Starting Chemo in JAN 2007

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  • Rebecca
    Rebecca Member Posts: 971
    edited June 2007
    Mel-I am still laughing about your baby elephant. That is so absolutely adorable! The best thing that was done for me was done by an absolute stranger when I was in the hospital. I was lying in bed feeling VERY sorry for myself with DH at my side. All of a sudden 4 people in traditional Asian Indian garb glided into the room. One of them handed me a single very beautiful flower, then they each filed past and smiled at me. It was in total silence, and done so quickly that I did not have time to feel uncomfortable. It was so wonderful and made me feel so happy in a time that I truly thought I would never be happy again. Any other stories out there?

    Terry-great to hear that Tae is doing well. There are many horror stories about Arimidex, but remember that horror stories make better reading than smooth sailing…..I am told that the reality of the drug is not the same as what you find on the message boards.

    Nancy that sounds like a great party! If there was ever a time that it would be ok to have your port show, that was it I think.

    I went to a party as well…and I think I had my first cancer-free experience! It was almost surreal. Off to Sunday activities…..check back later!
  • meliaanne
    meliaanne Member Posts: 682
    edited June 2007
    Hi All,
    Skye, love your new photo! And Mel, that baby elephant idea is the best; I would love that too. Your husband sounds like a typical male to me; mine was awful early on til I broke down one night, told him he was being a sh*t, and he hadn't seen it. He jumped in then and has been fine since. But I had the kids here during recovery from surgery, so I think he was off the hook early, and that once I was back at work he figured I was fine. I am actually doing less as time goes on b/c of the cumulative effect of the chemo, and the absolute lack of energy.

    Viddie, the taxol is def taking its toll on me emotionally and physically. I really have to fight feelings of depression and sadness, and I think it is the worst on Sundays. I get very sad as the next treatment gets closer. And this week my ankles swelled, I had lots of pain, and I really hit the wall. I take aleve, which I think Skye took. and it helps with the pain, but I do have vicodin if I need it. I am just overall tired of it all; no hair, no energy, etc. And the lack of eyelashes affects what gets in my eyes, which makes me cranky, the lack of pubic hair actually makes bike riding less comfy ... the lack of energy is so unlike me. It all added up Friday night into a major meltdown.

    We are going to look for a new bike for my husband today, out to lunch, stop by a farmer's market. I think it will be very good for me to get out today. I didn't do much yesterday at all, and the less I do, the sadder I get.

    Good to hear Tae is doing better. Jan, watch that strep. Love your dog! Viddie, enjoy your daughter.

    Melia
  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2007
    Skye – What a great picture. Thanks for posting it. I like the new wig.

    Viddie – While I am not a tazolian I did have a major crash day after every chemo that I contributed to the Decadron (hate that stuff). Always the same day each time that I would feel very sad, depressed, upset all day.

    Mel – your own baby elephant. That’s just about the coolest thing I have ever heard of.

    T4t – good to hear from you!

    DH and I went out to eat lat night. A lady walked by our table and gave me “the look.” Then before I new it she was over at our table, holding my hand, and telling me how she’s been were I am, etc. It was really very sweet, but took me so off guard I could hardly think of a thing to say to her. It’s the first time I’ve had that happen to me outside of a cancer event where I expect it more.

    Rebecca & Mel – in the nice things people have done category. My biggest one is probably that I went to a local support group just a few days before my mastectomy. I was in a pretty bad place emotionally and still feeling rotten from my first surgery. Anyway – although the group does just social get together’s vs. the traditional support group – they totally took me under their wings. After the social part of the evening was over all of these women stayed and told me about their surgeries, answered all of my questions, etc. Then when I was in the hospital one of them came to visit me and gave me a gorgeous supper soft robe that I really enjoyed snuggling up in as I was recovering from surgery. I still wear it all the time and feel so protected in it. This is the same group of gals who later threw a party for me in the chemo room on my birthday.
  • skyedivine
    skyedivine Member Posts: 839
    edited June 2007
    Quote:

    Hi all,
    Fellow Herceptinans,
    Any of you on tamoxofen or arimidex yet?

    Viddie, my onc says he will not start the tamo or arimidex, whichever he decides on, until after radiation. So it will be given along with the rest of the year's worth of Herceptin. As for the Taxol, I had so many weird reactions with it that I would not be surprised if it's to blame for your "see-saw." But those mental and emotional things were the first to clear for me, Viddie. Two weeks out I felt like I had my head back...mostly! :-) Do hang in there, dear.

