Spina Bifida Spina Bifida is a birth defect where the spinal cord does not develop correctly, or is not closed all the way while still in the mother. Back many years ago people who were diagnosed with spina bifida were not expected to live very long. Their lifespan was only about 6-12 months and then they would die. From having the spinal cord not developed it can cause massive defects on the child. It can be as simple as just a limp in the walk, but it can get as bad as not being able to use their legs at all. These children still have the right to work out and become stronger individuals. The children may also want to be involved in a sport. Many people may think this is impossible, but with slight modifications the child can participate …show more content…
Often times if the spina bifida is minor the surgery can almost completely solve the issues the person is having. These surgeries require many different procedures that normally include neurosurgical, orthopedic, and urologic. Infection is common among these patients especially after being operated on. They must be monitored very closely so the infection can be reversed. After the surgeries the orthopedic surgeon becomes the most important role. Their job is to monitor the range of motion, motor strength, skin irritation, and more. Many times the orthopedic surgeon will have to provide the person with braces. These braces will help the person stand the correct way if they can. That way when walking they can strengthen the muscles used to walk. This will get the person one step closer to living a close to normal …show more content…
Children can go under go a countless amount of surgeries to help them work through spina bifida, however it is almost impossible for the child to get through their lives without symptoms going unnoticed. There are many different stages of spina bifida going from minor symptoms like a limp in their walk to being pretty much completely paralyzed. There have been many famous people with spina bifida such as athletes, actors, writers, and more. By sharing these famous people with children with spina bifida it will help them look at life more positively. There are ways that parents can have a better chance at avoiding spina bifida, however there is no way to completely get rid of the chances of the child having the disease. Before scientists went into research on spina bifida the children were not likely to live past a year. Spina Bifida is a horrific birth defect, and hopefully with continuing studies spina bifida average rate will continue to
In Canada, a clinical study by De Wals et al was performed to assess whether or not folic acid fortification has an effect on the recurrence of NTDs (neural tube defects), especially on upper and lower birth defects called spina bifida (De Wals et al., 2008). The study was performed in three different regions in Canada: the eastern, western and central provinces (De Wals et al., 2008). Furthermore, the population of the study was conducted on three different types of births which were livebirths, stillbirths, and termination of pregnancies, and the study was carried out through three periods included prefortification, partial fortification and full fortifications (De Wals et al., 2008). The researchers followed the scientific investigation
The world as we know it has had many issues that has affected the lives of many people in our community. Some of these issues produce a negative response or unfair opportunities for the people with these issues. One type of issue that can be affected negatively in our community is child disabilities or any disabilities in general for that matter. The life of a person with disabilities could be a huge issue if the community keeps responding the way they have been responding.
Progeria takes more than a physical toll; however: the emotional impact for a child living with a rare and fatal disease can be terribly difficult and traumatic. Since children with Progeria have normal intelligence, most of them go to school like every other child. However, there can be a downside because these children have a far greater risk of being bullied. Additionally, these children are compelled to do physical activities somewhat differently. Since they are so petite and have fragile bones, it is hard for them to get involved in any sport. They also get tired very easily so they need to take constant breaks from strenuous activities. Even walking a short distance can cause harm to the body. Children with Progeria need to make sure to stay well-hydrated and have regular, minor physical activity (Diseases) that does not put them at risk for bone or cardiovascular injury. The emotional backlash
In the article Optimizing Health Care for Children with Spina Bifida Liptak discusses some of the struggles with healthcare for child with spina bifida. Liptak (2010) states that children with spina bifida “need specialists, generalists to deliver complex care.” Spina bifida is the most complex birth defect. Children with spina bifida can have “problems with breathing, a latex
Spina Bifida literally means “split spine”. It is the most common permanent disabling birth defect in the United States. It happens when the brain, spinal cord do not completely develop. It is the most common neural tube defect in the United States- affecting 1500 to 2000 of more than four million babies in each year. An estimate shows 166,000 individual lives with Spina Bifida in the United States. I choose this disorder because many people do not about the effects, causes, symptoms and treatments about the disorder and I wanted to know more about spina bifida.
