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Ditto. mikey.

– Hide quoted text — Show quoted text – He told me the first time, and again this time it didn’t matter to him one way or the other.  The most important thing to him is that when it was all over with, no matter what had to happen, is that I was still here with him. [...] He told me shortly after my surgery last year, when I was really getting so tired about this whole entire adventure we were on again "you’re not your breasts, or your hair, this body is just a shell, who you really are is inside, not on the outside" Yes, this is the heart of it. I didn’t fall in love and marry her because of her gorgeous bod and come-hither looks (although they sure didn’t hurt), it was because of her warmth, and her fire, and her laughter. None of that has changed. Thanks, Annie.

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I couldn’t find your original post {I’m on webtv/not showing up here} I saw parts of it cut/pasted into another of the posts here. But I was just going to make a comment about what you said about having a "Wilms Tumor" when you were a kid. My cousin also had that as a young girl {15 at the time/mid 40’s now} She was treated with something they called cobalt {similair to rads?} She however didn’t loose her kidney as a result of the cancer. They also treated her for nodules in her lung as well. Take care there dear I’m very sorry to hear that it has caused you to miscarry. My thoughts and prayers are with you. God bless Annie Ultimately…..we know deeply that the other side of every fear is a freedom. "Courage"…is *fear* that has said it’s prayers.

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Now that her prognosis seems hopeful, and we (or at least I) have gotten past the fears of imminent death, one scary part that remains is the question of where the hell this cancer came from. To my wife’s knowledge, cancer doesn’t run in her family, so it came as quite a surprise. And now I worry about our teenage daughter; is she at a greater risk for cancer at a young age? Damn; what an inheritance to pass on.

Don’t knock yourself out trying to figure out where it came from.    The potential for cancer is present in all of us, it’s really better to regard it as like a random part of the aging process rather than like an infectious disease that has a traceable cause.  Even when all the known hereditary, environmental, racial and lifestyle factors are taken into account, it only explains about 30% of the cancers that happen.  The rest is completely random to the best knowledge of medical science. As for heredity, without genetic testing, it is only reckoned that there is evidence of an inherited tendency to breast cancer only if it has occurred in three generations, so there is no reason to worry about your daughter. Tim Jackson

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Just what I think,looks are not everything, its who you are,i just want my wife with me and in good health. mikey.

– Hide quoted text — Show quoted text – There’s really not much I can add to those that have already posted back to you. I just wanted to let you know that this is all very new right now, and does indeed take some getting used to.. this is not easy by any stretch of anyone’s imagination. I’m in this mess for a second time. I was origianlly dx in 1999. I had a lumpectomy, radiation and chemo the first time. Prior to my recurrence showing up I had an infection in the breast from Feb-May of 02. "Group B Strep} I had it aspirated every week during that time period so my bc surgeon could get samples for cultures for path work..to monitor the effectiveness of the anti-biotics I was on. This left the breast very malformed, which translates to a very big dent. But like I told people "it’s not like I started out with Raquel Welches TaTa’s to begin with, soooo not a big deal really" But obviously you still concern yourself with what am I going to look like after this? Unfortunately, It’s such a "looks" oriented society we live in…you really can’t get away from feeling like this unless you really work hard at it. The recurrence showed up in 11/02.. I had surgery, a modified radical mastectomy, and immediate recon. On 6/6/03 I just finished doing 6 months of chemotherapy. {4 rounds of AC and another 4 rounds Taxotere} I worried about what I would look like after this was over, and what my hubby would think when he saw me. I’m still not finished with the recon..as chemo had to get in there first. So I do look abit mis-shapen to say the least. {one that I call my "perky 30 year old boob" one and one that’s still 53 years old, and heading south on vacation} This I hope will be resolved shortly..at least by the end of the year we’re hoping. This is if my HMO will co-operate with us about additional surgery I’m requesting. I’m requesting a prophylactic mastectomy for medical reasons/which has turned into quite an issue with the HMO. My hubby and I have been married almost 30 years and have 3 kids and 7 grandchildren. I suppose that might make a bit of difference in the way you look at things of this nature. He told me the first time, and again this time it didn’t matter to him one way or the other.  The most important thing to him is that when it was all over with, no matter what had to happen, is that I was still here with him. This time the poor guy is dealing with me with no hair, no eyelashes, and no eyebrows, and a mis-shapen set of TaTa’s to boot. I’ve nick named myself "alien lady" cute, huh? Better then "Mrs. Clean" I thought, everyone’s using that one…lol! He told me shortly after my surgery last year, when I was really getting so tired about this whole entire adventure we were on again "you’re not your breasts, or your hair, this body is just a shell, who you really are is inside, not on the outside" Who we are has not a thing to do with what we look like…it’s who we are as a person. And that’s all tucked away inside, and it’s only seen by those that know us the best, and love us the most. You’ve come to a great group of people. We will be here when you or your wife need us. Post often if you need to, and share so we can help you get through this. Good luck to you both.Take care there/God bless you both annie p/s sorry for the mini-series length post Ultimately…..we know deeply that the other side of every fear is a freedom. "Courage"…is *fear* that has said it’s prayers.

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He told me the first time, and again this time it didn’t matter to him one way or the other.  The most important thing to him is that when it was all over with, no matter what had to happen, is that I was still here with him. [...] He told me shortly after my surgery last year, when I was really getting so tired about this whole entire adventure we were on again "you’re not your breasts, or your hair, this body is just a shell, who you really are is inside, not on the outside"

Yes, this is the heart of it. I didn’t fall in love and marry her because of her gorgeous bod and come-hither looks (although they sure didn’t hurt), it was because of her warmth, and her fire, and her laughter. None of that has changed. Thanks, Annie.

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Hi Guitar, Welcome to the group, no-one likes to be in.

Thank you. I myself am only 34 and was diagnosed last Sept. I had a mastectomy chemo and have just finished my 3wks of radiotherapy. So i understand how your wife must be feeling.

Boy, this all really sucks. But I am glad it’s not worse, and I am very grateful for the sympathy which everyone here has expressed. Thanks, everyone. Now that her prognosis seems hopeful, and we (or at least I) have gotten past the fears of imminent death, one scary part that remains is the question of where the hell this cancer came from. To my wife’s knowledge, cancer doesn’t run in her family, so it came as quite a surprise. And now I worry about our teenage daughter; is she at a greater risk for cancer at a young age? Damn; what an inheritance to pass on. Your wife probably feels the same as you (not very sexy, after all shes been through!) Give her time, i know i need time to feel like a desirable woman again! Have you spoken to her about how you feel?

