Welcome to the official Army of Club Penguin! Established September 29th, 2006, we have been the largest and best Club Penguin community since. Enlist today and start your journey!
~ Roxy & Daniel
Ktman: Make sure to re-read The Battle of the Underground post for all the info on this upcoming practice battle.
http://blog.armyofclubpenguin.com/2009/09/05/the-battle-of-the-underground/
Date: Sunday, September 13th
Time: 1 P.M. EST
Place: Fjord, Snow Fort
Who: ACP and Nachos
Why: Fun
Filed under: ACP |
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Roxy, is currently serving as the 52nd Commander-in-Chief
Daniel, is currently serving as the 53rd Commander-in-Chief.
1st
2nd
3rd
10:00 PST, 11:00 Pacific, 12:00 Central, 1:00 Eastern, 2:00 Atlantic. 6:00 UK.
Matre10
so thats 10:00 PST
FINALLY gawsh
i can make it
http://i609.photobucket.com/albums/tt171/JediSethACPphotos/commanderfox1.gif deliver this pic to pack, i wont be here for 3 days, tell pack this is the beta version 😉
ill be there
9th
I should be able to make it 🙂 10th 8) !!!!!!!!!!
YUSH!!!!! Finaly an epic PB with the two strongust armies!!!! I’ll be there!!!
Ikr rider finally there is a pb or something around here I can make it! Btw from now on I won’t be able to make any pb or anything on saturdays after 2 o clock because I have catholic school but ill try my best to make some parts of the battles sometimes I might make the whole battle
I can make it!
why?fun! LOL
Oooh, A PB… Woot! I can make it 😀
~Pinkgirl1114
YAY!!! lets kick some major NACHO BUTT!
be there
you will see me there meat,
maniac
i am comming
Yo Meat,
Do you remember me?
I wanted to see if you wanted to help me with a new cp army.
Let me know.
cpsnowvikings.wordpress.com
you have to make the time exactly when I have to go to church? Its a half hour battle, and I can’t be there for any of it! Is it possible for you to change the time to something later?
i’LL BE THERE!!!!!
Adjunct General~Happyman444
I just came back from the doctor and it turns out I have swine flu!!!! 😮 It’s not really THAT bad, the worst part is my sore throat and headaches but its not to bad. If your scared of dying from it dont worry unless: You have asthma, in that case get to the doctor ASAP and if you have respritory (Chest, lungs, etc.) problems
~Lsund
IM COMING!!!!!!!!!!!!!!!!!!!!!!!!!! :):):):):):):):):):):):):):):):):):):):):):)):
I HAVE AN UPPER REPRITORY VIROUS AND I HAD TO GET AND INHAILER,COUGH SYRUP AND ANTIBYODIX.
Practice battle with nachos!
Posted on September 8, 2009 by Seanehawk aka Meat
Ktman: Make sure to re-read The Battle of the Underground post for all the info on this upcoming practice battle.
http://blog.armyofclubpenguin.com/2009/09/05/the-battle-of-the-underground/
Date: Sunday, September 13th
Time: 1 P.M. EST
Place: Fjord, Snow Fort
Who: ACP and Nachos
Why: Fun
Filed under: ACP
ill be there.
ill be there
ill make it
be there, and we will probley win cuz we always do!
Prolly.
cant mak it im fightin for ze nachoz
As of now I Lincoln31543 QUIT the ACP and shal never return. All i wanted to do is help capnhook and look where it put me, making this comment saying i quit. I did not want to but i half to. im not going to say y, but if you want to know email me at lincoln31543@yahoo.com. sorry but i cant take being here. i will miss all of you.
~Lincoln31543
I’ll be there,
I will try to make it, Oh and i recruited for you guys! 😀
Hey guys….
I, twingeh, have decided I will retire sometime after I overpass the legends line near to Christmas. Hopefully. Then i will retire totally.
With sad regards.
Twingy
p.s Sorry, but i will only be active now at weekends.
Lsund-
Thats too bad! Theres a person in some of my classes who has it, and like 8 at the high school. And yikes, I have athsma…. But its just excercise-induced, so i should be ok, right?
http://www.youtube.com/watch?v=CG9AjwL7Bgg CP NEWS VIDEO OF CURRENT ARMY AND WAR EVENTS!
i might make it
hello I’m Lincoln31543, I want it to end now I have proof that im leglley blind and I’m tired of everyone saying im not. I go to a school called ISBVI or Indiana School for the Blind and visually Impared, I’m Leglley blind in my right eye and totley blind in my left eye. I’m leglley blind because my dad William Ritchhart gave me this disease that is called Marfan syndrome (or Marfan’s syndrome) its a connective tissue disorder.
Here are some things that it can effect.
Symptoms
Although there are no unique signs or symptoms of Marfan syndrome, the constellation of long limbs, dislocated lenses, and aortic root dilation is sufficient to make the diagnosis with confidence. There are more than 30 other clinical features that are variably associated with the syndrome, most involving the skeleton, skin, and joints. There is a great deal of clinical variability even within families that carry the identical mutation.
Skeletal system
The most readily visible signs are associated with the skeletal system. Many individuals with Marfan syndrome grow to above average height. Some have long slender limbs with fingers and toes (arachnodactyly). This condition of elongated limbs is known as dolichostenomelia. An individual’s arms may be disproportionately long, with thin, weak wrists. In addition to affecting height and limb proportions, Marfan syndrome can produce other skeletal anomalies. Abnormal curvature of the spine (scoliosis) is common, as is abnormal indentation (pectus excavatum) or protrusion (pectus carinatum) of the sternum. Other signs include abnormal joint flexibility, a high palate, malocclusions, flat feet, hammer toes, stooped shoulders, unexplained stretch marks on the skin and thin wrists. It can also cause pain in the joints, bones and muscles in some patients. Some people with Marfan have speech disorders resulting from symptomatic high palates and small jaws. Early osteoarthritis may occur.
