Stem Cell Therapy

Stem Cell therapy is a stem cell that comes from a persons body. It can replicate itself and has the ability to make Stem_cell_treatments.svgspecialized cells for various tissues in the body. This includes the heart,brain, and liver. Stem cells can come from three different places. The embryo , bone marrow, and cord blood which comes from the umbilical cord after a babies born. The embryo method is the most affective method but also the most controversial. Public,politicians, and religious groups are against the embryo method because the embryo is destroyed after the stem cells are extracted. They believe it is equivalent to taking a life. That is why researchers have developed other methods. The bone marrow method is usually extracted from adults. These stem cells are limited in potential relative to embryonic stem cells. The cord blood stem cells hold enormous potential in treating diseases. I am for stem cell research I believe that it will help cure some diseases. Stem cell research is not illegal in the United States. There is however funding and use restrictions on it put in place by congress. The states that allow stem cell research California,Connecticut,Illinois,Indiana,Maryland,Massachusetts,New Jersey,New York, Washington,Wisconsin, and Virginia. Stem Cell research has been known to help people with Parkinson, Stoke, Alzheimer, and spinal cord injuries. Right now it is also being used to treat cancer such as leukemia. Stem cells not only help humans they also help animals. Alpine Animal Hospital in Pocatello, ID treats animals using stem cells. They do not use embryonic stem cells. Instead they take the fat tissue from the animal. They give them general anesthesia to obtain the fat tissue. It is either taken from the abdomen or the shoulder. They take the sample to the laboratory so they can harvest it to get the stem cells from the tissue. It usually takes 2-3 hours. They then sedate your pet and put the stem cells directly into where the disease or injury is. They give it to the persons animal intravenously. Meaning as a solution, nutrient or drug given through the vein. The stem cells have been known to help animals withpro-stem-cell-research

  •  Chronic Arthritis
  • Joint pain
  • Cartilage damage
  • hip displacement
  • tendon or ligament damage
  • Chronic illnesses such as autoimmune disease,live,kidney, and allergies.

Stem cell therapy can help a lot of people in the long run and with out the proper funding we really don’t know it’s potential. This is a good way to help cure diseases. It could is the medical future in cures.

 

Sources

“Alpine Animal Hospital.” Alpine Animal Hospital. N.p., n.d. Web. 27 Apr. 2014.
sites.psu.edu
“Stem Cell Research.” Embryonic and Fetal Research Laws. N.p., n.d. Web. 27 Apr. 2014.
“Stem Cells: The Facts.” Stem Cells: The Facts. N.p., n.d. Web. 27 Apr. 2014.
Wikipedia.org

Prosthetics just for humans?

Prosthetics help children who have disabilities. A prosthetic is a medical devices that doctors use. They put it on children who have lost or werHorsee born without certain limbs. There are other types of prosthetics leg braces and arm braces are an example. My daughter has been wearing them all ever since she could walk. Prosthetics help my daughter walk because her feet turn inward. They help to straighten her feet out. I got a hold of Hanger Inc. They are a prosthetics manufacturing business. I wanted to get a hold of someone who worked on prosthetics so I could learn more about them. Cindy Goodwin got a hold of me and said she would look more into my request. A week later she wrote back and said that she would get someone from Boise, ID to write me back via e-mail so I could conduct my interview. I am still waiting to hear back from him. Many people wear prosthetics even famous athletes. The fastest 100 meter dash was done by someone who wore prosthetics. He is an olympic champion named Usain Bolt. Prosthetics doesn’t limit a persons mobiity if they can dream it and work hard enough to acomplish something they can. All you have to do is set your mind to it. Prosthetics not only help people they also help animals as well. Orthopets. Is a prosthetic company that builds prosthetics strictly for animals. I watched an episode of Nature on bionic pets and how they get around. If ypu get a chance you should watch it. It’s very inspirational.  It amazes me how far tecnology has come and how caring people are that they would try to find a way to help animals. There waporkys a movie that came out in 2011 about a boy and a dolphin the dolphin got into an accident with a boat and had to get it’s tail amputated. It was based on a true story. The dolphins name is Winter and she had to learn how to re use her tail. It is an amazing movie. Animals aren’t to different from us they need help and have emotions just like us. I am glad tecnology has got advanced to were we can help them.

A link to Bionic pet video

Episodes

 

Sources

“Interesting Facts.” Corpus Christi Prosthetics. N.p., n.d. Web. 26 Apr. 2014.

