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,

I want to take the time to welcome you to the group. I am sorry that I haven't posted before now but it is better late than never. You will find a great deal of info and lots of love and support. I am very sorry that you have come to meet us all this way. We all sympathize and share those same feelings with you.

I saw that you take care of your mother. I know how hard that is. We live next door to my mom and we took care of my dad until he passed away Nov.98. He had suffered with Parkinson's disease for 20 years. It works alot like alzheimer's disease. I can also sympathize with you on this too. It is a very hard thing to do but one you won't regret. I think it would be great if you could get away for just a little while and take some rest. I wish we had someone that would have helped us with dad. I wouldn't feel so tired all the time now. It takes alot of energy and lots of patience with the sick as I know that you know. I am thinking about you and praying for you. If you ever want to email privately my email addy is nora@... . Please take care of yourself and have a great evening.

Nora

hello

Hi everyone,

I just wanted to say thank you for all the responses. I am excited to be a part of this group--as I am already feeling a little more positive about the future after reading the messages on this site.

My ob/gyn doesn't feel that we will get very far with any further testing. She feels that my past history with pre-cancerous cells on my cervix has something to do with it. I have had several surgeries.

I am still very " raw " from the loss. I am actually thinking of going away next week for a few days with my dh--just to get away from the family. We live my parents right now, my mother is a brittle diabetic with a heart condition and alzheimer's --so we help my father take care of her. Life hasn't dealt me many positive things lately.

Thank you all for listening. I need it.

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  • 3 weeks later...
Guest guest

,

Welcome to our group. I am so sorry that you have a reason to find us, but

glad that you did. You are at a very difficult point right now, but know

that we are here to help if you need us.

Take care,

Tara

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Guest guest

Dear ,

I am so sorry for you and your dh loss. I am glad you found this

group. I am sorry your ep was so hard for the drs. to diagnose.

Sometimes I get this crazy idea that I would like to start a group to

inform obgyns how to check for ectopics. The on-call doctor I called

the first night I had complications told me not to worry and gave me

no insturctions/precautions for signs to look for. I also think these

obgyns should belong or receive info on groups such as this so they

can be more sympathetic. (I am sorry for going on a soap box). As

for your other message, I am not a doctor but I don't think you

should go on the pill before ttc, it can really screw up your cycle.

Another thing my NEW obgyn said was to stay on the prenatals. We are

charting and using condoms until our " 3 month " wait is over. One

more thing, I am having an HSG done also before I TTC per my drs.

suggestion. I am here if you ever need to talk. I too am new, ep

3/13.

Take care,

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Guest guest

,

I am sorry you have a reason to come here, but glad that you found

us. My ectopic was 3/11/00 and resolved with methotrexate. I will not be

able to try until my third AF and I am expecting the first at any time.

Write anytime you need anything. I hope you post op appointment goes

well, Kim

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Guest guest

,

Welcome to the group. I'm sorry for your loss and the circumstances

that brought you to us, but I know that you will find great comfort and

support.

You are in my thoughts and prayers.

Big hug,

Jo-Ann

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  • 2 years later...
  • 3 years later...

thank you , that is a relief. i guess i should have looked

more closely at the finer details!

>

> hello all i am another new member. Like Naomi drugs (paroxetine)

made

> things so much worse. i was given 6 months 9 years ago after 10 mins

> with a psych and actually having an undiagnosed physical illness-my

> only symptom resembling depression was fatigue. since then i have

had

> chronic twitches of my head and persistent facial muscular tension.

> both very demoralising. until i saw sites like this i thought there

was

> nothing to be done. however, i recently tried 400iu of natural

vitamin

> e and after 2 days felt more like my old self than i had in 9

years. it

> did make me feel a bit hot and chesty though. unfortunately the

> physical illness chronic prostatitis persists and the vit e caused

some

> burning pain peeing. i have read lots of good stuff about magnesium

but

> have a concern about it causing candida overgrowth as per

Eby's

> website. with the prostate thing i have to take long courses of

> antibiotics at times, and candida would be most unwelcome! i wonder

if

> anyone has experienced or heard of problems with magnesium causing

> yeast probs. many thanks for listening.

