CdLS Foundation

Giving Tuesday
2025-12-02
Use GivingTuesday to Support the CdLS Foundation!
Mark your calendars for December 2. It is the annual celebration of GivingTuesday, a global movement that inspires people to give, collaborate, and make a difference. This special day is all about turning generosity into action, and it’s the perfect opportunity to support the CdLS Foundation.
Whether you choose to donate, share our mission on social media, host a fundraiser, or simply spread kindness, every act of generosity counts. Your support helps raise awareness and provide critical resources for individuals with CdLS and their families and professionals caring for them.
Together, we can transform compassion into real change. Join the CdLS Foundation this GivingTuesday and help us continue our mission of support, education, and hope.
Everyone has something to give; what will you give on December 2?

Stay Covered: Open Enrollment Essentials for Rare Disease Families
2025-11-19 14:00 - 15:00 UTC
Health Insurance is changing …are you ready? Join NORD on November 19 at 2:00PM EST for a webinar to help members of the rare disease community understand what to look for during open enrollment. We will provide tips for choosing the right health plan so you can keep getting the care and medicines you need.
Register here

CdLS Foundation November Virtual Support Group for Parents
2025-11-13 19:00 - 20:15 UTC
The CdLS Foundation is pleased to offer Virtual Support Groups for Parents, providing a consistent opportunity to connect, share, and support one another. The November Support Group topic will be resources.
Thursday, November 13, 2025
7:00 – 8:15 p.m. ET
📍Topic: Resources
We believe no parent should walk this path alone at the CdLS Foundation. As caregivers, you are the backbone of our community, and we see you. We understand the emotional and physical challenges that come with your role.
These virtual gatherings are here to help you:
• Connect with others who understand your journey
• Share and receive meaningful advice
• Feel heard, supported, and uplifted.
Whether you’re new to the CdLS community or have been walking this road for years, we invite you to join us for an hour of connection, understanding, and encouragement. You belong here.
Sessions will be held on the first Thursday of every month and will focus on connection and support.
To register, visit: https://bit.ly/cdlsnov25.

Parent University: Parent Panel – Let’s Share Experiences and Learn From Each Other. Search for Peace of Mind and How is it Best Created? – The Path to Peace of Mind
2025-11-13 12:00 - 13:00 UTC
We all have differing experiences as we think about the future. The best way to learn is from others. Le’t hear some great ideas and pitfalls to avoid. Share the best things to try, and what you might avoid. This is a HOPE session, and you will learn IT IS possible, but that you are probably never done. We will hear from parents who are veterans at this, and some who might be just starting their journey.
Register now

Honoring Our Love: Navigating Grief During the Holidays Support Group
2025-11-11 18:00 - 19:00 UTC
Honoring Our Love: Navigating Grief During the Holidays
A Supportive Gathering for Parents Who Have Lost a Child with CdLS
The holiday season is often described as a time of joy, celebration, and togetherness. But for parents who have experienced the profound loss of a child, these months can also bring waves of grief, longing, and tender memories. The sparkle of the season may feel dimmed when the absence of your child is so deeply felt.
The CdLS Foundation, in partnership with Courageous Parent Network, invites you to a heartfelt webinar created just for you—a safe and compassionate space to gather, reflect, and honor the love you continue to carry.
Event Details
Date: Tuesday, November 11, 2025
Time: 6:00 p.m. ET
Location: Online via Zoom
What to Expect
Together, we will gently explore:
Why grief can feel especially heavy during the holidays
Ways to hold both your sorrow and your love
Meaningful rituals to honor your child in holiday traditions
Practical tools for navigating family, social gatherings, and emotional triggers
How leaning into grief, rather than pushing it aside, can nurture healing
This gathering will be led by Jennifer Siedman, Director of Community Engagement at Courageous Parent Network and a bereaved parent herself. With wisdom, compassion, and lived experience, Jennifer will help guide a conversation of connection, hope, and remembrance.
You Are Not Alone
In this season when absence is deeply felt, community matters more than ever. By joining us, you’ll be among parents who understand, sharing a space where your child’s memory is honored, your grief is validated, and your love is seen.
Register Here
Let’s come together to honor our children, our grief, and our enduring love—finding comfort in each other’s presence this holiday season.

