NOUN: 2009

Wednesday, December 16, 2009

, , farewell

, , i just make our blog my public diary, , ,(sort of), , we just said our farewells to the man behind the discovery of this blogger by IV-newton, ,sir neil, , bye bye nah, , huhu, , we will miss you so much, ,
, , enks, , all, ,

, , maggraduate nah meh soon

Tuesday, November 10, 2009

PROYEKTO SA FILIPINO: MOVIE REPORT

JIREH CUARTO
IV-NEWTON

Ang sine ay pinamagatang “The chronicles of Narnia: The Lion, The Witch, and The Wardrobe” at ito ay dinirektuhan ni Harold Games. Ang musika ay nilapat ni Van Toffler na sadyang angkop-na-angkop sa lahat ng eksena, lalong-lalo na sa mga eksenang may drama at mga labanan. Ito ay pinagbibidahan ng apat na bata na sina George Henley, William Moseley, Skandra Keynes at Arma Popplewell na gumanap bilang Peter, Edmund, Sally at Lucy White, sila ay magkakapatid na napadpad sa mahiwaga at misteryosong kaharian ng Narnia. Ang kanilang kasuotan ay hango sa mga damit ng mga Prinsesa’t Prinsepe at ang iba naman ay kagaya ng sa mga sinaunag kasuotang panglaban noong unang panahon. Ang aral na natutunan ko sa sine ay ang pagiging matapat at matapang sa anumang mga pagsubok na ating haharapin.
Ang ikalawang sine na aking pinanood ay pinamagatang “The Golden Compass” na dinirektuhan ni Chris Weitz. Ang musika sa pelikulang ito ay nilapat ni Freddie Highmore na nagging angkop[ sa mga eksenang may halong drama. Ito ay pinagbibidahan ni Dakota Blue Richards na gumanap bilang Lyra sa pelikula. Ang kanilang kasuotan ay mga marangyang kasuotan noong unang panahon na ginagamit ng mga Nomads at Gypsies. Ang pelikula ay nagbibigay ng aral ukol sa pagiging masunurin at masipag na tao.
Sa dalawang nakakamanghang pelikulang aking pinanood,mas nakakaangat ang kagandahan at ang produksyon ng “The chronicles of Narnia: The Lion, The Witch, and The Wardrobe” sapagfkat mas naipapalahad ng mga artista o bida dito ang kanilang mga emosyon kaysa mga artista na nakikita natin sa “The Golden Compass”. Higit sa lahat, maliban sa magandang produksyon at cast ng Narnia, mas maraming aral ang matututunan ng mga manonood ng Narnia.

Thursday, October 8, 2009

Research Paper (second grading)

1.TITLE PAGE

2. ACKNOWLEDGEMENT

ACKNOWLEDGMENT

The researchers would like to express their warm grtitude to the following persons who extende their helping hands and encouragement in making this study a reality.

Mr. Neil Improgo, English Teacher, for his valuable and expert advise, knowledge and excellent ideas, thus supporting, advising, supervising and guiding the researches with utmost patience that inspire to complete the study;

Dr. Erlinda C. Chico, Secondary School Principal II of Manolo Fortich National High School, for her understanding and cooperation in allowing the researchers to use the Computer Laboratory for their research work;

Miss Methuselah K. Arenas, for her moral support;

To the parents of the researchers, for giving not just encouragement but also provide financial, physical, and mental supports;

And above all to God Almighty, for showering the researchers with lots of blessings everyday which give enlightenment, wisdom and courage so that the researchers will be able to finish the study.

3.DEDICATION

DEDICATION

To
our beloved parents,
relatives, friends,
classmates, our teachers,
our special someones and
most especially to
the school
MANOLO FORTICH NATIONAL HIGH SCHOOL
This work is dedicated.

4. Table of Contents

TABLE OF CONTENTS

Page

TITLE PAGE i ACKNOWLEDGMENT... ii

DEDICATION... iii

TABLE OF CONTENTS... iv

Outline 1

Introduction

Body

Conclusion

WORKS CITED 20

APPENDICES

-Pictures 21

-Video 22

-Concept Map

OUTLINE

Spinocelebellar Ataxia or Degeneration
I. Introduction
Spinocerebellar degeneration is the diagnose illness of Aya Ikeuchi, a 15-year old japanese girl. This illness was introduced to the public through the film ONE LITRE OF TEARS.

II.Spinocerebellar degeneration or ataxia is a disease in the nervous system.

A.It often occurs when parts of the nervous system that control movement are damaged.