Yes, some. But not much. It has been a while since we have taken the time to have a long talk – the day-to-day routine can get so busy! We can usually find a few moments in the evening to talk, but I think we really need a night out without the kids soon. Just be grateful that you still have your wife and 3 lovely children. I myself was not so fortunate! I lost 3 babies through miscarries. I am unable to carry them to full term, due to my cancer treatment i had as a child,(Wilms Tumour, kidney removed).

I’m so sorry to hear of your losses. I do feel very fortunate – I have had an easy life, never been poor, never lost anyone close to me before their time. I have good friends, a wonderful family, and of course the love of my life. So I guess I’m not used to any kind of pain or suffering. :-)

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<< I understand your problem.  When my wife elected to have a bilateral mastectomy, I kind of took my cue from the following. TRUE LOVE OF THOMAS MOORE by Galen Drake   Wow–thanks for sharing!

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There’s really not much I can add to those that have already posted back to you. I just wanted to let you know that this is all very new right now, and does indeed take some getting used to.. this is not easy by any stretch of anyone’s imagination. I’m in this mess for a second time. I was origianlly dx in 1999. I had a lumpectomy, radiation and chemo the first time. Prior to my recurrence showing up I had an infection in the breast from Feb-May of 02. "Group B Strep} I had it aspirated every week during that time period so my bc surgeon could get samples for cultures for path work..to monitor the effectiveness of the anti-biotics I was on. This left the breast very malformed, which translates to a very big dent. But like I told people "it’s not like I started out with Raquel Welches TaTa’s to begin with, soooo not a big deal really" But obviously you still concern yourself with what am I going to look like after this? Unfortunately, It’s such a "looks" oriented society we live in…you really can’t get away from feeling like this unless you really work hard at it.   The recurrence showed up in 11/02.. I had surgery, a modified radical mastectomy, and immediate recon. On 6/6/03 I just finished doing 6 months of chemotherapy. {4 rounds of AC and another 4 rounds Taxotere} I worried about what I would look like after this was over, and what my hubby would think when he saw me. I’m still not finished with the recon..as chemo had to get in there first. So I do look abit mis-shapen to say the least. {one that I call my "perky 30 year old boob" one and one that’s still 53 years old, and heading south on vacation} This I hope will be resolved shortly..at least by the end of the year we’re hoping. This is if my HMO will co-operate with us about additional surgery I’m requesting. I’m requesting a prophylactic mastectomy for medical reasons/which has turned into quite an issue with the HMO.     My hubby and I have been married almost 30 years and have 3 kids and 7 grandchildren. I suppose that might make a bit of difference in the way you look at things of this nature. He told me the first time, and again this time it didn’t matter to him one way or the other.  The most important thing to him is that when it was all over with, no matter what had to happen, is that I was still here with him. This time the poor guy is dealing with me with no hair, no eyelashes, and no eyebrows, and a mis-shapen set of TaTa’s to boot. I’ve nick named myself "alien lady" cute, huh? Better then "Mrs. Clean" I thought, everyone’s using that one…lol! He told me shortly after my surgery last year, when I was really getting so tired about this whole entire adventure we were on again "you’re not your breasts, or your hair, this body is just a shell, who you really are is inside, not on the outside" Who we are has not a thing to do with what we look like…it’s who we are as a person. And that’s all tucked away inside, and it’s only seen by those that know us the best, and love us the most.   You’ve come to a great group of people. We will be here when you or your wife need us. Post often if you need to, and share so we can help you get through this. Good luck to you both.Take care there/God bless you both annie p/s sorry for the mini-series length post Ultimately…..we know deeply that the other side of every fear is a freedom. "Courage"…is *fear* that has said it’s prayers.

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Hi Guitar, Welcome to the group, no-one likes to be in. I myself am only 34 and was diagnosed last Sept. I had a mastectomy chemo and have just finished my 3wks of radiotherapy. So i understand how your wife must be feeling. My Husband has been so understanding about everything, he doesn’t pressure me at all. He is waiting till i feel ready. He says that my appearance now, doesn’t make me any less desirable. Sex isn’t all there is to a marriage anyway, but time is a great healer! Your wife probably feels the same as you (not very sexy, after all shes been through!) Give her time, i know i need time to feel like a desirable woman again! Have you spoken to her about how you feel? Just be grateful that you still have your wife and 3 lovely children. I myself was not so fortunate! I lost 3 babies through miscarries. I am unable to carry them to full term, due to my cancer treatment i had as a child,(Wilms Tumour, kidney removed). So PLEASE, think of what you yourself have got and count your blessings! There are lots of others, including myself, that are not so blessed as you obviously are. Apprieciate your wife for who she is and not what she looks like, at the moment. After all, isn’t that what marriage is about? I hope in time you will get back to normal and spend the rest of your life happily together. Good Luck! Take care, Shaz x

