Wendy’s Story

Site created on December 11, 2018

I have followed quite a few CaringBridge sites over the years, but never imagined I would be here. BUT...here I am starting a site to keep friends and family updated in one place.

On December 7, 2018, I was diagnosed with a rare cancer called Ocular Melanoma in my left eye. I am still processing the news and probably still in a bit of denial about the whole thing, but I am moving forward with treatment. It's time to get this tumor outta here!!

A few facts about Ocular Melanoma (OM)

* OM is a distant cousin to skin melanoma, but they are not the same beast.

* OM is a slow growing, often aggressive form of cancer that does not respond to chemo.

* Radiation Therapy is the preferred treatment.

* It is the most common primary cancer of the eye in adults, but is still rare; your odds of getting it are about 6 in 1 million.

* Dr's don't know exactly what causes OM. However, people with fair skin, blonde or red hair, and light-colored eyes are more likely to get it.

* There is no hard evidence that links OM to ultraviolet rays.

* OM usually develops in the middle layer of the eyeball (choroid), which holds all the blood vessels that feed the inner eye.

* Symptoms include bulging eyes, change in color, poor vision, or red, painful eye, but most people do not have any noticeable symptoms.

I am sharing this with you because I gain strength from my community of family and friends. I am also a firm believer in the power of prayer and positive thoughts. Thank you for lifting me up in prayer and sending positive thoughts and love! I can't do this without it!!



Newest Update

Journal entry by Wendy Carpenter

Today is a great day!! 🩷🩷

Yesterday was my big appointment and everything looked good; the metabolic rate in the two known tumors has reduced and the spot on my shoulder blade was no longer there. All of this points to the treatment working, which is the best news possible. 

As thrilled as I am that the treatment is working, it has not come without some significant and harsh side effects, some may be life long…time will tell. Given my tumor burden is low and the immunotherapy will continue to work for some time, the team feels it is best to continue taking a break from more treatment. My body needs time to get back to a new baseline. This is another hard thing with cancer…always weighing the risk/benefit and sometimes feeling like you are making an impossible decision on what is best. I am relieved that they feel I can continue on this break and I feel so blessed to have a team that considers me as a whole person and not just treating the cancer. 

So what’s next…

I am so excited to finally be returning to work this coming Monday, April 15th. I had to postpone my original date due to the cold I picked up several weeks ago (side note: I now have a keen understanding of what a little cold will do to someone who is immunocompromised…it’s not fun!) I will continue working from home for a couple weeks as I ease back in, but I can’t wait to be back in person. 

For the next eight weeks I will continue letting my body recover. I will have another scan at the end of eight weeks to check up on everything and  we will use the data to help us decide next steps. A few years ago, I had a scare that put me on a three month surveillance plan and I HATED it…could not wait to go back to six months. Funny how things change…I am so excited that I don’t have to go back for two months…I feel like I won the lottery. Changed perspective…this is one of the silver linings of cancer. 

Over the next two months I would love prayers that my body continues to heal from the damage done by immunotherapy and that I can get back to my original baseline. Also, that I can successfully get and stay off the steroids. I am so close!! 

Thank you to everyone who has sent me cards, texts, called, stopped by and supported me. You will never know how it has carried me through some of the hardest days. 


Sharing a few fun pics from the past month that have brought me joy!


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