Tag: TCP


TCP happenings!

2
May

Hey all,

Wow where to even begin?? This week has been crazyyyyyy.

First I have to start with Beyond Limits, local Orange County-er Bonner Paddock stars in his own film where he climbs up Mt. Kilomanjaro in Tanzania, Aftica. I saw it Wednesday night, and I was in complete awe of his strength. The whole time I was just smiling and thinking to myself, wow I cannot believe this guy who has CP, did this climb…the altitude was insane..the temperature…all the natural elements battling against him, on top of his physical health….I am speechless. AND the coolest thing was….I got to meet him!! We talked for a bit, I think my dad and him hit it off nicely hah, but it was really great to be able to talk a bit about his climb, and his foundation that was introduced in his film as well, OM foundation (One Man One Mission) Check it out for yourself, http://www.beyond-limits.com/home.php http://1man1mission.org/projects/ props to all who journeyed up there with him for the support and the filming as well, you are all incredible!! I hope to get involved in your cause one day, and represent TCP and all those kids out there!

Okay hmm what else…our gym had a grand ‘ol party last night for our Takedown Challengers, who went through a six week weight loss program, it was a lot of fun and there was A LOT of food!! We made these cookies that are mini peanut butter ones in baby muffin tins with a reeses in the middle, they are killer! Congrats challengers. Oh and I think that I’m just going to have to upload like and entire album of pics from over a few weeks, because we have them on about three different cameras, I just need to sort through them! Sorry about that. :p Alsooo, last week was the Ragnar Relay  Race, a non-stop 200 miles race down the coast that my parents and sister did with a 12 man team called WTF ( Witness the Fitness) Ha! They ended up dominating their division, finishing in 28 hours on no sleep and got 5th out of 45 teams! GO WTF! :) I am especially so proud of my sister being the only teen on the team! She did so well and ran 3 legs of about 4-8 miles each time on extreme terrain with no sleep! Sara, you are amazing and I wish I could’ve seen you run! Love ya. I am very proud of my parents as well, my mom is a super star running maniac (like always) and my dad who basically turned himself into an avid runner and worked through his planter faciitis, a very painful problem with his tendons on one of his foot that he pushed through all during the face! My dad is also training for a body building competition memorial day weekend, so he is all about being hardcore right now with his overall health. Keep it up papa, you will do so well and I am excited to watch you win first place!

I am working on my left side a lot in the gym since I have been overcompensating a lot on my right side. I also started wearing my brace again, and I am trying to convince myself it’s not that bad since it is so crucial for my health. I feel very optimistic with where I am at in life, health wise, mentally, socially…I am on my way to better things and living life to the fullest. life is good. :)

Hmm what else… oh, the SAT was yesterday, eeeek that thing was hard! I think I was unprepared for the math portion. I loved the English part though, it’s my expertise. ;) I can always retake it, but I am fairly confident in my academic ability. Glad that is over with until I get my scores back. Although I am still en route to a few more important exams this year. AP tests this week, SAT subject tests, the ACT, and finals week all in June. Wow thats a mouthful! It’ll be nice to knock all that out, and then call myself a senior! Definitely got to look toward applying for college this summer! I might have to take a trip back East to keep my options open. This time in my life is all so exciting, and going by SO incredibly fast!! :)

I hope you all are in good spirits and health as well, summer will be here before you know it and we can all be kids again! ;p Thanks for being so supportive of me and reading my blog, this has been such a fun experience for me and I hope you enjoy this site as much as I do. I am open to ideas for expanding this site to bigger and better things, while still representing all you TCPer’s out there, so if you guys ever think of anything, please shoot me an email!

Thanks so much, have a nice Sunday afternoon. I vow to get pics up soon, I’m trying to manage my time better these days, its a challenge for sure!

-Katy

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Feeling a bit MIA

27
April

Hey Guys…

Sorry I haven’t posted in awhile, I have the SAT and AP tests creeping up on me and it’s time to get down to business!

Although I am going to the Newport Film Festival tomorrow for the last showing of Beyond Limits with CP star Bonner Paddock, to see his journey up a 19,000 ft mountain, can’t wait to mee him! :) Going to represent all the TCPers out there!

