Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Kenda, I'm delighted to hear you've decided against implants. That's one decision you'll never regret . . . If you have any second thoughts, please think of us. I think I can speak for all of us when I say that getting breast implants was the worst single decision we made in our lives. We're doing what we can to make a postitive experience out of it by helping others. It's always wonderful to know another woman won't have to go down that road. Please tell you friends! Hugs, Rogene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Hi and Welcome! As a mother of two boys that I breastfed, I totally can completely empathize with you regarding the change in your breasts. I too, had saggy breasts that my PS convinced me that implants would cure. After 3 surgeries for Capsular Contracture in less than a year, along with flu-like symptoms and fatigue, I decided to explant on March 17th, along with a full lift. How I wish I had gotten just the lift in the first place! They are exactly how I wanted them to be, and I would have saved thousands of dollars, as well as a lot of pain and heartache. I am so glad you found this site, and decided not to implant. I wish I had before I decided to have my implants. Best of luck to you! Cristinahomemadesoaper <kdskaggs@...> wrote: Hi Rogene,You are right, the voice in my head has been screaming at me to stop. I knew I wouldn't get support to get implants here, I wanted the truth because it seems few plastic surgeons give it. After reading here and talking to Dr. Melmed, I am totally convinced NOT to get implants. Since kicking fibro years ago and all the diseases I had along with it, I place much value in my health. Too much value to risk it for the sake of rounder breasts. Thank you for saving me from what so many of you are going through. You will never know how much I appreciate it.Kenda> Welcome . . . I'm sure you already know you won't be> encouraged to get implants here! Our ladies have had> ban experiences and stay around to help inform others.> > The most important, most powerful voice is that one in> your head that's telling you what you SHOULD do. . . > > Most of us heard it, and disregarded it.> > The nightmares that go with implants are too many to> list. Suicide is 4X's that among implanted women as> other plastic surgery patients . . . Is that enough to> know?> > Hugs and prayers,> > RogeneOpinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. "Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world." - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Hi Marie, I feel so lucky today, like someone (all of you and Dr. Melmed) saved me from a certain hell. Because I have had fibro and my ANA levels were elevated in the past, I am one who likely would develop autoimmune problems from implants. The plastic surgeons dismiss it and say that all of you would have had problems anyway. This is something I just couldn't accept. All of our bodies are different and some of us are more sensitive than others. To me that means that without the silicone trigger, you wouldn't have had the cause to get sick, it's simple cause and effect. My husband was never for the implant surgery, I had to push him into believing they were safe and that I would look and feel better with them -- something he never believed. Thank you so much for all the information you have given me and for posting publicly about your pain. You all have helped me more than you know. Kenda I am so > You should give yourself a pat on the back for doing such thorough research and finding this wonderful support group. > > I was in your situation in 2003. I researched implants and the pros and cons of them. I thought I knew what I was getting myself into. The plastic surgeons have a way of making everything sound so safe. The warning signs are all there but, " It will never happen to you " the saline implants are so safe. WRONG! > > I do hope you take the time to read some of the posts from some of the women on this site. If only I had found this site before my surgery last May, I would have saved myself a lot of heart ache...not to mention a lot of Hair! > > You see Kenda, I would consider myself one of the lucky ones. My only symptom is chronic hair loss. It is stated in the disclaimer you have to sign, but who would have thought it would happen to me. I have about 50% of the hair on my head that I had before implants. > > I had my implants in for only 9 Months and I had them removed. I put two and two together and knew that the implants were making my hair fall out. I also knew that if they were doing this to me this early on, what would my symptoms be like in a few months or a year from now? > > I am just trying to save you some grief. The implants only last between 7-12 years before you have to have them replaced. > They don't feel real while they are in your chest. > They make you very self conscience. > You have to massage them all of the time so you don't get capsular contraction. > Most likely you will have to have more than just one surgery. > You can't sleep on your stomach because you feel like you are balancing on two balls. > The list goes on and on! > > The most important thing is that you are taking a chance with your health. You might not get sick...or you might be just like one of us fighting for your health, and wishing you had those little boobs you had before the surgery. > > If your breasts are saggy from having babies, than I would highly recommend getting JUST a lift. It has done wonders for my breasts as they are as perky as a teenagers...just smaller. > > I love the way my breasts look now that I don't have those foreign objects tugging at my skin. I love that they are soft and fall like they are supposed to be. > > Save yourself the worry and not to mention the pain of implants. Love your body the way God made it. My vote would be NOT to get the implants! > > Do as you may, and know that we are all here for you. Ask as many questions as you need to before you make this decision. Best of Luck to you! > > Marie > > > New member > > > > Hi everyone, my name is Kenda and I am new to your list. I had an > initial > consultation with a plastic surgeon regarding breast implants. I am > 44 years old and > have wanted them for years. I am thin, 5'4 " , 100 pounds, and have > what I call 1/2 > breasts. After two pregnancies and breastfeeding, the upper outer > part of my > breasts are sunken. I went to three different plastic surgeons for > consults and all > were surprised that at my size I had as much breast tissue as I did > -- a perfect > candidate for implants! Excitedly I booked my surgery for 4/22. I > was happy about > my decision