Lisa O'Leary for Team Patrick
When it comes to love, they say when you know, you know. Well, my husband and I certainly proved that theory. Patrick and I fell in love hard and fast. I knew he was the one the first time we met for coffee, and he would have been the first to tell you the same. Patrick was the epitome of a gentleman and treated me and everyone around him with the utmost respect.
In September of 2014, Patrick suffered a seizure that landed him in the ICU. First they thought it was a stroke, then a benign cerebral deformity – all of which were scary but we knew at the end he would be okay. Unfortunately, they were wrong, and a short time later Patrick was diagnosed with glioblastoma. I promised him I would never leave his side and took a leave of absence from my job to assume the role of caretaker.
From then on our world became about surgeries, radiation, Temodar, and all that comes along with brain cancer. Patrick’s extremely complicated focal seizure condition which caused prolonged episodes of postictal psychosis led him to inpatient hospitalizations all in all totaling around five months. In the seemingly never ending confusion and turmoil, I made sure to be the one constant in his life. I made myself the best advocate I could be for his care and his number one cheerleader. There were many days when the man in front of me was not my Patrick, and I lived for the moments when I would see the switch in his eyes and he would come back to me. But no matter what we were faced with, there was never a day when Patrick didn’t know how loved he was.
Patrick and I were married on May 24, 2015. My brother-in-law performed the ceremony at our home, set to our favorite Motown hits. We knew we didn’t have long, but I wanted more than anything to know what it was like to be married to the love of my life and my best friend. Less than six weeks later on July 11, 2015, I held Patrick’s hand as he took his last breath. This was just ten months after that first seizure turned our lives upside down.
Since we said goodbye, I have struggled with all of the things that grief brings – anger, depression, a feeling of listlessness and lack of meaning. But I know that the best way to honor our love story is to keep moving forward and do what I can to fulfill Patrick’s legacy of love and service. I want to make him proud every day. I hope that sharing our story helps other caregivers understand that they are not alone, and that there will be life again – maybe just with a different soundtrack.
This year I am focusing my efforts on the Bay Area Brain Tumor Walk which will be held on 5/13/2017 at Crissy Field in San Francisco. I am a member of the planning committee and it has been a rewarding experience. I am passionate about this cause, so I’m taking action. I need your help in this fight. National Brain Tumor Society will not rest until a cure exists - but more needs to be done. Please join in my effort!
National Brain Tumor Society is fiercely committed to finding a cure for brain tumors. They are aggressively driving strategic research; advocating for public policies that meet the critical needs of the brain tumor community; and providing comprehensive patient, family and caregiver resources. Your support ensures this important work will continue.
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