    Caya the Herceptin makes me extra tired and sluggish for a week after I get it. I also have slight nausea from time to time but nothing like chemo. So I just try to plan plenty of naps, not much else to do about it and we really need the Herceptin. I see lots worse se's on the HER2 site than I have. I'm just hoping it isn't cumulative like the Taxol. -- skye
  • skyedivine
    skyedivine Member Posts: 839
    edited June 2007
    Mel you are the ONLY person I know with a baby elephant. It IS way cool. Congratulations!
    As for my baby woodchuck, I heard it squealing for a while last evening and am hoping something didn't get it. You're right Caya, it is much cuter than the returning luxuriant pubic hair will be. LOL! And yes, Rebecca, the author really wrote that! Did she think it would bring us comfort to imagine silken tresses flowing down around our knees?
    Caya the idea of manicure and pedicure sounds wonderful. I'm still holding my breath that my right thumbnail stays on right now so I'm afraid to have much done to them...I haven't put any polish on since the wedding as I'm paranoid about not being able to examine them every two hours. Maybe before our trip in August I'll have that done.
    Thanks to all the confirmations on my new wig. It's MUCH cooler to wear and I somehow feel more chic in it. We all need our illusions to get by. :-)
    Hope everyone is finding blessings in the day! - Skye
  • skyedivine
    skyedivine Member Posts: 839
    edited June 2007
    Puffball is still there; I found him lying under my hostas for shade when I went out to water the flowers. He doesn't look good. I put a little dish of water by him. Last night I left out a dish of milk which was gone this morning. Not much else I can do I guess, poor thing. - Skye
    image
  • IowaCindy
    IowaCindy Member Posts: 341
    edited June 2007
    Relay was an interesting experience for me. Last night was the first time I felt 'anger' at what had happened to me. The Survivor's Lap was nice but I didn't get emotional at all. It was just fun to walk with such a large group and see my friends, coworkers and family cheering on the side.

    It was during the luminary quiet lap that the anger started to come out. To realize that I was one of those lights really made me angry. Wow, it was a surprise to me to have the happen.

    The anger didn't last long. I've refused all along to give in to bitterness or anger. I'm not starting now that I'm three weeks from completing treatment. I'm not trying to brush aside what's happened. I'm just making a choice on how I want my life to reflect what's happened. I don't like angry people. I won't be one! (I do admit the occasional situations that frost my cookies though!)

    Relay started at 5 pm. I was there about 3:30 to set up our camp site. I stayed until about 10:15 but had to go home to check my dogs. I played with them, took a 3 hours nap and then was back at Relay by 3:45 AM to walk during the last two hours. It's a 25 mile trip from my house to where this Relay was held. I put one hundred miles on my car.

    I slept about 4 hours after I got home but my dogs won't let me sleep anymore. SO I'm unloading the cooler and stuff from Relay.

    Hope everyone has a good Sunday.

    Cindy
  • mer1957
    mer1957 Member Posts: 534
    edited June 2007

    Just lost my post...Rebecca, who were those Asian Indian people with the flower? How cool!

  • Rebecca
    Rebecca Member Posts: 971
    edited June 2007
    Quote:

    Just lost my post...Rebecca, who were those Asian Indian people with the flower? How cool!




    Mary-I have no clue who they were, that was the beauty of it. they went to every room on the oncology ward (and perhaps elsewhere) and gave everyone who was there a flower and a glorious smile. The ladies were in bright silk saris, and they walked in a row through the room and each made eye contact with me and then left. I actually still have my flower...I hung it upside down to dry when i got home, and it is still hanging by a string from the window by my bedside. It was so wonderful that I wanted to do it myself with my girl scout troop--but they voted it down. Ah well.

    cindy, the relay sounds like it affected you on a very profound level. I do think that we all have a right to be a bit angry...it is when you let that anger dominate your life that it is a problem. Feeling angry once in a while is as healthy as feeling sad about it. Experience your feelings or they will haunt you!
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited June 2007
    Hi,

    I feel so out of touch here; there are so many posts I'm about 300 behind, and that's no exaggeration. My browser is set to show 80 posts per page; my browser is now at page 53 on this thread and I still haven't read Page 50.

    However, I just wanted to pop in and say that I spent two weeks on tamo and was slowly transitioning from Prozac to Effexor at the same time. I had terrible stomach problems. Lots of gas, diarrhea, but constipation too, so I felt kind of like a large powder keg that couldn't explode. I felt awful. Mena had told me that she'd had a lot of stomach problems on tamoxifen so I decided to switch. I still had a prescription for Femara in my purse that the onc had written me before the bone scan was done.