– Hide quoted text — Show quoted text – First, welcome to the group where none of wants to be.  I am sorry that our connection with you is through this dreaded ‘beast’ (yes, ‘beast’ not ‘breast). I would like to suggest you contact a counselor who specializes in this area to help both you and your wife as soon as possible.  I have been fortunate in that my husband let me know immediately that he found me desirable (10 days after having a bilateral mastectomy–I still remember ;-) This is the third attempt I am making to answer your post.  I was knocked off-line twice before–am sure it’s an aol glitch–my turn ‘today’ but also see it as an opportunity to go beyond my initial reaction ;-) I do not want to discount your feelings.  We all respond differently and men are more influenced by visual stimuli.  However, this area can be so much further enhanced through exploration of other areas of sensuality–i.e. olfactory (different scents), touch, and through emotions, including spirituality.  Some cultures forbid lovemaking without covering of the body parts related to the act of making love as well as restrict time allowed for this (i.e. Orthodox Judaism–requires body parts to be covered and does not allow love-making during certain times of the month).  From what I have read and been told–the mystery surrounding those restrictions alone heightens their feelings and levels of satisfaction.  (Time restrictions were also thought to cut down on potential medical-related difficulties and more importantly (at one time) increase fertility). There is so much more to satisfaction from the intimacy of love-making than the visual alone.  Each of us comes to this, however, from a different perspective and ‘baseline.’  From what you describe, it sounds as if you need to explore these different avenues which, surprisingly, should greatly increase your fulfillment in this area–which it would most likely have even done if your wife never had b.c. to begin with. I know my husband is affected by the results of my surgery.  I am too. One way to look at it is that it has giving her/me a second chance at life–if one can get beyond the physical.  Because I know that my husband is affected  by it–often times I wear my bra with prostheses–which looks and feels quite ‘real’ (even though it is not the same and does limit what one might do with it).  Personally, though, I can still feel the same or at least similar pleasurable feelings in that area when pressure is placed in that area from on top of my bra.  Sure, it isn’t the same thing. Right now you are probably feeling alot of conflicting emotions–including fear and even possibly ‘disgust’ (not necessarily over the actual physical appearance) but what the whole experience of breast cancer represents and what it has the potential to become.   Some of your fears might include anger, fear of abandonment, helplessness, feelings of being overwhelmed, guilt, a need to share what is going on but at same time holding back because of what your wife is dealing with as well and not wanting to further burden her.  Again, from a personal female perspective, it is/was important to me to know that my husband still needed/needs me in the same ways as before.  Of course, the experience of b.c. alone changes us–and there is no way that things can be exactly the same.  However, it is a time for personal growth, too. One thing  that helped my husband and I was a book sent to me by a friend. KITCHEN TABLE WISDOM, by Rachel Remen (Reiman?), M.D.  It is a series of short inspirational stories.  I read aloud these aloud to my husband on the way to many of my dr.’s appt’s soon after diagnosis.  It was a springboard to sharing intimacy, and sometimes lead to further discussion.  Often times, there was no need to further discuss–the stories alone brought about increased feelings of shared inspiration and intimacy. My best thoughts are with you and your wife at this difficult time.  She so very much needs you in ways that you have not had a chance to experience. Use this time now to grow beyond the  superficiality of limited sensuality from only one sensual source.  Again, I am in no way denying the importance of its immediate impact but only letting you know there  is so much more. Breast cancer is so unfair–especially when it makes its ugly appearance in women so young.  Learn all you can about it so that you can be your wife’s advocate.  Look at different ways you can work together as a team–with her as well as with her physicians.  Involve your whole family from a positive perspective–take part in activities such as the "Relay for Life."  Check into available resources such as the "Wellness Center" and programs through the American Cancer Society.  Also make sure that there is time away from breast cancer–for you, your wife, and your children.  Use this time now to grow and become the best you can be in ways that you have not yet explored.  It can be done and the rewards will be beyond what you had never imagined or even thought possible, not only for yourself but for your wife and family.  Again, my best thoughts and prayers to you all.  {{{Hugs}}}

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<< Plus, anesthetics make her nauseous, which she really, really loathes. I also used to get quite nauseous with anesthesia.  However, after having gone through chemo with successful anti-nausea treatment, upon someone’s recommendation (not sure whom) I asked if I could have an anti-nausea medication (Zofran–which I had before chem) with the anesthesia.  They agreed.  I was fine when I woke up—first time ever I awoke after being ‘under’ without that horrid feeling one experiences as they ‘wake up’ after surgery.

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Kaye, thank you for your thoughts!

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Ann, Yah, it’s been only 12 weeks. Your description sounds a lot like what she’s going through right now. – Hide quoted text — Show quoted text – That was all a year ago now, and I look and feel quite normal. There is a scar near my arm and on the breast, even the indentation where they removed bopsy and surgical tissue has pulled together a little and isn’t as deep (looks like a very small golf divot!) I feel OK with it now, and that has encouraged my hsuband too, I think. [...] Try to talk when she seems to want to. Perhaps it’d be ok to tell her you’re worried about hurting her, or saying the wrong thing, and see how she responds. Counseling is a neutral ground to help you get started talking too. She will quite probably look normal again, with maybe a small divot or so, if indeed she had a lumpectomy. As the others said, looking normal isn’t important in love, but I know how the mind plays games. Try to get out of the game by talking it over together or with counselor. And watch how not only communication, but even looks improve. It does take about a year for healing to complete, for me anyway – no more redness at all…

Wow, that’s really encouraging! I hope I will be able to report the same in a year. Thanks for sharing your thoughts.

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More surgery? Yipes! She wouldn’t stand for it. She had three surgeries, two months apart, and by the end not only was she hurting a lot, but she was thoroughly sick of healing only to be cut open again along almost the exact same seam. :-) Plus, anesthetics make her nauseous, which she really, really loathes.

Whoops, my mistake. The procedures weren’t two MONTHS apart — they were two WEEKS apart. Not sure if that’s better, or worse.

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Don’t feel that this is a abnormal response. You are normal. But you are also human. Unlike animals, the human mind allows us to look beyond the physical and connect mentally. It sounds like you need a "mind tuneup". Get some help and you will feel better about what has happened to her. She is not your  toy. She is not broke. Don’t give up on her…ever. She has the best kind of this disease and she will soon be back. What you do now will always be remembered and if you give her enough hugs and encouragement…will be appreciated. Things will get better and soon from the sounds of it. Joe Joe

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Tim said it very well indeed.  There’s one little bit I’d add.  If you give it a little time and it doesn’t get better for you, you might want to consult a professional to counsel.  I wish you the best.

Thank you, Barb. Like I mentioned to Joe, I’ll keep it in mind.

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– Hide quoted text — Show quoted text – Hello everyone, I’m new to this group so please forgive me if I stumble over netiquette issues. My wife has breast cancer. I don’t remember the medical terms but it’s in her ducts and the doctor said it’s the most common type. She has had surgery to remove cancerous tissue in one breast, and some of her lymph nodes. She is in the tail end of a six-week-long radiation treatment, which is to be followed by five years of tamoxifen. She’s 36, and the doctor says that the reason they want to do such aggressive treatment is exactly because she’s so young – they want to make sure it doesn’t recur. All in all, I gather that hers seems to be a pretty successful case, as breast cancer cases go. I have every confidence that the doctor is doing what needs to be done. I am writing this post not because I am concerned for her life or her health, but because I am concerned about our marriage. To be blunt, I am afraid that I won’t be able to resume a normal sexual life with her because I am having a hard time with her changed appearance since her surgery. Her breast has big scars and is misshapen due to the tissue removal, and at present the whole area is also all bruised up and discolored from the radiation treatment. When I see her this way it is very hard for me to feel physical desire. I have never been good with blood or surgical procedures, and seeing her scarred breast actually makes me a little queasy. I love her dearly – we have been married more than 10 years and have three children together. She is everything to me. I feel so ashamed and angry at myself for not being able to get past her appearance. And I know that this isn’t even a really bad situation – I know people who are much worse off, and I feel guilty about whining over a relatively minor thing. But I can’t help it, this is how I feel. I hate it. I don’t know what to do, how to change myself to get over these feelings. Can anyone offer any advice? I sure need some.

