In Memory & Honor

Ann's Hope In Honor & Memory

A part of Ann’s Hope Foundation’s mission is to remember and honor those who have battled melanoma.

If you would like to have your loved one added to our memory page or to honor a survivor, please contact us at 262.305.1370 or send us mail at: Ann’s Hope Foundation
P.O. Box 376
Hartland WI 53029.

2018 Memorials

Jennifer Birney

Honorary Chair

Here’s my disclosure: 100% honest, my entire life I’ve been a lover of the sun.  I have had many glorious tans in my life, but I’ve also been sunburned more times than I’d like to admit.  Back as a teen I baked in tanning beds, even had a tanning lamp of my own, spent plenty of vacations and summers in the good ol outdoors probably with baby oil or some fabulous smelling tanning oil…and who am I kidding, I still love to absorb the sun now, just without oil.  Yes, I do now wear sunblock (most of the time) and have SPF in my daily face moisturizer, but I’m guilty of probably not always protecting my skin as much as possible or reapplying as recommended.

Here’s how my recent journey began…

My husband Steve must of been admiring my derriere (haha!) and brought to my attention a dark spot on my butt cheek.  Was it chocolate, lint, a wood chip, dust, dirt, anything I could flick off?  Nope…it was a very dark mole/freckle with regular boarders like an eraser top in size if not smaller. I was never aware of this spot and assumed it must of recently taken up real estate on my tush.  Seemed to be an odd spot since I don’t often sun my butt cheeks and I’ve never considered myself a moley person.  Sun spots, yes I have plenty of them on my shoulders, chest and back.  When my daughter was in elementary school, the Cheetah Girls were the big thing on Disney. She once asked me if she could take me to show and tell as a real live “Cheetah Girl” due to my sun spots. She thought I was legit part cheetah or probably a founder of the Cheetah Girls, ha!  Anyway, I thought about this new mole/spot, tried to brush off my thoughts figuring it’s fine right?!?!  But then realized, um Jen…pull it together, this is a red flag and anyone that knows me, knows I love the sun, and probably has a fair share of sun damage and over exposure in my life.  This was my wake up call that I’m grateful for.  I knew deep down that I need to be seen, checked over head to toe and leave it to the experts to determine if it’s something or nothing.

I made an appointment in early-mid September 2017 with my family doctor physicians assistant who I’ve known 30 plus years.  She checked me head to toe and the only spot that raised a red flag to her was indeed that dark spot on my butt cheek.  On 9/19/17, I had that spot surgically removed. The spot had regular borders, was dark in color and was just considered a nevus at that point.  Quick, easy, a few stitches and then we waited for the pathology.  I was told if it’s bad news, you’ll likely hear something quicker than if it’s benign.  Steve took out the stitches for me 10 days later (his first attempt at this and job well done I might add) and I still hadn’t received the results.  I felt relief knowing, no news is good news…or so I’d hoped.  I sent a message to the physicians assistant asking her to follow up and she had notified me that it was still being reviewed.  The biopsy had been read my multiple pathologists and was being forwarded on to an additional specialist as the results kept coming back as “small lesion challenging to decipher”.  The specialist reviewed it and brought back the final diagnosis.  On 10/3/17 I was diagnosed with “Malignant Melanoma In Situ”.

I took a picture of the spot before it was removed.  Why?  Just in case it was abnormal, I wanted people to see something that could seemingly appear to be fairly normal, can actually be abnormal. I (and thanks to Steve) indeed literally saved my ass and if I can help you save yours or others, that’s my whole reason for sharing this.  I don’t want or need sympathy or pity, but want to encourage you to get naked and get checked.  I avoid the spotlight most of the time.  Most people that know me or truly know me know that I’m actually quite shy or guarded (until I am comfortable with someone).  I don’t share too many intimate details of my personal life and family life online or social media.  I embrace and cherish my family so much and prefer to keep most of it all near and dear to me, live it, embrace it and not put my every thought, opinions and moments on social media for everyone else (even though I share many portraits) and fun events we’ve done or are doing.  I put some additional thought into my current situation wondering, do I keep it quiet and carry on or do I bring awareness and possibly shed some light.  I decided it’s the right thing for me to share this and if I can convince you to get checked, ask your friends and family to get checked, keep record of your spot/s, be aware and take action on any changes, it’s worth me bringing myself into the spotlight and sharing my current reality with you.

Now what?  I will be having some upcoming and ongoing follow ups, plus an additional wider excision procedure to remove more (even though the margins were all clear).  I won’t be sharing frequent updates online, but I want you to be aware of what my melanoma looked like and ask you to please check yourself and be seen if something raises a red flag for you. Better safe than sorry!  I’m sure all melanomas don’t look the same, but I have malignant melanoma and I’m sharing mine.  Be aware and don’t wait!

