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    <title>Breast Cancer Survivors</title>
    <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion</link>
    <description><![CDATA[All about breast cancer]]></description>
    <language>en-us</language>
    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/05/07/optional-surgery-or-not-axillary-node-dissection</guid>
      <title>optional surgery or not:  axillary node dissection</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/05/07/optional-surgery-or-not-axillary-node-dissection</link>
      <description><![CDATA[HI, &nbsp;I am waiting to hear if my surgeons/oncologists recommend I get an axillary node dissection to follow up my bilateral mastectomy &amp; sentinel node surgery. &nbsp;This would precede radiation to chest wall &amp; armpit region. &nbsp;I also have tissue expanders in ( just to complicate things a little more &nbsp;:) &nbsp;). I would love to hear from anyone who has gone through this surgery or down parts of this path before. &nbsp;I&#39;m also happy to share my experiences with breast cancer so far, also, if you want to talk about it. &nbsp;Thanks.]]></description>
      <pubDate>Mon, 07 May 2012 18:06:21 GMT</pubDate>
      <dc:creator>Felicity</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/05/01/aremedex</guid>
      <title>Aremedex</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/05/01/aremedex</link>
      <description><![CDATA[Was wondering if anyone else is on this cancer pill to help prevent the cancer from coming back
Am curious to hear what side effects you are experiencing if any
I am tired most of the time and very much pain in the joints and muscles
And unfortunately gaining weight even with trying not to through diet and exercise but was told all of the above are side effects
]]></description>
      <pubDate>Tue, 01 May 2012 17:09:38 GMT</pubDate>
      <dc:creator>Linnypoo</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/05/01/triple-negative-breast-cancer</guid>
      <title>Triple negative breast cancer</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/05/01/triple-negative-breast-cancer</link>
      <description><![CDATA[Hello all, I am one year post treatment for triple-negative breast cancer and have just been diagnosed with a local recurrence. I had 8 chemo treatments (AC-Taxol), bilateral mastectomy (no reconstruction) and 25 radiation treatments. I am now told that radiation is not an option, nor is surgery, so it looks like more chemo. Had a ct scan today, bone scan tomorrow and I&#39;m more than a little bit afraid of getting the results next week. Just wondering if there is anyone else out there in a similar situation? I have a fantastic support system and wonderful doctors, but none of them have had cancer!]]></description>
      <pubDate>Tue, 01 May 2012 12:59:13 GMT</pubDate>
      <dc:creator>not2yys</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/26/cancer-free</guid>
      <title>Cancer Free</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/26/cancer-free</link>
      <description><![CDATA[My surgeon met with me three days ago three weeks after my surgery to tell me that they got rid of the cancer.&nbsp; Yesterday, I&nbsp;saw my oncologist.&nbsp; He confirmed the great news that I am now cancer free.&nbsp; I am&nbsp;on Tamoxifen for the next five years.&nbsp; My radiation consultation is scheduled for&nbsp;May 15.&nbsp; I will have reconstruction surgery later in the year...probably around September.&nbsp; Currently, I am stuffing the left side of my bras with an uplift bra pad.&nbsp; I am planning on purchasing breast forms to make me look and feel whole again in the meantime.&nbsp;]]></description>
      <pubDate>Thu, 26 Apr 2012 16:56:11 GMT</pubDate>
      <dc:creator>Girl Lee</dc:creator>
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      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/21/good-news</guid>
      <title>Good News</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/21/good-news</link>
      <description><![CDATA[Yesterday&nbsp;I went for my axillary node dissection.&nbsp; As I was going into surgery my BS informed me that my cancer was HER2 Neg and that I may not require a lot of treatment; maybe only hormone therapy.&nbsp; Just have to wait to see if the rest of the nodes are clear.<br />
<br />
The surgery went well, however I was unable to keep anything down so I had to go to Emerg late last night to get some medication.&nbsp; Is everyone aware if you are in<b> Ontario </b>and have <b>homecare </b>you can <b>receiveve a medication card for persriptions (only pay $2 per fil</b>l)? The nurse in the Emerg informed me of this service,&nbsp;not my access centre.&nbsp; You just need to request a card through your case manager. This is a huge blessing for us, hope it helps someone else.]]></description>
