« Cross-Generational Cancer Chat | Main | Hobson and Holtz Talk Peas »

TrackBack

TrackBack URL for this entry:
http://www.typepad.com/services/trackback/6a00d8341c5ec453ef00e54fc5bbb48834

Listed below are links to weblogs that reference To Know: Social Realities of Loss and Suffering Following Mastectomy:

Comments

Mike Gunderloy

You could try emailing the lead author. This appears to be her contact info: http://ssis.arts.unsw.edu.au/staff/staff.php?first=Miroslava&last=Crouch

Susan Reynolds

Looks like a possibility for this one Mike. Good find. I wonder why it isn't standard practice to share research access when hiring a surgeon or oncologist.

I'd never thought of it but some of these people must have encountered the issue before. I think they want us to feel "cured" and therefore not needing anything else after they remove a primary tumor - at least that's the feeling I got from the surgeons.

Haven't seen the oncologist yet so there may be hope that s/he is more realistic about patients not feeling like one is cured just to have something removed. We will see.

whymommy

I wish I had info to help you on this, Susan, but I don't. I do have a lot of D.C. cancer info, though, so if I can help you navigate the local stuff, please feel free to email me. I've been in treatment for inflammatory breast cancer for 6 months now, doing the chemo thing, and getting a lot out of cancer yoga and a local women's group. There's also a wonderful Wellness Community for when you're feeling social and needing some support, relaxation, or exercise through chemo and whatever treatments you require. Each of us has a slightly different regimen, but we can all support each other.

Prayers and best wishes for a speedy mastectomy recovery. Thanks for blogging about the realities. It will help women who come after you ... I know, cause I'm one of them! I go to surgery next month, and I appreciate everything you have to say on this.

whymommy

I wish I had info to help you on this, Susan, but I don't. I do have a lot of D.C. cancer info, though, so if I can help you navigate the local stuff, please feel free to email me. I've been in treatment for inflammatory breast cancer for 6 months now, doing the chemo thing, and getting a lot out of cancer yoga and a local women's group. There's also a wonderful Wellness Community for when you're feeling social and needing some support, relaxation, or exercise through chemo and whatever treatments you require. Each of us has a slightly different regimen, but we can all support each other.

Prayers and best wishes for a speedy mastectomy recovery. Thanks for blogging about the realities. It will help women who come after you ... I know, cause I'm one of them! I go to surgery next month, and I appreciate everything you have to say on this.

The comments to this entry are closed.

About My Cancer

  • Invasive Lobular Carcinoma
    My form of breast cancer is less common than others. In fact only about 6 to 8% of cases of breast cancer are the invasive form that is based in the lobules, not in the milk ducts.

    Invasive, sometimes called Infiltrating, is a scary word. In most cases this form of breast cancer has been present for 8–10 years when detected by a mammogram or physical exam.

    In my case there was clearly an area that felt thickened or dense on December 6, 2007. A mammogram the next afternoon was not able to detect it but it clearly appeared on ultrasound and was confirmed by multiple biopsies the same day.

    During those 8 to 10 years the cancer took to become apparent to me, there has been plenty of opportunity for those invasive cells to get out of the breast and spread to the rest of the body.

    It is after all, by definition, an invasive form of cancer.

    Each year about 190 thousand women are diagnosed with invasive breast cancer in the US and about 40 thousand women will die of the disease. The larger the mass is when discovered the more risk. Mine had tentacled almost 5cm into the surrounding tissue and two other areas in the breast were discovered as well.

    My chances of living another 10 years without cancer in another area are about 40%. The likelihood of one of my other underlying health conditions doing the job before that is 20%. it took a few months to get used to that idea.

    Now though my attitude is that at least I know what I'm facing. It's just not what I expected. Life changes in an instant.

Funding Cancer Research


  • We Will Not Apeas Cancer

Iced Visitors


Blog powered by TypePad
Member since 08/2005

Twitter Updates

    follow me on Twitter
    My Photo

    -Contact-

    • Frozen Pea Fund Office Second Life:
      Frozen Pea Fund SL

      *Office hours Tues 5PM Eastern/ 2PM Pacific
      or just drop in & pick up a frozen pea t-shirt, pea beach-ball etc.
      *Drop a notecard to my SL avatar Tynan Clary anytime.
    • by mail
      Susan Reynolds
      1474 Northpoint Village Ctr #314
      Reston Virginia 20194

    Susan's Professional Blog

    Find me here

    43Things Delicious Facebook Facebook Flickr LinkedIn Ma.gnolia Other... Pownce Reddit Skype StumbleUpon Twitter Upcoming YouTube

    Psst...


    • Alltop, all the cool kids (and me)


    • my 'currently-reading' shelf:
       my currently-reading shelf

    • TwitterCounter for @susanreynolds

    Blog Catalog


    clickety

    • Clicky Web Analytics