News.yahoo.com

http://www.bornjustright.com

 

 

OCD

OCD is Checklista condition known as overactive compulsive disorder. What compulsive means is that you have the urge to do something even if you’re body is telling you no. Everybody has urges to do things whether it is to check and make sure your doors locked or to double check and make sure that you turned the oven off before you leave the house. People with OCD have these urges but they do them over and over again. Usually people with this condition have a routine they follow it’s the same routine everyday. For instance a person afraid of someone breaking in might lock and unlock their doors several times before they have to go to bed. People with this condition can’t just stop doing these routines. The disease just takes control of their body even if they wanCompulsivet to quit the compulsiveness won’t let them. Researches don’t really know why people have OCD. OCD can run in the family. Researches believe that if they study the part of the brain that runs on fear and anxiety that maybe they can come up with better treatment for this condition.  OCD starts out during childhood or teen years. People are usually diagnosed by the time they are 19. About 1/3 of adults who have OCD developed it as a child. OCD affects around 2.2 million Americans. Women and men are about equal when it comes to getting this condition. Some of the symptoms of OCD are

  • Can’t control their behaviors or thoughts
  • Do the same routine over and over again
  • Have repeated thoughts
  • Get relief when performing a routine
  • spend at least one hour a day on a routine

OCD can sometimes get better or it can get worse. It keeps people from working or doing responsibilities at home. It can also cause other problems like eating disorders, depression, or other anxiety problems. People who have OCD can get help. There is therapy they can take called cognitive behavioral therapy. It teaches people different ways to think and react in different situations. This helps to control their anxiety. There is also medication for people who have OCD. It has to be prescribed by a doctor. Most of the medication begins working right away but some could take up to 6 weeks.

 

 

Sources

“Obsessive-Compulsive Disorder, OCD.” NIMH RSS. N.p., n.d. Web. 20 Apr. 2014.

Psychcentral.com

Webpages.scu.edu

 

Down syndrome

Downs syndrome is a childhood disease. It happens when a child is born when a child is born with an extra copLangdony of chromosomes. A normal child is born with 23 chromosomes. A child with down syndrome has 21. This additional chromosome alters the way the child is born. Kids who have down syndrome usually have low muscle tone, small stature, and an upward slant of the eyes. One in every 691 babies in the U.S. are born with Down syndrome. It is the most common genetic disorder. There is approximately 400,00o Americans who have down syndrome. Down syndrome was first discovered in the nineteenth century by a English physician named John Langdon Down. He wrote a book on the accurate description of this genetic disorder. The book was published in 1866 and he was named the “father” of down syndrome. There are three different types of down syndrome. Trisomy 21, translocation, and mosaicism. Trisomy is caused when an embryo copies three chromosomes instead of two. This happens when the egg or spChromosomeerm fail to separate. This type accounts for 95% of the cases found. Translocation accounts for 4% of cases. In this type part of the chromosome breaks off during cell division and attaches to another chromosome. This is typically chromosome 14. Mosaicism occurs when the trisomy chromosome 21 takes in one of the initial cell divisions after fertilization. When this happens their is a mixture of two types of cells people usually contain 46 chromosomes. Those that have this type contain 47. Mosaicism accounts for only 1% of cases.

Sources

http://www.dovemed.com

http://www.langdondownmuseum.org.uk

“What Is Down Syndrome?” – National Down Syndrome Society. N.p., n.d. Web. 20 Apr. 2014.

Shyann had her second surgery March 27th, 2014. She had surgery on her right bone to straighten it out. After surgery everything was different because she could no longer use her right foot until it got all healed up. She had to figure out how to get from one place to another on just one foot. To make things easier NORCO provided her a wheel chair to use for the next 5 weeks. This made it easier for her to get from one place to another. It made it a lot harder for everyone else. The wheel chair doesn’t collapse very well and it’s really heavy making it a lot harder to get her to school and back. Not only did the surgery affect family it also affected her schooling. Sometimes she has to be carried places or hop from one place to another. children love pushing her around in the wheel chair but sometimes they can push her to fast which causes pain in her leg. She also has to go to different classrooms like for music she usually went downstairs but because she can’t use her one foot she has to go to a different room. She also can’t participate in certain events like fun runs or dancing. She doesn’t mind instead she will just move the upper half of her body. For the fun run she just waits at the end of the finish line cheering on her other classmates. The hardest part about the wheel chair is that we have steps in order to get into the house and it is really hard to carry a wheel chair up a bunch of steps. She also has to accommodate when it comes to doing things in the house. Not using her leg makes it a lot harder to get to the bathroom,go to bed, or sit at the dinner table. She has gotten pretty good at hoping from place to place but still needs help sometimes. I wish that they had light weight wheel chairs it would make it easier for everyone. She gets her cast off the 25th of April and will be able to use her foot again. She’s exited and can’t wait to do the things she used to