for less than a day and have been researching implants > for hours on end ever since. > > The reason I am here is that I want your opinions regarding saline > implant safety. > All of the doctors tell me there is NO risk and that the material > used is inert and the > fluid inside is saline water and will simply be absorbed by my body > if one should > rupture. After seeing your photos, I can't say that I'd want my body > to absorb that > fluid! I spoke with my ND and he said that if I ever had a positive > ANA test, I > should not have the surgery because I would be at a higher risk for > autoimmune > diseases. My current ANA is negative but two tests 12 and 10 years > ago I believe were > positive and speckled -- I'll have to have my ND interpret the tests for me when I > see him tomorrow. My health is not something I am willing to gamble for cosmetic > gain. I had fibromyalgia about 10 years ago and was very sick for about 5 years. I > beat it 5 years ago and don't ever want to feel that way again. Has anyone here > ever had their ANA tested either prior to > implantation or following? > > At this point in my life I am either going to go for it or put the > idea away > permanently. I am definitely leaning toward not having the surgery > but need the kick > in the butt from you who have already been there. I believe the doctors are lying to > me but also wonder if I am being paranoid. > > Thank you so much for your help. > > Kenda > > > > > > > Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. > > " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Hi Marie, I feel so lucky today, like someone (all of you and Dr. Melmed) saved me from a certain hell. Because I have had fibro and my ANA levels were elevated in the past, I am one who likely would develop autoimmune problems from implants. The plastic surgeons dismiss it and say that all of you would have had problems anyway. This is something I just couldn't accept. All of our bodies are different and some of us are more sensitive than others. To me that means that without the silicone trigger, you wouldn't have had the cause to get sick, it's simple cause and effect. My husband was never for the implant surgery, I had to push him into believing they were safe and that I would look and feel better with them -- something he never believed. Thank you so much for all the information you have given me and for posting publicly about your pain. You all have helped me more than you know. Kenda I am so > You should give yourself a pat on the back for doing such thorough research and finding this wonderful support group. > > I was in your situation in 2003. I researched implants and the pros and cons of them. I thought I knew what I was getting myself into. The plastic surgeons have a way of making everything sound so safe. The warning signs are all there but, " It will never happen to you " the saline implants are so safe. WRONG! > > I do hope you take the time to read some of the posts from some of the women on this site. If only I had found this site before my surgery last May, I would have saved myself a lot of heart ache...not to mention a lot of Hair! > > You see Kenda, I would consider myself one of the lucky ones. My only symptom is chronic hair loss. It is stated in the disclaimer you have to sign, but who would have thought it would happen to me. I have about 50% of the hair on my head that I had before implants. > > I had my implants in for only 9 Months and I had them removed. I put two and two together and knew that the implants were making my hair fall out. I also knew that if they were doing this to me this early on, what would my symptoms be like in a few months or a year from now? > > I am just trying to save you some grief. The implants only last between 7-12 years before you have to have them replaced. > They don't feel real while they are in your chest. > They make you very self conscience. > You have to massage them all of the time so you don't get capsular contraction. > Most likely you will have to have more than just one surgery. > You can't sleep on your stomach because you feel like you are balancing on two balls. > The list goes on and on! > > The most important thing is that you are taking a chance with your health. You might not get sick...or you might be just like one of us fighting for your health, and wishing you had those little boobs you had before the surgery. > > If your breasts are saggy from having babies, than I would highly recommend getting JUST a lift. It has done wonders for my breasts as they are as perky as a teenagers...just smaller. > > I love the way my breasts look now that I don't have those foreign objects tugging at my skin. I love that they are soft and fall like they are supposed to be. > > Save yourself the worry and not to mention the pain of implants. Love your body the way God made it. My vote would be NOT to get the implants! > > Do as you may, and know that we are all here for you. Ask as many questions as you need to before you make this decision. Best of Luck to you! > > Marie > > > New member > > > > Hi everyone, my name is Kenda and I am new to your list. I had an > initial > consultation with a plastic surgeon regarding breast implants. I am > 44 years old and > have wanted them for years. I am thin, 5'4 " , 100 pounds, and have > what I call 1/2 > breasts. After two pregnancies and breastfeeding, the upper outer > part of my > breasts are sunken. I went to three different plastic surgeons for > consults and all > were surprised that at my size I had as much breast tissue as I did > -- a perfect > candidate for implants! Excitedly I booked my surgery for 4/22. I > was happy about > my decision for less than a day and have been researching implants > for hours on end ever since. > > The reason I am here is that I want your opinions regarding saline > implant safety. > All of the doctors tell me there is NO risk and that the material > used is inert and the > fluid inside is saline water and will simply be absorbed by my body > if one should > rupture. After seeing your photos, I can't say that I'd want my body > to absorb that > fluid! I spoke with my ND and he said that if I ever had a positive > ANA test, I > should not have the surgery because I would be at a higher risk for > autoimmune > diseases. My current ANA is negative but two tests 12 and 10 years > ago I believe were > positive and speckled -- I'll have to have my ND interpret the tests for me when I > see him tomorrow. My health is not something I am willing to gamble for cosmetic > gain. I had fibromyalgia about 10 years ago and was very sick for about 5 years. I > beat it 5 years ago and don't ever want to feel that way again. Has anyone