I’ll be on in good time, still trying to get hike pics from my dad’s camera. Like I said, he’s a little slow when it comes to technology. :p Thanks for being patient for those of you who stay interested!!

Have a good one.

-Katy

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CP + Guilt Trip = Bad Monday

19
April

Maybe….

I should start stretching so my mom won’t say ” your castings were a complete waste of your time and a complete waste of our money.”

Because….

I know that is the truth. Yeah. Ouch. Ugh this morning was abnormally worse than most Monday’s. I need to stop screwing myself over if I’m going to do this right. At least my day got progressively better despite my depressing start in the AM. The weather is beautiful so I went outside for a loooong run/walk to contemplate my actions. Hmm. Fuuuun stuff we get to deal with huh?

I’m off to try and be productive and finish a thing or two for school. Hope your Monday morning was better than mine!

-Katy

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Push-ups & Hills

11
April

Hey Everyone!

Wow what a nice week off from school, although I didn’t have school I still felt busy with hittin’ the gym (and the beach of course ;p almost every day!) Actually, we had a great charity event just yesterday at our gym, I’ve mentioned it before…it was lots of fun! We raised a few thousand dollars for The Wounded Warriors Project by hosting a 90 second push up competition! We had many generous sponsorships and donations, and I can’t wait to get some pics up. Somehow, I was able to knock out 67 push-ups in 90 seconds and raise a few hundred dollars by doing so, so I am pretty stoked! My left arm was about to break off though, it was pretty funny… I tried not to laugh once my muscles were dead haha.

We did a very ambitious hike this morning as well through Peter’s Canyon in Irvine not too far from here. It had such gorgeous views of new homes and crevices in the land…but unfortunately I forgot my camera!! I was super bummed, but hopefully I can manage to get a few pics from others that went along. There were three majorly steep hills that I just about passed out on! My ankle is a little sore, but my dad noticed I am walking better–and coming from him that’s definitely a plus! Sometimes I worry that I won’t be able to do hikes like this, but I can really only take everything day by day.  There’s no use in worrying about something that’s either unpreventable, or years and years away.

Well thanks for the chat guys, but I have to hit the books before school in the morning ….which I am dreading terribly so.  Hope you had a great spring break and are all staying healthy! :) Pics will be coming eventually, so stay tuned.

-Katy

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Spring is here, summer is coming!

26
March

Hey Guys,

Hope you had a good week! I am happy that spring break is almost here, I think we could all use a well deserved break from reality every now and then.  I cannot believe it is already spring… next thing you know it will be summer…and the 1 year anniversary of TCP!Also my 18th birthday, but who’s counting. :p Speaking of turning 18, HAPPY BIRTHDAY to Greg!! (My awesome web manager guy) I hope you have a fabulous day, and may this year bring you the best days of your new life as an adult (at Stanfordin the fall might I add!)

 I have been doing cardio almost everyday, my body is exhausted! Although, it has been an adventure each day. Running along the beach is so much fun, I feel very thankful to live in such a beautiful place! The weather is so nice here as well, seems like summertime might come a bit early. :p

On Sunday a big group of the Takedown Challengers and I will be embarking on another hike around here. I don’t know what to expect, but I am sure it will be just as great as all my other hiking experiences. I feel like I have gotten to be a much stronger runnner these past few weeks. I am able to keep up with the crew these days. It’s a good feeling of accomplishment and I hope my body enables me to keep it up! I’ll be sure to post about the hike afterward to tell you how it went. Last Sunday we went to a big recreational park where they had horse trails and stables, and it was a few miles wide. Such a pretty sight, I had no idea this place even existed around here! It was in Irvine not too far from where I live.  I will try to get some pics up, as technologically inept as my dad is, he managed to snap a few pics of the scenery. :p

I have to confess something though…as much as I have been working out, I haven’t really kept up my stretching and brace wearing. :/ I need to get myself back on track because this is not a good pattern!! Yikess. I definitely don’t want to go through castings again…just gotta pull myself together a bit. It’s just all a big part of life with CP I guess. so have to remember to give my therapist a call, she is probably wondering if I fell of the face of the earth. :p

I am excited for next school year though (already, I know) But mostly because I will be a senior, and I might join ASB! Some of my best friends are on it and they said I would make a good addition, so I think I am going to apply for Commissioner of Community Service, pretty self-explanitory..but the position would just mean that I am in charge of representing HBHS at charity events, community service activities, that ASB attends. It might be a good idea to do something for UCP-OC, who knows, they might need a number of school spirited teens to support their cause at one point. :) I was also chosen to be a part of NHS National Honors Society for next year, and my amazing English teacher is the leader, I am so excited!’s a pretty special thing, only 20 seniors are involved in representing our school for it! It will be gratifying to get involved in the community and the school especially, since it is my last year! I have to make it the most memorable that’s for sure!