      <pubDate>Sun, 22 Apr 2012 00:44:00 GMT</pubDate>
      <dc:creator>Jen</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/18/prosthesis-shopping</guid>
      <title>Prosthesis shopping</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/18/prosthesis-shopping</link>
      <description><![CDATA[I thought it may be of&nbsp;interest&nbsp; : <a href="http://www.mlam.ca/products/been-a-boob-spirit">http://www.mlam.ca/products/been-a-boob-spirit</a>. &nbsp;Highly recommended&nbsp;place to anyone looking for post-mastectomy lingerie and breast prosthesis.&nbsp; Located in&nbsp;Hamilton ON.&nbsp;&nbsp;<br />
<br />
Another place to get&nbsp;unusual prosthesis:&nbsp;http://www.titbits.ca/v1/tb_faq.html<br />
<br />
Suzanne]]></description>
      <pubDate>Wed, 18 Apr 2012 19:48:15 GMT</pubDate>
      <dc:creator>SueCis</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/16/can-someone-ease-my-nerves</guid>
      <title>Can someone ease my nerves?</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/16/can-someone-ease-my-nerves</link>
      <description><![CDATA[I have to have the PCC catheter put in my arm to salvage my vein as my chemo is going to be aggressive. I am, for lack of better words, freaked out about having this in my arm for months and the care it requires. Can anyone ease my nerves about this? Share your experience with it?<br />
<br />
Tanner]]></description>
      <pubDate>Mon, 16 Apr 2012 22:59:40 GMT</pubDate>
      <dc:creator>Tanner</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/15/wig-shopping</guid>
      <title>wig shopping</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/15/wig-shopping</link>
      <description><![CDATA[Because I may start treatment this week and the Dr. anticipates my hair will start falling out about 9 days after my first treatment, two of my best girlfriends and I went to try to find me a wig. I made an appointment at a place I was referred to and it was the best experience I could ask for. Out of a basement of a house, two ladies make you feel amazing. It was neat, clean, professional but so much fun. We were there for two hours and I walked out with a wig I am so happy with. I must have tried on at least 35 and I left with a blonde bob style. The funny part is my natural hair is brown and medium length and VERY curly. The one thing I thought was, I have a fight on my hands and I need to take away anything good or what could be fun from this and looking for and deciding on a wig, proved to be one of those times. Never been a blonde before, this should be interesting!! lol Have a good day all!<br />
<br />
Tanner]]></description>
      <pubDate>Sun, 15 Apr 2012 13:06:32 GMT</pubDate>
      <dc:creator>Tanner</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/13/hamilton---ywca-encore-program</guid>
      <title>Hamilton - YWCA Encore Program</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/13/hamilton---ywca-encore-program</link>
      <description><![CDATA[For anyone in the Hamilton area -- post surgery -- there is a YWCA Encore program -- starting on Thursday April 19 to June 7 -- at the Ottawa Streeet North Y.<br />
This program is free to post surgery breast cancer clients.&nbsp;<br />
It offers gentle floor exercises, followed by a time of group discussion, special guest speakers an pool time (gentle and fun oriented exercise time)&nbsp; Wear comfortable clothes and bring your bathing suit.&nbsp; There was an orientation yesterday (April 12).&nbsp;<br />
If interested, call 905-545-6249, ext. 118<br />
<br />
I have registered and do not know anything more about it but I am looking forward to it --- maybe we can get some more out to it ----&nbsp;it sounds like a great opportunity to have fun together as a group as well as gain some valuable information.]]></description>
      <pubDate>Sat, 14 Apr 2012 02:57:18 GMT</pubDate>
      <dc:creator>Joanne_53</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/13/the-verdict-is-in</guid>
      <title>the verdict is in</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/13/the-verdict-is-in</link>
      <description><![CDATA[Well, I want to first say that my experience with the Dr.s and nurses at my cancer centre were pheonominal. I was treated with such warmth and integrity, it was amazing. My first visit after bloodwork was with the Radiation oncologist (he was so young, I was in shock.lol) One hour was spent with him because he went over everything with me, my results again and disected them a bit more for me so I could understand. He determined I will need 30 treatments in total. 25 for my whole breast, 5 more on targeted tumour area.<br />
