01. Help Maia Be More Independent
Maia is an 8-year-old girl with cerebral palsy. She has difficulty walking and talking, and she requires a range of therapies to help her live as independently as possible.
One of the most important things that Maia’s parents can do to help her become more independent is to provide her with opportunities to practice new skills. This could involve things like helping her to dress herself, brush her teeth, or make her own bed. It is also important to give Maia positive reinforcement when she succeeds so that she feels encouraged to keep trying.
Another way to help Maia become more independent is to teach her how to use adaptive equipment. This could include things like a wheelchair, a communication device, or a special spoon for eating. Adaptive equipment can help Maia to participate in activities that she would not be able to do without it, and it can also give her a sense of independence.
Finally, it is important to create a supportive environment for Maia. This means making sure that her home is accessible and that she has access to the resources she needs. It also means being patient and understanding and giving Maia the time and space she needs to learn new things.
With the right support, Maia can achieve her full potential and live a more independent life.
Just4Children
Just4Children is a charity that provides funding for children with disabilities to access quality of life-enhancing surgeries and treatments. They offer a range of services, including selective dorsal rhizotomy (SDR), stem cell therapy, mobility and sensory equipment, and more.
If you are interested in helping Maia be more independent, you can donate to Just4Children’s campaign. Your donation will help to fund the therapies and equipment that Maia needs to reach her full potential.
How You Can Help
There are many ways you can help Maia be more independent. Here are a few ideas:
- Donate to Just4Children’s campaign.
- Share Maia’s story on social media.
- Volunteer your time to help Maia with her therapy or to provide her with support.
- Advocate for better access to services for children with disabilities.
Every little bit helps, and together we can make a difference in Maia’s life.
02. Baseball as a Bonding Experience for Children with Disabilities
Baseball is a great way for children of all abilities to get exercise, learn teamwork, and have fun. But for children with disabilities, baseball can also be a special way to bond with their families and friends.
There are many ways that children with disabilities can participate in baseball. Some children may be able to play on a regular team, while others may need to play on a modified team or in a wheelchair baseball league. No matter what level of participation, baseball can be a great way for children with disabilities to feel included and accepted.
In addition to the physical and social benefits of baseball, the sport can also help children with disabilities develop important life skills. For example, baseball teaches children how to follow rules, how to work together as a team, and how to deal with disappointment. These are all skills that can help children with disabilities succeed in school, work, and life.
One child who has found great success in baseball is 10-year-old Maia. Maia has cerebral palsy, which affects her mobility. But that hasn’t stopped her from playing baseball. Maia plays on a modified team that uses wheelchairs. She loves the sport and says that it helps her to feel “normal.”
Maia’s parents are also big fans of baseball. They say that the sport has helped Maia to make friends and to build her confidence. They also say that baseball has taught Maia valuable life lessons, such as the importance of teamwork and perseverance.
If you have a child with a disability, I encourage you to consider getting them involved in baseball. It’s a great way for them to get exercise, have fun, and make friends. It can also help them to develop important life skills.
03. Tadpole Adaptive Provides Online Shopping and Crowdfunding for Equipment for Adults & Children with Special Needs
Tadpole Adaptive is an online retailer and crowdfunding platform that provides equipment for adults and children with special needs. The company was founded by Andy Huesing, who has cerebral palsy. Huesing wanted to create a company that would make it easier for people with disabilities to access the equipment they need to live independent lives.
Tadpole Adaptive offers a wide range of products, including strollers, bikes, standers, walkers, car seats, bath chairs, and more. The company also offers a crowdfunding platform that allows people to raise money for the equipment they need.
Tadpole Adaptive is committed to providing high-quality products at an affordable price. The company also offers a price match guarantee, so you can be sure you are getting the best possible deal.
In addition to its online store, Tadpole Adaptive also has a team of experts who can help you find the right equipment for your needs. The company also offers a variety of resources, including educational materials and a blog.
If you are looking for equipment for a loved one with a disability, Tadpole Adaptive is a great place to start. The company’s wide range of products, affordable prices, and knowledgeable staff make it easy to find the right equipment for your needs.
