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Medical Forum / Diseases and Disorders / Breast Cancer / October 2008

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October is Breast Cancer Awareness Month

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Mary Fisher - 01 Oct 2008 19:55 GMT
... and here we usually take the opportunity to have a roll call of present,
past and lurking members.

Who's going to kick off?

Mary
Trice M - 02 Oct 2008 03:31 GMT
>Who's going to kick off?

>Mary

I guess you just did, Mary, with your post.<g
So I will add myself, (unfortunately).   Here!

Trice (of the USA)

NO SPAM OR FORWARDS, PLEASE.
x{yz}enophil44@hotmail.com - 02 Oct 2008 18:30 GMT
>>Who's going to kick off?
>
[quoted text clipped - 4 lines]
>
>Trice (of the USA)

Geraldine here in Newcastle upon Tyne (UK)
Mary Fisher - 02 Oct 2008 20:06 GMT
> >Who's going to kick off?
>
[quoted text clipped - 4 lines]
>
> Trice (of the USA)

OK, I asked for that.

It would be good to know why you're here, what your experience of bc has
been and, yes, your geographical locality.

I'm Mary, now 69, from Leeds, Yorkshire, England. I was diagnosed with bc
after a routine mammogram in April 1988. I had a lumpectomy and radiation
courtesy of the British National Health Service and took part in a five year
(extended to ten years) research programme: ATAC - Arimidex or Tamoxifen,
Alone or in Combination. I've no idea which group I was in. There were few,
if any, side effects (except that the radiation was unpleasant). I'm still
going strong, very active and, to date, n.e.d.

Our system doesn't do automatic mammos after we're seventy - might even be
earlier, but I shall ask for them annually. I doubt that I'd be here if I
hadn't gone for that one at the mobile unit in the grounds of our local
hospital (so close I walked there in ten minutes) on 23 April.

I joined this group so that I could learn more about the condition and gain
support forom others - although at that time I didn't feel that I really
needed support, I had everything I needed from my breast care nurse but I
had a lot of time on my hands and had been shocked by the reaction of some
of my friends and family. This, I was to learn, is normal.

I have learned a lot here, loved, laughed and shed tears. Those I've met
physically or on-line have been a strength and a source of surprises. It was
worth coming.

So, over to the rest of you!

Mary.
A.P.Thorsen - 20 Oct 2008 21:07 GMT
> It would be good to know why you're here, what your experience of bc has
> been and, yes, your geographical locality.

Hi, all -

I'm Ann T., 8 year survivor of stage III locally advanced BC, now 52 y/
o, widowed, retired, no children.  5 tumors in left breast (largest
3.1 cm), 1 in right.   Bilateral mastectomies, no reconstruction.
Six months of chemo (4 x 3 weeks AC, 4 x 3 weeks Taxol), 6 weeks
radiation, Tamoxifen for 2.5 years, Arimidex since (going to stop at
the end of this year).  Enthusiastic member of a breast cancer
survivors' rowing team.

Used to hang around here a lot, but have slacked off since losing my
free & easy usenet access.

Nice to see y'all.

Ann T.
I don't much monitor the email address in my header, but can be
reached at ann thorsen (leave out the blank between first & last) at
yahoo dot com.
Tim Jackson - 20 Oct 2008 21:15 GMT
> Hi, all -
>
[quoted text clipped - 15 lines]
> reached at ann thorsen (leave out the blank between first & last) at
> yahoo dot com.

Hey Ann, nice to hear from you.  Sounds like the rowing has been good
for you and that you're doing OK. Great.

Tim
J - 20 Oct 2008 22:35 GMT
> Used to hang around here a lot, but have slacked off since losing my
> free & easy usenet access.

Hi Ann,
You could try http://news.motzarella.org/
A regular on the prostate cancer newsgroup has been using it for many years.
It's free and easy, I think.
J
news.central.cox.net - 21 Oct 2008 22:50 GMT
Hi, all -

I'm Ann T., 8 year survivor of stage III locally advanced BC, now 52 y/
o, widowed, retired, no children.  5 tumors in left breast (largest
3.1 cm), 1 in right.   Bilateral mastectomies, no reconstruction.
Six months of chemo (4 x 3 weeks AC, 4 x 3 weeks Taxol), 6 weeks
radiation, Tamoxifen for 2.5 years, Arimidex since (going to stop at
the end of this year).  Enthusiastic member of a breast cancer
survivors' rowing team.

