Jump to content
RemedySpot.com

Re: Thankful

Rate this topic


Guest guest

Recommended Posts

Guest guest

How very beautiful you are both out & especially IN. I am so pleased to

know you here in cyber world- You have given us all a new pair of eyes with

that lovely reflective post. Thank you sooooooo much for sharing. It helps

us all during our stress in caring and loving those with CF & those who

care for them, regardless of ages. LOVE is so pure & you have reminded us

all about that..........

Thank you & have a wonderful day-week,I do hope he is feeling well & will

even feel better :):)

LOVE & HUGS,

grandmomBEv

Thankful

I have just gone to Liams bed while hes having an afternoon nap and he is so

beautiful, sleeping spread out like a frog. I am so thankful for my son, at

that moment I was able to forget everything about CF and the stress of it

and just look at him as a beautiful pure baby. I thank God that he is in

my life, I am so thankful that he is my son even if he has CF. I dont often

have these times when I just can look at him for what he is, my mind is

always racing and trying to think of what I can do for him or give him to

make him live longer and be more healthy. I am slowly learning to Love my

son out of love and not out of fear. Just wanted to share this moment of

reflection.

Thank you to all of you out there as well who are all searching for more for

our precious children.

I am so glad that Liam is able to walk, see, hear and basically do anything

he wants to achieve in life, i am glad he is born in this era of time where

much is avaliable to him.

Its really important to look at what is good and what is well in life rather

than constantly looking at what is not.

proud mum to my baby boy 11 months old wcf. Also mum to my

beautiful girl Lily in heaven, I am also thankful but sad that we had Lily,

it was a short 8 days but very special. She was sent for reasons beyond my

minds eye.

EVERYTHING IN LIFE HAPPENS FOR A REASON HAPPY OR SAD

I have these moments where I just get mussy and reflective, bear with me.

LOL

Link to comment
Share on other sites

Guest guest

,

That was beautiful!!! Sometimes everyone needs to be reminded to just enjoy

our wonderful children and not always think of CF! Thank you for sharing it

with us, I know I appreciated it!!!

Vicki

Thankful

>

>

> I have just gone to Liams bed while hes having an afternoon nap and he is

so beautiful, sleeping spread out like a frog. I am so thankful for my son,

at that moment I was able to forget everything about CF and the stress of it

and just look at him as a beautiful pure baby. I thank God that he is in

my life, I am so thankful that he is my son even if he has CF. I dont often

have these times when I just can look at him for what he is, my mind is

always racing and trying to think of what I can do for him or give him to

make him live longer and be more healthy. I am slowly learning to Love my

son out of love and not out of fear. Just wanted to share this moment of

reflection.

> Thank you to all of you out there as well who are all searching for more

for our precious children.

> I am so glad that Liam is able to walk, see, hear and basically do

anything he wants to achieve in life, i am glad he is born in this era of

time where much is avaliable to him.

> Its really important to look at what is good and what is well in life

rather than constantly looking at what is not.

>

> proud mum to my baby boy 11 months old wcf. Also mum to my

beautiful girl Lily in heaven, I am also thankful but sad that we had Lily,

it was a short 8 days but very special. She was sent for reasons beyond my

minds eye.

>

> EVERYTHING IN LIFE HAPPENS FOR A REASON HAPPY OR SAD

>

> I have these moments where I just get mussy and reflective, bear with me.

LOL

>

>

>

Link to comment
Share on other sites

Guest guest

Oh , reading your post, specially the end brought tears to my

eyes, life is indeed strange but yet so precious. Remember the movie

Forest Gump, where he says life is like a box of chocolates, you

never know what you are going to get.

For me things happened backwards than for you, a was born so

healthy, so we thought, so we loved her out of pure love, last year

when she was diagnosed that feeling changed to love out of great

fear, I think now we are back to our love out of pure love.

Love to you and Liam,

mom of a 10 wcf, Venanzio 7 nocf, Pepe 3 nocf

>

>

> I have just gone to Liams bed while hes having an afternoon nap and

he is so beautiful, sleeping spread out like a frog. I am so

thankful for my son, at that moment I was able to forget everything

about CF and the stress of it and just look at him as a beautiful

pure baby. I thank God that he is in my life, I am so thankful that

he is my son even if he has CF. I dont often have these times when I

just can look at him for what he is, my mind is always racing and

trying to think of what I can do for him or give him to make him live

longer and be more healthy. I am slowly learning to Love my son out

of love and not out of fear. Just wanted to share this moment of

reflection.

