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Re: for Liz

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Dear Liz,

I read your letter yesterday and still can not stop thinking about

you...I am really very sorry that you have to go through such hard

chemo therapy treatment...I don't know what " wise " words I could say

to you....(I a mother of 16 years old boy myself...so you are just at

the same age...)

Liz, my thoughts and prayers are with you girl. I will pray for good

and prompt results of this treatment.

Taka care,

Elvira

In iga-nephropathy , " Liz Enza " <babyenza69@h...>

wrote:

> dear Rose

>

> Im very sad to hear about your son. I myself was diagnosed with IgA

just in

> January of this year, and i am only 15. I can say it was very hard

getting

> through treatments and still is , as i will be treated with

medications for

> the rest of 2003 and 2004. I had to endure some harsh chemo therapy

> treatments as to suppress my immnue system so it would not attack

my

> kidneys. I had all the side affects as people with cancer do when

being

> treated with chemo(e.x. my hair fell out). But i would have to say

one thing

> kept me under controll, my parents. My mother was so immportant to

me always

> there sitting with me during the night when the nausea and vomiting

and all

> the terrible things would happen, she would get up and feed me

bring

> breakfast in bed. she Helped me understand my homework as i missed

so much

> of the school time.And even though i was supposed to not go to

school i made

> the decision that i would take on as much as possible so i went.And

the days

> when i said i felt ok and im just tired and i don't wanna go she

was the one

> telling me there will be other times when you are more sick and you

will

> need to miss those days so you should go and have a nap in class.

It made

> all the difference in an education for me. As many parents do feel

when

> there child is sick, my father felt distressed and almost guilty,

he cryed

> when i found out i had IgA and then he explained to me that he

never even

> knew what it was yet he felt my pain and he also explained i shoudl

be

> healthy liek the rest of the 3 children he had, i am no

different ,and me

> being the youngest, it isn't fair to you at all that you should

have an

> abnormal childhood not being able to go out with your friends as

you once

> did. He still does not understand to this day,but i understand that

a parent

> should not have to see there child suffer, and a parent should not

have to

> think that they may have to burry there child before there child

burries

> them. Though he felt sad he still tryed as hard as he could to make

me

> smile, but whiped away tears as he could not control how he felt. I

would

> have to say if those two people where not there in my time of need

i would

> not have been able to be treated , therefore these people saved my

life,

> that is why i think that if a child so young will have to be

treated as i

> did then they should have both of there parents around not just one

because

> thet both make all the difference from breakfast in bed to a simple

smile on

> your face!

>

> >From: " Rose " <roseg_tex_3@y...>

> >Reply-To: iga-nephropathy

> >To: iga-nephropathy

> >Subject: I need your support

> >Date: Tue, 01 Jul 2003 17:37:25 -0000

> >

> > My son is 5 now he was diagnosed w/ IGA of March 2002. He has the

> >support of me and his father. My family is going through another

> >crises. iel's father is from Mexico and might be

deported,

> >we go to trial in August. I need some of you to explain how

important

> >it would be for iel to have both of his parents through out

his

> >illness. I put my sons medical records in the court files, with a

> >brief explanation of the diease so the judge can understand. I

think

> >hearing from people w/ this same disease and is going through what

> >iel will in the future will help the judge understand how

> >support is very important to iel.Thank you!

> >

> >

> > Rose

> >

>

> _________________________________________________________________

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