Jump to content
RemedySpot.com

and family support

Rate this topic


Guest guest

Recommended Posts

:

You have taken the first step to show you care by getting on this list. You

must really care.

I have two completely different experiences with great family support and

lack there of. My brother and his wife basically avoided us for a long time

after our son was diagnosed b/c they did not know how to deal with it. When

they finally did start coming around again they avoided asking about it and

never made any attempt to learn about CF. They're funny that way...they

tend to avoid any emotional situation like this. I try to be understanding

of this because its the way they are. I know they care though because they

did sell more raffle tickets to raise money for CF than any one else.

My husbands brother and his wife on the other hand were very supportive.

They came to see us right away after dx. They cried right along with us.

They also did a lot of research right away so that they understood more

about CF. They also learned all about doing my son's therapy and how to

give his meds so they could give us a break when we needed it. They were

never afraid to ask questions.

So my advice to you is to ask them if you can read everything they do after

they're done with it, learn how to look after your nephew so your sister can

get away,and be a good listner and shoulder to cry on...family support is

one of the most important things in this difficult time. Your sisters

future and that of her son's has been completely altered and right now

family is going to seem like the only thing that she can grab on to to keep

her from sinking.

It will get better over time for her.

Give her a big hug from all of us here at cfparents.

Tammy mom of Zack (almost 6wcf) and e (3nocf)

Re: Potty training

Hello everyone, my name is ,

this past week my nephew was tested and shown to have CF. I wish to support

my sister and nephew as much as I can can in this, any suggestions on the

best way to support a mother of a child with CF?

I have no kids, but am getting tested to see if I might be a carrier.

.

_________________________________________________________________________

Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com.

Share information about yourself, create your own public profile at

http://profiles.msn.com.

***********************

This is a secular list.

***********************

PLEASE do not post religious emails to the list.

--------------------------------------------------

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.

--------------------------------------------------

Our webpage is at http://www.eohio.net/malbright/cfparents.htm

_________________________________________________

Post message: cfparentsegroups

Subscribe: cfparents-subscribeegroups

Unsubscribe: cfparents-unsubscribeegroups

List owner: cfparents-owneregroups

_________________________________________________

WE HAVE A CHAT PAGE!!!

/chat/cfparents

_________________________________________________

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...