here > ever had their ANA tested either prior to > implantation or following? > > At this point in my life I am either going to go for it or put the > idea away > permanently. I am definitely leaning toward not having the surgery > but need the kick > in the butt from you who have already been there. I believe the doctors are lying to > me but also wonder if I am being paranoid. > > Thank you so much for your help. > > Kenda > > > > > > > Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. > > " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Hi Rogene, I am so thankful that all of you have made your voices heard so that some of us won’t endanger our health. It’s hard to discuss health issues with someone who has never been sick, they don’t seem to understand what it’s like. Having had fibro and other health issues, it’s a road I never want to go down again. My sister has 10 year-old silicone implants and has never had them checked out. She doesn’t understand my decision not to have the surgery. Nearly all of the women at the gym I go to have breast implants, it seems it’s the thing to do. I’ll remain a minority. Kenda Kenda, I'm delighted to hear you've decided against implants. That's one decision you'll never regret . . . If you have any second thoughts, please think of us. I think I can speak for all of us when I say that getting breast implants was the worst single decision we made in our lives. We're doing what we can to make a postitive experience out of it by helping others. It's always wonderful to know another woman won't have to go down that road. Please tell you friends! Hugs, Rogene Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Hi Cristina, The plastic surgeon said I don’t need a lift. Did you find someone other than the doc who implanted you to do the lift? I’m wondering if it would help for 1/2 breasts -- that’s what I call my breasts after breast feeding. Kenda Hi and Welcome! As a mother of two boys that I breastfed, I totally can completely empathize with you regarding the change in your breasts. I too, had saggy breasts that my PS convinced me that implants would cure. After 3 surgeries for Capsular Contracture in less than a year, along with flu-like symptoms and fatigue, I decided to explant on March 17th, along with a full lift. How I wish I had gotten just the lift in the first place! They are exactly how I wanted them to be, and I would have saved thousands of dollars, as well as a lot of pain and heartache. I am so glad you found this site, and decided not to implant. I wish I had before I decided to have my implants. Best of luck to you! Cristina homemadesoaper <kdskaggs@...> wrote: Hi Rogene, You are right, the voice in my head has been screaming at me to stop. I knew I wouldn't get support to get implants here, I wanted the truth because it seems few plastic surgeons give it. After reading here and talking to Dr. Melmed, I am totally convinced NOT to get implants. Since kicking fibro years ago and all the diseases I had along with it, I place much value in my health. Too much value to risk it for the sake of rounder breasts. Thank you for saving me from what so many of you are going through. You will never know how much I appreciate it. Kenda > Welcome . . . I'm sure you already know you won't be > encouraged to get implants here! Our ladies have had > ban experiences and stay around to help inform others. > > The most importa nt, most powerful voice is that one in > your head that's telling you what you SHOULD do. . . > > Most of us heard it, and disregarded it. > > The nightmares that go with implants are too many to > list. Suicide is 4X's that among implanted women as > other plastic surgery patients . . . Is that enough to > know? > > Hugs and prayers, > > Rogene Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Hi Sue, What type of products are you using to detox with? I have used so many over the years, I feel like an expert. Kenda Dear Kendra, Thanks for the reply its really kind of you to mention your ND, I live in England so its impossible for me but some of the ladies will find it useful, THANKYOU. I am so glad you have decided against implants, you are both lucky and clever to have researched things so well, if only 20 years ago I had the same opportunity to look into everything as you have done I would have my health. Keep well Kendra, I intend to keep dettoxing as much as I can. Keep intouch Sue. Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2005 Report Share Posted March 29, 2005 Kenda You sound like a very smart lady and I applaud your efforts to find out the truth. We all have heard the same old story about how saline implants aren't harmful. The hundreds of women on this site all with very similar stories prove otherwise. I never had my ana tested but, like you, I had fibromyalgia. I was diagnosed when I was 26 yr. old. Most of my symptoms weren't bad then--just annoying. They came and went and as long as I got my rest, it was no problem. When I was 35 I decided to get implants as I was terribly terribly flat and had always wanted to know what it would be like to actually have breasts. I had no shape whatsoever. None. My 2 sisters and best friend had gotten saline and assured me they were safe. As the years passed after I got implants, my fibromyalgia worsened. I had just about every symptom imaginable. I had more bad days than good, but never thought it was anything other than fibromyalgia. Then 4 years ago, over a few month period of time, my symptoms took on a sinister turn. I started developing many many new symptoms--frightening ones. My heart, skin, muscles, tendons, stomach, lungs, everything became involved. I had brain dysfunction so bad that I absolutely couldn't stand the way I felt. I kept hoping it would go away. I tried everything I knew to try. It didnt get better it got worse. I was scared to death I was dying. then God guided me to this site and I saw how similar my symptoms were to everyone elses. Immediately I scheduled an explant. Within weeks, my weirdest brain dysfunction left. I had to go on a therapy with antibiotics and have spent thousands of dollars to try and get better. I am much much better than I was. Even alot of my fibromyalgia symptoms are better (maybe they never were fibro symptoms. I mean most autoimmune diseases have many similar symptoms.) I still experience waxing and waning of fatigue, and muscle spasms mainly and I am trying hard to get the rest of my health back. I was diagnosed with Mixed Connective Tissue disorder which is an autoimmune disorder of unknown origin with features of more than one autoimmune disease. I had symptoms of lupus and scleroderma. This is what the implants did for me. And by