    After two weeks I switched to Femara (& no Effexor!!!). I do feel a lot better. My stomach is still pretty bad though, and I look pregnant and seem to be in discomfort most of the time. I don't know why I am still having problems, but I think once you have a really bad stomach episode, it damages the lining of your intestines and it takes a while for things to get back to normal.

    I am wondering if anyone else is having gastric problems on their hormonal medications?

    OK..I'll post more once I've *really* caught up.

    Mizsissy
  • meliaanne
    meliaanne Member Posts: 682
    edited June 2007
    Mizsissy, sorry about your stomach problems. I wish I could help, but triple neg here ...

    Skye, what type of treatment did your husband have to have for his prostate cancer? Was it found routinely? I can't get my husband to have his checked, cannot get him to a dr for anything. The kids are very upset about this; they told him they think he is being selfish, and I agree. We know he has high blood pressure for example. And you would think that watching my cancer discovered during an annual check would motivate him.

    Cindy, what an amazing, if exhausting, experience the relay must have been. And I agree with Rebecca, it's fine to feel the anger. There are so many emotions involved in this journey, and I guess we need to just work thru all of them.

    Mary and Mel, how are you feeling?

    Had a nice Sunday, got my husband a new bike, went to lunch, farmer's market, took a very short walk. I am so tired now. I am really going to have to work to get back in shape when chemo ends. I laid down to read after my walk and didn't so much fall asleep as pass out ... this fatigue is daunting. Viddie, four more treatments and we will be done! I am envious of those of you with hair; I do have fuzz and feel like it is making a valiant effort to grow, but the taxol must be slowing it down ... very tired of the wig, which I think is looking kind of ratty these days. I may need to get a new one, as I have worn this since Feb and figure I will need it at work til about November ...

    Melia
  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2007
    What do you all think about this wig:
    http://www.paulayoung.com/catalog/produc...p;size=Average#

    I would get it in brown.

    I'm really thinking about ordering it, but I can't decide. If I hate my $400 wig will I hate this one too? I'm just so sick of wearing scarves I thought I might be nice to go out in disguise once and awhile.
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited June 2007
    Jan, that wig is cute. I just ordered a very short lightweight one from Paul Young called "Ultimo" ...hasn't arrived yet.

    http://www.paulayoung.com/catalog/produc...1016&adsrc=

    I think a short fluffier style would look good on you. Also, maybe two-toned color. I bought a 350 dollar wig that I don't like; I've gotten lots of uncompliments on it.

    Mizsissy
  • viddie
    viddie Member Posts: 547
    edited June 2007
    Hi everyone,

    Once again, thanks for your sharing your experiences and for being there. I am feeling better today. I just have to resign myself to the fact that weekends for the next four weeks will be solely for r & r, and that’s okay.
    I finally have my appointment with the new breast surgeon about the Diep surgery on Wednesday. If all goes well and she agrees to do a prophylactic bilateral mastectomy, I will hopefully have my surgery on August 6.
    Caya,
    How are your choc. Chip cookies? I could enjoy one or two just about now. Having a manicure and pedicure: what a treat!!
    Mel,
    How are you feeling? I love the baby elephant gift. What a nifty idea.
    The countdown for your Diep surgery is around the corner. You are the first of many of us to have this procedure. You will be our very own pioneer.
    Terry,
    It is good to hear from you. I am glad to hear that Tae is doing so well. Sounds like you had a busy yet fun week.
    Nancy,
    That is amazing that there were so many people at the same party with cancer, and four with scarves. Did you all talk to each other? I hope you had a good time.
    Rebecca,
    That sounds like a surreal experience. That is a story worth remembering.
    Melia,
    We are getting to the end. Yippee!!! Sounds like you had a great day. You deserve it!! Now you can rest for the rest of the night.
    Jan,
    People who are in our club do seem to know what to say and do . Sometimes an acknowledging smile is alright also, especially at a restaurant. Your support group is so sweet. Coming to the chemo room on your birthday to throw you a party was so nice of them to do. Those are the moments we will treasure.
    One of my friends also gave me a super soft snuggly pink bathrobe. I also love to snuggle up to it.
    The wig is very nice and chic. It looks like Meg Ryan. Go for it!
    Skye,
    I love your new wig. I hope the woodchuck is okay. Puffball is so cute.
    Cindy,
    I also agree. It is okay to feel the anger. We need to feel it before we can let it go. Sounds like you had a very busy but rewarding night.
    Mizsissy,
    I hope you feel better soon.
    Catch you all later,
    Viddie
  • luckymel
    luckymel Member Posts: 643
    edited June 2007
    Jan, I think that wig is very cute. I can see you in it. It looks and sounds like it would be light and easy to wear,too - for $52, I'd jump on it. I think you might enjoy it, if you got the right one. Their prices are so good I wonder how they do it. Have you ever gone and tried on wigs anywhere? Or is that how you got the $400 one?

