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Newsletter #1

March 26, 2007

Dear Friends and Supporters of www.facingforwardllc.com ,  
I want to thank you all again for all your letters of 
support, encouragement, and for your interest in the 
direction I am taking with "Facing Forward" (and the recent 
newspaper article) and appreciating the unique nature of 
its concept. There was much that couldn't be covered in 
the article that Jerry wrote though he certainly gave me 
quite enough space to share as much as possible. I love 
hearing from in particular those of you who wrote and 
called who said "Your story sounds like mine!". Not 
because I want anyone to have to fight this battle of 
course, but because there is so much more than just 
awareness that needs to be shared, and many of us have 
experienced what appears to the world to be a "unique" 
situation only for us to find that there are many YOUNG 
women, women of DIFFERENT LIFESTYLES, and women with 
METASTASIS (or mets as those of us who grow tired of saying 
it call it.) I had wanted to wait until my website was 
much more full of information, and until the EBay links and 
MySpace links were in place. Of course beyond that there 
is the shooting of the DVD itself that has been challenging 
and the development of makeup and skincare products which 
also take time and a lot of Internet research. Its a far 
reaching project, and while initially we are still aiming 
for October for an official launch, it could be quite some 
time before the full concept is completed (if ever!!)  
There is so much that can be done with this and there are 
so many of you with wonderful ideas and offers of 
assistance that I myself am wondering how it will actually 
appear once it is launched. I would be remiss to not open 
my mind to newer ways to do things and I want to link to as 
large a community as possible, of course without losing 
touch of our real goal, and that is to help reach 
survivors.  
 
The advent of Elizabeth Edwards announcement has propelled 
me to go ahead and put the web address out there, along 
with this email because the timeliness and the circumstance 
surrounding her recurrence is so textbook in the way that 
it is unique to our approach. There are resources out 
there that tout awareness and we certainly want that. But 
there is much to be aware of and one of those concepts is 
the concept of metastasis, what it means, and how it 
changes the perception of our lives and the way we approach 
the illness. People don't often think of cancer as a 
chronic illness like diabetes or sickle cell, but once the 
illness spreads to another organ in the body, the disease 
has metastasized and is now considered incurable. That 
word incurable is so initially frightening. I remember 
when I found out just how serious my circumstances were.  
In the dark at 3am...they jumped out at me. The odds that 
stared me in the face...a 20% chance of surviving 5 years?  
What did this mean? Yet the doctors felt they could treat 
my recurrence fairly easily and I was being given great 
odds in the offices of the oncologists. The truth is there 
just aren't enough studies and information over time to 
understand approaching cancer as a chronic illness.  
Because of new treatments and approaches, sometimes the 
disease can be managed for many, many years. A full 
lifetime, if proper care is taken and of course the right 
amount of prayers and luck (depending on your beliefs) are 
involved. Here I am staring at my potential 5th 
recurrence. (The lung spot has cleared for the most part, 
but now a spot on the back needs to be investigated, the 
only symptom now is pain, so it isn't urgent yet.) I say 
this because I want people to see a woman LIVING with 
cancer, not dying from it, or simply surviving it. Mrs. 
Edwards is such a perfect example of this and her approach 
is so wonderfully optimistic, refreshing and empowering.  
Incurable doesn't mean deadly. Not always. We have to 
acknowledge the seriousness of what we are fighting. So it 
helps to know that cancer will always be a part of my/our 
lives in some way. But it doesn't have to overwhelm it. I 
read about a woman a couple of years ago who had fought 
Breast Cancer 30+ times. Now that's power.  
 
A few other facts you have probably heard mentioned now, 
but are not always as commonly known. Breast Cancer that 
has spread to the bone or liver is still BREAST CANCER.  
Cancer is defined by the type of cell involved not the 
location. Breast Cancer likes the bones, liver, lungs and 
brain. (I have had it more times in my bone than anywhere 
else-my breast has not been affected since the initial 
diagnosis 6 years ago.) Once it has spread it is 
classified as incurable. It will most likely recur, and 
though you cannot predict such timing, it seems to do so 
within a 5 year period. Survivors work hard to get as many 
years between occurrences as possible. Additionally, 
though not always the case, the disease tends to be more 
aggressive in younger women. I know more women in my own 
age range that have passed than those in older age 
brackets. If you are young and you have fought the 
disease...don't live in fear...but live in diligence. The 
tests we have are not as effective, the only indicator I 
had was pain. Severe pain in my sternum, and quick growth. 
So you must rely on your own knowledge of your body. And 
push for tests. PET scans in particular. Tumor/Blood 
markers were completely ineffective in most of my 
diagnoses. X-rays were not helpful. Pain which led to a 
CT scan was my savior. Consider how you look at pain. It 
saved my life. It can be your friend and it can be managed 
too. (All this said remember your doctor will probably not 
be as diligent as you are and may not be thrilled with your 
approach-ITS YOUR BODY, don't be paranoid, just be alert.)  
 
 
I will leave you all with all this to digest. I know it is 
lengthy, but it is the first official newsletter email and 
we needed to cover some ground. I have a small amount of 
my initial "mini book" "Don't Let the Cat Get Your 
Wig"...which have not been at Amazon for some time due to 
shipping issues, I will order more soon. But I will let 
these go first come first serve at $10 for coverage of 
start up costs here. Which are what they are! We are 
considering doing a fundraising event sometime soon check 
the "Save Our Boobies"/"Boobies Rock" page for details as 
they become available. Who knows, could become an annual 
event. And goodness knows the diva hasn't been singing 
enough lately!!!  
 
Much love to you all, take good care and thank you for 
taking time to read so much information. I promise more 
pictures, movies, art and fun for the future. Til then, 
wishing you good health, and do sign the guestbook if you 
will and let us know you are here. (And what you NEED and 
WANT to see!)  
 
Lauren Brower 
Facing Forward LLC 
www.facingforwardllc.com 
all emails blindcopied for privacy

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