Here are some of the benefits of shopping at Tadpole Adaptive:
- Wide range of products: Tadpole Adaptive offers a wide range of products for adults and children with special needs, including strollers, bikes, standers, walkers, car seats, bath chairs, and more.
- Affordable prices: Tadpole Adaptive is committed to providing high-quality products at an affordable price. The company also offers a price match guarantee, so you can be sure you are getting the best possible deal.
- Expert advice: Tadpole Adaptive has a team of experts who can help you find the right equipment for your needs. The company also offers a variety of resources, including educational materials and a blog.
If you are looking for equipment for a loved one with a disability, I encourage you to check out Tadpole Adaptive. The company’s wide range of products, affordable prices, and knowledgeable staff make it easy to find the right equipment for your needs.
04. The Newest Technology in Standing Frames
Standing frames are an assistive technology that can help people with disabilities to stand upright. They are often used by people with Rett Syndrome, a genetic disorder that affects the development of the brain.
There are many different types of standing frames available, but the newest technology is making them more accessible and effective than ever before. For example, some new standing frames use sensors to track the user’s movements and adjust the frame accordingly. This can help to ensure that the user is always in a comfortable and safe position.
Other new standing frames are powered, which means that they can be raised and lowered with the push of a button. This can be helpful for people who have difficulty standing or sitting on their own.
The newest technology in standing frames is making it possible for people with disabilities to stand upright more easily and safely than ever before. This can have a number of benefits, including improved circulation, muscle strength, and overall health.
A Blog to Tell the Story of Our Little Girl Grace
Our little girl Grace was diagnosed with Rett Syndrome when she was just two years old. Rett Syndrome is a genetic disorder that affects the development of the brain. It can cause a variety of symptoms, including intellectual disability, impaired speech, and motor coordination problems.
When Grace was first diagnosed, we were devastated. We didn’t know what the future held for her. But we quickly learned that Grace is a fighter. She is determined and always smiling.
One of the things that has helped Grace the most is standing frames. Standing frames allow Grace to stand upright, which helps to improve her circulation, muscle strength, and overall health. They also help to reduce the risk of scoliosis, a common problem for people with Rett Syndrome.
We are so grateful for the newest technology in standing frames. It has made a huge difference in Grace’s life. She is now able to stand for longer periods of time, which is helping her to reach her full potential.
We hope that this article has helped to raise awareness of the newest technology in standing frames. If you have a child with Rett Syndrome or any other disability, we encourage you to learn more about standing frames. They can make a real difference in the lives of children with disabilities.
How to Help Grace
If you would like to help Grace, you can do so by donating to her GoFundMe page. The money raised will go towards purchasing a new standing frame for Grace. You can also follow Grace’s story on her Facebook page.
Thank you for your support!
05. Little Fighter Harper to be Pain-Free After Life-Changing Operation
A four-year-old girl with cerebral palsy will be able to live without pain thanks to a life-changing operation this summer. Harper Sharrocks, from Norwich, has a form of cerebral palsy that causes her to have muscle spasms in her legs. These spasms can be very painful, and they have made it difficult for Harper to walk.
But thanks to the generosity of the Norwich community, Harper will be able to have a selective dorsal rhizotomy (SDR) operation. SDR is a surgery that can reduce the amount of muscle spasms in people with cerebral palsy.
The operation will be performed at Great Ormond Street Hospital in London. It is a complex surgery, but it has the potential to give Harper a significant improvement in her quality of life.
Harper’s parents, Natasha and Steve, are hopeful that the operation will allow Harper to walk without pain. They are also hopeful that it will give her the confidence to do more activities that she enjoys, such as swimming and dancing.
“We are so grateful to everyone who has donated to Harper’s fundraiser,” said Natasha. “This operation would not have been possible without their support.”
The operation is scheduled to take place in July. Harper’s family is hoping that she will be able to make a full recovery and start living a pain-free life.
About Selective Dorsal Rhizotomy
Selective dorsal rhizotomy (SDR) is a surgery that can reduce the amount of muscle spasms in people with cerebral palsy. The surgery involves cutting some of the sensory nerves in the spine. This reduces the amount of information that the brain receives about the muscles, which can help to reduce the amount of muscle spasms.