    Mizsissy, I like the one you picked out, too. Let us see a photo when it comes.

    I've got nothing but compliments on my wig, literally every time I go out someone says something. Part of it is that I got the right style right off the bat (thank you, wig store ladies) and part of it is that my wig has highlights and also goes darker at the roots, so it looks very natural. It also swings and moves like real hair. So I just put it on and went, right from the start, and always felt natural. I did wear it out, though, poor thing, and had to get a replacement.

    Mizsissy, I wondered where you had been the past couple days - but surely you're not all that far behind. You can't possibly have stopped reading at page 50, that was ages ago.
  • meliaanne
    meliaanne Member Posts: 682
    edited June 2007
    Viddie,
    Is your daughter gone? How was the visit?
    Jan, that's a darliing wig. How do the Paula Young wigs look in person? For that price, you aren't risking much, and I see one I like for me too. If they are any good at all, it's an inexpensive investment, and I think we are all tired of how we look!
  • Rebecca
    Rebecca Member Posts: 971
    edited June 2007

    Jan, I like it...but if you hate the wig you have why get more? On the other hand, I think it will be very fetching on you, and at that price it might be worth the gamble.

  • viddie
    viddie Member Posts: 547
    edited June 2007
    Melia,
    My daughter is coming home on Thursday. She is taking prerequisite courses here for graduate school. She wants to be a nurse practitioner. She is staying until August 18, two weeks after my surgery. That will be a treat. I am a little anxious about the fact that she quit her job. I know she hated her boss and in order to take these courses and return home she had no choice. I also know that she will probably be able to get a job as soon as she gets back to DC, but I am still a little nervous about that. Her health insurance ends on June 30, so she has to get health insurance here when she returns. In Ma. although it is quite expensive (around $350.00 for a 23 year old), it is good coverage. She can only use it here, except for emergency when traveling, so when she returns to DC, she has to get a job also for health insurance. I promised myself that I would not worry about that. Glad you asked?? LOL.
    Viddie
  • luckymel
    luckymel Member Posts: 643
    edited June 2007
    I had such a lazy day today. I stayed in my jammies and read the paper much more thoroughly than usual - didn't finish with it until 4pm or so, if you can believe that. I was interrupted by a couple of phone calls, but can't think what else I did. Larry has the virus I got before going into the hospital, so he's feeling a bit under the weather, so he was taking it easy today also, so NOTHING happened around here today. I'm feeling just fine - still coughing a bit from the virus, but as far as the surgery is concerned, I feel great. Haven't taken anything at all for pain today, and have no need for anything, even when I'm up doing something. I can put both arms over my head with no discomfort - it's just too good to be true. I'm sure the diep postop period will be more difficult, but I'm enjoying this, for now.l Tomorrow my mother in law is coming to spend the night - I don't really need any help, but she wanted to, so she is going to just come over and cook (or bring food) and go home the next day. She lives 90 min. away or so, so it's a bit much for her to drive over and back in the same day. So we'll have a nice visit. I have to stay home tomorrow, at least until my surgeon calls wtih the path report.

    Rebecca and Jan, I loved your "nicest thing someone did for you" stories. It's good to think of all the good things that happened, because there are a lot of positive things that happen on a journey like this. Maybe everyone should stop and think of the best thing, and share it with us. Your story, Rebecca, sounds almost mystical or something. Like something you'd see in a movie, perhaps - it gives me chills to read about it. Good chills, though. Jan, your story is just another example of the sisterhood that develops with other bc survivors. We all know how special that is.

    Cindy, your post really makes me wish I'd made it to a Relay. I'm guessing they are about all done for this year, right? Since this is cancer survivors' day, or week, or whatever.