Physical therapy

Ever since Shyann was 7 months old she has had a physical therapist. That is a person who specializes in helping peoplePhysical Therapy who need help physically. A physical therapist helps with all different type of physical problems like a car accident, sports injury, or a disability. Shyann’s first physical therapist was John Hurley he helped her out tremendously. He helped her with walking and balancing. He also was the one who first noticed problems in her feet. He helped get us into Shriner’s Hospital in Salt Lake City. Shriners is a hospital that helps disabled children with low income families. Shriners doesn’t make you pay anything because they believe that a child’s health and well being is more important than money. Shyann’s Doctor at Shriner’s was Doctor Carol she was the one who diagnosed her with tibial torsion and the mildest kind of Cerebral Palsy that could possibly be fixed with surgery. After Shriners we had to find a prosthesis business to make her a pair of braces so she could keep her feet straight. John was Shyann’s Physical theraPtpist until 3 years old. After that I had to find a new physical therapist. I went to Portenuf Physical medicine where I met Shannon for the first time. Shanon did some test on her to see if she qualified for physical therapy. Shyann qualified and is now 7 years old and Shanon has been her physical therapist ever since. Shanon has helped out my daughter so much and has made significant improvement in her physical abilities.

Sources

http://www.Baystatept.com

http://www.utica.edu

 

Postivie Story

Kimberley Carnevale is an author,motivational speaker, and disability advocate. Last year she had lost her home. Her daughter and service dogs had nothing in a blink or an eye. Kimberley had developed post traumatic stress disorder. That is an anxiety condition that happens aftelollipopr something extreme happens to a person. This was hard for Kimberley because she had a disability on top of everything. They had to depend on the kindness of others to provide shelter. Even though they had lost everything she needed to stay strong for her child. She would wait until after her daughter had gone to sleep before she would cry and let loose of everything she had built up. Kimberley thought of her self as a good person. They lost there house to a brutal attack from a family member that was an alcoholic. She had felt betrayed by her family member, and by god. It got to the point where she thought her daughter would be better off without her. That she deserved better a roof over her head and someone who could take care of her. Even though her daughter had known she had lost everything she never complained. She would never ask for things she wanted on the T.V. Or get upset when her mom couldn’t play with her because she was sick. One day Kimberley and her daughter went to the store she could tell her daughter really wanted a lollipop that was there. Her daughter never once asked for it or made any indication that she wanted it. Because of this Kimberley decided to buy it for her. It was near the end of the month and all she had left to her name was $1.35. Even though they didn’t have very much money left she still bought her the lollipop because she had been so good. Her eyes lit up and she said. ” Thank you mommy, your the BEST mommy.” She was so happy tears were running down her face. It was at that moment that the cloud that had been hovering over her had been lifted off her shoulders. She knew that the only thing the two of them needed was each other and that the rest was a bonus. It was the best she ever felt. She said., ” In the spirit of giving , I wish for your life be blessed with the insight of my little girl, the shedding of your wet coat, a new a positive perception on life….filled with an unlimited supply of lollipops.”

 

Sources

 

Carnevale, Kimberley. “E-Bility DisABILITY Information Resources.” Lollipop Lesson. N.p., 2007. Web. 06 Apr. 2014.

 

Make a Wish

Make a Wish Foundation is a non profit organization. It was founded in the United States. The idea of this organization is to give kids with life threatening illnesses a chance to make a wish or have aMake a wishn experience they have all ways wanted. The kid has to range from the age of 2-18 years of age. There doctor or physician will decide if the child is eligible to participate in this organization. Make a Wish is not only located in the united states it is also located in 42 other countries. This foundation has 62 different chapters in the United States. It’s main head quarters is located in Phoenix , Arizona. The president and CEO of this foundation is David A Williams. The most wishes given are to a professional wrestler names John Cena. Children have given this wish over 450 times. When I was younger I got a chance to be a part of make a wish. I really wanted to go to Disneyland but because of my condition it wasn’t an option. So I decided on a second wish and that wasOLYMPUS DIGITAL CAMERA to be on T.V. My doctor mom and make a wish thought that was a reasonable wish. I got a chance to be on KSL’s telethon they sat and talked to me about my brain tumor and my surgeries. It was more of an interview I believe. I don’t remember to much about it. I was 7 or 8 and I remember I was really exited about it. I told everyone that I was going to be on T.V. and to make sure and watch Chanel 8. I remember I had to travel to Idaho Falls where there station was located and they gave me a toy afterwords I believe it was a barbie. Make a Wish is a good foundation it gives children a chance to experience things they never thought was possible.

