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Apraxia Kids

Learn about this cause: What are the reviews? Is it Legit? Do I like the mission? What is the CEO's salary?

EIN: 251858159 ✦ Pittsburgh, PA ✦ Designated as a 501(c)(3)

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Overview

What is Apraxia Kids?

Apraxia Kids is a renowned nonprofit organization situated in Pittsburgh, Pennsylvania. With a mission to bolster the support systems for children suffering from apraxia of speech, they dedicate their efforts to educating professionals and families, fostering community engagement, and advocating for research. Their activities encompass providing resources, hosting support groups, and offering guidance to families and professionals alike. They also launch educational initiatives, such as the IEP Road Map, and engage in community outreach, including organizing national Walk for Apraxia events and distributing speech tablets to families in need. Their annual conference attracts a global audience, and they offer scholarships to further the education of families and aspiring speech language pathologists. With a commitment to their cause, Apraxia Kids continues to serve and support children with apraxia of speech, reaching out to communities across the nation.


Official website here: www.apraxia-kids.org

What are the reviews and ratings of this charity?

Charity Navigator Rating: 97% (Four-Star out of Four Star rating)

Apraxia Kids has achieved a notable Four-Star rating from Charity Navigator, reflecting its commitment to accountability and transparency. The organization boasts high scores in key areas such as Leadership & Adaptability (100), indicating a strong governance structure, and Culture & Community (97), which suggests effective engagement with stakeholders. With a program expense ratio of approximately 84%, a significant portion of funds is directed towards its mission-focused activities, ensuring that resources are utilized effectively.

User feedback highlights the crucial role Apraxia Kids plays in the lives of families affected by Childhood Apraxia of Speech (CAS). Many users express gratitude for the organization's efforts in raising awareness and providing resources that were previously lacking. The testimonials emphasize the emotional and financial burdens placed on families, stressing that the support offered by Apraxia Kids has made a substantial difference in their lives, both personally and collectively as a community.

While the organization has made significant strides, some challenges remain. The feedback indicates that families often face financial hardships that may limit their ability to contribute, particularly once their children begin to improve. Nonetheless, the organization's ongoing initiatives and community support help to ensure that they continue to foster awareness and provide essential resources for current and future families navigating the challenges of CAS.


This AI summary has been generated from information found on Charity Navigator and Great Nonprofits.

What do the Facebook reviews say about Apraxia Kids?

84% of 440 reviewers on Facebook recommend Apraxia Kids. Overall, the sentiment expressed reflects gratitude for the resources and support provided by the organization, especially for families navigating the challenges of speech apraxia.

Many families found the nonprofit to be a vital first step after receiving a diagnosis, highlighting the helpful and positive atmosphere that Apraxia Kids cultivates. Those who utilized their services felt reassured knowing they could access valuable information and support tailored to their needs.

The testimonials showcase an overwhelming appreciation for the organization, with many expressing relief and thankfulness for having a dedicated resource like Apraxia Kids available during a crucial time in their journey.


This AI summary has been generated from reviews found on Facebook.

Is Apraxia Kids legitimate?

Apraxia Kids is a legitimate nonprofit organization registered as a 501(c)(3) entity. Apraxia Kids submitted a form 990, which is a tax form used by tax-exempt organizations in the U.S., indicating its operational transparency and adherence to regulatory requirements. Donations to this organization are tax deductible.


Heare are some key statistics you may want to consider:

Executive Compensation: $135,061
Professional Fundraising Fees: $0
Other Salaries and Wages: $408,348

For more financial information, click here


Official website here: www.apraxia-kids.org

What is the mission statement of Apraxia Kids?

Apraxia Kids, as the leading nonprofit organization, is committed to strengthening the support systems for children with apraxia of speech. They achieve this by educating professionals and families, fostering community engagement and outreach, and advocating for research. Their mission is to empower families and improve the lives of these children by providing resources, guidance, and access to necessary educational services. Apraxia Kids invests in the future by supporting research, offering scholarships, and organizing events like the National Conference and Walk for Apraxia. They also provide resources such as the IEP Road Map and speech tablets to families in need.


Official website here: www.apraxia-kids.org

Who is the CEO of Apraxia Kids?

Angela Grimm is the Executive Dir. of Apraxia Kids.


Official website here: www.apraxia-kids.org

What is the revenue of Apraxia Kids?

Apraxia Kids's revenue in 2023 was $1,275,247.


Official website here: www.apraxia-kids.org

Who are the executives of Apraxia Kids and what are their salaries?

The average compensation at Apraxia Kids during 2023 was $67,926. There are 8 employees and 1600 volunteers at Apraxia Kids.