Children Have Spiritual Lives, Too. Exploring the Way Children Connect in Their World.
2025-11-10 20:00 - 21:00 UTC
Join CPN and chaplain and researcher Amanda Borchik, MDiv, BCC to learn about the ways children express their unique spirituality and to discuss ways that we as parents, caregivers and clinicians can nurture their spirit.
This event will take place on Monday, November 10th at 8:00 pm ET (7:00 pm CT, 6:00 pm MT, 5:00 pm PT).
Register here.

California Family Gathering
2025-11-08 11:00 - 15:00 UTC
Join families from California for a CdLS Foundation-sponsored Family Gathering.
Saturday, November 8, 2025
11:00 a.m. – 3:00 p.m. P.T.
Graciously hosted by: Traci, mother to Jacob Weber
Sweet Shade Ability Center
15 Sweet Shade
Irvine, CA 92606
Family Gatherings are planned with your whole family in mind. There will be activities for everyone. You’ll have the chance to meet families in the area who share similar challenges and triumphs as parents of children with CdLS.
CdLS Foundation staff, Clinical Advisory Board members, and local organization OC Music Services will be in attendance.

*Disclaimer: This event is a private reservation and is not endorsed by the City of Irvine.
Register here!

Cornelia de Lange Syndrome Foundation 11th Scientific Symposium
2025-11-07 08:30 - 17:00 UTC
Join us for the Cornelia de Lange Syndrome Foundation’s
11th Scientific Symposium
Toward Therapy for Chromatin Disorders: CdLS and Beyond
Friday, November 7, 2025
8:30 a.m. – 5:00 p.m. PT
Beckman Center of the National Academies of Science & Engineering
100 Academy Way
Irvine, CA 92617
We will explore some of the most exciting frontiers in science—delving into CdLS and related disorders of chromatin, transcription, and RNA dysregulation. Our challenge, and our shared opportunity, is to connect these insights into biology and mechanisms with pathways that lead toward meaningful therapies.
We are also proud to offer AMA PRA Category 1 Credits™ for continuing medical education.
Register now at https://cdlssymposium.com/cdls-foundation-scientific-symposium-registration-form/
Attend in-person or virtually.
We invite you to present your latest research in CdLS and related fields during our dedicated poster sessions. Poster abstract submission instructions can be found on the registration page.
For a detailed schedule, speaker bios, and more information, please explore our official event website: https://cdlssymposium.com/
We look forward to seeing you there!

Adolescent and Adult Multidisciplinary Clinic
2025-11-01 | Harvey Institute for Human Genetics, Greater Baltimore Medical Center, 6701 N. Charles St., Suite 2326, Baltimore, MD, 21204, United States
This Foundation-managed, free clinic occurs twice yearly at Greater Baltimore Medical Center (GBMC) in Baltimore, MD. Foundation Medical Director Antonie Kline, M.D., Director of Clinical Genetics at the Harvey Institute for Human Genetics at GBMC, has led these clinics since 2001. Any individual age 12 or older with CdLS can attend with their families.
Presentations on the following topics from CdLS Clinical Advisory Board members: Behavioral Psychology, Child Psychiatry, Gastroenterology, Genetics, Gynecology, Neurology, Pediatric Ophthalmology, Speech and Language, Urology. Live Q&A with CdLS Clinical Advisory Board Members.
For more information on the clinic or to secure your spot, contact Whitney Rinaldi or call 860.676.8166.

CdLS Foundation Texas Family Gathering
2025-10-19 11:00 - 14:00 (America/Chicago)
Join families from Texas and surrounding states for a CdLS Foundation Family Gathering.
Sunday, October 19, 2025
11:00 a.m. – 2:00 p.m. CT
Graciously hosted by: Tiffany, mom to Tristan and Olivia, and Bailey, mom to Carson
Windhaven Meadows Park
5400 Windhaven Pkwy
Plano, TX 75093
Family Gatherings are planned with your whole family in mind. There will be activities for everyone. You’ll have the chance to meet families in the area who share similar challenges and triumphs as parents of children with Cornelia de Lange Syndrome (CdLS).
Click here to register!