> Thank you to all of you out there as well who are all searching for

more for our precious children.

> I am so glad that Liam is able to walk, see, hear and basically do

anything he wants to achieve in life, i am glad he is born in this

era of time where much is avaliable to him.

> Its really important to look at what is good and what is well in

life rather than constantly looking at what is not.

>

> proud mum to my baby boy 11 months old wcf. Also mum to my

beautiful girl Lily in heaven, I am also thankful but sad that we had

Lily, it was a short 8 days but very special. She was sent for

reasons beyond my minds eye.

>

> EVERYTHING IN LIFE HAPPENS FOR A REASON HAPPY OR SAD

>

> I have these moments where I just get mussy and reflective, bear

with me. LOL

>

>

>

Link to comment
Share on other sites

Guest guest

I think that we all need these little moments in our days. Well like

for you they only come once in a blue moon, but the important thing is

that we still have them ( rare as they may be )

I lost 2 after my first son was born. I was pregnant so I am

sure the magnitude of loss was not as severe but definately there. One

was at 12 weeks and one at 16 weeks. Then my son Colgan who even with

this I would not trade for the world.

Thanks for sharing your moment with us

Ashauna

Link to comment
Share on other sites

Guest guest

i also had misscarriges, 3. first one was twins. then after my first son was

born, i fopund out i have graves disease, which is hyperthyroid. the doctor

told me, thyroid disease may have been the cause of my miscarriges. i tend

to think he was right. hope all is well

maureen mom of 3,, 2 with cf,, Noelle forever 20!

Maureen----->-@

>From: Ashauna_and_@...

>Reply-To: cfparents

>To: cfparents

>Subject: Re: Thankful

>Date: Thu, 7 Aug 2003 23:07:16 -0500 (CDT)

>

>I think that we all need these little moments in our days. Well like

>for you they only come once in a blue moon, but the important thing is

>that we still have them ( rare as they may be )

> I lost 2 after my first son was born. I was pregnant so I am

>sure the magnitude of loss was not as severe but definately there. One

>was at 12 weeks and one at 16 weeks. Then my son Colgan who even with

>this I would not trade for the world.

>

>Thanks for sharing your moment with us

>Ashauna

>

>

>

>-------------------------------------------

>The opinions and information exchanged on this list should IN NO WAY

>be construed as medical advice.

>

>PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR

>TREATMENTS.

>

>------------------------------------

>

>

>

Link to comment
Share on other sites

Guest guest

Yes I remember the movie!

It is really important to love them like they have not got an illness and I

find it hard.

Because I am a herbalist I find that drawing the line between work and Liams

life is very hard, when I read papers and information my mind always goes

back to CF and Liam, i feel like I am switched on all the time. My husband

keeps telling me to switch off but its hard when i see Liam all day I often

see CF. I am getting much better though, my hubby is brilliant at getting

me to talk it out, about my fears of him dying and things like that. I dont

want this disease to eat me up and consume me so I am trying to remind

myself all the time that he is my strong little boy who just wants to learn

and love and live life every day even if he has CF, he isnt sick he just has

something more to live with than others.

I was reading a site last night on the web and I just thought I am so gald

Liam dosent have cancer or leukemia or brain tumours etc. Some of these

poor children and their families. I am so blessed.

I am sure that we shape our children by our belief systems, our emotions of

fear or faith, our words of love or hate, our attitude of accepting CF=death

or not believing this and pushing away the fears that bind us and make us

accept the statitisics.

I really believe that words are powerful, I tell Liam every night real

positive stuff for his life, so he grows up knowing he is strong not weak,

healthy and not sick.

Well thats all from me I have to go and cook dinner

mum to baby Liam 11 months old with a zest for life

Re: Thankful

> Oh , reading your post, specially the end brought tears to my

> eyes, life is indeed strange but yet so precious. Remember the movie

> Forest Gump, where he says life is like a box of chocolates, you

> never know what you are going to get.

