This is the first in a series of articles built to highlight rare hereditary cancer syndromes. This month, Heather, @ZHeatherChamp, shares her story of living with Cowden syndrome.
Genetic Counseling Note: People who carry one mutation in the PTEN gene can have several different, but related, disorders, including Cowden syndrome. Cowden syndrome can also be caused by mutations in several other genes.
People with Cowden syndrome often have skin findings, including benign tumor-like growths called hamartomas. Hamartomas are often found on the skin, mucous membranes (mouth, lips, nose) and intestines. Other rare skin findings, including facial trichilemmomas, can also be seen with Cowden syndrome. A dermatologist, or a dermatopathologist, is often the first to diagnosis these skin findings.
Individuals with Cowden syndrome are at increased risk to develop several cancers, including cancers of the breast, thyroid and endometrium (lining of the uterus). Lhermitte-Duclos disease can also be a part of this syndrome.
Tell us a little about yourself, Heather.
I’m 43 years old, I like to read, crochet, and occasionally play the piano. I also love to do genealogy work and research my family history. I have two cats named Kona and Tigger. I live with my family – my mom is a huge support to me and I wouldn’t be where I am today without her.
Before being diagnosed with two brain tumors, I had hoped to be a special education teacher. I now work on call as a substitute teacher, but am having a difficult time maintaining FT employment because of my medical management (I’ve had 32 doctors appointments since June 2015).
How and when did you learn that you carry a PTEN mutation?
I experienced symptoms in July 2011 that warranted a brain scan, after which I learned I had two separate brain tumors. Following a 13 hour surgery, the tumors were found to be benign gangliocytomas, also known as Lhermitte-Duclos Disease.
My neurosurgeon said, “I think you have Cowden syndrome.” I had my blood drawn for genetic testing and learned I carry a mutation in the gene called PTEN, which means that I do, in fact, have Cowden syndrome. I had previously survived thyroid cancer in 2003. The thyroid cancer diagnosis makes complete sense now because I had a huge goiter that was 10x larger than normal. Since my diagnosis in the Fall of 2011 I have had my uterus and ovaries removed preventively.
Do any of your family members carry this mutation?
None of them have interest in being tested, which has been a hard pill for me to swallow. I have not one woman in my family who has breast, ovarian, uterine or thyroid cancer and have no known family history that is consistent with Cowden syndrome.
How has this information that you carry a PTEN mutation changed your life?
I struggle with feeling disconnected from people. My life now includes constant doctor appointments, and I sometimes miss my “old” life. Many people don’t understand this new life of mine and are unable to relate to it. Having the knowledge that I could potentially develop cancer someday makes me feel different, and I don’t like that – it is a constant struggle for me to manage the emotions surrounding this.
Has anything positive come from this diagnosis?
I see my family through different eyes – I’m appreciative, grateful and thankful for the family that I have. I don’t know if I can yet say I am “thankful” for the brain tumor diagnosis, but if it weren’t for that diagnosis I don’t know how I would have ever been diagnosed with Cowden syndrome. Through social media I have connected with amazing people who are also living with CS, who give me the strength and hope to take each new day as it comes. I know I have my own struggles, but connecting with others gives me the courage to take the next step. While I was recovering from the brain surgeries, I had many people praying for me, even strangers. Once I had hit the year mark of recovery, I decided to pay it forward and chose to volunteer as a Literacy Tutor.
What would you like people to know about PTEN and the associated syndromes?
That it is manageable. Although it’s considered ‘rare’, there are many of us out there. You are not alone. Once you get “used” to this finding, it does get easier. Four years ago when I found out about this I felt like my world was going to crumble. And then I met other people out there who are also carriers and it gave me strength --- you are not alone.
BRCA has received a lot of media attention since Angelina Jolie’s disclosure. How does that make you feel?
I want other women who are at high risk for breast cancer (but carry a mutation other than a BRCA mutation) to feel that they have a voice, too. Sometimes, because fewer people know about PTEN, it feels like our situation is less important and less serious. It’s not a competition of course, but it has encouraged me to be more vocal about my situation. I am not BRCA positive, but I am at high risk to develop breast cancer too. I wish Ms. Jolie would have raised awareness for ALL hereditary cancer syndromes – that is what I’m hoping and helping to do!
You can follow Heather's advocacy efforts and get involved in the conversation on Twitter.