 

Sources

“Make-A-Wish Foundation.” Wikipedia. Wikimedia Foundation, 04 May 2014. Web. 06 Apr. 2014.
secure.wish.org
simagjewelry.blogspot.com

Disabliity camps

Disabity camps

fsn.tamu.org

Being a kid with a disability is hard. Kids with disabilities need to have a place where they can be themselves and interact with other people like them. That way they don’t feel different. That is why there are disability camps. There are over 200 disability camps in the United States. If you go to fcsn.org they have a directory that categorizes the different disabilities and tells you what camps fits the child’s special needs. Wonderland Camp is a camp out in Missouri this camp takes children with all different types of disabilities. It has been running for the past 40 years.  There mission, “is to provide a fun, educational camp experience for children teenagers and adults with disabilities.”  The founder of this camp is Charles J Miller. He had a dream to put a residential summer camp on the property that him and his brother- in- law owned Harry brown. It’s located on a lake of the Ozarks. He wanted a place where people who were mentally and physically challenged could experience the outdoor life and be themselves. The camp first opened in 1972. They have a different variety of activities for the campers.

  • Swimming
  • Baoting
  • Fishing
  • Arts and crafts
  • MusicMarshmellos
  • Carnivals

This gives children with different disabilities a chance to be themselves and have fun with people just like them. When I was younger I got offered to go to disability summer camps. I always turned them down because I was afraid that I would get home sick and that I would have a hard time making friends. Looking back I wish I would of taken the opportunity to go and experience the camp life and meet people just like me. I think disability camps are a good idea because it helps builds their self esteem, gives them a chance to enjoy the outdoors, and shows them that they can do anything that they put their mind too.

 

 Nichy.org

Sources

“Federation for Children with Special Needs.” Federation for Children with Special Needs. N.p., n.d. Web. 05 Apr. 2014.
“Wonderland Camp – Mission & History of Wonderland Camp.” Wonderland Camp – Mission & History of Wonderland Camp. N.p., n.d. Web. 05 Apr. 2014.

Chemo When I was 8 years old I had to undergo chemo therapy. Which is the use of any drug to help prevent a disease. Chemo therapy is used a lot for cancer patients. The procedure required me to go to sleep. The surgeons had to drill a hole in my chest and put a main line in. A main line is a tube that they attach to a vein. It is used to give me medicine like saline and antibiotics. They were hoping that Chemo would help get rid of my brain tumor once and for all. There are a lot of side affects that come with it. Some of which include

  • Appetite Change
  • Bleeding problems
  • Hair loss
  • Nausea and VomitingMain line
  • Infection
  • Memory change

I experienced most of these side effects. It was really hard for me to be on Chemo as a kid. I wasn’t able to run, swim, do strenuous activities, or climb on things. The typical things that kids do.The reason was because if I was to trip and fall I would tear out my main line. That would cause internal bleeding and I would of possibly died. There was one time that my dad took me to Downata Hot Springs I wasn’t able to swim so I sat on the steps. I was playing ball with another little girl when it fell into the water. Without thinking I jumped into the water to retrieve the ball. My dad rushed me home as fast as he could to clean the main line and make sure no water had gotten into my veins. I was on Chemotherapy for a little over a year. I went to Primary Children’s Hospital to have it taken out. They told me that it had gotten rid of my brain tumor. I have been in remission now for 16 years I still have to go there every two years to make sure it doesn’t come back.

Sources

“Coping with Cancer: Supportive and Palliative Care.” Chemotherapy Side Effects Sheets. N.p., n.d. Web. 30 Mar. 2014.
“Mainline.” Dictionary.com. Dictionary.com, n.d. Web. 30 Mar. 2014.
“What Is Chemotherapy?” What Is Chemotherapy? N.p., n.d. Web. 30 Mar. 2014.