So I feel like I’m a little delayed and repetitive in my posts lately…are there any burning questions or topics you’d like to discuss? I’ve pretty much talked about CP related stuff in the past, but I know I’m only one in millons of teen with CP…so if you’re out there and always wanted to talk about a certain something you noticed, dealt with, confronted–anything CP related..just comment on this and see where it takes us! Thanks!

I’ll be on soon, hopefully with pictures of the hikes.

-Katy

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a Looking Glass into Cerebral Palsy

21
March

Hey there!

So I have been feeling like I am much more uneducated on CP than I should be, considering Im affected by it each minute I live! So here’s the deal, I did a little research and here is what I came up with, there are four types of  Cerebral Palsy…I let wikipedia break it down for ya :p I feel like they do a good job of encompassing all the FAQ’s. Hopefully it isn’t too much to take in, feel free to just skim over it…I bolded a few parts that caught my attention, as it applies to some commonalities of CP. I have a few more info to the right colums under “resources” that you maybe want to check out as well. I just thought you might want to go on here to read up on CP, as some other webs are a bit intimidating and hard to sort out. I’m not sure if you have already done any research on your own, nevertheless, this is here… who knows, maybe researching is how you came across my TCP web! :)

CEREBRAL PALSY

Spastic cerebral palsy is by far the most common type, occurring in 70% to 80% of all cases. Moreover, spastic CP accompanies one of the other types in 30% of all cases. People with this type are hypertonic and have a neuromuscular condition stemming from damage to the corticospinal tract or the motor cortex that affects the nervous system’s ability to receive gamma amino butyric acid in the area(s) affected by the disability. Spastic CP is further classified by topography dependent on the region of the body affected; these include:

  • Spastic hemiplegia (one side being affected). Generally, injury to muscle-nerves controlled by the brain’s left side will cause a right body deficit, and vice versa. Typically, people that have spastic hemiplegia are the most ambulatory, although they generally have dynamic equinus on the affected side and are primarily prescribed ankle-foot orthoses to prevent said equinus.[11] —-This is the definition of my case!
  •  
  • Spastic diplegia (the lower extremities are affected with little to no upper-body spasticity). The most common form of the spastic forms. Most people with spastic diplegia are fully ambulatory and have a scissors gait. Flexed knees and hips to varying degrees are common. Hip problems, dislocations, and in three-quarters of spastic diplegics, also strabismus (crossed eyes), can be present as well. In addition, these individuals are often nearsighted. The intelligence of a person with spastic diplegia is unaffected by the condition.
  • Spastic tetraplegia (all four limbs affected equally). People with spastic quadriplegia are the least likely to be able to walk, or if they can, to want to walk, because their muscles are too tight and it is too much effort to do so. Some children with quadriplegia also have hemiparetic tremors, an uncontrollable shaking that affects the limbs on one side of the body and impairs normal movement.

Occasionally, terms such as monoplegia, paraplegia, triplegia, and pentaplegia may also be used to refer to specific manifestations of the spasticity.

Ataxia (ICD-10 G80.4) type symptoms can be caused by damage to the cerebellum. The forms of ataxia are less common types of cerebral palsy, occurring in at most 10% of all cases. Some of these individuals have hypotonia and tremors. Motor skills such as writing, typing, or using scissors might be affected, as well as balance, especially while walking. It is common for individuals to have difficulty with visual and/or auditory processing.

