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Umar Mughal – One of the Famous People with Osteogenesis Imperfecta

Umar Mughal – One of the Famous People with Osteogenesis Imperfecta (Brittle Bone Disease)

The 28-year-old graphic designer Umar Mughal has suffered from genetic bone disorder Osteogenesis Imperfecta since birth. His soft, fragile bones frequently fractured while he was growing up, and poor healthcare in his home country Pakistan resulted in his tiny stature and deformed limbs.

FIND OUT how local doctors were responsible for ruining his body’s natural development.

Osteogenesis Imperfecta is an inherited bone disease that has no cure and is a lifelong condition. There are eight types of the disease, which can range from mild to fatal. Children born with Type II and Type III are typically born with bone fractures, and often die as newborns. The condition is very rare, and there are fewer than 20,000 cases reported a year world-wide.

Umar’s legs cannot support his body weight, and he gets around by scooting across the floor at home. He has to do physical therapy daily for the rest of his life to maintain mobility of his shortened limbs. The cost of his medical care is wildly expensive and recurring. He faces additional difficulties because of his rounded shoulders and scoliosis in his spine.While he can move about freely in his own home, Umar is completely reliant on others to carry him around when he’s out in public. He was largely dependent on his brother for transportation, but gradually became more autonomous after getting a job at a graphic design firm 10 years ago.

CHECK OUT

how he navigates the city.

Osteogenesis imperfecta (OI) is a genetic disorder that affects the production of collagen, a protein that is important for the strength and structure of bones. People with OI have bones that are fragile and break easily, and they may also have other abnormalities, such as short stature, hearing loss, and deformities of the teeth and limbs.

There are several types of OI, ranging from mild to severe, and the severity of the condition can vary widely within a family. Some people with OI may only experience a few fractures throughout their lifetime, while others may have frequent fractures and may require surgery or other medical interventions.

Treatment for OI may include medications to improve bone density, physical therapy to improve mobility and strength, and surgery to correct deformities or to stabilize bones. People with OI may also need to take precautions to prevent fractures, such as avoiding certain activities or wearing protective gear.

OI is a lifelong condition, but with proper medical care and management, people with OI can lead active and fulfilling lives.

Umar Working

When Umar got his first graphic design job, he worked his way up through every department, despite coworkers doubting his ability to perform at the same level able-bodied people can.

“Everyone in that studio thought that I would not be able to work. Even my manager thought the same thing… He said he would shorten the duration of my shift because he thought I couldn’t work for that long,” he remarked. “But I showed them I can work hard, and within the three months of learning, I amazed everyone. [They] started to support me as much as they could, and they all still do.”

Find out what Umar does for a living HERE.

Umar was taught by his mother to live his life like a normal healthy man, and began using ride share apps to hail motorcycle drivers for lifts. He now does everything on his own, including attending religious services, getting to and from work, and teaching graphic design to students.

SEE how Umar moves around in public.

In addition to growing his career, Umar has plans to give fellow disabled people a chance to thrive.

“I’m working on resources to open an institution where I will give jobs to people with disabilities,” he detailed. “I will make them independent by teaching them work and providing them jobs and shelter, so they don’t ask for help. Instead, they will be able to help someone else, making a chain.”

FIND OUT what Umar has planned for his institution.

Famous People With Osteogenesis Imperfecta

Osteogenesis Imperfecta is a genetic disorder that results in brittle bones that break easily and depending on the severity, can result in an early death for those who suffer from the disease.

Despite the high morality rate of Type II Osteogenesis Imperfecta, many people survive when diagnosed with one of the 20 other types of the degenerative disorder.

The disease is most prominently recognized by the general public due to a story line on ABC’s “Grey’s Anatomy,” when doctor’s Jackson Avery and April Kepner’s son dies within minutes of his birth, and from Samuel L. Jackson’s depiction of supervillain Elijah Price in M. Night Shyamalan’s “Unbreakable,” starring Bruce Willis.

However, most people don’t know that there are plenty of famous people with Osteogenesis Imperfecta thriving in the world.

Another famous person with brittle bone disease is actor Atticus Shaffer, who is most well known for playing Brick Heck on Patricia Heaton starrer, “The Middle,” has Type I Osteogenesis Imperfecta, which resulted in his sort stature of only 4’8.”

British actor Kerry Ingram, who played Shireen Baratheon on HBO’s “Game of Thrones,” and appeared in 32 episodes of Netflix series “Free Rein,” has a mild form of Osteogenesis Imperfecta.

Australian actor Quentin Kenihan was born with Osteogenesis Imperfecta, but appeared in 2015 “Mad Max: Fury Road” beside Charlize Theron and Tom Hardy, before his death in 2018.

famous people who have lived with osteogenesis imperfecta

There are many famous people who have lived with osteogenesis imperfecta (OI), a genetic disorder that affects the strength and structure of bones. Some examples include:

  • Abraham Lincoln: Lincoln is believed to have had a mild form of OI, which may have contributed to his tall and thin build and his difficulty in standing for long periods of time.
  • Tisha UnArmed: UnArmed is an actress, comedian, and disability rights activist who has OI and uses a wheelchair. She is known for her work in theater, film, and television, and is a prominent voice in the disability community.
  • Zach Anner: Anner is a comedian, author, and television host who has OI and uses a wheelchair. He is known for his work on the Oprah Winfrey Network and his popular YouTube channel, which features videos about living with a disability.
  • Paddy Rossbach: Rossbach is a disability rights activist and the founder of the National Spinal Cord Injury Association. She has OI and uses a wheelchair, and has been a leading advocate for the rights of people with disabilities for more than 50 years.

These are just a few examples of the many famous people who have lived with OI and made significant contributions to their fields.

Here are some facts about osteogenesis imperfecta (OI)

  • OI is a genetic disorder that affects the production of collagen, a protein that is important for the strength and structure of bones.
  • OI is also known as “brittle bone disease” because people with OI have bones that are fragile and break easily.
  • There are several types of OI, ranging from mild to severe. The severity of the condition can vary widely within a family.
  • OI can also cause other abnormalities, such as short stature, hearing loss, and deformities of the teeth and limbs.
  • OI is caused by mutations in the genes that produce collagen, and it is inherited in an autosomal dominant pattern, which means that a person only needs to inherit one copy of the mutated gene to develop the condition.
  • OI is a lifelong condition, but with proper medical care and management, people with OI can lead active and fulfilling lives.
  • There is no cure for OI, but treatment may include medications to improve bone density, physical therapy to improve mobility and strength, and surgery to correct deformities or to stabilize bones.
  • OI is a rare condition, affecting about 1 in every 15,000 to 50,000 live births.

Check out – > Famous Filmmakers in Pakistan

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