III.This disease has many different causes.
A.Most of its causes are hereditary.
1.Autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty one from the other parent.
2.Autosomal recessive, in which both parent pass on a copy of the faulty gene.
3. It can also be caused by having an extra copies of a normal protein, not just a mutated one.
B.Still, it can be acquired.
1.CSpinocerebellar degeneration is the diagnose illness of Aya Ikeuchi, a 15-year old japanese girl. This illness was introduced to the public through the film ONE LITRE OF TEARS.A.It often occurs when parts of the nervous system that control movement are damaged.A.Most of its causes are hereditary.
1.Autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty one from the other parent.
2.Autosomal recessive, iA.Most of its causes are hereditary.
1.Autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty one from the other parent.
2.Autosomal recessive, in which both parent pass on a copy of the faulty gene.
3. It can also be caused by having an extra copies of a normal protein, not just a mutated one.
B.Still, it can be acquired.onditions that can cause acquired ataxia include stroke, multiple sclerosis, tumors,alcoholism, metabolic disorders, and vitamin deficiencies.

IV.There are many types of ataxia.
A.Autosomal dominant spinocerebellar degeneration includes spinocerebellar ataxia (SCA) types 1,2,3 and 6.
1.SCA type 1 is characterized by either hypermetric or slow saccades.
2.SCA type 2 diminish velocity saccades areflexia.
3.SCA type 3 or the Machado-Joseph disease involves a rapid, involuntary, oscillatory motion of the eyeball and occasionally slow saccades.
4.SCA type 6 is shown by downbeating nystagmus,and positional vertigo.
B.Ataxias caused by other factors.
1.SCA 4, which usually results to the absence of neurologic reflexes.
2.SCA 5 has an average duration of 25 years.
3.SCA 7 is characterized by macular degeneration,and slow saccades.
4.SCA 8 is often shown by horizontal nystagmus.

V.Symptoms of ataxia are usually common among its categories or types.
A.Common symptoms observed in a person with ataxia are slow saccades, nystagmus and paralysis.

VI.Treatments are already catered to persons who have the spinocerebellar disease.
A.If the ataxia is caused by another condition, that underlying condition is treated first.
1.Ataxia caused by a metabolic disorder may be treated with medications and a controlled diet.
2.Vitamin deficiency is treated with vitamin therapy.
3.But some acquired ataxia are incurable.
3.1Those that are acquired through alcoholism for years..
B.However,there's no known cure for the hereditary ataxia.

VII.Our conclusion.
Spinocerebellar degeneration, a rare disease,yet it was able to be introduced to the public by the film about a true-to-life story of a 15-year old girl.It's incurable in some cases.That's why we must be very careful because it could also be acquired through alcoholism,which is undeniable in our country.

INTRODUCTION

Spinocerebellar degeneration or ataxia.A very rare disease yet it was able to be introduced to the public by the television drama "One Litre of Tears" based on the life of a 15-year old Japanese girl named Aya Ikeuchi.

BODY

Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a disease in its own right.
The hereditary ataxias are categorized by mode of inheritance and causative gene or chromosomal locus. The hereditary ataxias can be inherited in an autosomal dominant, autosomal recessive, or X-linked manner.

The hereditary ataxia is grouped into two.First, the autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty one from the other parent.Second, the autosomal recessive, in which both parents pass on a copy of the faulty gene.There are five typical autosomal recessive disorders in which ataxia is a prominent feature: Friedreich ataxia, ataxia-telangiectasia, ataxia with vitamin E deficiency, ataxia with oculomotor apraxia (AOA), spastic ataxia. Disorder Subdivisions: Friedreich's ataxia, Spinocerebellar ataxia, Ataxia telangiectasia, Vasomotor ataxia, Vestibulocerebellar, Ataxiadynamia, Ataxiophemia, Olivopontocerebellar atrophy, and Charcot-Marie-Tooth disease.

In the case of the acquired ataxia, conditions that can cause it include stroke, multiple sclerosis, tumors,alcoholism,smoking, metabolic disorders, and vitamin deficiencies.
And under these two categories of the ataxia are numbers of varying types of this disease which are known to affect different regions within the cerebellum.It's symptoms vary with the specific type and with the individual patient. Generally, a person with ataxia retains full mental capacity but may progressively lose physical control.

Until now, there is no known cure for spinocerebellar ataxia, which is a progressive disease-it gets worse with time- although not all types cause equally severe disability.

Treatments are generally limited to softening symptoms, not the disease itself. The condition can be irreversible. A person with this disease will usually end up needing to use a wheelchair, and eventually they may need assistance to perform daily tasks.
The treatment of incoordination or ataxia, then mostly involves the use of adaptive devices to allow the ataxic individual to maintain as much independence as possible. Such devices may include a cane, crutches, walker, or wheelchair for those with impaired gait; devices to assist with writing, feeding, and self care if hand and arm coordination are impaired; and communication devices for those with impaired speech.