I understand your problem.  When my wife elected to have a bilateral mastectomy, I kind of took my cue from the following. TRUE LOVE OF THOMAS MOORE by Galen Drake My favorite love story is also a true one. Soon after he was married, Thomas Moore, the famous 19th century Irish poet, was called away on a business trip. Upon his return he was met at the door, not by his beautiful bride, but by the family doctor. "Your wife is upstairs," said the doctor. "But she asked that you not come up." And then Moore learned the terrible truth; his wife had contracted small pox. The disease had left her once flawless skin pocked and scarred. She had taken one look at her reflection in the mirror and commanded that the shutters be drawn and that her husband never see her again. Moore would not listen. He ran upstairs and threw open the door of his wife’s room. It was black as night inside. Not a sound came from the darkness. Groping along the wall, Moore felt for the gas jets. A startled cry came from a black corner of the room. "No! Don’t light the lamps!" Moore hesitated, swayed by the pleading in the voice. "Go!" she begged. "Please go! This is the greatest gift I can give you now." Moore did go. He went down to his study, where he sat up most of the night, prayerfully writing. Not a poem this time, but a song. He had never written a song before, but now he found it more natural to his mood than simple poetry. He not only wrote the words, but he wrote the music too. And the next morning, as soon as the sun was up he returned to his wife’s room. He felt his way to a chair and sat down. "Are you awake?" he asked. "I am," came a voice from the far side of the room. "But you must not ask to see me. You must not press me, Thomas." "I will sing to you, then," he answered. And so for the first time, Thomas Moore sang to his wife the song that still lives today: Believe me, if all those endearing young charms, Which I gaze on so fondly today, Were to change by tomorrow and fleet in my arms, Like fairy gifts fading away, Thou wouldst still be adored, as this moment thou art — Let thy loveliness fade as it will, Moore heard a movement from the dark corner where his wife lay in her loneliness, waiting. He continued. Let thy loveliness fade as it will, And around the dear ruin each wish of my heart Would entwine itself verdantly still — The song ended. As his voice trailed off on the last note, Moore heard his bride rise. She crossed the room to the window, reached up and slowly drew open the shutters. Believe me, if all those endearing young charms Which I gaze on so fondly today Were to change by tomorrow and fleet in my arms Like fairy gifts fading away, Thou wouldst still be adored, as this moment thou art Let thy loveliness fade as it will, And around the dear ruin, each wish of my heart Would entwine itself verdantly still. It is not while beauty and youth are thine own, And thy cheeks unprofaned by a tear, That the fervor and faith of a soul may be known To which time will but make thee more dear! No, the heart that has truly loved never forgets But as truly loves on to close, As the sunflower turns on her god when he sets The same look which she turned when he rose. Thomas Moore

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This is difficult both for you and for her.  At first she is going.to feel that no-one would want her looking like this, and you are going to feel turned off by her mutilation.  BUT these feelings can pass and desire will return.  You will both get used to her new shape in time, and more easily once the bruising goes down.  Please don’t feel ashamed of how your body reacts, this is perfectly natural, but do give it time to come to terms with the situation.  The thing to feel ashamed of would be walking away from her when she needs you most, just for lack of patience.

Tim, thank you for the encouragement. I guess time and patience are really the key for me. You can do this.  You didn’t marry her tits.  We all age and suffer attrition to our bodies, at 36 we try not to think about it but it is there and it happens and we will have to face it sooner or later.  She is still the same woman.

You’re right. I didn’t marry her tits (nice though they were). In everything else outside of bed, she’s no different than before. Look at the other one.  It’s cute and sexy.

I laughed when I read this, because the doctor actually removed some tissue from the other side too, partly to get a biopsy there and partly to "even things out" so she wouldn’t look lopsided. Her nipple on that side went from a little downward-pointing to perkier than when she was a teenager! I am, actually, in awe of her toughness. Even though I know she must be wiped out from the radiation treatment, she is still carrying on more or less as she always does, with the only difference being that she takes a few more naps than before, and is currently complaining a little about the radiation burns. She has a much higher pain threshold than I do, and is (I think) more emotionally stable than me as well. She told me that when her doctor first told her that the biopsy had come back with a cancer detection, the doctor and her assistant left her alone for a few minutes, presumably so she could cry in private. Not my wife. She sat there twiddling her thumbs, patiently waiting for them to come back and finish the conversation and tell her what her options were. I, on the other hand, probably would have fallen apart just as they expected.

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Don’t feel that this is a abnormal response. You are normal. But you are also human. Unlike animals, the human mind allows us to look beyond the physical and connect mentally. It sounds like you need a "mind tuneup". Get some help and you will feel better about what has happened to her. She is not your  toy. She is not broke. Don’t give up on her…ever. She has the best kind of this disease and she will soon be back. What you do now will always be remembered and if you give her enough hugs and encouragement…will be appreciated. Things will get better and soon from the sounds of it.

Thanks, Joe. I have not had a chance to talk frankly to anyone about this and it’s a relief just to be able to put these words together on the screen. I know that this phase is only a short time compared to the decades that I expect and hope we will share in the future. I don’t know if I need professional help right now but I’ll keep it in mind just in case.

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My husband was great during my experience.  I had a masatectomy about 8 years ago and was pretty horrified when I first saw the scars.  I found that candles and some lacy little number did a great deal to help me feel sexy again.  It’s hard for both of you but it can be overcome.   As time passes you’ll get used to her new appearance.

Thanks, Lisa. I am sure you’re right, it’s just hard to believe emotionally right now. Time will tell. There’s always plactic surgery to make things look better if you choose to go that route.

More surgery? Yipes! She wouldn’t stand for it. She had three surgeries, two months apart, and by the end not only was she hurting a lot, but she was thoroughly sick of healing only to be cut open again along almost the exact same seam. :-) Plus, anesthetics make her nauseous, which she really, really loathes.

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"But I can’t help it, this is how I feel. I hate it. I don’t know what to do, how to change myself to get over these feelings. Can anyone offer any advice? I sure need some.

Tim said it very well indeed.  There’s one little bit I’d add.  If you give it a little time and it doesn’t get better for you, you might want to consult a professional to counsel.  I wish you the best. Barb

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Tim said it very well indeed.