Here’s the good news, I caught it early and I pray it doesn’t spread or reappear.  I am hopeful that I will be OK and will be hyperaware with anything I see.  I’m not going to lie…it made me feel like I been punched in the gut for no reason after being told I have malignant melanoma.  I’ve been feeling many emotions due to having a diagnosis that no one ever wants to hear, but I am strong, I will do everything I can to overcome this and I’ll tackle this being as positive and optimistic as I can. I will continue to work and live life to the fullest, just like I did before joining the cancer club…that will not change.  I have so much left to do here, so much more to give, experience and share…so cancer, you might be tough, but I’m going to show you just how strong I can be.

A few things I’ve recently learned about Malignant Melanoma. Melanoma only accounts for about 1% of all skin cancer cases, according to ACS.  But it’s the deadliest type of skin cancer, with more than 9,000 Americans dying from melanoma each year, according to the CDC.  It’s a cancer that arises from the melanocytes in your skin, which are the cells that produce the pigment of your skin and it causes new moles or changes existing ones into cancerous ones.  Researchers don’t know what causes melanoma, but being exposed to UV light increases your risk for developing it.  90% of melanoma cancers are due to skin cell damage from UV radiation exposure. Having fairer skin, history of blistering sunburns or a family history of skin cancer increase your risk as well. Luckily, melanoma is usually easily treated with surgical removal if caught in an early stage. If melanoma spreads beyond the skin, it can require more extensive treatment. Melanoma can develop in places that don’t see the sun…like between the toes, under your nails, in your eye, under a tattoo or even inside your lady parts. Get acquainted with your skin and get a thorough check by a doctor once a year. Do your own skin exams monthly. Try getting a partner, friend or family member to help out with those hard to see areas.

Follow the ABCDE Rule: A stands for asymmetrical, B stands for border, C stands for color, D stands for diameter and E stands for evolving.

When melanoma is found early, it is easily cured with simple outpatient surgery.  Melanoma can spread, come back or reappear at any time.  When found in later stages, it may become life-threatening, and there are few effective therapies to treat metastasized melanoma.

Take care, love the skin you’re in and get checked!

Jennifer Birney

2018 Memorials

Katie Haugen • 12/10/82 – 2/16/18

Katie Haugen, age 35, passed away on Friday, February 16, 2018 at home with her husband, parents and siblings by her side. Born in New Prague, MN on December 10, 1982 to Ray and Trudy Schueth. Katie was a graduate of Lourdes in Rochester, MN, 2001 and earned her Bachelor of Science Degree in Special Education form the University of Wisconsin, Eau Claire in 2006. Katie married Keith Haugen on December 11, 2010 and together they have a 3 year-old son, Hudson. Katie was a Special Education Teacher at Sam Davey Elementary in Eau Claire, WI for 10 years. While teaching, she also coached Special Olympics and provided respite care for children with disabilities. Katie’s world revolved around her little man whom she lovingly referred to as “H”. Together they went on many adventures while she taught Hudson about the world around him. Some of her favorite things to do were spending time with family and friends and focusing on her passion for health and fitness. She ran multiple long distance races, including half-marathons, 10k’s and 5k’s. She inspired others to be the version of themselves with her gentle encouragement, positivity and unwavering support.

Katie spent the past year inspiring all she came in contact with her grace and strength as she bravely fought Metastatic Melanoma.

Katie is survived by her husband of 7 years, Keith, her beloved son, Hudson, her parents Ray and Trudy Schueth, siblings Brad, Eric and twin sister Kari. She is further survived by her grandparents, nephews and nieces, aunts and uncles and cousins.

Craig Harasha


Craig Harasha was a man who lived his life with integrity. He was true to himself and deeply cared for those around him. Craig was a dedicated employee of Alliant Energy and a committed member of the Cascade Nation Ski Patrol. He was an outdoor enthusiast with a passion for skiing, hiking and biking. He also enjoyed reading and spending time with friends and family. He was quick to help anyone who needed a task completed and loved to give a helping hand.

Craig was diagnosed at the age of 42 with stage 4 melanoma after finding a lump on his upper back. His short battle with melanoma was fought with courage and dignity and he endured two rounds of chemotherapy, Gamma Knife, whole brain and other radiation. The beast known as melanoma took his life in just six short months.

Craig was a loving son, brother, uncle, friend and nephew and is deeply missed by all. They are each saddened that his life was cut short by this horrific disease.

Craig was alive at the inception of Ann’s Hope Foundation and we now continue these efforts in his memory. Life is all about the journey; Craig’s journey was comprised of simple pleasure and heartfelt giving.

Richard Cibula


Husband, father, grandfather, friend, Richard was 63 years old and just beginning to experience retirement when melanoma ended his life. Richard enjoyed many activities with his wife Jan and children Anne and Eric, including skiing, cycling and golfing. Richard volunteered in numerous charity events and loved giving back to his community.

Richard’s melanoma was first discovered with a black area on his toe. He endured surgeries and a year of Immunotherapy before relapsing and losing his two-year battle to melanoma. He lived long enough to see his third grandchild, Phoebe, born. Ann’s Hope Foundation was started in memory of Richard by his daughter, Anne Frentzel.

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