SDR is a complex surgery, but it has the potential to give people with cerebral palsy a significant improvement in their quality of life. The surgery can make it easier for people to walk, and it can also reduce the amount of pain that they experience.
SDR is not a cure for cerebral palsy, but it can be a very effective treatment for some people. If you are considering SDR for your child, it is important to talk to your doctor about the risks and benefits of the surgery.
How to Help Harper
If you would like to help Harper, you can donate to her GoFundMe page. The money raised will go towards the cost of the operation and the family’s travel expenses. You can also follow Harper’s story on her Facebook page.
Thank you for your support!
06. Kaiden’s CP Journey
Kaiden is a 7-year-old boy from Norwich, England who has cerebral palsy. He was born at 27 weeks gestation and diagnosed with periventricular leukomalacia (PVL) at 6 weeks old. PVL is a brain injury that can cause cerebral palsy.
Kaiden has spastic quadriplegia cerebral palsy, which means that he has muscle spasticity in all four limbs. This makes it difficult for him to walk, and he also has difficulty with his fine motor skills.
Kaiden’s family has been working hard to help him reach his full potential. They have enrolled him in physical therapy, occupational therapy, and speech therapy. They have also been working with Just4Children, a charity that provides funding for children with disabilities to access quality of life enhancing surgeries and treatments.
Kaiden is eligible for a selective dorsal rhizotomy (SDR) operation. SDR is a surgery that can help to reduce the amount of muscle spasticity in people with cerebral palsy. This can make it easier for them to walk and can also reduce the amount of pain that they experience.
Kaiden’s family is fundraising for the cost of the SDR operation. They have set up a GoFundMe page and have been holding fundraising events. They are also hoping to raise awareness of SDR and the importance of funding for children with disabilities.
Kaiden’s family is hopeful that the SDR operation will help him to walk more independently and to reduce the amount of pain that he experiences. They are also hopeful that the operation will give him the confidence to do more activities that he enjoys.
“We are so grateful for the support that we have received from the Just4Children charity and from the people who have donated to Kaiden’s fundraiser,” said Kaiden’s mother, Sarah. “We are so hopeful that the SDR operation will help Kaiden to reach his full potential.”
Kaiden’s story is a reminder that there is hope for children with cerebral palsy. With the right treatment and support, children with cerebral palsy can live full and happy lives.
How to Help Kaiden
If you would like to help Kaiden, you can donate to his GoFundMe page. The money raised will go towards the cost of the SDR operation and the family’s travel expenses. You can also follow Kaiden’s story on his Facebook page.
Thank you for your support!
07. Joshua’s SDR Journey
Joshua is a 7-year-old boy from Dumfriesshire, Scotland who has cerebral palsy. He was born at 32 weeks gestation and diagnosed with cerebral palsy at 6 months old.
Joshua has spastic diplegia cerebral palsy, which means that he has muscle spasticity in his legs. This makes it difficult for him to walk, and he also has difficulty with his fine motor skills.
Joshua’s family has been working hard to help him reach his full potential. They have enrolled him in physical therapy, occupational therapy, and speech therapy. They have also been working with Just4Children, a charity that provides funding for children with disabilities to access quality of life-enhancing surgeries and treatments.
Joshua is eligible for a selective dorsal rhizotomy (SDR) operation. SDR is a surgery that can help to reduce the amount of muscle spasticity in people with cerebral palsy. This can make it easier for them to walk and can also reduce the amount of pain that they experience.
Joshua’s family is fundraising for the cost of the SDR operation. They have set up a GoFundMe page and have been holding fundraising events. They are also hoping to raise awareness of SDR and the importance of funding for children with disabilities.
Joshua’s family is hopeful that the SDR operation will help him to walk more independently and to reduce the amount of pain that he experiences. They are also hopeful that the operation will give him the confidence to do more activities that he enjoys.