Here are 17 key members and their salaries:


Angela Grimm (Executive Dir.)
  • Compensation: $135,061
  • Related: $0
  • Other: $6,753
George Lin (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Sarah White (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Jonathan Spiegel (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Edwin Maas (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Neil Kilby (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Stephanie Fera (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Gary Fernando Md (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Lou La Vecchia (Chairman)
  • Compensation: $0
  • Related: $0
  • Other: $0
Jeffrey Mills (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Amber Vecchio (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Claudio Capone (Vice Chair)
  • Compensation: $0
  • Related: $0
  • Other: $0
Brennan Woods (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Alyson Taylor (Secretary)
  • Compensation: $0
  • Related: $0
  • Other: $0
Mark Conroe (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0
Amber Pinskey (Treasurer)
  • Compensation: $0
  • Related: $0
  • Other: $0
Matthew Stevens (Board Member)
  • Compensation: $0
  • Related: $0
  • Other: $0


Official website here: www.apraxia-kids.org

Where can I find the form 990 for Apraxia Kids?

Apraxia Kids's most recent form 990 was submitted in 2023 and can be accessed here.


Official website here: www.apraxia-kids.org

Learn more at the official website: www.apraxia-kids.org

Mission Statement of Apraxia Kids

Apraxia Kids, a leading nonprofit organization, is committed to strengthening the support systems in the lives of children with apraxia of speech. They achieve this by educating professionals and families, facilitating community engagement and outreach, and investing in the future through advocacy and research. Apraxia Kids' mission is to provide a robust network of resources and guidance for families affected by apraxia, empowering them to navigate the challenges associated with this speech disorder.

The organization's primary focus is on educating professionals and families. Apraxia Kids achieves this by offering a wealth of resources, including online materials and support groups, which enable families to connect with one another and seek advice from experienced professionals. Furthermore, they enhance their website to provide easier access to these resources, attracting over 1.1 million views during a specific period.

Apraxia Kids also invests in community outreach by developing statewide resources for their families. They organize annual conferences, both live and virtually, to bring together professionals, families, and individuals affected by apraxia. During these events, they provide valuable educational sessions, award scholarships to support families and future speech language pathologists, and offer community outreach programs like the Walk for Apraxia events, which raise awareness and donations in 64 cities.

Additionally, Apraxia Kids supports research by assisting researchers worldwide in recruiting subjects for apraxia studies. They also provide resources, such as speech tablets, to children from low to moderate income families, ensuring that no child is left behind in the pursuit of better speech abilities.

In essence, Apraxia Kids' mission is to provide comprehensive support to families and children affected by apraxia of speech. They achieve this by educating professionals and families, facilitating community engagement, and investing in research, ultimately empowering families to navigate the challenges associated with this speech disorder.

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Impact




October, 2024

Apraxia Kids significantly impacts the lives of children with apraxia of speech and their families by providing essential resources, education, and community engagement. In a recent period, over 73,500 members sought support through its platforms, utilizing resources and guidance from peers and professionals. The organization enhanced its outreach through a revamped website, generating over 1.1 million views and facilitating access to valuable downloadable educational materials.

A critical resource, the interactive IEP Road Map, was developed to help families navigate the complexities of acquiring appropriate educational services, empowering them with knowledge at each step. The annual conference, attended by 628 individuals from around the world, combined live and virtual formats, extending educational opportunities through additional sessions in July 2023. Moreover, the provision of 48 scholarships ensured that financially challenged families could participate, alongside 4 scholarships awarded to graduate students aspiring to become speech-language pathologists.

Community engagement efforts included the participation of more than 7,000 individuals in nationwide Walk for Apraxia events across 64 cities, enhancing awareness and fundraising efforts. Additionally, the speech tablet program provided crucial communication devices to low to moderate-income families, ensuring that access to speech support is available to those who need it most. Apraxia Kids also champions research advancement by assisting researchers in recruiting subjects for ongoing studies, thereby fostering further understanding and treatment of apraxia. Through these multifaceted initiatives, Apraxia Kids plays a vital role in strengthening support systems for children with apraxia and their families.




This information is meant to be a general summary of Apraxia Kids. Please take the time to review official sources before making any decisions based upon the content provided here.


Financials

This financial information is from Propublica.

Revenue
$1,275,247 (2023)
Expenses
$1,316,441 (2023)
Efficiency

Other financial information:

This information is from the most recently submitted tax form from this organization, which was in 2023.

  • Investment Income: -$1,097
  • Program Service Revenue: $132,984
  • Gross Receipts: $1,911,046

Assets and Liabilities:

  • Total Assets: $1,279,230
  • Total Liabilities: $336,033
  • Net Assets: $943,197

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Programs

Programs are reported by nonprofits in their tax forms and are normally their tax-exempt activities.

Conference Income

Revenue

$129,344

Contract Services

Revenue

$3,640

Organization Details

Founding Year

2000

Principal Officer

Angela Grimm

Main Address

1501 Reedsdale Street 202, Pittsburgh, PA, 15233

NTEE Category

Code: G98 - Disease

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