Walk for Will and Hope
2025-10-19 09:30 - 12:00 UTC
Time: Registration begins at 9:30; walk begins at 10.
– No advance registration required.
– 2-mile walk on Stony’s paved path at your own pace. We’ll have coffee, donuts, bagels and juice.
– Even if you can’t walk, it’s a wonderful opportunity to connect with other families impacted by CdLS. Last year, we had 4 families with direct CdLS connections — three who have children and whose daughter had CdLS and died as an infant.
– There is a $10 daily park entrance fee to get into the park unless you have an annual Huron-Clinton Metroparks pass.
– Dogs are welcome but must be on a leash.
– We walk in the rain or shine. We’ve done both!
– This is the only event of its kind in Michigan.
– Call/text Maureen Feighan-Kurth at 248 701-9955 with any questions.
The walk was started in 2009 in honor of Will Kurth and his sister, Hope, both affected by CdLS. Will was born in Royal Oak, Michigan in 2004 and spent three months in the NICU before he died from respiratory issues. His sister, Hope, was born three years later, in 2007, also with CdLS. She spent two weeks in the NICU before coming home and has been full of sass and determination ever since. She turns 18 on Oct. 31.
The walk aims to honor not just Will and Hope, but all people impacted by CdLS. More importantly, it raises awareness of this rare condition, bringing together other families impacted by the syndrome. Since it was created, approximately 10 families with children with CdLS have walked with us, along with their loved ones. We’ve also raised more than more than $70,000 for the CdLS Foundation over the last 16 years. The Smith family and their daughter, Liz, have been important partners in organizing the walk every year.
If you can’t join us on Oct. 19, we’d love your support no matter what. We’re so grateful to everyone who has played a role in raising awareness of CdLS and being a part of the walk.
To support the Walk for Will and Hope click here.

Date: Sunday, Oct. 19
Location: Stony Creek Metropark, 4300 Main Park Road, Shelby Township.
Starting from Baypoint Beach Picnic Shelter. Look for the “Will & Hope” signs.
Time: Registration begins at 9:30; walk begins at 10.

Baltimore Running Fest
2025-10-18 | Baltimore
It was an unforgettable weekend at the Baltimore Running Festival! Team CdLS Baltimore didn’t just cross finish lines; they surpassed their fundraising goal, raising over $16,700 for families affected by CdLS. Thank you to everyone who ran, cheered, and volunteered.
Congratulations to the Team on your incredible accomplishment! You committed months ago, trained through it all, and showed up ready to run for a cause bigger than yourself. Thank you to our Curb Crew for bringing the energy, signs, cheers, and love from sunrise to the finish line! And a special thank you to our Team Ambassadors Sydnie, Peyton, Amanda & Liam, you remind everyone why we run.

Thank you for every stride and see you in 2026!If you are interested in being on Team CdLS Baltimore 2026 or be a part of our Curb Crew, please email Lisa Schreoder, Event Manager at lschroeder@cdlsusa.org.
Event details will be posted when they become available.

We are delighted to invite you to become a part of Team CdLS Baltimore for the 25th Annual Baltimore Running Festival, taking place on Saturday, October 18, 2025! This exciting event promises a vibrant atmosphere filled with energy and camaraderie. As you lace up your running shoes, you’ll not only be participating in an exhilarating day of racing but also making a significant impact in the lives of those affected by Cornelia de Lange Syndrome (CdLS).
Together, we can rally to raise awareness and essential funds for the CdLS Foundation. Your involvement is crucial, and every step you take will help illuminate the path forward for this meaningful cause. Join us in making a difference! Your participation truly matters!
Contact Lisa Schroeder for more information!
Register Now!

Knowing The Rights for your RARE Child, (Or Yourself) Webinar
2025-10-16 12:30 - 14:00 UTC
Global Genes invites you to join us for the 8th and final session of our year-long virtual patient summit.
Knowing The Rights for your RARE Child, (Or Yourself)
📅 Thursday, October 16th | 🕑 12:30 – 2:00 p.m. ET
Understanding your legal rights is critical to effectively advocate for your child and yourself. Join us for an empowering panel discussion.
This session will cover essential topics such as:

Navigating insurance policies
Understanding education laws
Accessing healthcare services

You’ll leave with practical tools to advocate confidently, communicate persuasively, and lead effectively within complex systems. Together, let’s strengthen our voices and ensure every child has access to the rights and services they deserve.
Register here: http://bit.ly/4mRpUmT

37th Annual Amber Gaines Memorial Golf Classic
2025-10-13
Thank you to our sponsors, golfers, and donors who participated in this year MCWP & PLM’s 37th Annual Amber Gaines Memorial Golf Classic on October 13th. Your participation and generosity made this year’s event a tremendous success this year. Because of you we raised over $80,000.00 to support the CdLS Foundation. Your generosity empowers us to continue serving nearly 4,000 families across the United States and around the world. With your help, we will continue to fund vital programs and services that support families, their caregivers, professionals and research.
Your participation and contributions are making a tangible difference. Although the event is over, your continued support can still have a lasting impact on our community. If you missed it this year you can still, make a donation here.
Save the Date: October 12th, 2026, for our 38th Annual Amber Gaines Memorial Golf Classic! See you there.

