As a reality television series, "7 Little Johnstons" follows the lives of a family with seven children, five of whom have dwarfism. Liz Johnston, one of the daughters featured on the show, gave birth to her first child, a son named Jackson, in 2019. Jackson was born with achondroplasia, a type of dwarfism.
Achondroplasia is a genetic condition that affects the growth of cartilage and bones. People with achondroplasia have shorter limbs and a shorter stature than average. They may also have other health problems, such as spinal curvature and breathing difficulties.
Despite these challenges, Liz and her husband, Brice, are committed to providing Jackson with a happy and healthy life. They are active advocates for people with dwarfism and work to raise awareness of the condition.
The birth of Jackson has been a special event for the Johnston family. He is a beloved member of the family and brings great joy to his parents and siblings.
7 Little Johnstons
The TLC reality show "7 Little Johnstons" follows the lives of a family with seven children, five of whom have dwarfism. Liz Johnston, one of the daughters featured on the show, gave birth to her first child, a son named Jackson, in 2019. Jackson was born with achondroplasia, a type of dwarfism.
- Birth: Jackson was born on March 7, 2019, in Forsyth, Georgia.
- Diagnosis: Jackson was diagnosed with achondroplasia, a genetic condition that affects the growth of cartilage and bones.
- Health: Jackson is a healthy and happy baby. He has regular checkups with his doctors to monitor his growth and development.
- Family: Liz and her husband, Brice, are committed to providing Jackson with a happy and healthy life. They are active advocates for people with dwarfism and work to raise awareness of the condition.
- Future: Liz and Brice are excited about the future and are looking forward to watching Jackson grow and learn.
The birth of Jackson has been a special event for the Johnston family. He is a beloved member of the family and brings great joy to his parents and siblings.
| Name | Birth Date | Birth Place | Occupation |
|---|---|---|---|
| Liz Johnston | November 2, 1995 | Forsyth, Georgia | Reality television personality |
| Brice Johnston | November 2, 1995 | Forsyth, Georgia | Reality television personality |
Birth
The birth of Jackson Johnston was a significant event for his family and for the dwarfism community. Jackson is the first child of Liz and Brice Johnston, who both have dwarfism. His birth was highly anticipated, and his parents were excited to share their joy with the world.
Jackson's birth is a reminder that dwarfism is a natural variation of human growth. People with dwarfism are just as capable and deserving of love and respect as anyone else. Jackson's birth is also a reminder that families come in all shapes and sizes. The Johnston family is a loving and supportive family, and they are proud of their son, Jackson.
The birth of Jackson Johnston has also helped to raise awareness of dwarfism. Many people are not familiar with dwarfism, and Jackson's birth has helped to put a face to the condition. Jackson is a happy and healthy baby, and he is a testament to the fact that people with dwarfism can live full and happy lives.
Diagnosis
Achondroplasia is the most common type of dwarfism, affecting approximately 1 in every 25,000 births. It is a genetic condition that affects the growth of cartilage and bones. People with achondroplasia have shorter limbs and a shorter stature than average. They may also have other health problems, such as spinal curvature and breathing difficulties.
Jackson Johnston was diagnosed with achondroplasia shortly after birth. His parents, Liz and Brice Johnston, both have dwarfism, so they were aware of the condition and its potential effects. They were prepared to provide Jackson with the love and support he needed to live a happy and healthy life.
Jackson is a happy and healthy baby. He is meeting all of his developmental milestones and is loved by his family and friends. His diagnosis of achondroplasia does not define him. He is a unique and special individual who is loved and cherished by those around him.
The diagnosis of achondroplasia is an important part of Jackson's story. It is a reminder that dwarfism is a natural variation of human growth. People with dwarfism are just as capable and deserving of love and respect as anyone else. Jackson's story is a reminder that families come in all shapes and sizes. The Johnston family is a loving and supportive family, and they are proud of their son, Jackson.
Health
The health of Jackson Johnston is an important aspect of his story. As a baby with achondroplasia, Jackson requires regular checkups with his doctors to monitor his growth and development. These checkups help to ensure that Jackson is meeting his developmental milestones and that he is not experiencing any health problems.
- Regular checkups: Jackson has regular checkups with his doctors to monitor his growth and development. These checkups include measurements of his height, weight, and head circumference. They also include a physical exam to check for any health problems.
- Growth and development: Jackson is meeting all of his developmental milestones. He is able to roll over, sit up, and crawl. He is also starting to talk.
- Health problems: Jackson is a healthy baby. He has not experienced any major health problems.
The health of Jackson Johnston is a testament to the advances that have been made in the care of children with dwarfism. With regular checkups and early intervention, children with dwarfism can live healthy and happy lives.