When i was born, my spine was not fully formed at the bottom, leaving an opening that would be the cause difficulties my entire life. I was diagnosed with Spina Bifida Occulta. Spina Bifida is an incurable birth defect where the vertebrae is defective causing the spinal cord to fail a proper development. In most cases of Spina Bifida the person is wheelchair bound their entire life along with other major health problems. Despite this, step by step I began walking on my own just under one year old.
First, I am going to talk about what spina bifida is. It is a congenital disability from the spine
Because of your sponsorship of $700, a person with Spina Bifida can participate in a recreation or therapeutic activity of their choice to improve their physical and social health. This year, SBCC paid for 53 families to attend conferences, camps, adapted sports programs, and gave direct financial aid to several families when bills overextended
Spina bifida is a congenital condition in which the posterior aspects of the vertebrae fail to develop, thus exposing part of the spinal cord (Bontrager 2010, p. 333). Most of the time this defect happens at L5 of the spine but there are different degrees of severity of this condition. From least symptomatic to most symptomatic, the varying stages are spina bifida occulta, spina bifida meningocele, spina bifida myelocele, and spina bifida meningomyelocele. Each have their own ways of being diagnosed and treated. Some of these different imaging modalities used include sonography, x-ray, CT, and MRI. Sonography is a modality that is utilized while the baby is still in the womb. X-ray is usually how spina bifida is discovered if the condition is unknown at birth. CT and MRI are used to further evaluate the condition once it is
Disability: Any child that has a disability such as spina bifida or cerebral palsy could have a huge physical effect on how they will develop. Spina bifida takes place when a child’s spinal cord did not develop correctly while the mum was pregnant. As a result of this a child legs could be partially or fully paralysed and that they could have a curvature on their spine. They could have difficulties controlling themselves when going to the toilet and have deformities in their bones and joints. A child with a physical disability could be at a disadvantage in so many way for E.G. if it were that had restricted movement, then they could find it hard to join in with things just like sports, putting Lego together, staking up things, putting toys
Margaret has spina bifida, a condition in which one or more of her vertebrae did not form properly, leaving her spinal cord—the most vital component of the central nervous system—unprotected. She has had eight operations and wears braces on her legs to keep them in the proper positions. Throughout all of these ordeals, she has retained her outgoing personality and positive view of
The procedure always spoke to me as an embodiment of the human spirit. ‘ If we cannot fix it one way, we will do it another; If we cannot mend the brain, we will correct the feet.’ Ever since my operation, I have used this same outlook to overcome all the handicaps. When I came home from the procedure, I had both legs in soft-wrapped splints. I was to be non-weight bearing and to keep still. The recovery period was frustrating for me and absolutely maddening for my mother. I had no interest in being immobile. So within days of coming home in the splints, I had to be brought back to the hospital. I had snapped the splints in to by trying to crawl. Afterwards, I was put into hard castings and I was more cautious. Once out of my castings, I had to endure a year or more of physical therapy, because I had to learn how to walk again. To this day, I refuse to let my disability stunt my potential. I have tried at every available opportunity to challenge myself, to keep on fighting, and to invent ways around my
Sixteen years ago, Eric Bolnick and his wife eagerly awaited to find out the gender of their baby. As visions of blue and pink raced through their heads, no one could’ve predicted this day would turn into one that would change their lives forever. Within minutes, they found out they were expecting a baby girl. Overwhelmed with joy, they didn’t hear the words “permanently disabled” escape their doctor’s lips shortly after the big news. 5 months later, Kayla Bolnick was born with spinal bifida.
Spina Bifida is a very serious and unpredictable disease it affects many people their are numerous of symptoms that come with this disease it's growing worldwide which is an problem. This disease is a growing problem it's becoming a big problem because scientist are still trying to find a cure and leads to this disease and why is it affecting so many people it's growing rapidly.
The causes of Spina Bifida is a result of genetic and environmental factors also depends on family history , family members could have this defect and its passed on. Another reason Spina Bifida can be caused is by not having enough folic acid which is a type of vitamin that is in green vegetables , a pregnant women should eat green vegetables or any other types of foods that contain folic acid so that the baby is born healthy.