My nerves were the worst meeting with the chemo medical oncologist and my worst fears were confirmed. I have to have quickly (like next week) very aggressive chemo. I get a dose every 2 weeks ( the usual is every 3) with what he tells me is the best meds that are out there. So, 8 treatments every two weeks. I have to have the pcc catheter put in to take the chemo, sounds so gross I can&#39;t even think about it. Anyway, I haven&#39;t thrown any medication names out there because quite honestly I have a few days worth of readings here on all the different kinds and what they are doing that I need to wrap my head around it before I can speak of them all. So needless to say this wasn&#39;t great news, even after all of this treatment, my percentage odds of getting cancer elsewhere is still to high for my liking but I do feel like I&#39;m in good hands and I&#39;m going to fight this with everything that I have. I am only 37 ( as of April 11th) and I have a 17 year old daughter getting ready for prom, graduation, college. She just left today for a trip to Chicago for a few days. She has health problems too that she is fighting. Actually she has surgery next week. Ugh, but she is a tough cookie as well so I have high hopes that she will be fine. So, that is that for now. I will let you know how my appt next week goes. Fight, fight, fight...]]></description>
      <pubDate>Fri, 13 Apr 2012 10:54:41 GMT</pubDate>
      <dc:creator>Tanner</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/11/call-for-the-dr</guid>
      <title>Call for the dr</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/11/call-for-the-dr</link>
      <description><![CDATA[JuST an update to let you know that I got my call today to see two different doctors on April 24. The first dr. is for chemo and the other for radiation. I really pray that I dont need any chemo and just radiation. Its just for consultation so I hope if treatments are needed, I can start right away and not have to travel back and forth to my home. I must admit when I heard the dr. was for chemo I got a bit scared and nervous. So I am praying for the best. Have a great day everyone.]]></description>
      <pubDate>Wed, 11 Apr 2012 18:26:36 GMT</pubDate>
      <dc:creator>jobkat</dc:creator>
    </item>
    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/09/angry</guid>
      <title>angry?</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/09/angry</link>
      <description><![CDATA[Hi there,<br />
<br />
I was diagnosed with triple negative invasive ductal carcinoma in Feb 2011. This type of BC&nbsp;accounts for less than 15% of breast cancer diagnoses. The drivers are unknown, so there is the usual treatment is to simply hit it with the full hammer (surgery, chemo and radiation) and cross your fingers. I finished treatment Nov 29, 2011. I had several complications, allergic reactions and still suffer from some issues. I have been quiet for 13 months about how I feel about a number of things and I am hoping I am safe expressing how I feel here.<br />
<br />
I can&#39;t help but notice the overwhelming dominance of happy, positive and pink-ribbon laden rhetoric in cancerland.&nbsp;&nbsp;Does anyone also feel&nbsp;angry about the lack of focus on prevention&nbsp;when it comes to cancer? Am I the only one who wonders why there is so much emphasis on &quot;cure&quot; and precious little on &quot;cause&quot;?<br />
<br />
I often feel angry about the fact&nbsp;that there are known human carcinigens in the thousands of products that we&nbsp;use and that many of the companies selling these products&nbsp;do so in the name of breast cancer research/fundraising. Am I the&nbsp;only one who feels&nbsp;frsutrated by this?&nbsp;Am I the only one who worries about her child in light of this?&nbsp;&nbsp;<br />
<br />
Despite living in Canada, having provincial health insurance (OHIP in my case), having a&nbsp;&nbsp;job with benefits, having breast cancer still cost my approximately $20,000. This number is made up of lost income, special treatments, travel, parking, food cost increases due to several food intolerances brought on by chemo, lymphatic therapy and so on.&nbsp;I am in serious debt now. Many are in a much worse financial position than I am.<br />
Am I the only one who is frustrated by the injustice of this?<br />
<br />