Used to hang around here a lot, but have slacked off since losing my
free & easy usenet access.

Nice to see y'all.

Ann T.
I don't much monitor the email address in my header, but can be
reached at ann thorsen (leave out the blank between first & last) at
yahoo dot com.

Have missed you and your support, check in when you can!
formerly me2me, now LadyBoot
Ixia - 02 Oct 2008 22:38 GMT
> ... and here we usually take the opportunity to have a roll call of present,
> past and lurking members.

I'm Ixia, 55, Norwegian living in USA, not far from DC. I have a
supportive husband, 2 grown kids and a small grand-child.

I was diagnosed with stage 3A er+ /pr+  /her2+ breast cancer in the
spring of 2007, after my breast became painful.  2 positive nodes were
found at the same time. I was treated fwith dose-dense AC and then
with Taxol + Herceptin before surgery. At the time of my mastectomy no
live cancer cells were found, and my oncologist pronounced me
"theoretically cured".

Since then I have completed 6 weeks of radiation and have just
finished a year of Herceptin. Yay! That completes my initial
treatment.

I'm on daily Tamoxifen, vitamin D, and Zometa infusions every 6
months.

I have recovered from chemo, surgery and radiation by now, and feel
good. I have had no reconstruction, and so far I feel comfortable with
that: I'm tired of being a patient, and I want to enjoy my life with
no big "procedures" hanging over me, to recover from, or to cause
unexpected side-effects and problems - if I can help it.

I enjoy this group and being able to touch base with others whose
lives have been impacted by this disease.

Ixia
Tim Jackson - 02 Oct 2008 23:14 GMT
> ... and here we usually take the opportunity to have a roll call of present,
> past and lurking members.
>
> Who's going to kick off?
>
> Mary

My wife died of breast cancer in March 2000, about three years after
originally finding a lump.  It was a steep learning curve at the time so
I stuck around to try to make things a bit easier for those who had to
follow the same path.

I've a daughter now about to turn 15 who was six at the time of her
mother's death, and a stepson of 27 in the British army.  Both great kids.

I'm 57, a freelance engineer and live in north-west England.

Tim Jackson.
Eva - 04 Oct 2008 03:19 GMT
> ... and here we usually take the opportunity to have a roll call of
> present, past and lurking members.
>
> Who's going to kick off?
-------------
Eva Destruction here in New York, diagnosed with Stage 3 BC in June 2004,
nearly died from having my life saved, still here thus far, hope the Angel
of Death doesn't see this post. (:^)
Mary Fisher - 04 Oct 2008 09:31 GMT
>> ... and here we usually take the opportunity to have a roll call of
>> present, past and lurking members.
[quoted text clipped - 4 lines]
> nearly died from having my life saved, still here thus far, hope the Angel
> of Death doesn't see this post. (:^)

How did you nearly die by having your life saved?

It's not far to say that without more details :-)

Mary
Eva - 04 Oct 2008 13:16 GMT
>>> ... and here we usually take the opportunity to have a roll call of
>>> present, past and lurking members.
[quoted text clipped - 8 lines]
>
> It's not far to say that without more details :-)
---------------
Sorry, I thought I'd told the story one time too many....my oncologist said
I had the worst side effects of chemo she'd ever seen.  I was so sick and
weak I couldn't walk a block without needing a rest, and that's only the
start of it.  I actually don't want to think about it any more.  I only want
to reassure others, that no matter how desperately ill you get from chemo,
just keep putting one swollen foot in front of the other and SURVIVE!

Eva
Mary Fisher - 04 Oct 2008 13:45 GMT
>>>> ... and here we usually take the opportunity to have a roll call of
>>>> present, past and lurking members.
[quoted text clipped - 16 lines]
> from chemo, just keep putting one swollen foot in front of the other and
> SURVIVE!

