Starting chemo Sept 05
Comments
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Good to hear everyone still doing fine. Sandra, glad to hear your MRI was fine. How is the ringing in your ears now? Enjoy the visit with Sandra.
Maxine - check in soon. Worried about you.
I had such weird experience this morning. I was speaking to a mother at my son's school who does not know about my bc. Her father just had a biopsy to test for prostrate cancer, which was B9. She said that she was relieved, because "once you get cancer, that is it, it or the associated problems will kill you." I was dumb struck and did not say anything, but it has been bugging me. Not nice to hear other people sort of pronouncing a death sentence on you....
On a nicer note - I saw Celine Dion in concert this weekend!! She was amazing!! I was in tears half the time. Apart from the fact that I love her music, I just think she is a wonderfully rounded person and a good role model. I also admire her for how she put her career on hold after her husband's dx and her son's birth. She seems so normal in a world of people like Britney Spears!
Keep well everybody!!
Liezel
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Hello everyone! Sorry for being MIA for so long. I've read back a few pages trying to catch up. I'm glad to see good news from recent test results for everyone!
Sandra / Susan: Enjoy your time in London. I'd love to see some pictures after your return!
Peg - I read about your recent mammo. I can sympathize with your fears. I have not had one since my diagnosis that was ‘all clear'. Last year I had a b9 lump removed, and my mammo a few months ago showed calcifications near the scar tissue. My breast surgeon reviewed the films along with the radiologist, and both felt it was from trauma and/or radiation and put me on the 6 month wait and see. My breast surgeon was adamant last time for a surgical biopsy, so his agreement that "it is probably nothing" this time made me feel much better. I go back in April. I'm hoping that just once I can leave there NOT in tears!
I am doing well and staying very busy. I still work a full time job, take care of 2 kids and my aging parents while still trying to stay involved with other committees and activities. I guess it's my own way of thumbing my nose at this whole cancer thing. I find that I tire much easier, but I try to keep moving forward. In my last post I did mention that I do have some really rough times mentally and emotionally. I called it my "2 year fear " - can anyone else relate?
To everyone else - here's to year 3 of continued health and happiness!
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hopeful,
so good to see your screen name again. We have missed you. Okay, can't speak for the group.... _I_ have missed you. Will post pictures of Sandra and I from London. Can't wait to meet her!
*susan*
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Hi hopeful - we can all relate - pop in and share your fears whenever you can - it helps to 'talk'.
Hey Tina - it's all happening - enjoy being port-free.
I will be packing my overnighter this day next week - London here I come - getting a little nervous now too.
Speak soon.
Sandra from the UK
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Hey Tina! Port free! ... and a farm! Congratulations!
Liezel, there's a lot of misinformation and superstition out there about cancer. Unfortunately we've all become experts.
Great to hear from you Hopeful! 3 years and counting!
Susan have a wonderful trip! Can't wait to see those pictures! -
Sandra,
Three days until I am on your time zone. I am not nervous, I am thrilled to be making a trip. I spend way too much time travelling, but it makes me happy. And I didn't survive cancer to NOT have fun. Can't wait to see your face in person.....
Be well,
*susan*
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Just packing my overnight bag ready for trip to London to meet Susan - watch this space ;-)
Sandra from the UK
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I'm anxiously awaiting to hear how the meeting between Sandra and Susan went today.
I had my own bc.org adventure today meeting up with 14 posters and chatters at a restaurant in NYC. We had a great time. I wish you all could have been there.
(Don't forget, if any of you are ever passing through NY, please let me know!)
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Susan and I get on really well and I am really glad I made the trip to London. I got to meet Lesley (hubby) and their lovely daughter Lauren. When I sort out reducing the piccie size, I will post.
Peg, who joined you in NYC restaurant?
Speak soon.
Sandra from the UK
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I'm glad Susan and Sandra had a good time.
I'm looking forward to seeing the pictures.
The photos of my event have been posted on the Get Together Forum. -
Hi everyone
I have been off work all this year, my hands are slowly getting worse, but at last, I heard today, I will go to Southampton on 31st for more testing. I will probably be admitted for 3 days or so.
Thank you all for thinking of me. I will let you know how I get on.
Maxine
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Sandra is one helluva woman! What a wonderful time we had.... I suspect we could have spent days together and still had things to talk about. Just home now, and will start downloading photos from my camera soon.
Sandra, thank you for taking the time and expense to come down to meet with me. Listen to this... sandra made a chocolate bar with our pictures on the wrapper. How cool is that?
Love to all....
*susan*
p.s. the intellectual one????