Yes, indeed and as one who has been there, he sure knows his stuff. My husband was great during my experience.  I had a masatectomy about 8 years ago and was pretty horrified when I first saw the scars.  I found that candles and some lacy little number did a great deal to help me feel sexy again.  It’s hard for both of you but it can be overcome.   As time passes you’ll get used to her new appearance. There’s always plactic surgery to make things look better if you choose to go that route. Good luck. Take care. …lisa

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First, welcome to the group where none of wants to be.  I am sorry that our connection with you is through this dreaded ‘beast’ (yes, ‘beast’ not ‘breast). I would like to suggest you contact a counselor who specializes in this area to help both you and your wife as soon as possible.  I have been fortunate in that my husband let me know immediately that he found me desirable (10 days after having a bilateral mastectomy–I still remember ;-) This is the third attempt I am making to answer your post.  I was knocked off-line twice before–am sure it’s an aol glitch–my turn ‘today’ but also see it as an opportunity to go beyond my initial reaction ;-) I do not want to discount your feelings.  We all respond differently and men are more influenced by visual stimuli.  However, this area can be so much further enhanced through exploration of other areas of sensuality–i.e. olfactory (different scents), touch, and through emotions, including spirituality.  Some cultures forbid lovemaking without covering of the body parts related to the act of making love as well as restrict time allowed for this (i.e. Orthodox Judaism–requires body parts to be covered and does not allow love-making during certain times of the month).  From what I have read and been told–the mystery surrounding those restrictions alone heightens their feelings and levels of satisfaction.  (Time restrictions were also thought to cut down on potential medical-related difficulties and more importantly (at one time) increase fertility). There is so much more to satisfaction from the intimacy of love-making than the visual alone.  Each of us comes to this, however, from a different perspective and ‘baseline.’  From what you describe, it sounds as if you need to explore these different avenues which, surprisingly, should greatly increase your fulfillment in this area–which it would most likely have even done if your wife never had b.c. to begin with. I know my husband is affected by the results of my surgery.  I am too.  One way to look at it is that it has giving her/me a second chance at life–if one can get beyond the physical.  Because I know that my husband is affected  by it–often times I wear my bra with prostheses–which looks and feels quite ‘real’ (even though it is not the same and does limit what one might do with it).  Personally, though, I can still feel the same or at least similar pleasurable feelings in that area when pressure is placed in that area from on top of my bra.  Sure, it isn’t the same thing. Right now you are probably feeling alot of conflicting emotions–including fear and even possibly ‘disgust’ (not necessarily over the actual physical appearance) but what the whole experience of breast cancer represents and what it has the potential to become.   Some of your fears might include anger, fear of abandonment, helplessness, feelings of being overwhelmed, guilt, a need to share what is going on but at same time holding back because of what your wife is dealing with as well and not wanting to further burden her.  Again, from a personal female perspective, it is/was important to me to know that my husband still needed/needs me in the same ways as before.  Of course, the experience of b.c. alone changes us–and there is no way that things can be exactly the same.  However, it is a time for personal growth, too. One thing  that helped my husband and I was a book sent to me by a friend. KITCHEN TABLE WISDOM, by Rachel Remen (Reiman?), M.D.  It is a series of short inspirational stories.  I read aloud these aloud to my husband on the way to many of my dr.’s appt’s soon after diagnosis.  It was a springboard to sharing intimacy, and sometimes lead to further discussion.  Often times, there was no need to further discuss–the stories alone brought about increased feelings of shared inspiration and intimacy. My best thoughts are with you and your wife at this difficult time.  She so very much needs you in ways that you have not had a chance to experience.  Use this time now to grow beyond the  superficiality of limited sensuality from only one sensual source.  Again, I am in no way denying the importance of its immediate impact but only letting you know there  is so much more. Breast cancer is so unfair–especially when it makes its ugly appearance in women so young.  Learn all you can about it so that you can be your wife’s advocate.  Look at different ways you can work together as a team–with her as well as with her physicians.  Involve your whole family from a positive perspective–take part in activities such as the "Relay for Life."  Check into available resources such as the "Wellness Center" and programs through the American Cancer Society.  Also make sure that there is time away from breast cancer–for you, your wife, and your children.  Use this time now to grow and become the best you can be in ways that you have not yet explored.  It can be done and the rewards will be beyond what you had never imagined or even thought possible, not only for yourself but for your wife and family.  Again, my best thoughts and prayers to you all.  {{{Hugs}}}

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My opinion, YMMV: It has probably only been 3 months or so since surgery? I had a lumpectomy, which sounds like what  your wife had. It looked so ugly I wouldn’t undress around my husband, and wouldn’t go to the pool or anywhere else with common showers etc. I was bruised gtpm botched biopsy, swollen from lymphedema in that arm, even tho only 9 nodes were taken, and have punch scar from biopsy as well as a 2" cut near the nipple, and a 6" or so cut under the front of that arm for nodes. They oozed and were red all thru my chemo, as things don’t heal too well during chemo. I thought I’d never feel whole again! After they’d healed enough for radiation, I’d just begun to feel sort of OK with myself, still couldn’t undress in front of hubby, tho he was totally fine with it, I was like you are, embarrassed, afraid, whatever. Then came radiation, with more swelling, some bruising, the scars stood out more, etc. I felt abused again, but no pain, just mental pain. That was all a year ago now, and I look and feel quite normal. There is a scar near my arm and on the breast, even the indentation where they removed bopsy and surgical tissue has pulled together a little and isn’t as deep (looks like a very small golf divot!) I feel OK with it now, and that has encouraged my hsuband too, I think. Perhaps your wife is also feeling as you are, and can’t share it with you as I couldn’t with my husband. We finally had the chance during a phone call about someone else with cancer to talk it thru (funny how its easier to talk about difficult subjects on the phone, or even email!) Try to talk when she seems to want to. Perhaps it’d be ok to tell her you’re worried about hurting her, or saying the wrong thing, and see how she responds. Counseling is a neutral ground to help you get started talking too. She will quite probably look normal again, with maybe a small divot or so, if indeed she had a lumpectomy. As the others said, looking normal isn’t important in love, but I know how the mind plays games. Try to get out of the game by talking it over together or with counselor. And watch how not only communication, but even looks improve. It does take about a year for healing to complete, for me anyway – no more redness at all… Ann in PA

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Hello everyone, I’m new to this group so please forgive me if I stumble over netiquette issues. My wife has breast cancer. I don’t remember the medical terms but it’s in her ducts and the doctor said it’s the most common type. She has had surgery to remove cancerous tissue in one breast, and some of her lymph nodes. She is in the tail end of a six-week-long radiation treatment, which is to be followed by five years of tamoxifen. She’s 36, and the doctor says that the reason they want to do such aggressive treatment is exactly because she’s so young – they want to make sure it doesn’t recur. All in all, I gather that hers seems to be a pretty successful case, as breast cancer cases go. I have every confidence that the doctor is doing what needs to be done. I am writing this post not because I am concerned for her life or her health, but because I am concerned about our marriage. To be blunt, I am afraid that I won’t be able to resume a normal sexual life with her because I am having a hard time with her changed appearance since her surgery. Her breast has big scars and is misshapen due to the tissue removal, and at present the whole area is also all bruised up and discolored from the radiation treatment. When I see her this way it is very hard for me to feel physical desire. I have never been good with blood or surgical procedures, and seeing her scarred breast actually makes me a little queasy. I love her dearly – we have been married more than 10 years and have three children together. She is everything to me. I feel so ashamed and angry at myself for not being able to get past her appearance. And I know that this isn’t even a really bad situation – I know people who are much worse off, and I feel guilty about whining over a relatively minor thing. But I can’t help it, this is how I feel. I hate it. I don’t know what to do, how to change myself to get over these feelings. Can anyone offer any advice? I sure need some.