Many patients with hereditary or idiopathic forms of ataxia have other symptoms in addition to ataxia. Medications or other therapies might be appropriate for some of these symptoms, which could include tremor, stiffness, depression, spasticity, and sleep disorders, among others.

Both onset of initial symptoms and duration of disease can be subject to variation. If the disease is caused by a polyglutamine trinucleotide repeat CAG expansion, a longer expansion may lead to an earlier onset and a more radical progression of clinical symptoms.

CONCLUSION

The researchers therefore say that this disease must not be taken for granted only because it's rare.This disease could be acquired through smoking or alcoholism, which are included in the life-style of almost every individual. The researchers also recommend further studies and research about this deadly degeneration of the cerebellum.

WORKS CITED

Dr. Arke, Is there a cure for spinocerebellar degeneration disease?,
http://wiki.answers.com/Q/Is_there_a_cure_for_spinocerebellar_degeneration_disease

"The Nervous System", Genes and Diseases,National Library of Medicine, http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowSection&rid=gnd.section.218

Ikeuchi Aya, film: "Ichi Rittoru no Namida / One Litre of Tears / A Diary of tears"
http://wiki.d-addicts.com/Ichi_Rittoru_no_Namida

The American Council on Science and Health, "What Every Teen Should Know About Tobacco", http://thescooponsmoking.org/xhtml/effects/spinocerebellarDegeneration.php

Timothy C. Hain, MD , Northwestern University Medical School, Chicago IL, USA. , http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowSection&rid=gnd.section.218

Wikipedia, http://en.wikipedia.org/wiki/Spinocerebellar_ataxia

APPENDICES

PICTURE

Thursday, June 11, 2009

WHO ARE WE??

GIF animations generator gifup.com
Nickname: Ji-Ji, "gong gong"
Address: Lingi-on. Manolo Fortich, Bukidnon, Mindanao, Philippines
Birthday: October 28, 1994
Birth Place: Maternity Hospital. Cagayan de Oro City
Friendster Account: jireh@hotmail.com

April 2, 2009, how could i forget the day of my most memorable, adventurous, audacious, temerarious, funny, and scary experience with my dear classmates and friends?

I woke up. I'm still sleepy, but the excitement that is within me is more powerful than the dizziness that i feel.
April 2,2009, the date that me and my classmates in III-William Shakespeare contemplated to have our adventurous outing at Sampiano, Sto. Nino, Manolo Fortich Bukidnon.

First, i was very worried =( , because i was the only one at the plaza, where we planned to meet, and i thought that my friends is really not going.
I checked my cellular phone, there were 10000000000 messages!!! and 1000000000 miss calls!!! by my friends and classmates (well, that's how they love me, can't blame them for it. LOL)
They were at the terminal waiting for me the whole time, while i was in the plaza crying myself out!!!
With abatement, i walk briskly and instantaneously towards the terminal station. There i saw nine (9) persons i call friends.(sighs)

I was very happy when i saw their funny faces.
They were Irene Gaspi (our tour guide. LOL), Alemar Genabio, Edwina Lerongan, Evelyn Vitor, Glen Mark Enloran, Jaime Hayson, Archie Cabacab, Sherlyn Tunhawan and of course ME (LMAO)

We All Have Favorites
Singer: Mariah Carey
Song: BYE-BYE

Bye Bye - Mariah Carey
FREE MP3 DOWNLOADS @ MP3-CODES.COM

Name:Donessa Teologo Carampil
Nickname:Donnah, Qkyw-qkyw
Address:Blk 5, Lot 13, CRistan Villa Subd., Dicklum, Manolo Fortich, Buk.
Birthday:19th of July, 1993
Birthplace:Camp 3, Manolo Fortich, Buk.
Cellular Number:09057709904
FAVORITES!!!!
Color:red and sky blue
Flower:red roses
Food:leche flan
Actor/Actress:Senior Chiaki/Nodame
Singer:Leona Lewis
Movie/Film:Nodame Cantabile
Song:Footprints in the Sand-Leona Lewis
MORE ABOUT ME!!
Hobbies:eating, texting, watching television
Personalities:talkative, optimistic,
Motto:"A NO uttered with deepest conviction is better and greater than a YES merely uttered just to please or, what is worst, to avoid trouble."
Ambition:I want to be a CERTIFIED PUBLIC ACCOUNTANT

A Day to be Remembered!!F-O-R-E-V-E-R!!!

It was almost 12 noon when we,together with my classmates, decided to take a glimpse of the star cast of the movie "Love Me Again-Land Down Under" in the track 'n field of Impasugong Central Elementary School.

