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Being relatively new to the profession, I am happy there are so many wonderful places to go to share info. Thanks for starting another resource!

Jodi VanDenHeuvel, RD, CD

-----Original Message-----From: fieberl Sent: Wednesday, May 21, 2003 10:19 PMTo: rd-usa Subject: HelloHi everyone. Good to see there is a another option out there for non ADA members.Many thanks to those who got this up and running. K. Fieber

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  • 2 weeks later...
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Way to go Donna! Wish more were like you, me included!

-Carol

hello

This is a nice idea. Good job rds. I quit posting on the ada-dce

listserve because of 'big brother' posts. Its really annoyed me that

whoever was taking it upon themselves to monitor the list notified the

ncdbe (org for cdes) we were talking in general terms about the cde

exam. So, a nonADA org posted a 'do not discuss' note. Made me sick.

Just after that ada posted one about 'do not discuss' salaries. Yuk

again. Some RD must have been a great 'hall monitor' as a kid, and is

still doing so. I dont believe any of us need to be 'monitored', its

insulting and kills communication. I'm on the ada mainlist, and

monitor a couple others (dce and ncc), but mainly lurk on those.

I think its good to shake RDs up every now and then. Otherwise

there are oo many 'tow the liners' keeping the status quo. I used to

get intimidated by the faceless rd mob, dont really care too much now.

I'm just careful what and how i post things.

I'm currently getting my job and salary 'upped' and am very happy,

and nervous. I have jumped through hoops and gotten in people's faces

at the hospital to get a jump in classification and recategorized job

title. It puts me from $27/hr @32 h/week to $31/hr @40h/wk or about

$63k/year. I'm a little scared its going to bottom out at the last

minute, I still havent signed the bottom line, should do so in the

next week or 2. I cant believe my good luck/hard work has finally paid

off. I'm not rich, but I sure feel like my worth is improving. The

cap in this new classification is about 89k, so i've got a hope to get

there one day and make TIME magazines benchmark.

Glad to be here, I put a picture of me and my two girls on my signture

page. I'm going to try to upload some more later of my garden and dog.

Very unprofessional, I love this. thanks for the rd-usa list.

Donna in LA

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  • 2 years later...

Sylvia,

It is going to be slow, but they may get here at some point. My DH

does not share his feelings, most days he denys he has any. A large

part of the family MO is to hide this and cover it and make excuses

for it. It is still so hard for my DH to face this, when he would

rather burry. He gets very upset if we talk about this too much. He

still, in so many ways, idolizes them. My sister-in-law is fed up

with everything right now, but I plan to tell her about this group

and gently introduce her. She has not read any books on BPD, but I

plan to buy her the one on being a daughter of a BPD. She has been

listening the boundary books on tape. She is a lovely woman and a

very Christian person. Since this all began a year ago, she and I

have become very close. We have a wonderful and sisterly relationship

outside of all of the BPD crisis. This would not have been possible

without the crisis at Easter. This has been the best part of clearing

the smoke and mystery, exposing it to light. We got to meet each

other again and become better friends and a closer family, but

farther apart from my MIL and FIL.

I find it so hard to get my mind around all of the abuse. I ache for

my SIL and husband. I want in some ways to take away their pain and

make it all better for them. I tried for a while to buffer my DH from

his parents and to help take care of them, but as you all have said

my MIL is a bottomless pit of need and hurt.

I am also amazed by the wonderful courage I see in all of the posts.

I see the hurt, but inside I also see the empathy and an amazing

amount of caring and giving. It makes me wonder again how my DH

turned out so well with such absentee parents.

Dawn

> > > My name is Dawn and I am a Non-BPD (39 years of age). Within

the

> > past

> > > year I have become the caretaker of a N/BPD the mother of my DH

> of

> > 4

> > > years. We have two kids, my son 3 and daughter 11 months. My

SIL,

> > my

> > > DH's older sister, has cut off all contact with her mother, the

> BPD

> > in

> > > question and father who is a co-dependent facilitator. My dh

and

> I

> > are

> > > in marriage counciling, my SIL is in group therapy. We

pressured

> my

> > > MIL and FIL into counciling with a therapist and thier

minister.

> > Both

> > > therapist and minister have diagnosed my MIL with BPD. MIL also

> has

> > > fibromyalgia, arthritis and depression. She is 65. She lives

less

> > than

> > > 100 yards from my SIL and 20 minutes from us. My father-in-law

> has

> > had

> > > major health problems which has left my DH and I to care for my

> MIL

> > > and FIL at our house on and off because we live near the

hospital.

> > >

> > > I have come under a barrage of unexplainable behavior. I can

not

> > make

> > > sense of all the things my BPD-MIL says, does and has done to

my

> > SIL

> > > and DH in the past. I am overwhelmed, hurt, angry and fed up,

but

> > not

> > > willing to give up.

> > >

> > > May I join this discussion group or do I have to have a mother

> who

> > is

> > > a BPD? I will understand if the answer is no.

> > >

> > > Dawn

> >

> >

> >

> >

> > Send questions and/or concerns to ModOasis-owner

> > " Stop Walking on Eggshells, " a primer for non-BPs, can be ordered

> via 1-888-35-SHELL () and for the table of contents, go

> to:

> > http://www.BPDCentral.com

> >

> >

> >

> >

> >

> >

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  • 3 years later...
Guest guest

hi gang happy late mothers day to all my girls!!!! and welcome to our new

members i am glad you found us and we are all in this boat together,so if i can

be of any help please let me know. i am barby caregiver for my husband who has

esld due to hep.c. he stays tired swolled and in pain, so i understand what you

all are saying. just know you are in GODS hands and you have come to a great

place for knowledge and support. welcome ,much love barby

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  • 2 months later...
Guest guest

i am inereseded in thei same.  Wha ios HCV?????????????????

Thanks be to God for he creates our tomorrows Love, Lyncia

 

 

Subject: hello

To: livercirrhosissupport

Date: Monday, July 27, 2009, 8:47 AM

 

Hello all- I am not a very active member,sorry. It seems I have only so much

time for networking  but am getting better. I have a Facebook page and have

hooked up with old friends. I am helped by all your posts and realize that one

day at a time is sooooo important. I need reminders of that fact often. I have

had HCV for quite a few 24 hrs. and who knows what the course of disease will

bring me in the future. Today is what is important. Who knows if we'll even be

around tomorrow- hope so though,always act as if. Take care all,

 Linnea

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