New member

Posted May 20, 2001 · May 20, 2001

Hi " Pappy " , My name is Myrna and I was diagnosed in

Feb.01, ttin March 01 due for RAI in July 01. I have

been reading and learning so much from this group. I

am scared about what my body is going through. But I

do appreciate what everyone else has been through and

what to expect. The scary part for me is knowing that

it could and might spread to other parts of my body.

I got my pathology report from the doctor and i didn't

like what I saw. I have been through cancer, my

father died of prostate cancer in '98 and my mom is a

breast cancer survivor. God knows how I feel about

this deasease. Hope to hear from you, Myrna

--- michaluk51@... wrote:

> -

> ME,ME,ME!

> I was diagnosed in December, surgery in January

> (pap, st11 w/ 2+

> nodes) had my trace dose of RAI yesterday for my

> scan on Monday. It's

> all been very odd, sometimes I feel completely all

> right with this

> and other times I recognize I'm moving through the

> stages to

> acceptance.

> Drinking from a lead lined container with nuclear

> signs on it was a

> tad weird. And I've had CT scans before so I guess

> Monday won't be so

> bad. I'll let you know as I go along. It'll be good

> therapy for me

> and I'd be very happy to answer ANY question you

> have

> Be good to yourself there fellow " pappy " (I just

> made that up!)

> Carol

>

> -- In Thyca@y..., baz42@a... wrote:

> > I am a new memeber of this group I look forward to

> hearing from

> other people

> > going through treatment for papillary thyroid

> cancer

>

__________________________________________________

Posted November 26, 2001 · November 26, 2001

.. Is there anyone else who has continued to miscarry

>after removal of their septum or is anyone aware of any other

>procedures?

Hello,

I am so sorry about your losses. I also have a uterine septum and I am

waiting to have surgery after 2 miscarriages - one at 12 weeks, one at 8

weeks. Removing the septum would have removed that as a causal factor in

miscarrying, from what I understand. I think the only way surgery could

have caused a problem is if the surgery itself caused scar tissue, which I

think is not very common with septum resections. I say this based on

research I've done on the net, and what I've heard from this group.

Did you have any residual septum left post surgery, or was it all removed?

I hope someone else in this group can give you some more insight. Again, I

am very sorry for your losses.

_________________________________________________________________

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Posted November 27, 2001 · November 27, 2001

--,

Thank you for responding. I am sorry for your losses and wish you

the best with your surgery. I was told that the septum was

completely removed and later they checked for scar tissue and none

was found. It's just a frustrating mystery.

Theresa

- In MullerianAnomalies@y..., " kathryn golbeck " <kathryngolbeck@h...>

wrote:

> . Is there anyone else who has continued to miscarry

> >after removal of their septum or is anyone aware of any other

> >procedures?

>

> Hello,

> I am so sorry about your losses. I also have a uterine septum and

I am

> waiting to have surgery after 2 miscarriages - one at 12 weeks, one

at 8

> weeks. Removing the septum would have removed that as a causal

factor in

> miscarrying, from what I understand. I think the only way surgery

could

> have caused a problem is if the surgery itself caused scar tissue,

which I

> think is not very common with septum resections. I say this based

on

> research I've done on the net, and what I've heard from this group.

> Did you have any residual septum left post surgery, or was it all

removed?

> I hope someone else in this group can give you some more insight.

Again, I

> am very sorry for your losses.

>

> _________________________________________________________________

> Get your FREE download of MSN Explorer at

http://explorer.msn.com/intl.asp

Posted November 27, 2001 · November 27, 2001

Hi Theresa,

I'm so sorry for your losses. It sounds like you've worked so hard to

figure out what's going on - you must be so frustrated! I'm glad you

found our group ... aside from the mullerian anomalies, there are

many women here who are coping with complicated fertility issues.

Welcome and take care!

Posted December 27, 2001 · December 27, 2001

Hello and welcome. I am so sorry about your losses. I just recently had

a loss at 13 weeks and mine was also a missed m/c. I think that stinks that

they won't do further testing right now. I have one loss and my dr is doing all

kinds of testing. I had an HSG last week and the dr believes I have a t-shaped

uterus (not good, trust me), but I am having an MRI on Monday to confirm his

diagnosis.

I hope that you get the answers you deserve and I hope that you never have to go

thru another loss. You will receive a lot of support on this site and these

ladies are so knowledgable. Good luck.

New Member

Hello,

My name is and I am 26 years old. I am recently married and Hubby & I

would love to start a family soon. I live in Hertfordshire, England.

I have had two miscarriages so far and I have just recently been told I have a

BU. The local hospital have told me this is not connected to the miscarriages

and that they will not look into anything any further until I have had at least

three miscarriages. Hubby & I have been through so much (The miscarriages were

close together and both times I had reached 12 weeks, thought I was 'safe' and

then discovered that I had had a 'missed miscarriage'.) I would really like to

know more about this BU condition. Everyone keeps telling me it is nothing to

worry about but I am not so sure!

I am joining this group, hoping to hear of people that have this BU (or

similar) condition and have had normal, healthy babies. I would also be

grateful for any information or website links that provide information.

Thanks in advance!

Posted December 27, 2001 · December 27, 2001