“We are so grateful for the support that we have received from the Just4Children charity and from the people who have donated to Joshua’s fundraiser,” said Joshua’s mother, Sarah. “We are so hopeful that the SDR operation will help Joshua to reach his full potential.”
Joshua’s story is a reminder that there is hope for children with cerebral palsy. With the right treatment and support, children with cerebral palsy can live full and happy lives.
How to Help Joshua
If you would like to help Joshua, you can donate to his GoFundMe page. The money raised will go towards the cost of the SDR operation and the family’s travel expenses. You can also follow Joshua’s story on his Facebook page.
Thank you for your support!
About Selective Dorsal Rhizotomy (SDR)
Selective dorsal rhizotomy (SDR) is a surgery that can reduce the amount of muscle spasticity in people with cerebral palsy. The surgery involves cutting some of the sensory nerves in the spine. This reduces the amount of information that the brain receives about the muscles, which can help to reduce the amount of muscle spasms.
SDR is a complex surgery, but it has the potential to give people with cerebral palsy a significant improvement in their quality of life. The surgery can make it easier for people to walk, and it can also reduce the amount of pain that they experience.
SDR is not a cure for cerebral palsy, but it can be a very effective treatment for some people. If you are considering SDR for your child, it is important to talk to your doctor about the risks and benefits of the surgery.
Thank you for your support!
We hope that you will consider donating to Joshua’s GoFundMe page. Every little bit helps, and together we can make a difference in Joshua’s life. Thank you for your support!
08. Levi’s Wish to Walk
Levi is a 6-year-old boy from Reading, Berkshire who has cerebral palsy. He was born 13 and a half weeks premature, and he was diagnosed with cerebral palsy spastic diplegia with a quadruple pattern at the age of 11 months old. This means that Levi will never walk unaided.
Despite his disability, Levi is a happy and active boy. He loves to play with his friends, and he enjoys swimming and playing football. However, Levi’s dream is to be able to walk.
Levi’s family is fundraising for a selective dorsal rhizotomy (SDR) operation. SDR is a surgery that can help to reduce the amount of muscle spasticity in people with cerebral palsy. This can make it easier for them to walk and can also reduce the amount of pain that they experience.
The SDR operation is not a cure for cerebral palsy, but it can be a very effective treatment for some people. If Levi is able to have the surgery, he will have a much better chance of being able to walk independently.
Levi’s family is hopeful that the SDR operation will help him to achieve his dream of walking. They are also hopeful that the operation will give him the confidence to do more activities that he enjoys.
“We are so grateful for the support that we have received from the Tree of Hope charity and from the people who have donated to Levi’s fundraiser,” said Levi’s mother, Sarah. “We are so hopeful that the SDR operation will help Levi to reach his full potential.”
Levi’s story is a reminder that there is hope for children with cerebral palsy. With the right treatment and support, children with cerebral palsy can live full and happy lives.
How to Help Levi
If you would like to help Levi, you can donate to his GoFundMe page. The money raised will go towards the cost of the SDR operation and the family’s travel expenses. You can also follow Levi’s story on his Facebook page.
Thank you for your support!
About Selective Dorsal Rhizotomy (SDR)
Selective dorsal rhizotomy (SDR) is a surgery that can reduce the amount of muscle spasticity in people with cerebral palsy. The surgery involves cutting some of the sensory nerves in the spine. This reduces the amount of information that the brain receives about the muscles, which can help to reduce the amount of muscle spasms.
SDR is a complex surgery, but it has the potential to give people with cerebral palsy a significant improvement in their quality of life. The surgery can make it easier for people to walk, and it can also reduce the amount of pain that they experience.
SDR is not a cure for cerebral palsy, but it can be a very effective treatment for some people. If you are considering SDR for your child, it is important to talk to your doctor about the risks and benefits of the surgery.
Thank you for your support!
We hope that you will consider donating to Levi’s GoFundMe page. Every little bit helps, and together we can make a difference in Levi’s life. Thank you for your support!
09. Utah Mom Chooses to Illegally Treat 3-Year-Old Daughter with Cannabis Oil
A Utah mother is facing legal trouble after she was caught illegally treating her 3-year-old daughter with cannabis oil. Sarah Ellett, 43, of Nephi, Utah, has been using cannabis oil to treat her daughter Remie’s severe seizures since she was just 18 months old.