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Look at the other one.  It’s cute and sexy. This is difficult both for you and for her.  At first she is going.to feel that no-one would want her looking like this, and you are going to feel turned off by her mutilation.  BUT these feelings can pass and desire will return.  You will both get used to her new shape in time, and more easily once the bruising goes down.  Please don’t feel ashamed of how your body reacts, this is perfectly natural, but do give it time to come to terms with the situation.  The thing to feel ashamed of would be walking away from her when she needs you most, just for lack of patience. Once upon a time it was a hot day and we found ourselves passing a bridge where the river had been dredged to make a bathing area.  On impulse we stopped, stripped to minimal clothes and took a dip.  As we swam and played in the water I realised that the sight of her one large braless breast floating under her thin wet blouse was seriously turning me on, and I really wanted to make love to her there and then.  Unfortunately this was a family trip, so "not in front of the children" and I had to wait. I suppose it took me about six months to get used enough to the scarring where her left breast used to be that I would caress it when we made love. It took her longer to accept it. You can do this.  You didn’t marry her tits.  We all age and suffer attrition to our bodies, at 36 we try not to think about it but it is there and it happens and we will have to face it sooner or later.  She is still the same woman. Good luck Tim Jackson

– Hide quoted text — Show quoted text – Hello everyone, I’m new to this group so please forgive me if I stumble over netiquette issues. My wife has breast cancer. I don’t remember the medical terms but it’s in her ducts and the doctor said it’s the most common type. She has had surgery to remove cancerous tissue in one breast, and some of her lymph nodes. She is in the tail end of a six-week-long radiation treatment, which is to be followed by five years of tamoxifen. She’s 36, and the doctor says that the reason they want to do such aggressive treatment is exactly because she’s so young – they want to make sure it doesn’t recur. All in all, I gather that hers seems to be a pretty successful case, as breast cancer cases go. I have every confidence that the doctor is doing what needs to be done. I am writing this post not because I am concerned for her life or her health, but because I am concerned about our marriage. To be blunt, I am afraid that I won’t be able to resume a normal sexual life with her because I am having a hard time with her changed appearance since her surgery. Her breast has big scars and is misshapen due to the tissue removal, and at present the whole area is also all bruised up and discolored from the radiation treatment. When I see her this way it is very hard for me to feel physical desire. I have never been good with blood or surgical procedures, and seeing her scarred breast actually makes me a little queasy. I love her dearly – we have been married more than 10 years and have three children together. She is everything to me. I feel so ashamed and angry at myself for not being able to get past her appearance. And I know that this isn’t even a really bad situation – I know people who are much worse off, and I feel guilty about whining over a relatively minor thing. But I can’t help it, this is how I feel. I hate it. I don’t know what to do, how to change myself to get over these feelings. Can anyone offer any advice? I sure need some.

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Question:

Yesterday was the first month anniversary death of my husband..He defeated pancreatic cancer by dying and so killing the monster as well. All the support has left and family have gone home. I will face a Christmas at home with a fireplace and my dog. Oh how I dread it. And following that will be my birthday and our would be 20th wedding anniversary. I am trying hard, but sometimes it is a very rough road. hugs to all. patty-anne

Patty-Anne, I am so sorry that you are having to go through Christmas alone this year.  My 3 year old daughter died of Wilms Tumor – a childhood kidney cancer – on the 23rd September, and so I too am dreading the holidays.  Not so much a Happy Christmas, but a Crappy Christmas for us I think. I have joined a Yahoo group for parents who’s children died of cancer, and it is what gets me through each day at the moment, talking with other people who truly understand.  There is a "grieving" mailing list at ACOR ( http://www.acor.org/ ) called "facing-ahead" which may provide a similar support for other bereaved people – it is a private list and so I cannot see what kind of topics are discussed without joining the list.  (I know that someone has mentioned ACOR before on this thread, but not this support group, ACOR is always worth a visit for anyone involved with cancer.)  The mailing lists work much like these news groups, except the emails come direct to your inbox, and they are for "members only" so they don’t get troubled by *salespeople*. I hope it is not as bad as we are anticipating. With you in thought, Harri T.

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Patty-Anne and Hari, I’m a member of two groups on ACOR and they have been incredibly helpful. I’m on the AML and Caregivers lists.  The people have been amazing. Yesterday was the first month anniversary death of my husband..He defeated pancreatic cancer by dying and so killing the monster as well. All the support has left and family have gone home. I will face a Christmas at home with a fireplace and my dog. Oh how I dread it. And following that will be my birthday and our would be 20th wedding anniversary. I am trying hard, but sometimes it is a very rough road. hugs to all. patty-anne

Patty-Anne, I am so sorry that you are having to go through Christmas alone this year. My 3 year old daughter died of Wilms Tumor – a childhood kidney cancer – on the 23rd September, and so I too am dreading the holidays.  Not so much a Happy Christmas, but a Crappy Christmas for us I think. I have joined a Yahoo group for parents who’s children died of cancer, and it is what gets me through each day at the moment, talking with other people who truly understand.  There is a "grieving" mailing list at ACOR ( http://www.acor.org/ ) called "facing-ahead" which may provide a similar support for other bereaved people – it is a private list and so I cannot see what kind of topics are discussed without joining the list.  (I know that someone has mentioned ACOR before on this thread, but not this support group, ACOR is always worth a visit for anyone involved with cancer.)  The mailing lists work much like these news groups, except the emails come direct to your inbox, and they are for "members only" so they don’t get troubled by *salespeople*. I hope it is not as bad as we are anticipating. With you in thought, Harri T.