For me, cancer treatment wasn&#39;t a &quot;gift&quot;, an experience that &quot;made me a better person&quot; and it certainly wasn&#39;t&nbsp;a rite of passage accompanied by loads of pin acoutrements. I do not deny that I have had incredible moments of calrity and&nbsp;earth shaking&nbsp;perception shifts, but it has simultaneously been horrific, painful and&nbsp;awful.<br />
<br />
My brain no longer works properly since chemo. It has been 6 months since my last treatment. It is frustrating. I am struggling to see the &quot;positive&quot; side of this side effect of treatment.<br />
<br />
Am I the only one that feels this way?<br />
<br />
d]]></description>
      <pubDate>Tue, 10 Apr 2012 01:56:33 GMT</pubDate>
      <dc:creator>dani</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/09/looking-for-advise-have-fibrmyalgia-and-considerin</guid>
      <title>Looking for advise! Have fibromyalgia and considering breast reconstruction</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/09/looking-for-advise-have-fibrmyalgia-and-considerin</link>
      <description><![CDATA[Hi I am new to this site hope I am putting this info in correct place. In 2010 i was diagnosed with her2 positive breast cancer and had a mastectomy on my right breast, followed by chemo and herceptin for six months ( was suppose to be a year but due to my heart functions decreasing herceptin was stopped at 6 months) I am now considering reconstruction with implants and I am very confused and stressed, I have an appointment to have the expander put in in May and don&#39;t know what to do, I have to have a 650cc expander inserted which seems kinda large to me, also I need a reduction on the other side to match. I suffer from fibromyalgia and I am worried it will just make issues worse, wondering if anyone had a similar situation that could help me make a decision if this is the right thing to do, or if I should accept the way I am and get on with life.Hi I am new to this site hope I am putting this info in correct place. In 2010 i was diagnosed with her2 positive breast cancer and had a mastectomy on my right breast, followed by chemo and herceptin for six months ( was suppose to be a year but due to my heart functions decreasing herceptin was stopped at 6 months) I am now considering reconstruction with implants and I am very confused and stressed, I have an appointment to have the expander put in in May and don&#39;t know what to do, I have to have a 650cc expander inserted which seems kinda large to me, also I need a reduction on the other side to match. I suffer from fibromyalgia and I am&nbsp;]]></description>
      <pubDate>Mon, 09 Apr 2012 17:30:27 GMT</pubDate>
      <dc:creator>hunnyb</dc:creator>
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    <item>
      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/09/looking-to-connect-with-others</guid>
      <title>Looking to connect with others</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/09/looking-to-connect-with-others</link>
      <description><![CDATA[Hi everybody, glad to have this opportunity to be with others like myself. I&#39;m a very energetic 64 year old (still teaching) diagnosed with BC in January. Had a lumpectomy in February, started on Letrozole 2 weeks ago, going to PMH next week re my radiation therapy. Hope to connect with ladies in a similar situation.]]></description>
      <pubDate>Mon, 09 Apr 2012 14:37:01 GMT</pubDate>
      <dc:creator>Scottie</dc:creator>
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      <guid isPermaLink="true">http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/03/surgery-overwaiting-for-next-steps</guid>
      <title>Surgery over...waiting for next steps</title>
      <link>http://cancerconnection.ca/groups/breast_cancer_survivors/discussion/2012/04/03/surgery-overwaiting-for-next-steps</link>
      <description><![CDATA[Hi everyone,<br />
<br />
I had my partial mastectomy on March 20, it was alot more painful than I had anticipated but it is starting to feel better now. I find that I still need to put some ice on the area because it is still swollen. I got my pathology report last week&nbsp;and I am happy to say that the margins were clear and both lymph nodes were negative.<br />
I was referred to the Cancer Clinic and I am now just waiting to get my appointments for the next leg of my journey. My surgeon seems to think that I will definitely need radiation but will let the medical oncologist decide whether I need chemo or not. All this waiting is really hard!]]></description>
      <pubDate>Tue, 03 Apr 2012 12:51:22 GMT</pubDate>
      <dc:creator>Rachel</dc:creator>
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