This long-standing Missouri golf outing is one of the CdLS Foundation’s largest fundraisers. Last year’s MCWP & PLM’s 36th Annual Amber Gaines Memorial Golf Classic did not disappoint. 132 golfers enjoyed a day of golf, a light breakfast, lunch and awards dinner at the Tapawingo National Golf Club, over $92,000 was raised! Thank you to the amazing committee who organized the event, the volunteers, golfers, donors and sponsors. With your continued support we can continue to support individuals with CdLS, their families and those who care for them. Join us again this year on Monday, October 13th, registration for 2025 will begin in July.
Tapawingo National Golf ClubSunset Hills, MO

Missouri Family Gathering
2025-10-12 14:00 - 17:00 UTC
Join families from Missouri and surrounding states for a CdLS Foundation Family Gathering.
Sunday, October 12, 2025
2-5 p.m.
Graciously hosted by: Haylee and Josh, parents to Charlee
Hercules Residence
2283 Marilyn Drive
Wentzville, MO 63385
Family Gatherings are planned with your whole family in mind. There will be activities for everyone. You’ll have the chance to meet families in the area who share similar challenges and triumphs as parents of children with Cornelia de Lange Syndrome (CdLS).
Register Here!

You’re invited to the Amber Gaines Memorial Golf Classic the next day!
Not a golfer, not a problem, you can volunteer, attend lunch or dinner, and be a part of this annual event going into its 37th year.
Click here for more information.

2025 Bank of America Chicago Marathon
2025-10-12
Running for those who cannot!
Thirty athletes from all over the globe will be running the 26.2 miles thought the street of Chicago as Team CdLS participates in our 26th at The Bank of America Chicago Marathon. They will go through countless hours of physical and mental training all while raising awareness and funds for the CdLS community. You can support the Team, by donating here. All donations will be posted on our Team CdLS Chicago page.
Funds raised through Team CdLS provide resources, research and crucial support services. Together, we can continue reaching out, providing help and giving hope to individuals and their families impacted by CdLS
Event Details
2025 Bank of America Chicago Marathon
Race Day: Sunday, October 12, 2025
Where: Grant Park, Chicago
If you are interested in being a team sponsor, please contact Lisa Schroeder, Events Manager.
Another fun way to support the team is to sign up for Curb Crew; we would love to have you as part of the “crew” and share in the fin and excitement of marathon weekend!
Thank you on behalf of Team CdLS 💜

7th Annual Whole Hog to Benefit CdLS Foundation
2025-10-11 16:00 - 19:00 UTC

You Can Never Be Too Prepared: Pediatric Disaster and Emergency Preparedness
2025-10-09 20:00 - 21:00 UTC
Children have unique medical, emotional, and developmental needs during disasters, and preparing to meet those needs is essential for effective response and recovery. This is even truer for children with a serious medical condition.
This event will provide a platform for learning and sharing best practices to create an actionable plan that prioritizes the safety and care of children in times of crisis. And include action items you can take now as the caregiver to make sure you are always prepared for the unexpected.
This event will take place on Thursday, October 9th at 8:00 pm ET (7:00 pm CT, 6:00 pm MT, 5:00 pm PT).
Register Here

Parent University: Sibling Panel – Let’s Talk About What Sibs Need to Know, When They Need to Know It, and Why. Let’s Hear Experiences From Siblings Themselves – The Future Without Us Peace of Mind
2025-10-09 12:00 - 13:00 UTC
Many of us are going to count on the siblings or other family members to step into our shoes. What jobs are they taking on? Do they feel like we have prepared them? What do they want to know yet? Have they already experienced the responsibilities? Have we as parents even talked with them, and how much of the nitty gritty do they NEED to know?
Register here

Every Voice Matters: Advocating for Person-Centered Medical Care Webinar
2025-10-07 20:00 UTC
Caring for a loved one who needs ongoing support is never simple—and when serious medical challenges arise, the journey can feel overwhelming.
In this heartfelt and practical webinar, Bettie Bell shares the story of her autistic son Maurice’s stage 4 cancer diagnosis and the powerful lessons they discovered along the way. Together, Bettie and Maurice offer insight into what it means to navigate healthcare with courage, advocacy, and compassion.
What You’ll Learn
Participants will walk away with strategies to make healthcare more collaborative, person-centered, and supportive.
Key Takeaways:

Practical Advocacy Tools – Communicate effectively with healthcare teams and ask for accommodations that truly matter.
Supporting Self-Advocacy – Empower individuals with disabilities to express choices, preferences, and fears during medical care.
Building Comfort & Connection – Maintain routines, reduce stress, and honor what matters most in challenging times.

