so it all started about 2 months ago. i started seriously worrying about my weight and the food i was consuming. so at first it started as just a diet but then it grew to become more serious. so i just started not eating. i dont want to be fat and gaining weight to me is like stabbing me with a knife. it hurts. i am scared...and lonely. but i would love to say i was improving but i am not.... i am getting worse. sometimes when i feel forced to eat or i get so hungry that i cant stand it i will just eat and then later i will make myself throw up. why? i really dont know... just to be skinny. Most people already think i am skinny enough but appariently they have never seen me in a bathing suit. i feel so alone and underestamated. i know though that God is here for me. And when i cry out to Him He hears me.. but sometimes its hard to believe. I feel Him there but He doesnt seem close enough. i need Him. i need His help... and i need Him to give me the power to tell Satan to "shut up!!!!"
so on a happier note i am doing well with my singing and progressing well in school.
Math: A
Language arts: A
Science: B
Social Studies: B
Key boarding: B
Chorus: A+ (imagine that!)
so i guess that is all i have to say!!!!!
♥ erin
- Music:106.9 - Edge
- Mood:
excited - Music:none
well lets just say i have been researching a little bit.. (okay maybe a lot) but i have found out SO much about stem cell therapy and what kind of reasearch they are conducting for it!! i really dont have time right now to explain all i have found but here is one of the sites i learned alot from..... www.cnsfoundation.org .
but i am going to the doctor for a check-up sometime in febuary and that is when we are going to ask about what he thinks we should do (hopefully he will say yes)
p.s - either answer komen gives us will require alot of support and alot of prayers. If he says no that will be a very emontionaly hard time for me and my family. If he says yes (hopefully) that will be a very emontionaly and physically hard time for myself and my family also. So please keep my family, my doctor, and I in your prayers that the right decision will be made (and once again hopefully yes!!!). Also keep in your prayers that when the decision is made that there will be alot of support, and kindness from others. And that no matter what happens that we will find the strength and courage to carry on.
Thank-You!!! any questions??? e-mail me at : cerebralpalsyhope@yahoo.com or www.myspace.com/istilllovehim88
- Location:home
- Mood:
distressed - Music:none
okay lets try this one more time!!!! hope you u like it!!! this is just me..... ffar from perfect... far from beautiful.... far from normal... just me!!! i like erin... but i dont like the girl with cerebral palsy. i feel like i live two lives, cerebal palsy life, and normal live.... but it gets to a point where they crash. and what i mean is that i can no longer have 2 lives.... i have to deal with just one and that is hard. in elemtary school the teachers pro tected my 2 lives but i am 7th grade now and that has changed.... but this is my life.. no (s) just life. i hope u like the pics!
- Mood:
anxious - Music:Colbie Caillat - Bubbly
i made this slide show so that people could see the real me!!! i hope you like it!!!
<div><embed src="http://www.onetruemedia.com/view_slidesh
it will soon be my birthday and i decided to make a slide show of all the years me and my dad had together!! hope you like it!!!
- Mood:
impressed
so i have had my cast off for a while but have really not seen much difference in anything... : (..... which is always a dissapointment. but i am getting a new brace soon that will just be clear w?pink straps because they didnt have the color i wanted..... but all is going okay for me.... but my friend nathaniel who also has C.P which also effects his hearing got put in the e.c class because he didnt understand what the interpreter was signing about and didnt really understand what it was all about. i think it is because they let him do anything he wanted last year and he never learned anything so this year he dosent understand..............
Never Alone 4:30 Barlow Girl Barlow Girl Christian 2 10/26/2007 1:57 PM
- Mood:
why him?
- Location:home
- Mood:
crazy
- Mood:
te he!
- Location:home
- Mood:
its 10:15 pm
- Stuck in Neutral by: Erin Collins
You would never expect anything from me would you? I'm always sitting here just watching you. Do you even think about how I feel? I always hope for the best, but prepare for the worst. I don't expect you to understand, but I will try to explain. When you sit there and laugh, I know it's about me... I can hear it all. I have feelings too, please try to understand that, I may be different, but it's not funny what I have to go through. Don't laugh at me, don't call me names, don't get your pleasure from my pain. In God's eyes we're all the same, someday we'll all have perfect wings. Don't laugh at me. We are all different in many ways, but laughing at me won't make anything better. Things are different from my point of view, you're not going to go through what i have to go through, so be happy about that. You don't go through the pain, disapointment, or the hurt, you are not made fun of or laughed at. As long as it,s not happening to you, right? My name is Erin, I'm living my life with Cerebral Palsy, I can only only explain so much, and you still won't understand.
i wrote this poem when i was in 2nd grade. my second grade year was probably the worst year i have ever had. i was made fun of all year with no stop! but i soon realized that normally people make fun of you to help themselfs feel better. but i also learned that sometimes people laugh because they like you, somtimes they laugh to hurt you. it is sad but it's soooooo true. thankfully no one has really made fun of me this year. most kids think it is so cool that i get to ride in a wheel chair and get to be on cruthes.... but anyway i guess thats life!!!!! i hopw you like my poem!
i would like to hear from you!!!!!! if you know someone who has cerebral palsy, want to know more about it, or just want to get to know me, e-mail me at....... cerebralpalsyhope@ yahoo.com or myspace me... myspace.com/istilllovehim88 thanks!!!!!!!! <3
- Location:home
- Mood:
(sigh) - Music:none
- Location:aunt's house
- Mood:
new car jitters - Music:none
well i have this orange and black cast that is striped that i picked out for halloween.... and unfortunatly i am pretty sure it probably won't be off till near that time (otc.29) but i just relized that my whole team at school is going on a REALLY fun field trip to the ropes course. which i am pretty sure will be like a HUGE obsticle course in mid air..... but it is on the 22nd and 23rd.......(sigh)... and i REALLY want to go on the field trip but i will still have a cast on. but we are hoping that maybe we can talk the doctor into taking it off sooner so that i can go on the really fun field trip. and here is what most people dont understand about C.P is that it's the little things that get on your nerves like not being able to go on a field trip because of a cast. the big things like having another surgery dosen't bother me as much (though it does get annoying also.) well i guess i will have to wait and see!!!!!!...(sigh)..... i sure do hope the doctors will have some compassion for me!
- Mood:
(sigh)
- Location:home
- Mood:determined
well..... it is always hard for me to explain what cerebral palsy is, or why i have it. I often times just tell people... " it is where your arms and legs dont work the way they are supposed to" but i wish it was really that simple.... so here i go i will try to explain...well it is a non-progressing disease that normally occurs during pregnacy, or shortly after. to me the statement "non-progressing" dosent make sense because mine seems to be getting worse with age. it can also be due to "birth trama" which is what the doctors suspect happened to me. cerebral palsy happens in the brain (cerebrum) and palsy refers to disorder of movement. so c.p can affect the brain, and always effects the movement. C.P hasn't effected my brain, except for the fact that only half of my brain works!!!!! (which is pretty cool) but there is no known cure for C.P which is very discouraging. but there are four different types of cerebral palsy... mine is Spastic Diplegia, which is where all of my limbs are affected, but my legs are affected more. some treatment options are Botox, Hyperbaric Oxygen (which is what we are now looking into), braces, surgery, etc.
sooooooo it may not make sense but its really not supposed to at first........ it is hard to understand and i dont see how i even do. but i guess u learn it after 12 yrs. living with it......... so that is cerebral palsy for you.....now that you know a little about what it is it will be easier for me to talk about what i am feeling or going through.
- Location:home
- Mood:determined
- Music:none