the way, I have a negative ana. ANA's are helpful in diagnosing autoimmune illness, but not necessary to have one. Dr. don't seem to get that. YOu can die from an autoimmune illness like lupus, scleroderma, etc and still have a negative ana. But the fact that you had a positive ana at one time should be a neon sign flashing " DANGER, DANGER " to you. Your body is already sensitive that way. You are a very lucky lady if you overcame fibromyalgia and I guarantee you are playing with fire if you should get implants. Run, don't walk as far away from implants as you can get. And read the posts from many ladies here who are glad to have their small soft breasts back and be rid of those unnatural looking and feeling implants. Putting a foreign object in your body is just looking for trouble. Believe me, you will never regret not getting implants, but you may very well regret it if you do. The women on this group are just so happy to regain their health--- like you said, cosmetic appearance just means so little compared to health. So spend you money on a fabulous vacation instead. God bless. Hugs Kathy --- In , " homemadesoaper " <skaggs@c...> wrote: > > Hi everyone, my name is Kenda and I am new to your list. I had an > initial > consultation with a plastic surgeon regarding breast implants. I am > 44 years old and > have wanted them for years. I am thin, 5'4 " , 100 pounds, and have > what I call 1/2 > breasts. After two pregnancies and breastfeeding, the upper outer > part of my > breasts are sunken. I went to three different plastic surgeons for > consults and all > were surprised that at my size I had as much breast tissue as I did > -- a perfect > candidate for implants! Excitedly I booked my surgery for 4/22. I > was happy about > my decision for less than a day and have been researching implants > for hours on end ever since. > > The reason I am here is that I want your opinions regarding saline > implant safety. > All of the doctors tell me there is NO risk and that the material > used is inert and the > fluid inside is saline water and will simply be absorbed by my body > if one should > rupture. After seeing your photos, I can't say that I'd want my body > to absorb that > fluid! I spoke with my ND and he said that if I ever had a positive > ANA test, I > should not have the surgery because I would be at a higher risk for > autoimmune > diseases. My current ANA is negative but two tests 12 and 10 years > ago I believe were > positive and speckled -- I'll have to have my ND interpret the tests for me when I > see him tomorrow. My health is not something I am willing to gamble for cosmetic > gain. I had fibromyalgia about 10 years ago and was very sick for about 5 years. I > beat it 5 years ago and don't ever want to feel that way again. Has anyone here > ever had their ANA tested either prior to > implantation or following? > > At this point in my life I am either going to go for it or put the > idea away > permanently. I am definitely leaning toward not having the surgery > but need the kick > in the butt from you who have already been there. I believe the doctors are lying to > me but also wonder if I am being paranoid. > > Thank you so much for your help. > > Kenda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2005 Report Share Posted March 30, 2005 Kathy, Thank you so much for telling me about yourself. All of your stories have made my decision so much easier. I actually was happy today as I told my family and friends that the surgery was off — for good! I will call the plastic surgeon’s office tomorrow to cancel with him as well. It’s terrible how a lot of us feel that we would be more attractive or more womanly if we had larger breasts. I read a website that listed 48 reasons not to get breast implants. One of the reasons was would we (as women) look at a man with a penile implant as being more attractive. I had to laugh because it seemed so ridiculous, of course a man wouldn’t be more attractive with a penile implant. So what is it that made me think I would be more attractive with larger breasts. I was in my late 20’s when I was first diagnosed with fibro as well, much younger than the typical patient. My symptoms weren’t bad in the beginning, similar to the way you explain yours. In time, they were debilitating. Any time I would overdo something, like clean house too long or attempt to exercise, I would spend two weeks in bed. I now exercise at the gym three days a week with a trainer and take yoga lessons twice a week. I also cycle from time to time. All things I couldn’t do with fibro. I even went skiing for the first time in over 20 years last week. Fibro is difficult to kick but in time I believe each of you can and will. You all have so much determination and strength to get your health back. I admire each of you. Kenda Kenda You sound like a very smart lady and I applaud your efforts to find out the truth. We all have heard the same old story about how saline implants aren't harmful. The hundreds of women on this site all with very similar stories prove otherwise. I never had my ana tested but, like you, I had fibromyalgia. I was diagnosed when I was 26 yr. old. Most of my symptoms weren't bad then--just annoying. They came and went and as long as I got my rest, it was no problem. When I was 35 I decided to get implants as I was terribly terribly flat and had always wanted to know what it would be like to actually have breasts. I had no shape whatsoever. None. My 2 sisters and best friend had gotten saline and assured me they were safe. As the years passed after I got implants, my fibromyalgia worsened. I had just about every symptom imaginable. I had more bad days than good, but never thought it was anything other than fibromyalgia. Then 4 years ago, over a few month period of time, my symptoms took on a sinister turn. I started developing many many new symptoms--frightening ones. My heart, skin, muscles, tendons, stomach, lungs, everything became involved. I had brain dysfunction so bad that I absolutely couldn't stand the way I felt. I kept hoping it would go away. I tried everything I knew to try. It didnt get better it got worse. I was scared to death I was dying. then God guided me to this site and I saw how similar my symptoms were to everyone elses. Immediately I scheduled an explant. Within weeks, my weirdest brain dysfunction left. I had to go on a therapy with antibiotics and have spent thousands of dollars to try and get better. I am much much better than I was. Even alot of my fibromyalgia symptoms are better (maybe they never were fibro symptoms. I mean most autoimmune diseases have many similar symptoms.) I still experience waxing and waning of fatigue, and muscle spasms