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That is one thing that is consistent in this group, kindness. Thanks. I appreciate the offer. I have however two dogs that are still looking for Jim, so we will do our Christmas, such as it is, together. But hey if you ever want to visit West Coast Canada. Give me a shout. A stupid women emailed today saying**.  Have a beautiful Christmas with fond memories of Jim.  I am sure he his watching over you and smiling.  I know you will get through it too.** As if Jim would smile at the hell I go through. What any of us go through. Some folks shouldn’t be near computers. Love to all.. peace..patty-anne

– Hide quoted text — Show quoted text – Patty-Anne, If you live anywhere near Reno, Nevada, you would be welcome to spend the holidays with my wife and I.  Or, if you would just like to visit Reno. You would be welcome with open arms, and lots of love and kisses from us both. We also have a cheery fireplace, but no dog. Berky the Warrior Folie

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Tracy, Try looking through the web-sites listed on http://www.acor.org/ped-onc/hp/wilmspages.html , these are personal stories of children who have had or still have Wilms’, most sites give further links. Also  http://www.geocities.com/karemel5/wilms.html is the web-site of a lady who was treated for Wilms in 1954, also gives more links. Harri T. Mother of 3 1/2 yr-old with stage IV, unfavourable Wilms. – Hide quoted text — Show quoted text – My son was diagnosed in March with a Wilms tumor at the age of 5 1/2 months. It was a Stage I Favorable histology.  He will be receiving his last treatment 7/30 (as long as the MRI, CT Scans, and U/S come back normal). Has anyone had experience with this that may tell me any long term effects? He is being treated with combo vincristine and actinomycin-D. Thanks! Tracy

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I am interested to find how his scans come out. I personally hope they go well and pray for it too. Is a very hard thing to watch all this happening to your child I know. Did they have to take the kidney? I have researched wilm’s extensively. He will survive I am VERY sure. My son died from the unfavorable last month.(clear cell sarcoma) Took only 8Mo. one kidney, 2 rounds of chemo, 2 surgeries and radiation. He was only 10. Please let me know how it goes? I wish the best for your little one:) Thankyou, Frank in Little Rock

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Frank, I am so sorry to hear about your son.  It’s good to hear that you have faith to help you in this difficult time.  I think it’s sad when people have no faith that are dealt with a personal crisis. I read somewhere about a woman whose child was diagnosed with a stage I favorable, and she mentioned how many times people told her how "fortunate" she was that it was a Wilms.  She replied that she didn’t feel fortunate at all.  Well, of course I wish that my son had a perfect life with no complications (don’t we all?) but it is a fact: we ARE fortunate that our little Drew has a very treatable cancer.  I wouldn’t have said that on the fateful Friday morning that I barely remember when we first found out it was a Wilms, though. They did take his right kidney, but the tumor was completely encapsulated – nothing in the lymph nodes, so the doctors are very optimistic.  We had a little scare last week, they had found lesions on his liver and ordered an immediate ultrasound.  After consulting with our oncologist and a GI physician, we determined that it was not a tumor, nor did they think it was malignant.  The weird thing is that they weren’t your typical "spotty" lesions, but marbleized all over the liver.  Since they did not do a biopsy, I am fairly convinced that it was nothing significant.  They will be keeping an eye on it, though. Were you part of the Wilms Tumor Study Group.  What do you think of that? Finally, I can only imagine how difficult all those stages of treatment were for you and your son.  Just the chemotherapy has been almost more than we can stand (and my son has had almost no side effects).  I’ll let you know when the final results come in. Any links you can give me regarding Wilms I would appreciate, and I’ll pray for you. Tracy in Louisville

– Hide quoted text — Show quoted text – I am interested to find how his scans come out. I personally hope they go well and pray for it too. Is a very hard thing to watch all this happening to your child I know. Did they have to take the kidney? I have researched wilm’s extensively. He will survive I am VERY sure. My son died from the unfavorable last month.(clear cell sarcoma) Took only 8Mo. one kidney, 2 rounds of chemo, 2 surgeries and radiation. He was only 10. Please let me know how it goes? I wish the best for your little one:) Thankyou, Frank in Little Rock

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My son was diagnosed in March with a Wilms tumor at the age of 5 1/2 months. It was a Stage I Favorable histology.  He will be receiving his last treatment 7/30 (as long as the MRI, CT Scans, and U/S come back normal). Has anyone had experience with this that may tell me any long term effects? He is being treated with combo vincristine and actinomycin-D. Thanks! Tracy

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Question:

Congratulations..survivor!! It’s always good to hear this….I hope you are investing in other kids that are now in the fight. It would be nice to be able to give some of these tags, to other survivors.. There’s a frieind, who’s child just finished her treatment, on july 4th…so they celebrated two independance days! :) Robin…mom to hannah,aka "wild thing".1/17/98 – 9/1/00  wife to E….the other love of my life.

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I am a survivor of childhood cancer. It has been 17 years or so since my last chemo treatment. I have lived a very normal and great life thanks to the support of people like you guys, family and God. Now that I am 30 I reflect on it quite a bit. I feel as if I fought a war. I don’t want to ever forget the experience but I don’t want to dwell on it as well. So I started wearing Dog Tags that have my name and the type of cancer that I beat on them. I noticed that this helped me and many others that I ran into that beat cancer as well. So I am offering these to anyone who would like to order them. They are actual dog tags that a guy in VA makes for the military. You can have anything printed on them. 5 lines 14 spaces per line.I have my name and Wilms Tumor 1979 on them.  $20 per pair and that includes shipping and everything. If anyone would like a picture of them or

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Question:

when my husband was being treated for osteo-sarcoma with chemo, his kidneys showed signs of strain and was put on dialisis for a while. has this happened to anyone else?

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when my husband was being treated for osteo-sarcoma with chemo, his kidneys showed signs of strain and was put on dialisis for a while. has this happened to anyone else?

My five year old daughter has been fighting wilms’ tumor (kidney cancer) for the last three years. The chemo that she was on damaged her remaining kidney. The condition she has is called "renal tubal acidosis or post chemo Fanconi’s syndrome". Her kidney leaks electrolytes from her blood into her urine, so we must replenish the electrolytes several times a day. Hopefully she will grow out of it. Because the kidneys filter the blood, they are in direct contact with the chemo, and can suffer from it. Hopefully your husband’s condition is temporary.   best wishes and good luck     Randy Mulligan

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Question:

I have to agree with Laura.Childhood cancer is more of a problem than most people realize. My son is one of the lucky one’s.He was 9 months old when he was diagnosed with wilm’s tumor. He will turn six in July. People keep telling me it’s time to get over it and put it in the back of my mind.I can’t do that. I tell everyone I can about Nicholas.It’s not the most pleasant topic but a necessary one.I was shocked at how many kids have this disease. we must never stop talking about childhood cancer until we have a 100% cure rate in all types of cancer.

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I am the mother of a cancer survivor.It is five years this past may since his diagnosis. Nicholas will turn 6 the end of July. He was 9 months old when he was diagnosed with Wilm’s Tumor.I never thought it would happen to anyone I know ,at least of all my son.But as we all know this disease is non-discriminating.I’ve heard of kids as young as 2 days old being diagnosed with cancer and I think it is high time that more research is done for childhood cancer. It’s amazing of how many cancers there are that attack our kids every year.Until my son was diagnosed, I had never even heard of anything but leukimia.Now, I read everything I can .Anyone who is going through this now feel free to e-mail me, and KEEP THE FAITH.