Athetoid or dyskinetic is mixed muscle tone — People with athetoid CP have trouble holding themselves in an upright, steady position for sitting or walking, and often show involuntary motions. For some people with athetoid CP, it takes a lot of work and concentration to get their hand to a certain spot (like scratching their nose or reaching for a cup). Because of their mixed tone and trouble keeping a position, they may not be able to hold onto objects (such as a toothbrush or pencil). About one quarter of all people with CP have athetoid CP. The damage occurs to the extrapyramidal motor system and/or pyramidal tract and to the basal ganglia. It occurs in 10% to 20% percent of all cases. In newborn infants, high bilirubin levels in the blood, if left untreated, can lead to brain damage in certain areas (kernicterus). This may also lead to athetoid cerebral palsy.

People with hypotonic CP appear limp and can move only a little or can’t move at all.

***I feel they don’t touch on social development very much… in my opinion, I believe it is one of any parents biggest worries to see their child be socially inept. With that said, it is essential to help integrate children with CP into “normal” activities with other children, in hopes that they will feel as equally accepted, loved, and respected, regardless of their disability or insecurity. However, I do realize that there are serveral more severe cases of CP where social situations cannot be implemented in one’s therapy, or develpment program and growth, due to the severity of his or her CP. So, this could mean the simplest of activities toward progression– from learning how to tie their own shoes, to riding a bike, or painting a picture with their classmates. Anything that creates a healthy source of interaction among children will help the child feel important, and included. Yet in every human being’s life there comes a time when they just need to be told that they are loved and befriended.  Support is HUGE in the development of a child–with or without CP. A child needs nothing more than the love and acceptance of their parents, family, and peers. If you give them that– dont fret, they will grow into the beautiful human beings you always hoped they’d be. There will be times of frustration, confusion, and hopelessness, but you will get through those hardships. See that you really make an attempt to understand that person around you with CP–whether they be your child, friend, brother or mother, and know that that is all you can do. That is all they want. To be understood.***

  • Symptoms

All types of CP are characterized by abnormal muscle tone (i.e. slouching over while sitting), reflexes, or motor development and coordination. There can be joint and bone deformities and contractures (permanently fixed, tight muscles and joints). The classical symptoms are spasticities, spasms, other involuntary movements (e.g. facial gestures), unsteady gait, problems with balance, and/or soft tissue findings consisting largely of decreased muscle mass. Scissor walking (where the knees come in and cross) and toe walking (which can contribute to a gait reminiscent of a marionette) are common among people with CP who are able to walk, but taken on the whole, CP symptomatology is very diverse. The effects of cerebral palsy fall on a continuum of motor dysfunction which may range from slight clumsiness at the mild end of the spectrum to impairments so severe that they render coordinated movement virtually impossible at the other end the spectrum.

Babies born with severe CP often have an irregular posture; their bodies may be either very floppy or very stiff. Birth defects, such as spinal curvature, a small jawbone, or a small head sometimes occur along with CP. Symptoms may appear or change as a child gets older. Some babies born with CP do not show obvious signs right away. Classically, CP becomes evident when the baby reaches the developmental stage at six and a half to 9 months and is starting to mobilise, where preferential use of limbs, asymmetry or gross motor developmental delay is seen.

Secondary conditions can include seizures, epilepsy, apraxia, dysarthria or other communication disorders, eating problems, sensory impairments, mental retardation, learning disabilities, and/or behavioral disorders.

Speech and language disorders are common in people with Cerebral Palsy. The incidence of dysarthria is estimated to range from 31% to 88%. Speech problems are associated with poor respiratory control, laryngeal and velopharyngeal dysfunction as well as oral articulation disorders that are due to restricted movement in the oral-facial muscles. There are three major types of dysarthria in cerebral palsy: spastic, dyskinetic (athetosis) and ataxic. Speech impairments in spastic dysarthria involves four major abnormalities of voluntary movement: spasticity, weakness, limited range of motion and slowness of movement. Speech mechanism impairment in athetosis involves a disorder in the regulation of breathing patterns, laryngeal dysfunction (monopitch, low, weak and breathy voice quality). It is also associated with articulatory dysfunction (large range of jaw movements), inappropriate positioning of the tongue, instability of velar elevation. Athetoid dysarthria is caused by disruption of the internal sensorimotor feedback system for appropriate motor commands, which leads to the generation of faulty movements that are perceived by others as involuntary. Ataxic dysarthria is uncommon in cerebral palsy. The speech characteristics are: imprecise consonants, irregular articulatory breakdown, distorted vowels, excess and equal stress, prolonged phonemes, slow rate, monopitch, monoloudness and harsh voice. Overall language delay is associated with problems of mental retardation, hearing impairment and learned helplessness. Children with cerebral palsy are at risk of learned helplessness and becoming passive communicators, initiating little communication. Early intervention with this clientele often targets situations in which children communicate with others, so that they learn that they can control people and objects in their environment through this communication, including making choices, decisions and mistakes.

