest, kindest to his people." This, too, is true of Joe.

 
 
 


Kyle Edvard Ericksen was born on 1/14/1971 and died 9/25/2000. He was 29. Kyle only lived 15 months after he was diagnosed with the beast. His treatment was experimental and it failed. He loved music, the ocean, skateboarding, his dog Tucker, his family, and life. He was the light of our life; a very big and painful hole will always remain in our hearts. We miss him so very much. He has one sister Kindra.

The following is a poem that I once saw posted on MPIP, I borrowed it, and had it put on a tile for Kyle's headstone. Music was so important to him.

Kyle, your music will always continue life is much like music. A well-lived life plays on forever in the minds, and the hearts, and in the very souls of all who hear it. Each life's song is but a blend of the notes given to us by God at the moment of our birth. We put the story to the melodies that we choose by the way we live each day. Throughout our lives, we add to this mix the notes from the lives of all who touch us deeply. And they, in turn, live on in us… and the music continues. Let Kyle's "Song" be remembered... and live on… in all who knew him.

We love you Kyle,
Mom, Dad and Kindra

 
 
 

This is my husband Randy. He was first diagnosed with melanoma in June of '95 when he had a mole removed. In January of '96, during a routine check-up, his doctor felt an lump in his neck. The following biopsy revealed what we had feared: the melanoma had spread to his lymph nodes. Randy underwent extensive surgery (modified radical neck dissection) and started a one year Interferon therapy right afterwards. He tolerated the IFN very well; he felt great and started to run again (some of you might remember his runner's story). In May 1998, the melanoma returned! It had spread to his liver, spine, adrenal gland and pancreas. He underwent Bio/Chemo-Therapy and had a partial response; meaning, that he only had a few spots in his liver and his spine left. Then, in March of 2000, he - once again - had new tumor growth in his abdomen. Unfortunately, all the therapies and surgeries he again underwent couldn't help save his life. He passed away on February 16, 2001 -- only 12 days after his 35th birthday.

Randy was the most wonderful, honest, inspiring and courageous person I've ever met. He changed my life forever and I hope, with all my heart, that he's still watching over me.

"Some people come into our lives and quickly go. Some people move our souls to dance. They awaken us to new understanding with the passing whisper of their wisdom, and make the sky more beautiful to gaze upon. Some people stay in our lives awhile, leave footprints on our hearts, and we are never, ever the same again."

~ Author unknown

 
 
 


Kenneth L. Luke
Age 44
Mar 2, 1956 -
April 18, 2000
Caregiver was Mom (Jan)

Diagnosed in June, 1994, primary mid-upper back: malignant melanoma - superficial spreading type, 0.62, Clarks Level III. He had a WLE at a major hospital specializing in MM. The SNB had not yet been developed. Other than periodic checkups, no further treatment was ordered.

In April, 1999 the melanoma returned with a vengeance, resulting in a complete left axilla lymphadenectomy (26 positive nodes). Over the next 9 months, Ken was treated at three well-known hospitals, all melanoma specialists. He had numerous surgeries, received two different vaccines, IL-2, DTIC and radiation but the melanoma continued to spread. He encountered many problems along the way and his condition deteriorated rapidly. By the end of January his liver had suddenly exploded with tumors, he experienced severe problems with IL-2, treatment was stopped and he was released from the NIH trial. In early February, a JWCI doctor said they had nothing for him and I was advised to "just keep him comfortable". Shortly thereafter, he went on hospice and passed away during Holy week, on April 18, 2000.

Ken always looked younger than his years, still played sports, loved to do stats and was known for his infectious smile and winning personality. His devotion to his family, loyalty to his friends, pride in his work, passion for sports and great sense of humor made up his wonderful persona. As a corporate accountant, preparing financial statements for an international corporation, Ken met and worked with people around the world. When he passed away, condolences poured in from all corners of the globe, each remembering a man with a great smile, a magnetic personality and one who always carried himself with class and dignity.

Throughout his battle, when bad news seemed to be the only news, Ken always remained positive, vowing that the "beast" would never steal his spirit. Ken never knew how many lives he touched and how his courage became an inspiration to all. He was truly a very special person, a brave warrior and our hero.