>

> Omer>>

>

>

>

> ** Magnesium does not cause candida. It helps candida. If

yours worsens with magnesium, look at the additives in the magnesium

and instead, get pure magnesium by Gillham at www.vitacost.com

>

>

> Here is what Eby says. If you read it carefully, you'll see it

is nothing but pure conjecture. He is very careful to state this.

Note the phrases " I believe " and " my intuition only, no facts here " .

>

> I disagree with him on his conclusions. There are many

examples of magnesium helping candida. If a malabsorption problem

exists, it is usually much more complicated than Eby presents. The

malabsorption problem itself feeds the candida, not the magnesium.

>

>

> Eby says:

>

> " Some people can't absorb ionizable magnesium compounds since

they have intestinal problems, such as candida albicans infection and

other problems perhaps of a medical nature, and they develop diarrhea

with relatively small doses of ionizable magnesium like magnesium

chloride, citrate, lactate, glycinate and so on. I believe they can't

absorb ionizable magnesium since ionizable magnesium first feeds

candida albicans fungus or other infective agent in the guts, thus

worsening intestinal health and diminishing absorption. I don't know

if this condition is rare or common, but suspect it is rare in well

people but more common in sick people such as depressives. Perhaps

leaky gut syndrome is present. There are fascinating tidbits of

information that suggests magnesium oxide will not be absorbed by

candida albicans (my intuition only - no facts here), yet the human

gut absorbs it. "

>

> --

>

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  • 1 year later...
Guest guest

Hi. I'm new to the group. My mother is a BP although I didn't know what

her condition was called until a few months ago when I did extensive reading

on the net. She's not been officially diagnosed though. I'm not a doctor.

I'm 45 and she is now 70. Over the last 10 years or so, her symptoms have

really intensified. It's hard to take, and hard to try and stay on her good

side. She holds an inheritance over my head and has already cut from her

will 2 siblings for blown out of proportion reasons. I have to admit that

if it weren't for the will, I wouldn't put up with someone behaving to me

like she does. The older I get, the less I can put up with dramatics, both

from her, and even from myself (learned response behaviour I think).

I'm looking forward to reading what others have gone through and how they

cope. I'm glad I found this group. :)

Skunky

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Guest guest

Welcome Skunky,

Hopefully you find this group as helpful as I have. The people on here are

wonderful, and always available to give advice for your particular situations

that your BPD will and has put you in.

T

Hello

Hi. I'm new to the group. My mother is a BP although I didn't know what

her condition was called until a few months ago when I did extensive reading

on the net. She's not been officially diagnosed though. I'm not a doctor.

I'm 45 and she is now 70. Over the last 10 years or so, her symptoms have

really intensified. It's hard to take, and hard to try and stay on her good

side. She holds an inheritance over my head and has already cut from her

will 2 siblings for blown out of proportion reasons. I have to admit that

if it weren't for the will, I wouldn't put up with someone behaving to me

like she does. The older I get, the less I can put up with dramatics, both

from her, and even from myself (learned response behaviour I think).

I'm looking forward to reading what others have gone through and how they

cope. I'm glad I found this group. :)

Skunky

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Guest guest

Hey Skunky,

Wow,...very similar.  I've already been cut out and am NC with Nada. 

Welcome to the group!

Kindest regards,

Mercy

Subject: Hello

To: WTOAdultChildren1

Date: Sunday, July 20, 2008, 8:28 AM

Hi. I'm new to the group. My mother is a BP although I didn't know what

her condition was called until a few months ago when I did extensive reading

on the net. She's not been officially diagnosed though. I'm not a doctor.

I'm 45 and she is now 70. Over the last 10 years or so, her symptoms have

really intensified. It's hard to take, and hard to try and stay on her good

side. She holds an inheritance over my head and has already cut from her

will 2 siblings for blown out of proportion reasons. I have to admit that

if it weren't for the will, I wouldn't put up with someone behaving to me

like she does. The older I get, the less I can put up with dramatics, both

from her, and even from myself (learned response behaviour I think).