In the venue,we saw Piolo Pascaul, Angel Locsin, Erich, Aj Dee, Nash,and John Manolo playing "seven-seven up."Even if it's already lunch break the site was still very crowded.We saw many people who just visit there to take a look of there favorite stars.

After taking our lunch at our friend's house, we went back to the elementary school.We were very amazed to see our high school teachers disguised in civilian clothes watching the shot.We begged our adviser,Mrs. Oliver to allow us to watch the taping but she didn't allow us to not unless we are willing to absent from our classes that afternoon.Of course we are so sad about that but we were delighted right after we saw our top-rank classmates in the venue.We decided to refrain from our classes that afternoon.It's very funny thinking that only seven of our classmates were able to attend the first period in the afternoon.We just laugh about it.They're very loyal.

After the first period in the afternoon, our classmates who attended the class were able to join us there which made us a whole section.Can you imagine that, a third-year top section class absents and cuts classes to watch a taping?Unbelievable but it did come to life!

The next morning we were called to report to the Guidance Office to get our admission slip.But of course we can't get one since we don't have excuse letters, not even one.So, using our powers of begging, we ask our adviser to sign our excuse letter since she's also the mother of Maril, one of our classmates.

See?nothing is impossible for III-Gumamela, the world where I lived for a year!

_donessat.carampil

Wednesday, June 10, 2009

Sentence Outline

Title/Topic:
Spinocelebellar Ataxia or Degeneration
I. Introduction
Slide 3

Spinocerebellar degeneration is the diagnose illness of Aya Ikeuchi, a 15-year old japanese girl. This illness was introduced to the public through the film ONE LITRE OF TEARS.
II.Spinocerebellar degeneration or ataxia is a disease in the nervous system.

A.It often occurs when parts of the nervous system that control movement are damaged.
III.This disease has many different causes.
A.Most of its causes are hereditary.
1.Autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty one from the other parent.
2.Autosomal recessive, in which both parent pass on a copy of the faulty gene.
3. It can also be caused by having an extra copies of a normal protein, not just a mutated one.
B.Still, it can be acquired.
1.CSpinocerebellar degeneration is the diagnose illness of Aya Ikeuchi, a 15-year old japanese girl. This illness was introduced to the public through the film ONE LITRE OF TEARS.A.It often occurs when parts of the nervous system that control movement are damaged.A.Most of its causes are hereditary.
1.Autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty one from the other parent.
2.Autosomal recessive, iA.Most of its causes are hereditary.
1.Autosomal dominant, in which the affected person inherits a normal gene from one parent and a faulty one from the other parent.
2.Autosomal recessive, in which both parent pass on a copy of the faulty gene.
3. It can also be caused by having an extra copies of a normal protein, not just a mutated one.
B.Still, it can be acquired.onditions that can cause acquired ataxia include stroke, multiple sclerosis, tumors,alcoholism, metabolic disorders, and vitamin deficiencies.
IV.There are many types of ataxia.
A.Autosomal dominant spinocerebellar degeneration includes spinocerebellar ataxia (SCA) types 1,2,3 and 6.
1.SCA type 1 is characterized by either hypermetric or slow saccades.
2.SCA type 2 diminish velocity saccades areflexia.
3.SCA type 3 or the Machado-Joseph disease involves a rapid, involuntary, oscillatory motion of the eyeball and occasionally slow saccades.
4.SCA type 6 is shown by downbeating nystagmus,and positional vertigo.
B.Ataxias caused by other factors.
1.SCA 4, which usually results to the absence of neurologic reflexes.
2.SCA 5 has an average duration of 25 years.
3.SCA 7 is characterized by macular degeneration,and slow saccades.
4.SCA 8 is often shown by horizontal nystagmus.
V.Symptoms of ataxia are usually common among its categories or types.
A.Common symptoms observed in a person with ataxia are slow saccades, nystagmus and paralysis.
VI.Treatments are already catered to persons who have the spinocerebellar disease.
A.If the ataxia is caused by another condition, that underlying condition is treated first.
1.Ataxia caused by a metabolic disorder may be treated with medications and a controlled diet.
2.Vitamin deficiency is treated with vitamin therapy.
3.But some acquired ataxia are incurable.
3.1Those that are acquired through alcoholism for years..
B.However,there's no known cure for the hereditary ataxia.
VII.Our conclusion.
Spinocerebellar degeneration, a rare disease,yet it was able to be introduced to the public by the film about a true-to-life story of a 15-year old girl.It's incurable in some cases.That's why we must be very careful because it could also be acquired through alcoholism,which is undeniable in our country.