Hi Cathy,  I am the father of a five year old girl who is also a survivor of wilms’ tumor. She was diagnosed when she was 2 1/2 years old. She finished treatment after six months, only to relapse two months later. She went through hell the second time around, and is still suffering some side effects from the treatment. The good news is that she has been off treatment for 1 1/2 years, and is still in remission. We used to have a little group of parents up at the hospital that would get together after the kids were asleep. We were our own little support group. I still can’t believe that my daughter is the only child left, out of eight. Childhood cancer, and all childhood diseases, seems to get a little more press up here in British Columbia. We have a huge three day telethon every year to raise funds for the Children’s Hospital, along with the Child Run and other fundraisers. I don’t know what we would do without all these good people. Glad to hear that Nicholas is doing well. It must feel great that he has reached the five year mark, and is presumably considered cured.Feel free to e-mail me at any time     Randy Mulligan

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My son Kenny is almost 4.  He was diagnosed right before Christmas of 96 with stage IV rhabdomyosaromca.   Kenny had been misdiagnosed a year prior when his biopsy slide was "misread" so we lost a whole year of treatment.   When people of think of cancer, they typically do not associate it with children.  However, CANCER is the number #1 killer of children between the ages of 2 – 15!!!  We lose 6 children a day to some form of cancer.  There will be some 9000 children diagnosed this year alone.  Do we ever hear any talk of it in the media?   Nope.  All we hear is how treatable childhood cancer has gotten.  What they fail to mention is the "after-effects" from the chemo and radiation to the child’s body.   Most of our children will never be able to have children.  I know my son has suffered balance and muscle control/coordination. We don’t even know if he is going to grow.   PLEASE!!! I urge anyone touched by cancer to walk in the MARCH in DC on 9/26th.  Almost every state will be represented with a Childhood Cancer Quilt.  We will be linking these quilts together to represent all the children who have fought, still fighting, or have died from this horrible disease. Sorry to be so long winded.  Please e-mail me for more info on the project, or for links associated with parents of children with cancer, or for Kenny’s awesome story. God Bless,

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Laura, My daughter died of Wilm’s tumor in March, and six of our young friends died since last December. A friend of mine is coordinating the quilt project in our city, and she got a quilt club to make a square for my daughter.  The problem is far worse than people know, but very few people care because they are just children.  Not a vocal political group.  The parents I know are taking on the problem and hopefully will get some more funding and attention as to what is causing this in our children. Colleen

– Hide quoted text — Show quoted text -My son Kenny is almost 4.  He was diagnosed right before Christmas of 96 with stage IV rhabdomyosaromca.   Kenny had been misdiagnosed a year prior when his biopsy slide was "misread" so we lost a whole year of treatment. When people of think of cancer, they typically do not associate it with children.  However, CANCER is the number #1 killer of children between the ages of 2 – 15!!!  We lose 6 children a day to some form of cancer.  There will be some 9000 children diagnosed this year alone.  Do we ever hear any talk of it in the media?   Nope.  All we hear is how treatable childhood cancer has gotten.  What they fail to mention is the "after-effects" from the chemo and radiation to the child’s body.   Most of our children will never be able to have children.  I know my son has suffered balance and muscle control/coordination. We don’t even know if he is going to grow. PLEASE!!! I urge anyone touched by cancer to walk in the MARCH in DC on 9/26th.  Almost every state will be represented with a Childhood Cancer Quilt.  We will be linking these quilts together to represent all the children who have fought, still fighting, or have died from this horrible disease. Sorry to be so long winded.  Please e-mail me for more info on the project, or for links associated with parents of children with cancer, or for Kenny’s awesome story. God Bless,

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Last night I attended our hospital parent bereavement group.  All but one them had lost their children to cancer. Every time I bring up the subject of more funding for childhood cancer research, I get irate  notes from those who think chidren do not deserve more funding because it will take away from adult research. I don’t understand this attitude at all.  You are very lucky to still have your son with you.  My daughter died of Wilm’s in March.  I will be atttending a conference in August that will hopefully give me more insight into what we can do, and a group of parents I know will be attending the March on Washington DC in September.  I can tell you one thing.  The parents I know will not stop until we get more funding, and any money we raise will go only to individuals who are researching cures for childhood cancer. Colleen – Hide quoted text — Show quoted text – I am the mother of a cancer survivor.It is five years this past may since his diagnosis. Nicholas will turn 6 the end of July. He was 9 months old when he was diagnosed with Wilm’s Tumor.I never thought it would happen to anyone I know ,at least of all my son.But as we all know this disease is non-discriminating.I’ve heard of kids as young as 2 days old being diagnosed with cancer and I think it is high time that more research is done for childhood cancer. It’s amazing of how many cancers there are that attack our kids every year.Until my son was diagnosed, I had never even heard of anything but leukimia.Now, I read everything I can .Anyone who is going through this now feel free to e-mail me, and KEEP THE FAITH.

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I am the mother of a cancer survivor.It is five years this past may since his diagnosis. Nicholas will turn 6 the end of July. He was 9 months old when he was diagnosed with Wilm’s Tumor.I never thought it would happen to anyone I know ,at least of all my son.But as we all know this disease is non-discriminating.I’ve heard of kids as young as 2 days old being diagnosed with cancer and I think it is high time that more research is done for childhood cancer. It’s amazing of how many cancers there are that attack our kids every year.Until my son was diagnosed, I had never even heard of anything but leukimia.Now, I read everything I can .Anyone who is going through this now feel free to e-mail me, and KEEP THE FAITH.

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Question:

As mentioned in a prior posting my 12 yr old daughter was diagnosed with Acute Lymphocytic Leukemia and Lymphoma (but the Doctors cannot tell me what type of Lymphoma).  Her body is not responding to the Chemotherapy as we had hoped and quite a few people have mentioned these Clinics in Mexico where they build up the immune system to help fight the cancer.  I have heard unbelievable stories but I don’t want to be a desperate mother who would believe anything but I do however have an open mind.  So, my questions are: Does anyone know about the Chelation Clinics in Mexico?  Has anyone gone there for treatments?  I would like to hear any stories  - good and bad or just your thoughts. Thank you. Nadine Saskatchewan, Canada

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I too would appreciate any information about the chelation treatments.  My 10 year old daugher has relapsed Wilms’ tumor and is not responding well to Phase II chemotherapy and radiation.  I am very interested in any alternatives.

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I too would appreciate any information about the chelation treatments.  My 10 year old daugher has relapsed Wilms’ tumor and is not responding well to Phase II chemotherapy and radiation.  I am very interested in any alternatives.

 Chelation of what?  EDTA chelates on to calcium, but what does it mean in this context?

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