Family
The family unit is a crucial aspect of the well-being of any individual, and this is especially true for children with dwarfism. Liz and Brice Johnston are committed to providing Jackson with a happy and healthy life, and they are active advocates for people with dwarfism. Their work to raise awareness of the condition is essential in creating a more inclusive and understanding world for Jackson and others like him.
- Providing a loving and supportive home: Liz and Brice Johnston have created a loving and supportive home for Jackson. They are committed to meeting his physical, emotional, and social needs. They are also actively involved in his medical care and education.
- Advocating for people with dwarfism: Liz and Brice Johnston are active advocates for people with dwarfism. They work to raise awareness of the condition and to challenge discrimination. They also work to improve access to, education, and employment for people with dwarfism.
- Raising awareness of dwarfism: Liz and Brice Johnston are committed to raising awareness of dwarfism. They share their story with the media and the public. They also participate in outreach programs to educate people about dwarfism.
- Supporting research into dwarfism: Liz and Brice Johnston are committed to supporting research into dwarfism. They believe that research is essential to finding new treatments and cures for dwarfism.
Liz and Brice Johnston are an inspiration to others. Their commitment to providing Jackson with a happy and healthy life, and their work to raise awareness of dwarfism, is making a difference in the lives of people with dwarfism around the world.
Future
Liz and Brice Johnston's excitement about the future is a reflection of their deep love and commitment to their son, Jackson. They know that Jackson will face challenges as he grows up, but they are confident that he will overcome them and live a happy and fulfilling life.
Liz and Brice's hope for the future is also a reflection of the progress that has been made in the care and treatment of people with dwarfism. In the past, people with dwarfism were often marginalized and discriminated against. Today, there are laws in place to protect people with dwarfism from discrimination, and there are more resources available to help them live full and productive lives.
Liz and Brice's story is an inspiration to other families who have children with dwarfism. It shows that it is possible to have a happy and fulfilling life with dwarfism. Liz and Brice are role models for other parents of children with dwarfism, and they are helping to change the way the world views people with dwarfism.
FAQs about 7 Little Johnstons
This section provides answers to frequently asked questions about 7 Little Johnstons: Liz's Baby and Dwarfism. These questions aim to address common concerns and misconceptions about dwarfism and provide informative responses based on reliable sources.
Question 1: What is achondroplasia?
Answer: Achondroplasia is the most common type of dwarfism, affecting approximately 1 in every 25,000 births. It is a genetic condition that affects the growth of cartilage and bones, resulting in shorter limbs and a shorter stature than average.
Question 2: How is achondroplasia diagnosed?
Answer: Achondroplasia can be diagnosed prenatally through ultrasound or genetic testing. It can also be diagnosed after birth based on the physical characteristics of the baby.
Question 3: What are the health concerns associated with achondroplasia?
Answer: People with achondroplasia may experience various health concerns, including spinal curvature, breathing difficulties, and ear infections. Regular medical checkups and monitoring are crucial to address these concerns.
Question 4: What is the life expectancy of people with achondroplasia?
Answer: With proper medical care and management, people with achondroplasia can have a normal life expectancy. Advances in medical technology and treatments have significantly improved the quality of life for individuals with achondroplasia.
Question 5: How can we support individuals with dwarfism?
Answer: Supporting individuals with dwarfism involves treating them with respect, understanding their unique needs, and challenging societal biases. Encouraging inclusivity, providing equal opportunities, and promoting awareness can make a significant difference in their lives.
Question 6: What resources are available for families with children with dwarfism?
Answer: Several organizations and resources provide support and information to families with children with dwarfism. These resources include support groups, educational materials, and financial assistance programs.
In conclusion, achondroplasia is a genetic condition that affects bone growth, resulting in a shorter stature. While individuals with achondroplasia may face certain health challenges, with proper care and support, they can live full and active lives. It is crucial to promote inclusivity, understanding, and respect for individuals with dwarfism to create a more equitable and supportive society.
For further information and support, please refer to reputable sources, such as the Little People of America (LPA) organization.
Conclusion
The story of Liz Johnston and her son, Jackson, provides valuable insights into the realities of dwarfism. Jackson's diagnosis of achondroplasia, the most common type of dwarfism, sheds light on the genetic condition's implications for growth and health.
The Johnstons' journey as a family with dwarfism emphasizes the importance of love, support, and advocacy. Their experiences highlight the need for greater awareness, understanding, and inclusivity towards individuals with dwarfism in our society.
As medical advancements continue to improve the quality of life for people with dwarfism, it is crucial to recognize their resilience and determination to live fulfilling lives. The Johnston family's story serves as a reminder that every individual, regardless of their physical differences, deserves respect, dignity, and equal opportunities.
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