Maggie goes to Washington
Kerrington’s Heart is taking a team, of those most interested, to Washington (virtually) this year. Read about Maggie’s 2020 visit to Washington and how you can partake in this years’ virtual advocacy event.
Merriam-Webster defines an advocate as “one who supports or promotes the interests of a cause or a group.” While this is an accurate and succinct definition of the word, being an advocate is as complex as it is gratifying, as frightening as it is empowering, and as draining as it is rewarding, and every advocate’s experience is as unique to them as their reasons for sacrificing so much of their time and energy for it are. My reasoning? HER. My beautiful little bundle of fire and sass whose sweet smile lights up every room and whose full bellied laugh makes it impossible to stay upset with her when she’s being mischievous is my motivation and my constant. She is my gentle, and sometimes not so gentle, reminder that not only her story but mine as well matters.
A year ago, I had the opportunity to advocate for Evelyn and the CHD community on a national level in Washington D.C. To say that I was terrified and intimidated would be a gross understatement, and I made my usual joke to Christy, with Kerrington’s Heart, that my fear of public speaking made me an unusual PR Director. Still, I’d been feeling moved to participate in the Conquering CHD Legislative Conference every year since Evelyn was born, so I buried my fear under too many coffees and an eagerness to make a difference and headed to the US Capitol.
The first day of the conference was intense to put it mildly. It was informative and emotionally charged and really emphasized the responsibility we were carrying as representatives of all heart families from each of our states. We heard from Congressional aides about what to expect and were given their assurances that the people we would be speaking with HEAR us and that our words and us being there carried much weight with them. We also heard from CHD warriors about their journeys and what our passion and presence meant to them. We heard from a nurse and a mother who told her heart wrenching journey of losing her child to CHD. By the end of the day, there wasn’t a dry eye in the room and you could feel how charged the atmosphere had become with renewed fervor for our cause.
The second day of the conference was comprised of our actual meetings at the Capitol. I was a jumble of anxiety but knowing that my fellow advocates would be with me and that we would get through it together bolstered me, while thinking of Evelyn and the many CHD children who were counting on me to be one of their voices, gave me the courage I needed to calm my trembling nerves. The meetings were incredible and empowering and every new person who I spoke with just fueled my passion for conveying the importance of what we are fighting for even more. Every person we met with asked questions not only just about CHDs in general but about each of our children as well. It was a long day full of walking all over the Capitol, sharing information and journeys, and sometimes even tears, but when I left the Capitol building after the last meeting, I felt energized in spite of the physical exhaustion, knowing that I had made a difference, that WE had made a difference.
This year we will be taking a team, of those most interested, to Washington (Virtually). We ask that only those who can attend, register. Please register at the link below. We will then provide you with all the necessary information to attend the virtual event! Deadline is Friday, February 12th to register with Kerrington’s Heart. If you would like to purchase tickets please visit the Conquering CHD link below.
Registration is required for the Conquering CHD Virtual Advocacy Conference.
Advocacy Conference + Pre-Conference Health Disparities Meeting
$25.00 per attendee
This ticket includes virtual admission to pre-conference meeting, advocacy conference day one, and advocacy conference day two (legislative visits)
Due to the cost of scheduling visits, registration is non-refundable after January 1, 2021
Attendance at Advocacy Conference day one is required to participate in Advocacy Conference day two
Advocacy Conference ONLY
$25.00 per attendee
This ticket includes virtual admission to advocacy conference day one and advocacy conference day two (legislative visits)
Due to the cost of scheduling visits, registration is non-refundable after January 1, 2021
Attendance at Advocacy Conference day one is required to participate in Advocacy Conference day two
Click here to see the agenda: Agenda Virtual 2.1 (conqueringchd.org)
Meet Lincoln
Child's Diagnosis: Hypoplastic Left Heart Syndrome
Has Kerrington’s Heart impacted your journey? If so, how?: Having the relationships that I've formed from meeting other heart moms, as well as a medical resource for experienced parents of these children, and the financial support often given has made our journey much easier to navigate. I have never felt alone, and always have someone who checks in on us or that I can contact if anything is needed. Before Lincoln was born, I would have never known that I would have needed this much guidance, so I am so very thankful that they were there from the beginning to see us along every step of the way!
What’s one thing you wish you’d been told at the beginning of your journey?: You think it takes a village to raise one child...try raising a special needs child! They have truly been the support system I never would have thought I'd need, and if I must be a member of such a somewhat unfortunate, unexpected 'club', I'm glad I'm in good company with all these heart mommas and families! There is nothing I regret about being accepted into the world of CHD, Lincoln makes it all so easily worthwhile!
Please share a little bit about your story: Lincoln Clay Shockey was born with Hypoplastic Left Heart Syndrome in April of 2015, and has been stealing hearts since the moment we found out his little heart was broken. Diagnosed prenatally at 24 weeks, he has undergone a series of surgical and medical procedures, including the 3 stage open-heart repair known as the Norwood, Glenn, and Fontan surgeries to treat his condition, all by the age of 2. He is spunky, super high energy, very empathetic and loving, and has yet to meet a stranger! Born to 4 older brothers, he was made to be a warrior, and enjoys crafts, playing outside, music, and of course, all things B-O-Y! Given that his medical condition is treated in Philadelphia, he was born a traveler and tourist, and visits his 'extended family' in Philly at least once a year. Most days Lincoln is playing, learning, and interacting like any other 5 year old boy, and aside from his initial condition, he has had only minor delays and minimal medical intervention since the completion of his surgical treatment. He is the center of attention and the rock of our family...even though he is little, he is mighty strong! There is nothing that can stop our little hero, and we cannot wait to see what goodness he brings to this world!