Well said! I think the same is true of radiation too (not the same kind of
syumptoms of course), they're the best weapons available at the moment.
Well, with drugs. Nothing is without side effects but they're all better
than the alternative. I'm glad you're surviving, along with the rest of us.

I'm sorry if I've read your story before, Eva, my memory isn't what it used
to be. Well, everything's still in there but the retrieval system isn't
working well.

Mary
x{yz}enophil44@hotmail.com - 04 Oct 2008 14:22 GMT
>>>> ... and here we usually take the opportunity to have a roll call of
>>>> present, past and lurking members.
[quoted text clipped - 13 lines]
>weak I couldn't walk a block without needing a rest, and that's only the
>start of it.

I was like that too.  I wasn't very nauseated because they gave me
medication for it, but for months I couldn't stir out of bed before
lunchtime.  I do wonder whether it also contributed to my worsening
heart problem, although they kept testing me and finiding nothing amiss.
To be fair, it didn't start till 8 or 9 months later.

>I actually don't want to think about it any more.  I only want
>to reassure others, that no matter how desperately ill you get from chemo,
>just keep putting one swollen foot in front of the other and SURVIVE!

I don't mind thinking about it, but maybe that's because I had little
sickness or nausea.  Although I could hardly stay awake long enough to
listen to a play on the radio, or concentrate enough to read a book,  I
found it a strangely pleasant, peaceful time for rest and reflection. My
dear pussy cat Phoebe spent a lot of time just sitting on my bed with
me, which was very comforting.

And since I managed to do quite a lot of writing, a line at a time, it
was surprisingly productive.

Thinking back on it, I'm amazed at how calm and peaceful I felt.  We
could have had the roof fall in, or the bailiffs at the door, I just
wouldn't have cared.

Signature

"It's easier to get forgiveness than permission."
Rear Admiral "Amazing" Grace Hopper

Barb - 11 Oct 2008 00:57 GMT
> ... and here we usually take the opportunity to have a roll call of present,
> past and lurking members.
>
> Who's going to kick off?
>
> Mary

Hello Group.  I'm Barb, soon to be a 25 year survivor of stage 2
breast cancer.  I had a right modified radical mastectomy in Nov. of
1983, followed by a year of CMF chemo.  I continued to teach
kindergarten through my treatment, and recently retired after thirty
years in the classroom.  I live in rural north central Pennsylvania
with my husband.

I am needing to have a hysterectomy the end of the month for a pre-
cancerous condition and am really hoping that no co-existing cancer is
found!  Keep fingers crossed for me, please.....

This has been a super group of very caring people, who truly have
shared laughs and tears over the years.  Here's hoping continued good
health for all of us!

Barb
Mary Fisher - 11 Oct 2008 10:01 GMT
> Hello Group.  I'm Barb, soon to be a 25 year survivor of stage 2
breast cancer.

What a model! We tend to think that the most up to date remedies are the
best, you show that it's not necessarily so.

> I had a right modified radical mastectomy in Nov. of
1983, followed by a year of CMF chemo.  I continued to teach
kindergarten through my treatment, and recently retired after thirty
years in the classroom.  I live in rural north central Pennsylvania
with my husband.

> I am needing to have a hysterectomy the end of the month for a pre-
cancerous condition and am really hoping that no co-existing cancer is
found!  Keep fingers crossed for me, please.....

I'm crossing everything!

> This has been a super group of very caring people, who truly have
shared laughs and tears over the years.

Indeed.

> Here's hoping continued good
health for all of us!

Seconded!

Mary
Barb - 11 Oct 2008 13:24 GMT
Hello Dear Mary,

It was so good to hear from you.  Of all my online friends, you are
the one least likely to spend any time worrying---and I'll confess,
this upcoming surgery makes me nervous. It's not the procedure itself
(although abdominal surgery doesn't sound like any fun).  I'm
concerned about them finding a co-existing cancer.  I've "talked
turkey" to myself a few times, reminding me that even if it is another
cancer, the hysterectomy could be curative if it's early stage.  I
know that worry doesn't do anything positive, but my tummy "flips"
periodically anyway.  Some good common sense advice would be most
appreciated, Mary.