    Melia and Viddie, I wish you guys were done with Taxol! It was so hard for me to drag myself through those last 3-4 weeks. You'll make it though, soon. I was thinking today, that maybe why I had such a hard time with Taxol at the very end was that I worked every single day up until the very end...I really didn't cut myself much slack. I did everything around home that I always do, all the errands, didn't ever get enough sleep...wonder if that's why I hit rock bottom when it finally hit me. Just a thought. I hear some people saying it was pretty easy, but at the end there, for me, I just flat couldn't put one foot in front of the other.

    Viddie, I know I said this yesterday, but the I spent the day today in the transition gown (too lazy to dress) and was impressed again by how perfect it is. It was so obviously designed by someone who had the same drains in the same places for the same reasons....it really is just the thing. Definitely get one.

    Melia, what kind of bike did you get your dh? I have a great bike - wonder when it would be safe to get on it? Does no exercise mean no biking? He said no exercise for 4 weeks, then I have my diep. I've got to do something!

    Skye, please don't tell me if your little hedgehog doesn't make it. He's so cute. I'll bet he's an orphan - is there a wildlife rescue organization around there?

    Terry, glad to hear Tae is doing better. Hope the progress continues.

    Hope all the rest of you had a wonderful day today. Love you all.
  • Lynn12
    Lynn12 Member Posts: 1,008
    edited June 2007
    Hi Ladies,

    Real quick check in. We went to friends to watch the last Sopranos. The day started cloudy and rainy, but by 5pm the sun was shining. They live on a lake, so we bbq'd, ate on the deck and went for a boat ride. Got back around 8:30 and sat by the bonfire until 9, watched Sopranos, then back outside at the bonfire. They are such nice people and so easy to get along with. We had a lovely time.

    Tomorrow I get my port out, I can't wait! I have no idea if it will be like getting it in as far as anesthesia, but it doesnt' matter to me, I just want it out.

    I'll catch up on all the posts tomorrow, hope everyone had a nice weekend!

    hugs,
    Lynn
  • skyedivine
    skyedivine Member Posts: 839
    edited June 2007
    Melia, my dh had NO symptoms and supposedly not old enough to really have to worry but it was found on a routine check and followed by a persistent urologist until dx. It's crazy for men not to have that done, like a woman refusing to have mammograms. I'd keep encouraging him, better to catch these things early...or be reassured when the tests come out negative!

    I think Puffball is still with us, he seemed to be moving around more which is good.

    Gearing up for first rads tomorrow...did anyone else here use pure aloe plant juice straight from the plant? A friend of mine swears by that. - Skye
  • Nancyab
    Nancyab Member Posts: 276
    edited June 2007
    Jan, I love that wig! Viddie, I did speak with 2 of the other ladies. One of the gals doesn't have a good prognosis, but she seemed well.
    The kids all went canoeing today so the house was quiet and I snuck in a nap. My leg muscles ( if any are left) hurt so bad when I stand or walk.
    The kids had a mishap canoeing and didn't get home until 6 I was getting worried, because they left at 11! I know they are old enough to take care of themselves but you never stop worrying do you?
    My daughter Kelly is 26 and her Husband Nick were with them but heck I was worried about them too. Turns out Nick's cousin lost his wallet in a deep fast moving part of the river ( why take your wallet?) and they were trying to find it. No luck! If anyone finds it they'll have a soap stars wallet and probably sell it on E-bay LOL!!! He should look there for it. Kids they all come with a boat load of stress don't they? Oh well they had fun. I wish I wasn't "considered" an oldie because I would of love to go canoeing.
  • mer1957
    mer1957 Member Posts: 534
    edited June 2007
    I found out the hard way that exercise makes the drains drain more and it takes longer to get them out. Try just walking around the house to start with!

    I'm feeling much better from my surgery--less tight. I was able to exercise with weights at a class yesterday and feel fine today. (That's usually the trick - to feel good and not sore the next day). Tomorrow starts rads. Good luck today Skye at rads. I know my whole routine is going to change with this rads appt every day.

    Mizsissy, I'm not on Tamox yet. Hope you feel better soon.
  • meliaanne
    meliaanne Member Posts: 682
    edited June 2007
    Mel and Mary, Glad to hear you are feeling better. The surgery wasn't as bad as I had feared, and I am glad you are finding that it wasn't a terrible ordeal also.

    Viddie, I guess it's chemo brain; I thought you were having a visit from a daughter. I knew about the one that was moving back for school. It's good she will be there for your surgery. I found my daughters to be much more sensitive and proactive than my son or husband during my recovery; little things like offering tea or soup, not waiting for me to ask. The guys just hung around waiting for requests, hard for me. Much better when one of the girls would just bring me tea and yogurt with my pain pill.