Remie was born with a rare condition called Aicardi syndrome, which causes her to have frequent and severe seizures. The seizures have left Remie with developmental delays and other health problems.
Ellett said that she tried everything she could to help Remie, but nothing seemed to work. She eventually turned to cannabis oil, which she said has been a miracle drug for her daughter.
“The seizures stopped,” Ellett told People magazine. “She started sleeping through the night. She started talking. She started walking.”
However, cannabis oil is illegal in Utah. Ellett was arrested in February after a caseworker from the Utah Division of Child and Family Services (DCFS) found out that she was using the drug to treat Remie.
Ellett is facing charges of child abuse and neglect. She could face up to 15 years in prison if she is convicted.
Ellett’s case has sparked a debate about the use of cannabis oil to treat children with seizures. Some people believe that cannabis oil is a safe and effective treatment, while others believe that it is dangerous and should not be used.
The American Academy of Pediatrics (AAP) does not recommend the use of cannabis oil to treat children with seizures. The AAP says that there is not enough scientific evidence to support the use of cannabis oil for this purpose.
However, some parents of children with seizures say that cannabis oil has been a lifesaver for their children. They argue that the AAP’s position is based on outdated research and that cannabis oil is a safe and effective treatment for seizures.
Ellett’s case is still pending, but it is likely to have a significant impact on the debate about the use of cannabis oil to treat children with seizures. If Ellett is convicted, it could discourage other parents from using cannabis oil to treat their children. However, if Ellett is acquitted, it could pave the way for other parents to use cannabis oil to treat their children with seizures.
The Future of Cannabis Oil
The future of cannabis oil for treating children with seizures is uncertain. The AAP’s position on the use of cannabis oil is likely to remain unchanged, but more research is being done on the potential benefits and risks of the drug.
It is possible that the FDA will eventually approve cannabis oil for the treatment of seizures. However, this is likely to be a long process. In the meantime, parents of children with seizures who are considering using cannabis oil should talk to their doctor about the risks and benefits of the drug.
10. Buddy Roamer: More Than Just a Walker
Buddy Roamer is a posterior walking aid that provides partial weight bearing postural support with mobility. The ergonomically designed frame supports body weight while allowing the child to walk around freely and unaided. Buddy Roamer has been designed to meet the needs of mild, moderate and complex users.
Buddy Roamer is a great option for children with cerebral palsy, spina bifida, and other conditions that affect their ability to walk. The walker is lightweight and easy to maneuver, making it ideal for use in both indoor and outdoor settings. Buddy Roamer also features a number of safety features, including a padded seat and a safety belt.
In addition to providing postural support and mobility, Buddy Roamer can also help to improve a child’s balance and coordination. The walker’s adjustable height and width allow it to be customized to fit the individual child, and the walker’s design encourages the child to use their own muscles to walk.
Buddy Roamer is more than just a walker. It is a tool that can help children with disabilities to live more independent and active lives. The walker can help children to participate in activities that they would not be able to do without it, such as playing with friends, going to school, and even traveling.
If you are looking for a walker that can help your child to reach their full potential, Buddy Roamer is a great option. The walker is safe, effective, and easy to use. It is also a great way to improve your child’s balance, coordination, and overall mobility.
Benefits of Buddy Roamer
- Provides partial weight bearing postural support
- Allows children to walk around freely and unaided
- Lightweight and easy to maneuver
- Features a number of safety features
- Can help to improve balance and coordination
- Encourages children to use their own muscles to walk
- Can help children to participate in more activities
If you are considering Buddy Roamer, here are a few things to keep in mind:
- The walker is designed for children with mild, moderate, and complex disabilities.
- The walker is adjustable to fit the individual child.
- The walker is safe and easy to use.
- The walker can help to improve balance, coordination, and overall mobility.
If you think that Buddy Roamer might be a good fit for your child, talk to your doctor or physical therapist. They can help you to determine if the walker is right for your child and can provide you with more information.