About the Presenters
Maurice Bellstewart lives in Newport News, Virginia, and is a graduate of Heritage High School and Wilson Workforce Rehabilitation Center, earning certifications in Food Services, Dishwasher Handling, and Food Safety Handling. He has been featured in national publications for his innovative work as an intern with the CROP Foundation, a nonprofit focusing on hospitality, food sustainability, and restaurant innovation. Maurice is a passionate self-advocate for himself and his community.
Bettie Bell, Maurice’s mother, has spent her life supporting his autonomy and independence. She celebrates his ability to advocate for his needs and creatively explore options for his future. Bettie is an endorsed PBS Facilitator, a BCBA, and a technology consultant who helps people with disabilities live their best lives with the supports they need.
Register Here.

Virtual Support Groups for Parents
2025-10-02 19:00 - 20:00 UTC
The CdLS Foundation is pleased to offer Virtual Support Groups for Parents, providing a consistent opportunity to connect, share, and support one another.
🗓 Thursday, October 2, 2025
🕖 7:00 – 8:15 p.m. ET
We believe no parent should walk this path alone at the CdLS Foundation. As caregivers, you are the backbone of our community, and we see you. We understand the emotional and physical challenges that come with your role.
These virtual gatherings are here to help you:

Connect with others who understand your journey
Share and receive meaningful advice
Feel heard, supported, and uplifted

Whether you’re new to the CdLS community or have been walking this road for years, we invite you to join us for an hour of connection, understanding, and encouragement. You belong here.
Sessions will be held on the first Thursday of every month and will be dedicated to connection and support.
To register, click here.

A Lifetime of Moments: Building Memories and Living your Child's Legacy Together
2025-09-22 20:00 UTC
Time together making memories as a family may feel especially precious when the child is living with a life-threatening medical condition. Making memories and sharing experiences that become part of the child’s legacy and the family’s treasure box can take many forms and can happen anytime: special occasions or a typical weekday.
There is meaning and legacy in experiences together; there is meaning and legacy in the concrete items that emerge from these experiences, such as photos, art, handprints, music.
Join researcher and Child-Life Specialist Dr. Jessica Boles and Soulumination’s McKenzie Johnson to learn about processes of making memories and building legacy that endure in your home and your heart.
This event will take place on Monday, September 22nd at 8:00 pm ET (7:00 pm CT, 6:00 pm MT, 5:00 pm PT).
Register here

Parent University: Protection and the Ways to Put It In Place – How Does Insurance Fit Into Our Planning – Safety Peace of Mind
2025-09-11 12:00 - 13:00 UTC
We know that insurance is a necessary part of our planning. Do we really need it if we have enough money? What if we can’t afford what we need? There are so many kinds of life insurance – between term life insurance, permanent life insurance, long-term care insurance and so many variations. Let’s have a basic class to identify the types of protection available, what to buy when, and when don’t we need it any more.
Register here

Virtual Support Groups for Parents
2025-09-04 19:00 - 20:00 UTC
The CdLS Foundation is pleased to offer Virtual Support Groups for Parents, providing a consistent opportunity to connect, share, and support one another.
🗓 Thursday, September 4, 2025
🕖 7:00 – 8:15 p.m. ET
We believe no parent should walk this path alone at the CdLS Foundation. As caregivers, you are the backbone of our community, and we see you. We understand the emotional and physical challenges that come with your role.
These virtual gatherings are here to help you:

Connect with others who understand your journey
Share and receive meaningful advice
Feel heard, supported, and uplifted

Whether you’re new to the CdLS community or have been walking this road for years, we invite you to join us for an hour of connection, understanding, and encouragement. You belong here.
Sessions will be held on the first Thursday of every month and will be dedicated to connection and support.
To register, click here.