    Mel, I am listening to you about the taxol and not doing too much up to the end. I am working and certainly hope to do so throughout, but a desk job is much diff from a nursing job. I have cut out the gym, just am way too tired to do that, am looking forward to returning mid July. I try to take short walks and we like to bike ride on weekends, but the rides are much shorter and less challenging. And I have cut errands back a lot too. Steve does the grocery shopping, which I hate even when healthy, so that has been a treat. I just overlook all the funny impulse buys. So even though the taxol is going on FOREVER, or so it seems, I am hoping to avoid the terrible side effects you had at the end. The ankle swelling went away after 24 hours, so that was encouraging. But who knows; if things get bad, I can certainly take some time off. My biggest fear about staying home is dwelling on it and getting depressed.

    Nancy, I know what you mean about worrying about adult kids. I like it better when I don't know til afterwards about their adventures.

    My bras/prosthesis were bothering me so much that I was worried about lymphedema. I went to the wonderful specialty shop where I got them, and the lady gave me expanders. What a difference. They just hook onto the back of the bra and effectively give you extra room, so the pros isn't so tight against my chest. Hopefully this will make me more comfy and I won't tear the bra off the minute I get home.

    Have a good day all; off to work.
    Melia
  • Dar1
    Dar1 Member Posts: 146
    edited June 2007
    Cindy, I felt the same way when I saw all the luminaries. It was a shocker to see several "In Memoriam" for my dentist, whom I just saw in late Dec. before I started chemo! She had sent a letter out in January, saying that she had cancer and would be leaving her practise, but I don't know what kind. Couldn't have been breast cancer to move that fast - very sad. My feeling was - cancer is such as thief - it robs people of years they should have, and survivors of peace of mind, body parts, etc. Made me want to do more to contribute, so I think I will volunteer again with the Cancer Society.
    We had a good weekend, but I still find the fatigue is there. I find it difficult to rest - guess it's still a lesson to learn, that I don't always have to be doing something. I was thinking of increasing my hours at work, but after how tired I was yesterday, I don't know. Maybe just 2 afternoons a week - I feel like such a wuss!
    I'm donating my wig to the Cancer Society - heard they have a good selection - has anyone checked it out?
    Mizsissy - hope you get feeling better!
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited June 2007
    Good morning gals,

    I just devoted a couple of hours to catching up on posts here. Wow, we're a busy group. I went back to page 50 and now we're on 53.

    Sorry I've missed the chats. My husband gets up very early (around 5:30) and I try not to sleep too much later, so by 8:30 I'm usually done for the day. I do feel though that things are coming back...energy, exercise, feeling better, except for my bad tummy.

    I don't know why my problems seems to be so much different from everyone else's..maybe this gastric problem is just totally unrelated to BC. Yesterday started out pretty good, but they DH & I were out in the car, delayed lunch a little, then it was all downhill from there. My stomach is enormous again, and I was in discomfort for most of the afternoon and evening.

    Today I am going to try something new. I am going to eat nothing but oatmeal and see if that helps, and I'll have frequent small meals. I am so tired of having a bad stomach. This has been going on for three weeks now. My stomach muscles are so tired and stretched out from being so distended all the time; I hope I don't end up with a permanent enormous potbelly.

    On a completely different subject, I now, very unexpectedly, have found a wonderful model for my dress designs!! I was in the local pharmacy, which operates kind of like a general store, and there, standing by the photo machine, is a georgeous, tall olive-skinned young lady with a figure like a Barbie doll. At first I can't believe she is real. A few months ago, when I had an outfit in a fashion show, I was asked to find a model and I had no idea where to find one, but here she was. Lovely figure and coloring, perfect!!!

    So I stood there a minute and thought, what am I going to do: just walk out of here and remember that I saw the perfect model without doing anything about it, or do something? So I approached her and explained that I design clothes, and would she be interested....?!! And it turns out she is very interested!!

    So now I have a new project, and that is getting ready for some photo shoots. I've got plenty of outfits..enough to make a winter line and a summer line, and I've just got to figure out how and where to set up a photo shoot. I have no idea where this will lead---if anywhere--but it is fun to do and it will be exciting to see my clothes on a really beautiful model.

    Who of us are getting zapped now? Joni, with all those zaps are getting very, very tired? I hope not too much. Radiation seemed like nothing at first and got very tiring towards the end.

    Melinda, congratulations on getting through your surgery which we all know is a huge emotional step as well as a physical one, but you seem to be sailing through with flying colors!!!