Early Nutritional Support In one cohort study of 490 premature infants discharged from the NICU, the rate of growth during hospital stay was related to neurological function at 18 and 22 months of age. The study found a significant decrease in the incidence of cerebral palsy in the group of premature infants with the highest growth velocity. This study suggests that adequate nutrition and growth play a protective role in the development of cerebral palsy.

Physiotherapy (PT) programs are designed to encourage the patient to build a strength base for improved gait and volitional movement, together with stretching programs to limit contractures. Many experts believe that life-long physiotherapy is crucial to maintain muscle tone, bone structure, and prevent dislocation of the joints.

Occupational therapy helps adults and children maximise their function, adapt to their limitations and live as independently as possible.

Orthotic devices such as ankle-foot orthoses (AFOs) are often prescribed to minimise gait irregularities. AFOs have been found to improve several measures of ambulation, including reducing energy expenditure and increasing speed and stride length. —very helpful!

Speech therapy helps control the muscles of the mouth and jaw, and helps improve communication. Just as CP can affect the way a person moves their arms and legs, it can also affect the way they move their mouth, face and head. This can make it hard for the person to breathe; talk clearly; and bite, chew and swallow food. Speech therapy often starts before a child begins school and continues throughout the school years.

Hyperbaric oxygen therapy (HBOT), in which pressurized oxygen is inhaled inside a hyperbaric chamber, has been used to treat CP under the theory that improving oxygen availability to damaged brain cells can reactivate some of them to function normally. Its use to treat CP is controversial. A 2007 systematic review concluded that the effect of HBOT on CP is not significantly different from that of pressurizened room air, and that some children undergoing HBOT will experience adverse events such as seizures and the need for ear pressure equalization tubes; due to poor quality of data assessment the review also concluded that estimates of the prevalence of adverse events are uncertain.

Nutritional counseling may help when dietary needs are not met because of problems with eating certain foods.

Both massage therapy and hatha yoga are designed to help relax tense muscles, strengthen muscles, and keep joints flexible. Hatha yoga breathing exercises are sometimes used to try to prevent lung infections. More research is needed to determine the health benefits of these therapies for people with CP. –LOVE YOGA!

Surgery for people with CP usually involves one or a combination of:

  • Loosening tight muscles and releasing fixed joints, most often performed on the hips, knees, hamstrings, and ankles. In rare cases, this surgery may be used for people with stiffness of their elbows, wrists, hands, and fingers. —this is what serial casting did for me, yet a more mild, prolonged form of aid!
  • The insertion of a Baclofen Pump usually during the stages while a patient is a young adult. This is usually placed in the left abdomen. It is a pump that is connected to the spinal cord, whereby it sends bits of Baclofen alleviating the continuous muscle flexion. Baclofen is a muscle relaxant and is often given PO to patients to help counter the effects of spasticity.
  • Straightening abnormal twists of the leg bones, i.e. femur (termed femoral anteversion or antetorsion) and tibia (tibial torsion). This is a secondary complication caused by the spastic muscles generating abnormal forces on the bones, and often results in intoeing (pigeon-toed gait). The surgery is called derotation osteotomy, in which the bone is broken (cut) and then set in the correct alignment.
  • Cutting nerves on the limbs most affected by movements and spasms. This procedure, called a rhizotomy, “rhizo” meaning root and “tomy” meaning “a cutting of” from the Greek suffix ‘tomia’ reduces spasms and allows more flexibility and control of the affected limbs and joints.
  • Botulinum Toxin A (Botox) injections into muscles that are either spastic or have contractures, the aim being to relieve the disability and pain produced by the inappropriately contracting muscle. — Did this at age 10, more mild form of aid as well!

A new study has found that cooling the bodies and blood of high-risk full-term babies shortly after birth may significantly reduce disability or death.