mainly and I am trying hard to get the rest of my health back. I was diagnosed with Mixed Connective Tissue disorder which is an autoimmune disorder of unknown origin with features of more than one autoimmune disease. I had symptoms of lupus and scleroderma. This is what the implants did for me. And by the way, I have a negative ana. ANA's are helpful in diagnosing autoimmune illness, but not necessary to have one. Dr. don't seem to get that. YOu can die from an autoimmune illness like lupus, scleroderma, etc and still have a negative ana. But the fact that you had a positive ana at one time should be a neon sign flashing " DANGER, DANGER " to you. Your body is already sensitive that way. You are a very lucky lady if you overcame fibromyalgia and I guarantee you are playing with fire if you should get implants. Run, don't walk as far away from implants as you can get. And read the posts from many ladies here who are glad to have their small soft breasts back and be rid of those unnatural looking and feeling implants. Putting a foreign object in your body is just looking for trouble. Believe me, you will never regret not getting implants, but you may very well regret it if you do. The women on this group are just so happy to regain their health--- like you said, cosmetic appearance just means so little compared to health. So spend you money on a fabulous vacation instead. God bless. Hugs Kathy --- In , " homemadesoaper " <skaggs@c...> wrote: > > Hi everyone, my name is Kenda and I am new to your list. I had an > initial > consultation with a plastic surgeon regarding breast implants. I am > 44 years old and > have wanted them for years. I am thin, 5'4 " , 100 pounds, and have > what I call 1/2 > breasts. After two pregnancies and breastfeeding, the upper outer > part of my > breasts are sunken. I went to three different plastic surgeons for > consults and all > were surprised that at my size I had as much breast tissue as I did > -- a perfect > candidate for implants! Excitedly I booked my surgery for 4/22. I > was happy about > my decision for less than a day and have been researching implants > for hours on end ever since. > > The reason I am here is that I want your opinions regarding saline > implant safety. > All of the doctors tell me there is NO risk and that the material > used is inert and the > fluid inside is saline water and will simply be absorbed by my body > if one should > rupture. After seeing your photos, I can't say that I'd want my body > to absorb that > fluid! I spoke with my ND and he said that if I ever had a positive > ANA test, I > should not have the surgery because I would be at a higher risk for > autoimmune > diseases. My current ANA is negative but two tests 12 and 10 years > ago I believe were > positive and speckled -- I'll have to have my ND interpret the tests for me when I > see him tomorrow. My health is not something I am willing to gamble for cosmetic > gain. I had fibromyalgia about 10 years ago and was very sick for about 5 years. I > beat it 5 years ago and don't ever want to feel that way again. Has anyone here > ever had their ANA tested either prior to > implantation or following? > > At this point in my life I am either going to go for it or put the > idea away > permanently. I am definitely leaning toward not having the surgery > but need the kick > in the butt from you who have already been there. I believe the doctors are lying to > me but also wonder if I am being paranoid. > > Thank you so much for your help. > > Kenda Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2005 Report Share Posted March 30, 2005 I used the same doctor who implanted me to remove the implants and capsules, and perform the lift at the same time. I am not sure if it would help you. My breasts were a B cup, but after breast-feeding, I lost a lot of tissue and had a lot of sag. My nipples also pointed down. With the lift, my nipples now are eye level, and the sag is gone. Luckily, I had a lot of tissue. I think I have ended up being a small B cup now. Before children I was a large B. I am fine with them though. . Kenda Skaggs <kdskaggs@...> wrote: Hi Cristina,The plastic surgeon said I don’t need a lift. Did you find someone other than the doc who implanted you to do the lift? I’m wondering if it would help for 1/2 breasts -- that’s what I call my breasts after breast feeding. :)Kenda Hi and Welcome! As a mother of two boys that I breastfed, I totally can completely empathize with you regarding the change in your breasts. I too, had saggy breasts that my PS convinced me that implants would cure. After 3 surgeries for Capsular Contracture in less than a year, along with flu-like symptoms and fatigue, I decided to explant on March 17th, along with a full lift. How I wish I had gotten just the lift in the first place! They are exactly how I wanted them to be, and I would have saved thousands of dollars, as well as a lot of pain and heartache. I am so glad you found this site, and decided not to implant. I wish I had before I decided to have my implants. Best of luck to you! Cristinahomemadesoaper <kdskaggs@...> wrote: Hi Rogene,You are right, the voice in my head has been screaming at me to stop. I knew I wouldn't get support to get implants here, I wanted the truth because it seems few plastic surgeons give it. After reading here and talking to Dr. Melmed, I am totally convinced NOT to get implants. Since kicking fibro years ago and all the diseases I had along with it, I place much value in my health. Too much value to risk it for the sake of rounder breasts. Thank you for saving me from what so many of you are going through. You will never know how much I appreciate it.Kenda> Welcome . . . I'm sure you already know you won't be> encouraged to get implants here! Our ladies have had> ban experiences and stay around to help inform others.> > The most importa nt, most powerful voice is that one in> your head that's telling you what you SHOULD do. . . > > Most of us heard it, and disregarded it.> > The nightmares that go with implants are too many to> list. Suicide is 4X's that among implanted women as> other plastic surgery patients . . . Is that enough to> know?> > Hugs and prayers,> > RogeneOpinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. "Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world." - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2005 Report Share Posted March 30, 2005 I don’t think there is anything that can be done with me, I’ll just have to learn to love me the way I am. I don’t have a droop, just not a nice round breast like before breastfeeding. Aging is tough! Kenda I used the same doctor who implanted me to remove the implants and capsules, and perform the lift at the same time. I am not sure if it would help you. My breasts were a B cup, but after breast-feeding, I lost a lot of tissue and had a lot of sag. My nipples also pointed down. With the lift, my nipples now are eye level, and the sag is gone. Luckily, I had a lot of tissue. I think I have ended up being a small B cup now. Before children I was a large B. I am fine with them though. . Kenda Skaggs <kdskaggs@...