    Mary, I am so glad to know your tightness is loosening up. You are very strong willed when it comes to fitness and I'm sure you'll be back in top shape in no time.
  • NOLONGERREADINGORPOSTING
    NOLONGERREADINGORPOSTING Member Posts: 778
    edited June 2007
    (con'td)

    Joni, I want you to know that your Van Gogh slide show has really got me going. I just found a marvelous book at Borders that documents Van Gogh's growth as an artist through his letters to his brother and personal diary, with sketches. I've ordered a copy and am going to read it, maybe as a way of helping with my own art block.

    Melia, I am fascinated with your trip to the Wolf Preserve. Let's hear more about those wolves. What are they like? I wonder how closely related they are to coyotes; do they interbreed?

    I'd better stop now before I give you gals TOO MUCH too read. Hope to make it to chat one of these nights.

    Mizsisy
  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2007
    Lynn – what did you think about the last Sopranos? I like the way they ended it.

    Nancy – Here’s a wallet story for you. A few years ago my dad stopped on the way to the lake to put gas in his boat. He didn’t realize it at the time, but as he was filling the boat he left his wallet on the small swim platform on the back of the boat. He drove to the lake, put the boat into the lake, and stayed out all day on the water before he realized that his wallet was gone. At that point he had no idea where he left it. Well, 2 weeks later he gets a phone call from a man who has found my Dad’s wallet. He was fishing in the lake and caught it! He returned it all soggy but with its contents still inside. This is a lake that is 100’ deep in places. So maybe there is still hope….

    Mel – Do NOT risk the exercise until the doc says it’s OK. I wouldn’t want you to have any problems that would delay your diep.

    Speaking of diep I saw the plastic surgery show on Discovery Health last night with Dr. Allen. They did a sgap on the show. I’d set my DVR to record all of the plastic surgery shows that were on this week hoping to catch it. Anyway, it was pretty interesting, they showed a lot of the surgery.

    Melia – I hope the bra expanders work. I still can’t stand to wear my prothesis but try my best to at least stay dressed until after dinner when I switch into my PJs.

    Mizsissy – My tummy problems didn’t leave after chemo either. I feel like I am still bloated and wake up every morning with a stomach ache. It’s not as bad as what you are describing – but I think it must be related to chemo. Congrats on the model – that is so exciting.

    Mary - what day is it that you start rads? I can't remember already.

    I ordered the wig – I figure I can send it back if I don’t like it. For some reason I am just so sick of bald right now. More than I have been at any point before. It was easier to deal with during chemo for some reason. And UGH the eyebrows – I want them back!!! Whaaa….

    The girls are feeling better after the strep throat. My DH has it now and I think I do to. I am going in to the doc this morning to find out.

    Have a good day!
  • Amera
    Amera Member Posts: 452
    edited June 2007
    Quote:

    And UGH the eyebrows – I want them back!!! Whaaa….




    Jan, that was the thing that made me look the most sick and strange. When my brows came back, it happened fairly quickly. It was hard to draw them on while they were growing in. It looked like a dark line in the middle of a bunch of fuzz.

    My hair is really showing a hairline at this point. It's very curly though so it's hard to tell how long it is and looks much shorter. Although, it's really only about 1/2 inch maybe at this point. I noticed a girl at church yesterday that had her hair intentionally this short. It looked good on her although she is about 20 and wears very funky clothes etc. Not sure I can pull off the same look as a suburban mom. I am really sick of the scarves at this point as well. I've started to go topless around the house all the time and in front of my kid's friends. They don't seem to notice or care. I am really hoping that by next month it will look more like an intentional cut rather than the chemo cut.
  • Dar1
    Dar1 Member Posts: 146
    edited June 2007
    I just got an email from my SIL with a lot of "helpful" info about cancer:
    "1. Every person has cancer cells in the body. These cancer cells do not show up in the standard tests until they have multiplied to a few billion. When doctors tell cancer patients that there are no more cancer cells in their bodies after treatment, it just means the tests are unable to detect the cancer cells because they have not reached the detectable size.
    2. Cancer cells occur between 6 to more than 10 times in a person's lifetime.

    3. When the person's immune system is strong the cancer cells will be destroyed and prevented from multiplying and forming tumors.

    4. When a person has cancer it indicates the person has multiple nutritional deficiencies. These could be due to genetic, environmental, food and lifestyle factors.

    5. To overcome the multiple nutritional deficiencies, changing diet and including supplements will strengthen the immune system.