Cord Blood Therapy: There are no published randomized controlled trials or meta-analysis of this treatment modality in cerebral palsy. In March 2008 a boy diagnosed with cerebral palsy appeared on the Today Show with his family. The parents noted that he could not walk on his own and appeared to be “swallowing his tongue” at times. He was eventually diagnosed with cerebral palsy and could only walk with the aid of a walker for a short time. Earlier that year he participated in a clinical trial involving his own cord blood that his parents had saved when he was born. His parents reported that within 5 days after the procedure he was walking on his own and talking, something his mother said he was not capable of on his own and it was doubtful he would ever be able to do on his own. They also reported that the doctors also told them that if his rate of progress continues uninterrupted until he is 7 he will be pronounced cured.

Conductive education (CE) was developed in Hungary from 1945 based on the work of András Pető. It is a unified system of rehabilitation for people with neurological disorders including cerebral palsy, Parkinson’s disease and multiple sclerosis, amongst other conditions. It is theorised to improve mobility, self-esteem, stamina and independence as well as daily living skills and social skills. The conductor is the professional who delivers CE in partnership with parents and children. Skills learned during CE should be applied to everyday life and can help to develop age-appropriate cognitive, social and emotional skills. It is available at specialized centers.

Biofeedback is an alternative therapy in which people with CP learn how to control their affected muscles. Some people learn ways to reduce muscle tension with this technique. Biofeedback does not help everyone with CP.

Neuro-cognitive therapy. It is based upon two proven principles. (1) Neural Plasticity. The brain is capable of altering its own structure and functioning to meet the demands of any particular environment. Consequently if the child is provided with an appropriate neurological environment, he will have the best chance of making progress. (2) Learning can lead to development. As early as the early 1900s, this was being proven by a psychologist named Lev Vygotsky. He proposed that children’s learning is a social activity, which is achieved by interaction with more skilled members of society. There are many studies, which provide evidence for this claim. there are however, as yet no controlled studies on neuro-cognitive therapy.

Patterning is a controversial form of alternative therapy for people with CP. The method is promoted by The Institutes for the Achievement of Human Potential (IAHP), a Philadelphia nonprofit, but has been criticized by the American Academy of Pediatrics.[The IAHP’s methods have been endorsed by Linus Pauling, as well as some parents of children treated with their methods.

Ok so that pretty much covers the mechanics of it, I think. Haha… I bolded some stuff I found interesting, as it applies to my life with CP. Seeing as Spastic CP ( I have that!) is the most common, I found this other article:

http://www.indianchild.com/CerebralPalsy/spastic-cerebral-palsy.htm

On a less informative note, I had another soccer game today! It was pretty awesome if I do say so myself. :) I almost scored a goal, except one girl got in my way. My my my it was such an inconvenience. :p I stretcheed really well afterwards, hopefully I’ll stay this limber, otherwise this running will do no good for me in the future. I feel like I have really kicked up the gears lately, I can run about 3 miles now at a steady pace without stopping, I am so happy. :) My parents, a few others ( and my sister!!) are doing a 200 mile relay race from Santa Barbara to Dana Point, alllll down the Pacific Coast Highway for about two days non-stop! It is a 12 man team, and each runner has 3 legs of different times and milage. I am so excited for them to kick some butt! I will be waiting for them here as they travel down the coast. Yay! :) I sometimes wish I could run that much, but it is just too hard on my body and I dont want to risk my health at this point in my life. Trying to be smart about it is all! Life is about keeping everything in moderation.

Hope all is well! Can’t wait for spring break, are you all counting down the days or what!?  Be on soon,

-Katy

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11 comments » | Exercising, Random, Teen Cerebral Palsy

Short Story–disability related

19
March

Hey ya’ll

Real quick–

There is this modern short story I was just assigned to read, and I thought you might find it as interesting as I did! I think this “He” has CP! Let me know what you think, I have so many curious thoughts about it, since modernism is known for its ambiguity and vagueness within the text. I can’t wait to talk about it in class tomorrow to hear my teachers’ opinion on it. Take a look! Also, those 2 questions we had to answer were so self-reflective, I really enjoyed answering them and being able to give examples from personal experience. I always learn so much about myself when asked such subjective questions like those ones.

http://q4honors.edublogs.org/files/2010/03/He-by-Katherine-Anne-Porter-short-story.pdf

Comment on this! Readers, let’s get a little discussion going…opinions, analyzations, conclusions, all of the above! :) Parents, you can join in too if you so wish!  The mom plays such a significant role in her nameless son’s life.