> wrote: Hi Cristina, The plastic surgeon said I don‚t need a lift. Did you find someone other than the doc who implanted you to do the lift? I‚m wondering if it would help for 1/2 breasts -- that‚s what I call my breasts after breast feeding. Kenda Hi and Welcome! As a mother of two boys that I breastfed, I totally can completely empathize with you regarding the change in your breasts. I too, had saggy breasts that my PS convinced me that implants would cure. After 3 surgeries for Capsular Contracture in less than a year, along with flu-like symptoms and fatigue, I decided to explant on March 17th, along with a full lift. How I wish I had gotten just the lift in the first place! They are exactly how I wanted them to be, and I would have saved thousands of dollars, as well as a lot of pain and heartache. I am so glad you found this site, and decided not to implant. I wish I had before I decided to have my implants. Best of luck to you! Cristina homemadesoaper <kdskaggs@...> wrote: Hi Rogene, You are right, the voice in my head has been screaming at me to stop. I knew I wouldn't get support to get implants here, I wanted the truth because it seems few plastic surgeons give it. After reading here and talking to Dr. Melmed, I am totally convinced NOT to get implants. Since kicking fibro years ago and all the diseases I had along with it, I place much value in my health. Too much value to risk it for the sake of rounder breasts. Thank you for saving me from what so many of you are going through. You will never know how much I appreciate it. Kenda > Welcome . . . I'm sure you already know you won't be > encouraged to get implants here! Our ladies have had > ban experiences and stay around to help inform others. > > The most importa nt, most powerful voice is that one in > your head that's tellin g you what you SHOULD do. . . > > Most of us heard it, and disregarded it. > > The nightmares that go with implants are too many to > list. Suicide is 4X's that among implanted women as > other plastic surgery patients . . . Is that enough to > know? > > Hugs and prayers, > > Rogene Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2005 Report Share Posted March 30, 2005 I hear you! . You know, after going through all this, I wish I had learned to love myself the way I was. It is a wonderful gift, but it would have been much easier, and much less expensive to love myself the way I was before the surgery, not after. Just wanted to let you know this, because I believe with all of my heart that you have made the right decision. Kenda Skaggs <kdskaggs@...> wrote: I don’t think there is anything that can be done with me, I’ll just have to learn to love me the way I am. I don’t have a droop, just not a nice round breast like before breastfeeding. Aging is tough! :)Kenda I used the same doctor who implanted me to remove the implants and capsules, and perform the lift at the same time. I am not sure if it would help you. My breasts were a B cup, but after breast-feeding, I lost a lot of tissue and had a lot of sag. My nipples also pointed down. With the lift, my nipples now are eye level, and the sag is gone. Luckily, I had a lot of tissue. I think I have ended up being a small B cup now. Before children I was a large B. I am fine with them though. . Kenda Skaggs <kdskaggs@...> wrote: Hi Cristina,The plastic surgeon said I don‚t need a lift. Did you find someone other than the doc who implanted you to do the lift? I‚m wondering if it would help for 1/2 breasts -- that‚s what I call my breasts after breast feeding. :)Kenda Hi and Welcome! As a mother of two boys that I breastfed, I totally can completely empathize with you regarding the change in your breasts. I too, had saggy breasts that my PS convinced me that implants would cure. After 3 surgeries for Capsular Contracture in less than a year, along with flu-like symptoms and fatigue, I decided to explant on March 17th, along with a full lift. How I wish I had gotten just the lift in the first place! They are exactly how I wanted them to be, and I would have saved thousands of dollars, as well as a lot of pain and heartache. I am so glad you found this site, and decided not to implant. I wish I had before I decided to have my implants. Best of luck to you! Cristinahomemadesoaper <kdskaggs@...> wrote: Hi Rogene,You are right, the voice in my head has been screaming at me to stop. I knew I wouldn't get support to get implants here, I wanted the truth because it seems few plastic surgeons give it. After reading here and talking to Dr. Melmed, I am totally convinced NOT to get implants. Since kicking fibro years ago and all the diseases I had along with it, I place much value in my health. Too much value to risk it for the sake of rounder breasts. Thank you for saving me from what so many of you are going through. You will never know how much I appreciate it.Kenda> Welcome . . . I'm sure you already know you won't be> encouraged to get implants here! Our ladies have had> ban experiences and stay around to help inform others.> > The most importa nt, most powerful voice is that one in> your head that's tellin g you what you SHOULD do. . . > > Most of us heard it, and disregarded it.> > The nightmares that go with implants are too many to> list. Suicide is 4X's that among implanted women as> other plastic surgery patients . . . Is that enough to> know?> > Hugs and prayers,> > RogeneOpinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. "Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world." - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 30, 2005 Report Share Posted March 30, 2005 I am truly happy today that I did make the decision I did. I take yoga lessons and really wish I could adopt a more yogic attitude about my body. I’m trying. Kenda I hear you! . You know, after going through all this, I wish I had learned to love myself the way I was. It is a wonderful gift, but it would have been much easier, and much less expensive to love myself the way I was before the surgery, not after. Just wanted to let you know this, because I believe with all of my heart that you have made the right decision. Kenda Skaggs <kdskaggs@...