I'm looking forward to reading what others have gone through and how they

cope. I'm glad I found this group. :)

Skunky

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Guest guest

Thanks for the welcome. My latest contact with my mother was when she

called me a couple of days ago. She was weepy and said she was depressed

and sorry that she had promised everyone that she wouldn't suicide again.

Then she suddenly changed and said hey listen. She thinks she has an old

bank account that she forgot about from years ago, and she wants me to find

out on the internet. I told her that's not the kind of thing I could find

on the internet, you would have to go to the bank and prove who you are.

Then she started crying and said ok, if you don't want to bother... I said

it's not a matter of bothering, that's not the kind of thing that would be

publicly available on the net. She cried that she couldn't talk anymore and

hung up on me.

Argh. I'm going to call her back tonight and try to somehow smoothe things

down, maybe distract her with some other topic to make her forget she was

mad at me.

Re: Hello

Welcome Skunky,

Hopefully you find this group as helpful as I have. The people on here are

wonderful, and always available to give advice for your particular

situations that your BPD will and has put you in.

T

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Guest guest

Thanks for the welcome. Does NC stand for no contact? I couldn't find it

in the abbreviation list. It's anyone's guess if I'll be cut out of, or in,

the will at the time she dies. She changes her will more often than her

clothes! I've mentally prepared myself for being cut out because she is so

volatile right now.

Re: Hello

Hey Skunky,

Wow,...very similar. I've already been cut out and am NC with Nada.

Welcome to the group!

Kindest regards,

Mercy

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Guest guest

Yes NC=No Contact, LC=Low contact.

Re: Hello

Hey Skunky,

Wow,...very similar. I've already been cut out and am NC with Nada.

Welcome to the group!

Kindest regards,

Mercy

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Guest guest

Thanks. I guess I'm LC. She lives on the west coast, and I'm in the

Toronto area. The distance helps.

Re: Hello

Yes NC=No Contact, LC=Low contact.

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Guest guest

Nice, I wish i had some geographic space from my BPD. I live 20 minutes away,

so it is very easy for them to come barging into my house. After getting back

from Italy on vacation, i seriously talked to my wife about moving there, but i

even questioned if the Atlantic would prevent my mom from getting to me :)

Re: Hello

Yes NC=No Contact, LC=Low contact.

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Guest guest

Yeah,...sorry NC is no contact. I need to remember when those

appreviations are second nature to me. My Nada changed her will

years ago. I've been disinherited for as long as I can remember.

Mercy

>

> Thanks for the welcome. Does NC stand for no contact? I couldn't

find it

> in the abbreviation list. It's anyone's guess if I'll be cut out

of, or in,

> the will at the time she dies. She changes her will more often

than her

> clothes! I've mentally prepared myself for being cut out because

she is so

> volatile right now.

>

>

> Re: Hello

>

>

> Hey Skunky,

> Wow,...very similar. I've already been cut out and am NC with Nada.

> Welcome to the group!

> Kindest regards,

> Mercy

>

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Guest guest

Welcome, Skunky.  An awesome group of people here and lots of support.  I've

also been 'cut' from the will.  I figure my integrity and happiness outweighs

any money though.  I just recently went to NC, again, after 'giving it another

shot'.  I hope we can help you in the many ways that I have received it from

here!

 

Take Care Of You,

JaneSoul

Hello

Hi. I'm new to the group. My mother is a BP although I didn't know what

her condition was called until a few months ago when I did extensive reading

on the net. She's not been officially diagnosed though. I'm not a doctor.

I'm 45 and she is now 70. Over the last 10 years or so, her symptoms have

really intensified.. It's hard to take, and hard to try and stay on her good

side. She holds an inheritance over my head and has already cut from her

will 2 siblings for blown out of proportion reasons. I have to admit that

if it weren't for the will, I wouldn't put up with someone behaving to me

like she does. The older I get, the less I can put up with dramatics, both

from her, and even from myself (learned response behaviour I think).

I'm looking forward to reading what others have gone through and how they

cope. I'm glad I found this group. :)

Skunky

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