Hugs,
Barb
pumpkin - 15 Oct 2008 06:06 GMT
october is also "bald and free" month, I just read (it refers to men, rather
unfairly)....

I don't like awareness months.....most people are "aware" of what's
impacting them most immediately in a moment....hurricane, autism, leukemia,
MS, financial stress, divorce, weight gain/loss, poor vision, great
love/passion, new pet, new house, burned down house.....

I think breast cancer awareness in the U.S. is pretty good.

On Oct 1, 2:55 pm, "Mary Fisher" <mary.fis...@zetnet.co.uk> wrote:
> ... and here we usually take the opportunity to have a roll call of
> present,
[quoted text clipped - 3 lines]
>
> Mary

Hello Group.  I'm Barb, soon to be a 25 year survivor of stage 2
breast cancer.  I had a right modified radical mastectomy in Nov. of
1983, followed by a year of CMF chemo.  I continued to teach
kindergarten through my treatment, and recently retired after thirty
years in the classroom.  I live in rural north central Pennsylvania
with my husband.

I am needing to have a hysterectomy the end of the month for a pre-
cancerous condition and am really hoping that no co-existing cancer is
found!  Keep fingers crossed for me, please.....

This has been a super group of very caring people, who truly have
shared laughs and tears over the years.  Here's hoping continued good
health for all of us!

Barb
Mary Fisher - 15 Oct 2008 10:28 GMT
> october is also "bald and free" month, I just read (it refers to men,
> rather unfairly)....

I didn't know that. I like bald men. I was bald during May and June of 1993,
I made everyone aware of it :-) Perhaps bald women should rejoice in their
condition too and stake their claim for inclusion.

> I don't like awareness months.....most people are "aware" of what's
> impacting them most immediately in a moment....hurricane, autism,
> leukemia, MS, financial stress, divorce, weight gain/loss, poor vision,
> great love/passion, new pet, new house, burned down house.....

Awareness months, days, weeks, years, whatever, aren't to make those with
experience of any condition aware of what they're experiencing, they're to
raise awareness among everyone else.

In the case of bc it's an opportunity for all of us to spread the word about
diagnosis, treatments and outcomes to all those other people who've never
thought about it. In that way we might save some from feeling panic if they
think they might have a lump.

Traditionally the 'roll call' has happened in this group simply because
October, being bc linked universally, is a good aide memoir for those (most
I suspect) of us who'd forget otherwise :-)

> I think breast cancer awareness in the U.S. is pretty good.

Good. I think it is here too - but that's because people have been MADE
aware of it by publicity - especially during October :-) And because we wear
our pink ribbons at all times and are happy to talk about it to anyone who
asks.

I've seen complaints from men with prostate cancer in both USA and UK that
bc is better publicised than pc - because, they say, women have made a fuss
about it and why can't pc be as well publicised? My answer is that THEY
should make a fuss too :-)

Mary
Ixia - 21 Oct 2008 02:27 GMT
> Hi, all -
>
[quoted text clipped - 5 lines]
> the end of this year).  Enthusiastic member of a breast cancer
> survivors' rowing team.

Hi Ann,

It's great to hear from a person with stage III who has been well for
8 years. It gives me hope!

> Used to hang around here a lot, but have slacked off since losing my
> free & easy usenet access.

Have you tried using Google-groups? It's free: http://groups.google.com/
Up in the right-hand corner there should be a 'help' link explaining
the various features of the service.

Be well. Hope to see you here again.

Ixia
pumpkin - 28 Oct 2008 06:16 GMT
October is also, always has been, my favorite month, but this little
addendum I could do without.
I'm pretty sure EVERY month is about BC, at least it certainly seems so from
the profusion of fundraisers, articles, pink everything, celebrity "brave
battles" and "personal stories".....zzzz.....

> ... and here we usually take the opportunity to have a roll call of
> present, past and lurking members.
>
> Who's going to kick off?
>
> Mary
 
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