    6. Chemotherapy involves poisoning the rapidly-growing cancer cells and also destroys rapidly-growing healthy cells in the bone marrow, gastrointestinal tract etc, and can cause organ damage, like liver, kidneys, heart, lungs etc.

    7. Radiation while destroying cancer cells also burns, scars and damages healthy cells, tissues and organs.

    8. Initial treatment with chemotherapy and radiation will often reduce tumor size. However prolonged use of chemotherapy and radiation do not result in more tumor destruction.

    9. When the body has too much toxic burden from chemotherapy and radiation the immune system is either compromised or destroyed, hence the person can succumb to various kinds of infections and complications.

    10. Chemotherapy and radiation can cause cancer cells to mutate and become resistant and difficult to destroy. Surgery can also cause cancer cells to spread to other sites.

    11. An effective way to battle cancer is to starve the cancer cells by not feeding it with the foods it needs to multiply.

    CANCER CELLS FEED ON:

    a. Sugar is a cancer-feeder. By cutting off sugar it cuts off one important food supply to the cancer cells. Sugar substitutes like NutraSweet, Equal, Spoonful, etc are made with Aspartame and it is harmful. A better natural substitute would be Manuka honey or molasses, but only in very small amounts. Table salt has a chemical added to make it white in color. Better alternative is Bragg's aminos or sea salt.

    b. Milk causes the body to produce mucus, especially in the gastrointestinal tract. Cancer feeds on mucus. By cutting off milk and substituting with unsweetened soya milk cancer cells are being starved.

    c. Cancer cells thrive in an acid environment. A meat-based diet is acidic and it is best to eat fish, and a little chicken rather than beef or pork. �Meat also contains livestock antibiotics, growth hormones and parasites, which are all harmful, especially to people with cancer.

    d. A diet made of 80% fresh vegetables and juice, whole grains, seeds, nuts and a little fruits help put the body into an alkaline environment. About 20% can be from cooked food including beans. Fresh vegetable juices provide live enzymes that are easily absorbed and reach down to cellular levels within 15 minutes to nourish and enhance growth of healthy cells. To obtain live enzymes for building healthy cells try and drink fresh vegetable juice (most vegetables including bean sprouts) and eat some raw vegetables 2 or 3 times a day. Enzymes are destroyed at temperatures of 104 degrees F (40 degrees C).

    e. Avoid coffee, tea, and chocolate, which have high caffeine. Green tea is a better alternative and has cancer-fighting properties. Water-best to drink purified water, or filtered, to avoid known toxins and heavy metals in tap water. Distilled water is acidic, avoid it.

    12. Meat protein is difficult to digest and requires a lot of digestive enzymes. Undigested meat remaining in the intestines become purified and leads to more toxic build-up.

    13. Cancer cell walls have a tough protein covering. By refraining from or eating less meat it frees more enzymes to attack the protein walls of cancer cells and allows the body's killer cells to destroy the cancer cells.

    14. Some supplements build up the immune system (IP6, Flor-ssence, Essiac, anti-oxidants, vitamins, minerals, EFAs etc.) to enable the body's own killer cells to destroy cancer cells. Other supplements like vitamin E are known to cause apoptosis, or programmed cell death, the body's normal method of disposing of damaged, unwanted, or unneeded cells.

    15. Cancer is a disease of the mind, body, and spirit. A proactive and positive spirit will help the cancer warrior be a survivor. Anger, unforgiveness and bitterness put the body into a stressful and acidic environment. Learn to have a loving and forgiving spirit. Learn to relax and enjoy life.

    16. Cancer cells cannot thrive in an oxygenated environment. Exercising daily, and deep breathing help to get more oxygen down to the cellular level. Oxygen therapy is another means employed to destroy cancer cells."

    There are many items in here that I agree with - chemo is toxic, cells can become resistant, nutrition is important, etc., but it upsets me - I often feel an element of smugness from this individual. Guess I am angry and unforgiving! I feel defensive, as though it was my fault I got cancer. I'll get over it, but just can't see her as supportive - I feel judged.
    There was nothing wrong with my immune system - I rarely got colds, etc. even when everyone around me was! I think that people don't want to accept that cancer can happen to anyone - sure there are risk factors and things we can do in improve our chances, but - and I'm sure we've all felt this - why me and not that other person who 1) drinks more, 2) weighs more, 3) has whatever unhealthy life style.
    OK I'll get off the soap box now, and try to be more loving and forgiving.

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