> For me things happened backwards than for you, a was born so

> healthy, so we thought, so we loved her out of pure love, last year

> when she was diagnosed that feeling changed to love out of great

> fear, I think now we are back to our love out of pure love.

>

> Love to you and Liam,

>

> mom of a 10 wcf, Venanzio 7 nocf, Pepe 3 nocf

>

>

>

>

>

>

>

> >

> >

> > I have just gone to Liams bed while hes having an afternoon nap and

> he is so beautiful, sleeping spread out like a frog. I am so

> thankful for my son, at that moment I was able to forget everything

> about CF and the stress of it and just look at him as a beautiful

> pure baby. I thank God that he is in my life, I am so thankful that

> he is my son even if he has CF. I dont often have these times when I

> just can look at him for what he is, my mind is always racing and

> trying to think of what I can do for him or give him to make him live

> longer and be more healthy. I am slowly learning to Love my son out

> of love and not out of fear. Just wanted to share this moment of

> reflection.

> > Thank you to all of you out there as well who are all searching for

> more for our precious children.

> > I am so glad that Liam is able to walk, see, hear and basically do

> anything he wants to achieve in life, i am glad he is born in this

> era of time where much is avaliable to him.

> > Its really important to look at what is good and what is well in

> life rather than constantly looking at what is not.

> >

> > proud mum to my baby boy 11 months old wcf. Also mum to my

> beautiful girl Lily in heaven, I am also thankful but sad that we had

> Lily, it was a short 8 days but very special. She was sent for

> reasons beyond my minds eye.

> >

> > EVERYTHING IN LIFE HAPPENS FOR A REASON HAPPY OR SAD

> >

> > I have these moments where I just get mussy and reflective, bear

> with me. LOL

> >

> >

> >

Link to comment
Share on other sites

Guest guest

,

I agree that what we think and what we say is very powerful. One of

the techniques that I use when I say my special thoughts is to see

whoever I am thinking about very healthy and full of life.

Liam will grow up believing that he can do anything he is set out to

do.

Love and good vibes your way!!

mom of a 10 wcf, Venanzio 7 nocf, Pepe 3 nocf

> > >

> > >

> > > I have just gone to Liams bed while hes having an afternoon nap

and

> > he is so beautiful, sleeping spread out like a frog. I am so

> > thankful for my son, at that moment I was able to forget

everything

> > about CF and the stress of it and just look at him as a beautiful

> > pure baby. I thank God that he is in my life, I am so thankful

that

> > he is my son even if he has CF. I dont often have these times

when I

> > just can look at him for what he is, my mind is always racing and

> > trying to think of what I can do for him or give him to make him

live

> > longer and be more healthy. I am slowly learning to Love my son

out

> > of love and not out of fear. Just wanted to share this moment of

> > reflection.

> > > Thank you to all of you out there as well who are all searching

for

> > more for our precious children.

> > > I am so glad that Liam is able to walk, see, hear and basically

do

> > anything he wants to achieve in life, i am glad he is born in this

> > era of time where much is avaliable to him.

> > > Its really important to look at what is good and what is well in

> > life rather than constantly looking at what is not.

> > >

> > > proud mum to my baby boy 11 months old wcf. Also mum

to my

> > beautiful girl Lily in heaven, I am also thankful but sad that we

had

> > Lily, it was a short 8 days but very special. She was sent for

> > reasons beyond my minds eye.

> > >

> > > EVERYTHING IN LIFE HAPPENS FOR A REASON HAPPY OR SAD

> > >

> > > I have these moments where I just get mussy and reflective, bear

> > with me. LOL

> > >

> > >

> > >

Link to comment
Share on other sites

Guest guest

That was a beautiful e-mail..Reminded me of Dorothy in the Wizard of Oz at

the end when she awakens after the storm........

I think for many of us thats the problem - we awoke after the storm and know

whats impt. and whats not...but most people don't so its a difficult world to

live in. The knowledge and wisdom I have achieved cannot be taught, bought or

learned. I wouldn't wish it on anybody yet I am a better person...albeit a

sad, tired and cranky one!

I am stepping down from my pulpit for tonight..........LOL LOL....my luck I

would trip and break my good arm........

Rosemary in NY with 3 children (13, 10.6 and 6.6)

with CF. I have a dog named TOBI and have

coined the phrase " BREATHE DAMMIT "

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...