-Katy

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Woo!

20
February
Hey Guys!

Happy Saturday first of all, my favorite day of the week. :)

Good News, I won the “Apple of Our Eye” award for Education! I also received quite a few certificates that were signed by members of the Senate, and the House of Representatives! It was so great, I feel very honored! The Dayle McIntosh Center www.daylemc.org  recognized me and my blog for being an exceptional leader in the CP community, especially for teens…I was very overwhelmed by the amount of recognition that was given to me and my cause, I cannot thank everyone enough at the DMC, and everyone else out in the persons with disabilities community. I appreciate all your support of my blog, and how much you really care about our world of CPers and such. I’d like to take the time to thank Pam Hope and Greg Greiner as well for the support, I appreciate all your time and effort into getting my name out there, and really believing in me. Check out www.cnsfoundation.org  , Pam works with this foundation, and I also have a forum on the website, that is open to public discussion. It is just a great place to visit for any of you who are curious, and want to donate and advocate, to help scientific research for children with disabilities as the research is greatly under funded.

And thanks Sara for coming with me :p Also, thanks Mom and Papa, and you too, Melanie ;) for always being there, even though you couldn’t make it yesterday..it is always nice to know you are always there for me. :) Love you all.

My biggest thanks goes to you all who follow my blog, you are amazing and I cannot express my gratitude enough. Go TCP :)

I hope that you all enjoy your weekend! Talk to you soon.

-Katy

"Apple of Our Eye"

Cerebral Palsy Help

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Thoughts

15
February

Do you ever wonder what it means to be alive? Or what defines happiness? Success? Truth? Beauty?

I can’t wait to take Theory of Knolewledge, Philosophy, Psychology, Sociology…. all those classes seem so intriguing. They have so much to do with us and the reasoning behind everything that is essential to our lives.

In class the other day we took personality tests, and the one I found most accurate (and cool) was this one:

www.humanmetrics.com ….if you want to take it heres how, it’s way worth it! I learned so much about myself and why I think the way I do.

-Open up that web page, click on Jung Typology Test to your left, click ‘Do it’.

-Take the test (give yourself about 15 min.)

-When you finish, memorize the four-letter code you recieve (mine was INFJ.)

- Go to www.personalitypage.com and click the Shakespeare looking icon in the center of the homepage.

-Scroll down to your type, and read away!

It’s pretty awesome, there are other sections of your type to look at as well, what careers you’ll fit into, your strengths and weaknesses… its all hopefully fairly relevant to you and your personality.

Hope you had a great weekend, I enjoyed getting in a few extra hours of sleep and a trip to the beach! Wow the weather is amazing here… now I’m going to start my homework, and applyng for scholarships. Yay, what a fun process. Haha.

-Katy

Cerebral Palsy Help

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Yay for good news!

8
February

Hi Everyone!

I hope you all had a fantastic Superbowl Sunday! It was such a fun day here, my mom and sister both ran the half marathon held here every year, and then we hosted a huge party at out house for the superbowl! I’m not much of a football follower, but it was fun seeing everyone get together and have a good time. Did you guys do anything fun this weekend?

I just had my therapy appointment, andI left with such a positive attitude! My therapist measured by flexibility, and since the castings, I have improved tremendously! I almost have my foot at a 90 degree angle, and my ankle improved by 15 degrees, when I flex it. I go back in two weeks for a check  up, and get an update on wearing my brace, and doing my at home stretching. I am so happy, I didn’t realize that the casting did that much for me! I am walking more evenly, and able to exercise still, with a stronger pace and fluency. I can’t wait to keep moving forward and see more improvements on my own! Wish me luck.

I hope you all have a fabulous week, I am about to attack my load of homework since I’ve put it off this weekend, and get these next two Monday’s off with thanks to the past Presidents of our country. Wish me luck for this one too. Haha…I’ll be on again soon!

-Katy

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