News from the NODCC

Celebrating 20 Years of the NODCC 2003-2023

Founder Barbara Fonseca on Regional Gatherings - The Community Lifeblood

of the NODCC


By Miriam Bernard


What it What it all comes down to, according to NODCC founder Barbara Fonseca, is families gathering together

to form a new type of community - a DCC community. As Barb aptly puts it, “It’s a place where you don’t have to explain yourself.” For a family member of a person with a DCC – a disorder many are not familiar with - this feels like a welcome break. That sentiment is where it all started in 2001 as a small assembly of just a few dozen families and individuals in the DCC community decided to become an official nonprofit to reach a wider swath of people and bring more resources to the DCC community. 


Barb’s son Nate, now (24), was diagnosed with a DCC at nine months old. The Fonseca’s were fortunate to be able to attend their first small family gathering shortly after diagnosis. It was the first time Barb and her husband, Anthony, interacted with anyone else whose child had an DCC, and it was life-changing. At this gathering they met a family whose son was 9 years old. That family had plans to go to a gathering in Columbus, Ohio, and encouraged the Fonseca’s to attend. Their family understood how meaningful and educational a trip like this would be and decided to pitch in to pay for them to attend the family gathering in Ohio a month later.


That time in Ohio changed everything, and Barb knew she wanted to be involved. She offered to host the next gathering near her home in Yorba Linda, California. At that time, events were nothing like the official conferences of the NODCC today. It took place at their local community center, and Barb and her family cooked spaghetti dinner for everyone in attendance. In 2003, that group achieved their 501C3 status, and the NODCC was officially born. Contrast that with the conventions of the last few years, attended by hundreds of people and epicenters for expert panels and specialized breakout groups, and you’ll have an inkling of how much the NODCC has grown in 20 years.


Still today, small gatherings are the lifeblood of the NODCC, because they are the literal origins of the organization. Before conferences, before research committees and databases, it was just families, sitting down together, to enjoy food, share their life experiences, and “not have to explain themselves”. This is

why the NODCC is excited to carry on and expand the important tradition of regional gatherings as they enter their next 20 years. What it all boils down to is having a community of people around you who support and understand you. Barb states, “We have developed lifelong friendships that we may not have

experienced if we did not attend that first gathering. Our hope is that everyone can have the same opportunity.”


There a several areas in the country that need a passionate individual or small group ready to help host a regional gathering. Our team is ready to offer tips, tools, resources, and training to anyone interested in bringing regional gatherings to your area. Please reach out to us at [email protected] with any questions or interest.


There are several regional gatherings planned around the US in the coming months, including the following.

St. Louis, Missouri: April 22, 2023: 2 - 4 pm, Washington University in St Louis,

School of Medicine Campus at 660 S. Euclid Ave., St Louis 63110. 

Any family, or individual, interested in attending can contact Lisa Mackenzie at [email protected] or 314-337-3380.

Yorba Linda, California: May 13, 2023: More info to come. Email Barb at [email protected]

Washington DC: July 2023: More information to come

Painted Post, New York: July 29, 2023: https://www.eventcreate.com/e/regionone For additional information contact Kathe Gee at [email protected]

Illinois (Chicago area) – Summer 2023


For more information on these, please check the events section of upcoming NODCC newsletters & the NODCC website https://nodcc.org/conferences-and-events/local-events/ or email [email protected]


This article is the first in a limited series called “Celebrating 20 Years of the NODCC – 2003-2023” – keep your eyes open in future months this year for additional anniversary pieces looking back on the history and legacy of the NODCC. To learn more about Barb’s story, click here to see a video interview about Barb and her family featured on the NODCC YouTube channel.

Be on the Lookout for Olam's Piggybank Grant Info

More information coming soon!

https://nodcc.org/resources/grants/

We Want to Hear from You!


Have you ever taken a trip to a destination that made life simple for you or your family member with a DCC? The NODCC wants to suggest DCC-friendly Vacation Destinations to our readers! We'd love to hear about the

location and what made it so great. Please take a moment to share your experience with us at the link below!

https://forms.gle/dArJ4PeZif1pvmsbA

Here are the latest opportunities to get involved with the NODCC community.

April Schedule


Connecting people affected by disorders of the corpus callosum is at the heart of what we do at the NODCC. We are excited to increase and improve our community sessions this year and offer presentations and discussions with experts.


Full session descriptions and registration links for each call are included below. Register for the upcoming calls and watch for details on more sessions coming soon!


Dads of the NODCC

April 25, 2023

4:30 pm PST / 5:30 pm MST/

6:30 pm CST / 7:30 pm EST

This is a meet and greet session for dads who have a child with a disorder of the corpus callosum. 

Register Here


Grandparents of the NODCC

April 29, 2023

8:30 am PST / 9:30 am MST/

10:30 am CST / 11:30 am EST

This is a meet and greet session for grandparents who have a grandchild with a disorder of the corpus callosum. 

Register Here


Expectant Parents and Parents of Newborns with a DCC

April 29, 2023

11:00 am PST / 12:00 pm MST/

1:00 pm CST / 2:00 pm EST

This is a meet and greet session for parents who have newborns or are currently pregnant with a baby with a disorder of the corpus callosum.

Register Here


To suggest a topic for a virtual session, please contact our Community Committee at [email protected].


April Regional Gathering

April 22, 2023

2 - 4 pm

The venue will be on the

Washington University in St Louis,

School of Medicine Campus at

660 S. Euclid Ave.,

St Louis 63110. 


Any family, or individual, interested in attending can contact Lisa Mackenzie at 

[email protected] or 314-337-3380. 


Adults with a DCC

May 4, 2023

4:30 pm PST / 5:30 pm MST/

6:30 pm CST / 7:30 pm EST

This is a meet and greet session for adults with a disorder of the corpus callosum. For registration link email Jasmin at [email protected]


Siblings Ages 10-15

May 7, 2023

11:00 am PST / 12:00 pm MST/

1:00 pm CST / 2:00 pm EST

This is a meet and greet session for siblings of DCCers ages 10-15 years. 

Register Here


Moms of the NODCC

May 11, 2023

4:30 pm PST / 5:30 pm MST/

6:30 pm CST / 7:30 pm EST

This is a meet and greet session for moms who have a child with a disorder of the corpus callosum. 

Register Here

Fundraisers & Donations

Matching Gifts

​Don’t forget to check for matching funds from your employer. Many companies have matching gift programs that will equal or exceed employees’ charitable donation amounts.

Facebook Fundraisers

Fundraising for charities on Facebook is an easy way to help raise money for the NODCC. Simply click on the “Support Nonprofit” option when creating a new Facebook post and select the NODCC as the recipient. Birthdays, memorials, remembrances, and celebrations are great events to encourage giving from your family and friends.


Looking for other ways to support? The NODCC is searching for sponsors and partners who want to support our organization. We encourage all readers of the newsletter to send company names or potential company contact information to [email protected].


Donate to keep our

community thriving!

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Contact Us

(714) 747-0063 I [email protected] I nodcc.org

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