> wrote: I don’t think there is anything that can be done with me, I’ll just have to learn to love me the way I am. I don’t have a droop, just not a nice round breast like before breastfeeding. Aging is tough! Kenda I used the same doctor who implanted me to remove the implants and capsules, and perform the lift at the same time. I am not sure if it would help you. My breasts were a B cup, but after breast-feeding, I lost a lot of tissue and had a lot of sag. My nipples also pointed down. With the lift, my nipples now are eye level, and the sag is gone. Luckily, I had a lot of tissue. I think I have ended up being a small B cup now. Before children I was a large B. I am fine with them though. . Kenda Skaggs <kdskaggs@...> wrote: Hi Cristina, The plastic surgeon said I don‚t need a lift. Did you find someone other than the doc who implanted you to do the lift? I‚m wondering if it would help for 1/2 breasts -- that‚s what I call my breasts after breast feeding. Kenda Hi and Welcome! As a mother of two boys that I breastfed, I totally can completely empathize with you regarding the change in your breasts. I too, had saggy breasts that my PS convinced me that implants would cure. After 3 surgeries for Capsular Contracture in less than a year, along with flu-like symptoms and fatigue, I decided to explant on March 17th, along with a full lift. How I wish I had gotten just the lift in the first place! They are exactly how I wanted them to be, and I would have saved thousands of dollars, as well as a lot of pain and heartache. I am so glad you found this site, and decided not to implant. I wish I had before I decided to have my implants. Best of luck to you! Cristina homemadesoaper <kdskaggs@...> wrote: Hi Rogene, You are right, the voice in my head has been screaming at me to stop. I knew I wouldn't get support to get implants here, I wanted the truth because it seems few plastic surgeons give it. After reading here and talking to Dr. Melmed, I am totally convinced NOT to get implants. Since kicking fibro years ago and all the diseases I had along with it, I place much value in my health. Too much value to risk it for the sake of rounder breasts. Thank you for saving me from what so many of you are going through. You will never know how much I appreciate it. Kenda > Welcome . . . I'm sure you already know you won't be > encouraged to get implants here! Our ladies have had > ban experiences and stay around to help inform others. > > The most importa nt, most powerful voice is th at one in > your head that's tellin g you what you SHOULD do. . . > > Most of us heard it, and disregarded it. > > The nightmares that go with implants are too many to > list. Suicide is 4X's that among implanted women as > other plastic surgery patients . . . Is that enough to > know? > > Hugs and prayers, > > Rogene Opinions expressed are NOT meant to take the place of advice given by licensed health care professionals. Consult your physician or licensed health care professional before commencing any medical treatment. " Do not let either the medical authorities or the politicians mislead you. Find out what the facts are, and make your own decisions about how to live a happy life and how to work for a better world. " - Linus ing, two-time Nobel Prize Winner (1954, Chemistry; 1963, Peace) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 6, 2005 Report Share Posted April 6, 2005 Welcome, le!! My name is Marina. I live in Ohio, too. It has been wonderful today, I spent soo much time outside!! You are in the right place for support. This is a wonderful group to be a part of. My doctor told me the same thing, about finding a support group. Sounds like you are in the same boat as I am. I was diagnosed when I was 32, I'm now 34 (almost 35). The Ra has affected me in all the same areas as yours has. I hope things get better for you. Take care.....Marina > > > Hi! My name is le and I am new to this web site and to RA. My > Rheumatologist recommended I find a support group to talk to about > learning to deal with a chronic illness. There are not any meetings > in my area, so here I am searching the net for others like me. I am > 30 years old and I was diagnosed with RA 5 months ago. I am taking > methotrexate only right now but it is not working at all. My sed rate > is escalating and the pain is no better.She wants to add another > medication next month if there is no change. I can't remember the > name of it, but it is a drug that acts similarly to methotrexate. I > am a senior at Miami University-Ohio majoring in early childhood > education and it is truly a battle to get out of bed right now. I > think focusing on my education is keeping me going right now, and my > daughter who is 10. I find it hard to believe that I am having to > deal with this as young as I am. Last week I recieved a permanent > disability placard for my car, wow that was hard! But it made my > commute to the campus easier today. The walking was killing me! I > currently have RA in my hips, ankles, feet, knees (she thinks) and my > feet. I hope you all don't mind this long message, and I look forward > to talking with anyone who can relate and hearing helpful information > or about resources for learning how to cope. I am not coping very > well right now, and my husband doesn't acknowledge that I am sick and > suffering. I think it is because it is something he can't see. Hope > to hear from you, and I hope everyone is enjoying the beautiful > weather, at least it is in Ohio! le Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 6, 2005 Report Share Posted April 6, 2005 Hello, le My name is Angie. I also live in Ohio. Where exactly do you live I live in lin. I am 31 years old and have been diagnosed with RA for about 9 months I am currently on methotrexate, hydroxchoroquine, naproxen and prednisone for my RA I work in the early childhood field I teach 2 1'2 to 3 year old kids Some days are extremely hard to keep up with the kids I also have a sone who will be 10 in June. Welcome to the group you have came to a great place From Angie > > > Hi! My name is le and I am new to this web site and to RA. My > Rheumatologist recommended I find a support group to talk to about > learning to deal with a chronic illness. There are not any meetings > in my area, so here I am searching the net for others like me. I am > 30 years old and I was diagnosed with RA 5 months ago. I am taking > methotrexate only right now but it is not working at all. My sed rate > is escalating and the pain is no better.She wants to add another > medication next month if there is no change. I can't remember the > name of it, but it is a drug that acts similarly to methotrexate. I > am a senior at Miami University-Ohio majoring in early childhood > education and it is truly a battle to get out of bed right now. I > think focusing