Parent University: Can I Really Retire? What Needs to Be Considered? What If I Move to Another State? What If I Want My Child to Move, Too? – Retirement Peace of Mind
2025-08-14 12:00 - 13:00 UTC
Retirement usually is a goal, right? We might love what we do, but the goal to retire securely and find that security to do so is usually a goal of our own planning. When should we take Social Security? If we move, what has to change? Do we need to update our estate planning documents? If our child moves with us, what happens to their benefits? Is a retirement plan just about money? What are we retiring TO?
Register here

Virtual Support Groups for Parents
2025-08-07 19:00 - 20:00 UTC
The CdLS Foundation is pleased to offer Virtual Support Groups for Parents, providing a consistent opportunity to connect, share, and support one another.
🗓 Thursday, August 7, 2025
🕖 7:00 – 8:00 p.m. ET
We believe no parent should walk this path alone at the CdLS Foundation. As caregivers, you are the backbone of our community, and we see you. We understand the emotional and physical challenges that come with your role.
These virtual gatherings are here to help you:

Connect with others who understand your journey
Share and receive meaningful advice
Feel heard, supported, and uplifted

Whether you’re new to the CdLS community or have been walking this road for years, we invite you to join us for an hour of connection, understanding, and encouragement. You belong here.
Sessions will be held on the first Thursday of every month and will be dedicated to connection and support.
To register, click here.

CdLS Foundation-Sponsored Northeast Family Gathering
2025-07-12 14:00 - 18:00 UTC
Join families from New York and the Northeast for a CDLS Foundation-sponsored Family Gathering.
Saturday, July 12, 2025
2 – 6 p.m. ET
The Arp Home
9B Sandpiper Lane
Rexford, NY
(9B is on the white mailbox with a long driveway)
Graciously Hosted by Jennifer and Nicholas Arp, parents to Jenna.
Bring your swimsuit and towel to enjoy the pool!
Bring the whole family and join us for a casual backyard get-together! You’ll have the chance to meet families in the area who share similar challenges and triumphs as parents of children with Cornelia de Lange Syndrome (CdLS).
SPECIAL GUESTS: The CdLS Foundation Family Service team will be available to answer questions
Pizza, sub sandwiches, and beverages provided. Please bring a snack or dessert to share.
Questions? Email Family Service

Register here: bit.ly/negathering25

Parent University: What Really Needs to Happen when We Die? How is This Plan We Put in Place Administered Properly? – After We Are Gone Peace of Mind
2025-07-10 13:00 - 17:00 UTC
We will walk thru an estate and financial plan and learn how it is “activated”. Who does what, who knows where everything is, and how can we make sure the family knows what to do? It is not fun to think about, but it is certainly an important topic that we all need to make sure we understand.
Register here

Virtual Support Groups for Parents
2025-07-03 19:00 - 20:00 UTC
The CdLS Foundation is pleased to offer Virtual Support Groups for Parents, providing a consistent opportunity to connect, share, and support one another.
🗓 Thursday, July 3, 2025
🕖 7:00 – 8:00 p.m. ET
We believe no parent should walk this path alone at the CdLS Foundation. As caregivers, you are the backbone of our community, and we see you. We understand the emotional and physical challenges that come with your role.
These virtual gatherings are here to help you:

Connect with others who understand your journey
Share and receive meaningful advice
Feel heard, supported, and uplifted

Whether you’re new to the CdLS community or have been walking this road for years, we invite you to join us for an hour of connection, understanding, and encouragement. You belong here.
Sessions will be held on the first Thursday of every month and will be dedicated to connection and support.

Register Here!

Parent Perspectives: Insights into Medical Decision-Making
2025-06-25 12:00 - 13:00 UTC
Making major decisions about interventions such as feeding tubes or tracheostomies is one of the greatest responsibilities caregivers face for their child, weighing not only risks and benefits but also the goals of care for their child. Join a panel of experienced parents as they share valuable insights into their decision-making journeys. Discover the factors that influenced their choices, the challenges they faced, and the lessons they learned along the way. Hear how they worked with their child’s care team and ultimately made their decisions. Don’t miss this opportunity to learn from real-life experiences and gather practical advice to support your own decision-making process.
This session will be moderated by Gabrielle Conecker, who has more than 20 years of experience in advocating for and advancing public health.
This event will take place on Wednesday, June 25th at 12:00 pm ET (11:00 am CT, 10:00 am MT, 9:00 am PT).
Register here
