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MPS SuperHero Foundation

Mps Super Hero Foundation

Non Profit Organization Management, Po Box 171770, Hialeah, Florida, 33017, United States, 11-50 Employees

mpssuperhero.org

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phone no Phone Number: +14*********

Who is MPS SUPERHERO FOUNDATION

Kalels MPS Superheroes Foundation is a non-profit organization created to spread awareness, save lives and find a cure for Mucopolysaccharidosis II (MPS II), also known as Hunters Syndrom...

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  • Po Box 171770, Hialeah, Florida, 33017, United States Headquarters: Po Box 171770, Hialeah, Florida, 33017, United States
  • 2017 Date Founded: 2017
  • 11-50 Employees: 11-50
  • dollar-icon Revenue: $50 Million to $100 Million
  • tech-icon Active Tech Stack: See technologies

industries-icon Industry: Non Profit Organization Management

SIC SIC Code: 5511 | NAICS Code: 441110 | Show More

checked-icon Does something look wrong? Fix it. | View contact records from MPS SUPERHERO FOUNDATION

MPS SuperHero Foundation Org Chart and Mapping

Employees
Michelle Paz

Michelle Paz

Board Member

Avram Joseph

Avram Joseph

Vice President/Co-Founder

Michelle Menendez

Michelle Menendez

Board Member

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Frequently Asked Questions Regarding MPS SuperHero Foundation

Answer: MPS SuperHero Foundation's headquarters are located at Po Box 171770, Hialeah, Florida, 33017, United States

Answer: MPS SuperHero Foundation's phone number is +14*********

Answer: MPS SuperHero Foundation's official website is https://mpssuperhero.org

Answer: MPS SuperHero Foundation's revenue is $50 Million to $100 Million

Answer: MPS SuperHero Foundation's SIC: 5511

Answer: MPS SuperHero Foundation's NAICS: 441110

Answer: MPS SuperHero Foundation has 11-50 employees

Answer: MPS SuperHero Foundation is in Non Profit Organization Management

Answer: MPS SuperHero Foundation contact info: Phone number: +14********* Website: https://mpssuperhero.org

Answer: Kalels MPS Superheroes Foundation is a non-profit organization created to spread awareness, save lives and find a cure for Mucopolysaccharidosis II (MPS II), also known as Hunters Syndrome. A rare metabolic disease which affects the joints, the liver, the spleen, the airway, the heart, and in most cases, the brain. Our goal is to raise $2.5 million which will be used to fund the cure (Gene Therapy) and to speed up the process of getting it approved by the FDA.

Answer:

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