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Hi everyone, It's been a while since I have posted. I been reading on the posts. Great to know that you ladies are still really active with the group. I have started a bc support group here in brownsville texas and I have a group of about 15 or so lovely ladies. I have been well, so far so good. Struggling with weight issues (too much pizza and tacos) and osteopenic bones but other than that I am well and so is my family. Robert and I will be traveling to Las Vegas next week. Everysince bc we promised that we would take a nice trip once a year together and another with the kids. Last year New York and Florida with the kids. This year Las Vegas and Hersey Penn with the kids (anybody been to Hersey - I hear its fun). Glad to know that all of you are well. God Bless Marg
PS nice to see on the boards hopeful - i believe we use to email eachother back in the chemo days.
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Sandra and Susan have afternoon tea in London
Well, for some reason I can't get the photos to show. Very annoying.
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Hello ladies. I am really going to make an effort to ‘stay in touch'.
It sounds like Sandra and Susan had a wonderful time. What a great experience for the both of you. I think all of us were there with you in spirit! I saw some of the postings about the NYC get together that Peg attended. It looks like it was a huge success. I have never met anyone from these boards in person. I'm a little jealous of those that have had the opportunity to do so. Peg - we are in the process of planning a ‘girls' trip to New York for a friend's 40th birthday. It will be somewhere in the August timeframe. If it works out, I would love to meet you!
Marg - it's good to see you! Sometimes the chemo days seem like a lifetime ago. I guess that's a good sign of moving on. I was in Vegas a few weeks ago. We had a GREAT time. Enjoy your trip.
Now the latest on the gift that keeps on giving: At a routine check up last week my GYN found a ‘lump' in the neck area. Could be a number of things, but he is leaning towards thyroid problems. I do have a family history (mom and 2 sisters with thyroid problems), so I'm going with that. When he mentioned the possibility of an enlarged lymph node I must admit that I was/am very scared. Started the testing this week with a neck ultrasound and lots of blood work. No results yet. My GP is a good friend of mine from college. I am confident that he will take very good care of me!
On the positive side - I leave for Florida 2 weeks from today! Spring break for my kids and a well deserved break for me.
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Hey, Susan thanks for the kind comments - I will be posting some piccies soon - after this week my work will be somewhat less and I will have time to play. Susan did the piccies get through to you from me?
Hi hopeful - funny Susan and I were talking thyroid when we met in London and how often it crops up amongst us - yep, the 'lump' will be something you can deal with - chin up.
Speak soon.
Sandra from the UK
I would love to meet Peg in NY too - who knows what the future holds.
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Maxine, you must be feeling pretty low? - here's hoping Southampton brings you relief.
Keep us posted.
Sandra from the UK
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Results are in and I do have a thyroid condition. Funny how I am celebrating a goiter! I started the medication this week and I am very releived to find out what it is.
Maxine - Will be thinking of you on the 31st.
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Hello all you wonderful ladies!
Things are going well here and I finally got my DRIVING privleges reinstated! OMG its been since early August since I have driven (other then to the corner quickie mart - one mile from home).
I go in on the 4th for my 1/2 yearly CT scan. I am really not worried about it to much. It is just something I have to do!
I have been following a 1300-1500 calorie daily intake (not a diet!) menu. So far I have lost 2 pounds this week and things are going well. I am going to start up in the next month at the gym with a good friend of mine (she already goes and has lost 40 or so pounds). I am bound and determined to be my own "biggest loser". I have between 100-130 pounds to lose! If anyone would like a copy of my menu please let me know. I am not really giving up any food group, just watching portions and eat 5-6 times a day instead of 2-3.
I will try to write more later....
Luv to all my sisters..... Good Friday and Happy Easter to those who celebrate it.
Tina
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I having trouble posting a couple of piccies from when Susan and I met up in London - I know I shouldn't say "something is impossible when it is only difficult" but I am giving up for now!
Speak soon.
Sandra from the UK xxxxx
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a gentle bump..... today is a hard one... my dead brother's birthday and we discovered that my father's heart defect has gotten worse. He will need full open heart surgery. This getting old is only for the most strong.
I wish I could share the photos with Sandra. If anyone wants my two photos, email me at smcmtucker at prettycoolsolutions dot com. I will send them directly.
Be well my dear friends...
*susan*
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I did it!!!! Here are two pictures from London from my wonderful visit with Sandra.
*susan*
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Here is a picture of us in front of Sandra's house. [Oh of course not. This is the Somerset House, a property right on the Thames that houses part of Kings College.]
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Hello hello my lovely sisters!
Firstly let me say how much I loved catching up on the previous posts and how gorgeous the photos are of Sandra and Susan's catch up! I would love to come to NY as I have an aussie friend living there now and have made a few bc friends as well. Definately on my to do list!
I think a few of you may have updated your pics for your profile? And how lovely they are! Glad to see us looking so good
Things have been okay here with us. Last week I had my 5th (!!!) boob operation as after the last one some internal stitches popped giving a very awkward shape so that had to be fixed as well as some nasty scars that needed revising. Just a minor op in the scheme of things and all went well.