EYES
Lens dislocation in Marfan’s syndrome, the lens was kidney-shaped and was resting against the ciliary body.Marfan syndrome can also seriously affect the eyes and vision. Nearsightedness and astigmatism are common, but farsightedness can also result. Subluxation (dislocation) of the crystalline lens in one or both eyes (ectopia lentis) (in 80% of patients) also occurs and may be detected by an ophthalmologist or optometrist using a slit-lamp biomicroscope. In Marfan’s the dislocation is typically superotemporal whereas in the similar condition homocystinuria, the dislocation is inferonasal. Sometimes eye problems appear only after the weakening of connective tissue has caused detachment of the retina.[10] Early onset glaucoma can be another related problem.
Cardiovascular system
The most serious signs and symptoms associated with Marfan syndrome involve the cardiovascular system. Undue fatigue, shortness of breath, heart palpitations, racing heartbeats, or Angina pectoris with pain radiating to the back, shoulder, or arm. Cold arms, hands and feet can also be linked to Marfan’s syndrome because of inadequate circulation. A heart murmur, abnormal reading on an EKG, or symptoms of angina can indicate further investigation. The signs of regurgitation from prolapse of the mitral or aortic valves (which control the flow of blood through the heart) result from cystic medial degeneration of the valves which is commonly associated with Marfan’s syndrome (see mitral valve prolapse, aortic regurgitation). However, the major sign that would lead a doctor to consider an underlying condition is a dilated aorta or an aortic aneurysm. Sometimes, no heart problems are apparent until the weakening of the connective tissue (cystic medial degeneration) in the ascending aorta causes an aortic aneurysm or aortic dissection, a medical emergency. An aortic dissection is most often fatal and presents with pain radiating down the back, giving a tearing sensation.
Because of the underlying connective tissue abnormalities that cause Marfan syndrome, there is an increased incidence of dehiscence of prosthetic mitral valve.[11] Care should be taken to attempt repair of damaged heart valves rather than replacement.
During pregnancy, even in the absence of preconceived cardiovascular abnormality, women with Marfan syndrome are at significant risk of aortic dissection, which is often fatal even when rapidly treated. For this reason, women with Marfan syndrome should receive a thorough assessment prior to conception, and echocardiography should be performed every six to ten weeks during pregnancy, to assess the aortic root diameter. For most women, safe vaginal delivery is possible.[12]
LUNGS
Marfan syndrome is a risk factor for spontaneous pneumothorax. In spontaneous unilateral pneumothorax, air escapes from a lung and occupies the pleural space between the chest wall and a lung. The lung becomes partially compressed or collapsed. This can cause pain, shortness of breath, cyanosis, and, if not treated, death. Marfan syndrome has also been associated with sleep apnea and idiopathic obstructive lung disease.
(BTW: Remember when I told you all about my Lung Callapsing? well thats the reason why.)
Central nervous system
Another condition that can reduce the quality of life for an individual, though not life-threatening, is dural ectasia, the weakening of the connective tissue of the dural sac, the membrane that encases the spinal cord. Dural ectasia can be present for a long time without producing any noticeable symptoms. Symptoms that can occur are lower back pain, leg pain, abdominal pain, other neurological symptoms in the lower extremities, or headaches. Such symptoms usually diminish when the individual lies flat on his or her back. These types of symptoms might lead a doctor to order an X-ray of the lower spine. Dural ectasia is usually not visible on an X-ray in the early phases. A worsening of symptoms and the lack of finding any other cause should eventually lead a doctor to order an upright MRI of the lower spine. Dural ectasia that has progressed to the point of causing these symptoms would appear in an upright MRI image as a dilated pouch that is wearing away at the lumbar vertebrae.[10] Other spinal issues associated with Marfan include degenerative disk disease and spinal cysts. Marfan syndrome is also associated with dysautonomia.
Well I hope you all will think before you act i was hert by all of you and its hard being the one that can see better then your mouther. Because my mom is almost totley blind because she was born too early., and my brouther he is severley Autistic. So I half to do all the shopping for my familey. My friend Pyton Mannin, who still needs a rank here in ACP, he knows me in real life. When he gets ungrouned on monday he can tell you about me.
And to all of ACP I’m so sorry that it was this long I did not know it would be this long. And I hope that you will understand what I am going through, because I’m under stress right now and sooner or later I might not be on for some time. I might be helping my mom or helping my brouther so if I’m not on for a while you know what I maybe doing.
~Lincoln31543
Im staying in ACP
Dryvit: Glad to hear you are staying Lincoln. Very sorry to read about your vision problems. I am sure everyone in ACP will send up a prayer or good thought your way. Thank you for sharing that with us. Everyone learns Lincoln.
wow lincoln. That’s allI can say. It must be really hard. I’ll be praying for you, thats for sure.
You should be fine Little guy, but if you have swine flu, dont go exersising. I have great news! I’ll be completely healed by either tommorow or SUnday, but im not allowed to go places or anything till monday Ill live! 😀
~Lsund
I wont be able to make it cause i will still be camping with my Scout Troop, I will be able to make it at like after 6 or 7.
I might be able to make it as im Australian try and make times good for Australians!
wow lincoln. im visually impaired but not that badly.
twingeh
i cant join the army how do i !!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
its ok lincon! btw i cant make the PB sorry dryvit its mah birthday party
I can’t make it I have a football game
I’m there
What a useful post here. Very informative for me..TQ friends…