 
 
 

Shayna who was born on March 1st 1974 at 3:53 pm on a Friday, Shayna kept me in labor for 36 hrs (pain) and when she was born I knew she would be my life. What a beauty, she would make people stop in their tracks and say how beautiful she was, I even entered her in beauty pageants and she won 1st place every time. Aside from her beauty she was mine and I loved and doted on her. She was an only child for almost 10 yrs and wanted a baby sister or brother so much that the day I told her she was going to get her wish, she cried with joy. Shayna was born in Southern California but when she was 14 we moved to Nebraska to give the kids a better "safer" upbringing. Shayna struggled through her teen years and at the age of 20 gave birth to her daughter, the child she wanted more than anything else in the world. Shayna finally got her act together and was such a good mom. She went back to school so she could become a nurse and was working full time and taking care of her daughter. Her life was coming together when she got sick and before she knew what was going on she had a hysterectomy and all kinds of invasive things done to her body. It took my breath away that if she wouldn't have had her daughter she would never have the chance to have a child of her own. Shayna was dx. on December 21st 1996, but the worst was yet to come. She had just been given a death sentence because her cancer was so aggressive and so fast spreading that they knew it would be very hard to stop it. Melanoma a simple SKIN cancer, that is what most people think, that you cut it off and its gone, well its not a simple SKIN cancer at all. PLEASE read about it and learn because what you don't know can and will kill you. Shayna lost her fight to melanoma on September 1st.1998 at 1:04 am at her home with her daughter sleeping soundly not really "knowing" Mommy was gone for always. Shayna fought hard but it (melanoma) was to deadly to beat, she left her little sister(14) and twin brothers(6) along with her little girl(4) and a devastated Mom. Our lives here will never be the same without Shayna, but not a day or night goes by without us talking and thinking about her. A mom is NEVER ready to lose a child, it changes you forever, it is so unnatural to outlive your "baby" but because I have the blessings of my other children I will survive.
 
 
 

I am submitting this photo of my wife, Kathy Salling. The photo was taken in 1960, the year we married and the year she became a Registered Nurse (RN). Kathy was born Sept. 3, 1939 and lost her battle with Melanoma on Mar. 28, 2000. In between we had 4 kids and 7 grandkids. Kathy's primary tumor appeared in 1976 and after surgery and an experimental immuno therapy program she was pronounced "cured." In 1998 she suffered a recurrence in the form of skin mets and sub-Qs on her upper body plus liver mets. After 5 cycles of Bio/Chemo (Legha Protocol) cleared the liver mets, we started Varidose Vaccine at JWCI ( Dr. Glenn Tisman.) She subsequently developed mets to the bone ( a titanium rod replaced the humerus in her left arm), brain mets requiring radiation, stomach lining and small intestine mets plus numerous sub-Qs returned. She also had mets in her abdominal cavity outside her colon. During her 2 year fight after the recurrence, she had about 40 tumors surgically removed but in the end we just couldn't remove them all. It seems she had mets everywhere in her body except the lungs.
 
 
 

Sally & Dickey Stilwell
This is a photo of me and my husband, Dickey, who lost his battle with Melanoma at the age of 29. We were together in total just over 3 years but had only been married 5 months. There aren't words to describe how Dickey changed my life. I now know the meaning of true love. So now he is my guardian angel and I only hope that he can take care of me from the heaven's above.
 
 
 

This is Beth Brawn (on right) and her sister, Brenda L. Cervi, March 21, 1963 - March 30, 2000. Original mm removed from back in 1996, lymph nodes were clear. New spot (unrelated to first according to Dr.) appeared in October 1999. Removal and biopsy done in Nov 99. CT scan done in December as soon as biopsy came back and MM had already spread to lungs, liver and brain. She refused all treatments as they gave her 2 months to live. She opted for better quality of life rather then effects of some of the treatments she was given the choice of.
 
 
 

  Name: Paul Schmidt
  Born: 2/10/1961
  Family: Husband and father of four.
  Diagnosed stage 1: June 1999
  Diagnosed stage 4: Jan 2000
  Died: June 25, 2000
 
 
 

This is Cindy Blanc.
The MPIP is dedicated to the continued struggle against the disease which took Cindy's life but could not conquer her spirit.

We have a memorial page on the MPIP in Cindy's honor.
 
 
 

If you would like to submit a picture for inclusion on our Memorial Page, please send us an email.

Memorial Page 1  |  Memorial Page 2

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