My onc has referred me onto a gyn-onc for discussions about what to do now I have finished zoladex. I suppose I am officially finished treatment?? My 2yrs of herceptin was up at Christmas and my last zoladex was a week ago. However the gyn-onc and my onc both feel I should have at least an ooph if not full hyst. I was very upset at that as I am still mourning my oldself and was really looking forward to her returning once zoladex was done. I feel so cranky, moody, tired, etc with the menopause symptoms however this new onc said "rather than fighting the beast you need to learn to stroke it" so he is aiming to do a more multidisciplinary approach to managing my symptoms rather than me constantly fighting to rid of them completely. I am going to bite the bullet and go ahead and book either the ooph or hyst next Monday so I will let you know when THAT surgery date is over. I am hoping then to be rid of the port as well! My final legacy!
Toben as you may remember was having some serious issues since my illness with anxiety/ADD symptoms and Post traumatic stress. He has finally been seeing someone very experienced with this sort of thing on a weekly basis which seems to be helping. He has his ups and downs but we are learning to manage them slightly better at least. Liezel I remember your son was having some similar issues, how is he?
Scott has taken up his new posting with the army which is 15hrs away. He works for 10weeks away from home then is back for a week. Not the most idea situation however it is much needed for both of our sanities I feel. Long story really but much of the same ups and downs.
Tina I would love to have a copy of your restricted calorie food plan (notice me not using the word "diet"!) please. Do you have my email address? it is my user name at hotmail dot com. I have put on alot of weight (again with zoladex and menopause) and am an eating machine! I need to plan better however as I have never needed to watch what I eat don't know where to start. Once my operations are out of the way I hope to get into the gym
I have to dash as I am expecting a client any minute (I am just doing beauty stuff from home for some pocket money at the moment)!
love to you all and please know that even if I don't post I often lurk and think of you always
xooxoxoxo -
Tina- i tell a lie, my email address is actually leannemyles at hotmail dot com !! Chemo brain??? Still??!!
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Leanne! It's so good to hear from you. I was thinking about you when I was trying to catch up on the boards. I'm sorry to hear about your latest potential surgeries, but congrats on finishing treatment! I know it's been a long hard road for you. You were (and are) a true inspiration to me. May you find huge success with "stroking the beast". And yes - I still use the "chemo brain" excuse all of the time!
Susan, I wish I had words that could comfort you regarding your brother. It must be a very tough time for you and your family. My thoughts and prayers are with you. I can relate to the issues with aging and ailing parents. It makes me feel like a helpless little girl at times. Keep us posted.
Leizel - I had a similar experience as you did earlier this week. Was among a group of friends and we were talking about a friend who is battling cancer for the second time and the prognosis is not good. Someone made the brilliant statement that it was ‘only a matter of time' before it came back. The whole recurrence fear is bad enough - I don't need someone telling me that it is only a matter of time. It really bugged me too.
Sending positive thoughts for Maxine on the 31st and Tina on the 4th .... I'll be away on Spring Break, but will definitely check in on my return.
Marg - how was Vegas?
I seem to only have time to check in during work hours, and I can't view the pictures from here! I really want to see the pics from the London trip. I'll send a PM to Susan with my email address.
Take care all!
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Hi Everybody!
Leanne, so good to hear from you again! At last finished - I can imagine that rather than stroking this beast, you want to kick his behind! Good luck with your decision on the ooph or hyst. I would not be able to make that decision..... Connor still having the same problems, but we are also slowly learning to live with it. I spoke to a counsellor the other day, and she said that kids their age make up their own reality if we do not explain everything to them. When they saw us sick, stressed and worrying, and maybe could not understand our explanations, they made up their own story, and this is scaring them. They are protecting themselves in a way from potential hurt. All we can do is talk to them, spend alone time and refer to our sickness and how much we missed them in that time. It is working slowly, but I find I do not have as much patience as before, so 1 day at a time.
Susan, I can really relate to your feelings at this time around your brother. The 18th was my sister's bday, and it is 10 yrs now that she has been dead. Time has not healed the wounds, but I have learned to live with it. It is just so difficult at this time of year.....
My cousin's son's wife has left him all alone with 1yr old twin girls. He can not cope and has left them with my cousin and his wife. They are battling financially, and now the girls might be taken away. My mom has asked if I would be willing to take them in. I would really love to have more kids, but do not know how DH would react. They are on the furthest side of the country from me, and it won't be that easy for them to keep seeing their parents. My first reaction is to take them, but there is so many logistical and financial things to consider. Think of me while I battle with this...
Maxine, good luck for Monday, and Tina for the 4th. My follow up also in April, after I was hoping to ignore it, they phoned to remind me. Going to ignore it for a few weeks more I think.....
Keep well all.....
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