on my education is keeping me going right now, and my > daughter who is 10. I find it hard to believe that I am having to > deal with this as young as I am. Last week I recieved a permanent > disability placard for my car, wow that was hard! But it made my > commute to the campus easier today. The walking was killing me! I > currently have RA in my hips, ankles, feet, knees (she thinks) and my > feet. I hope you all don't mind this long message, and I look forward > to talking with anyone who can relate and hearing helpful information > or about resources for learning how to cope. I am not coping very > well right now, and my husband doesn't acknowledge that I am sick and > suffering. I think it is because it is something he can't see. Hope > to hear from you, and I hope everyone is enjoying the beautiful > weather, at least it is in Ohio! le Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 6, 2005 Report Share Posted April 6, 2005 Hello le, WELCOME! I am Jen in Fl and I was just diagnoised a few weeks ago. Havent been to the Specialist yet. I have found this group to be incrediably supportive and knowledgable. I have only been in the group myself for 3weeks. I have learned alot here. Hope you get to feeling better soon. Jen in Fl In Order To Live Life, You Must Enjoy Life. --------------------------------- Messenger Show us what our next emoticon should look like. Join the fun. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2005 Report Share Posted April 8, 2005 le, welcome to the group! I am so sorry that you are hurting. It's a lot to take in when you're first diagnosed. I remember when I got my handicapped placard- it felt like I was giving in to the disease on some level, which didn't make any sense but I still felt that way. I Do you think your hubby would maybe be interested in seeing what the Arthritis Foundation website says about your disease? It's very informative in my experience. Try to listen to your body, I know it seems like it's speaking a foreign language right now. Rest when you can. I know that's easy to say, but you have a pretty full plate even for a healthy person- going to college and raising a family. Talk to your doc about your pain level- does she know how severe it is? It is so important that we communicate with our docs. I am fortunate that mine encourages an open line between patient and doc. You are still so young- my 27 year old daughter is in the process of being tested- she is having extreme fatigue, joint pain everywhere she has a joint...and she is normally wonder woman- 3 kids, stay at home mom, a little dynamo- takes care of elderly neighbors, PTA president, avid gardener and crafter. Hang in there, try to stay positive, and know that we are all holding good thoughts and wishes for pain free days. This is such a great place for good information and for understanding hearts. God bless Jane --- In , " danielle8750 " <dlr12994@p...> wrote: > > > Hi! My name is le and I am new to this web site and to RA. My > Rheumatologist recommended I find a support group to talk to about > learning to deal with a chronic illness. There are not any meetings > in my area, so here I am searching the net for others like me. I am > 30 years old and I was diagnosed with RA 5 months ago. I am taking > methotrexate only right now but it is not working at all. My sed rate > is escalating and the pain is no better.She wants to add another > medication next month if there is no change. I can't remember the > name of it, but it is a drug that acts similarly to methotrexate. I > am a senior at Miami University-Ohio majoring in early childhood > education and it is truly a battle to get out of bed right now. I > think focusing on my education is keeping me going right now, and my > daughter who is 10. I find it hard to believe that I am having to > deal with this as young as I am. Last week I recieved a permanent > disability placard for my car, wow that was hard! But it made my > commute to the campus easier today. The walking was killing me! I > currently have RA in my hips, ankles, feet, knees (she thinks) and my > feet. I hope you all don't mind this long message, and I look forward > to talking with anyone who can relate and hearing helpful information > or about resources for learning how to cope. I am not coping very > well right now, and my husband doesn't acknowledge that I am sick and > suffering. I think it is because it is something he can't see. Hope > to hear from you, and I hope everyone is enjoying the beautiful > weather, at least it is in Ohio! le Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Hi Vera, I took Remicade and four days later experienced pancreatitis. Also had near death experience due to servere infections. It was discovered after remicade I had a non-cancerous stricture of the common bile duct. I don't believe the remicade was responsible for the stricture. However, I can tell you that it was probably the cause of the pancreatitis and most definitely the horrible infections. It was the infections that they told me were going to kill me. I did have surgery twice and that has helped. Although to this day I can not fight a simple cold. If I get a cold, virus, anything it will last for a long time and it will be hard to get over it. I had the flu a year and a half ago, it lasted over four weeks. I did call the people who makes remicade and they have advise me to never take it again. Of course it has never been a thought to that it again. Hope this helps, if need any more information just let me know. Lynn and Vera Penick wrote: > My name is Vera and I have joined your wonderful group. > > My husband has had RA since he was 27 and is now 71. His medications > stopped working so his Rheumatoligist suggested Remicade. After the first > infusion of Remicade he began having pain in his lower back then both legs > and the front of one thigh have become numb. He's been x-rayed and back > problems are ruled out. So the thinking is his problem is a side effect of > the Remicade. Any problems such as he's having are listed as possible side > effects in the litature. > > Have any of you experienced such side effects after you were given > Remicade?? Did it clear up over time?? > > Thank you, > Vera/Central Florida > > -- > No virus found in this outgoing message. > Checked by AVG Anti-Virus. > Version: 7.0.323 / Virus Database: 267.7.5/18 - Release Date: 6/15/2005 > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 2005 Report Share Posted June 17, 2005 Welcome, Vera! Sorry to hear that your husband is having such troubles. I don't recall anyone having symptoms like this with Remicade, but there have been a few similar reports with Enbrel in the group. How many infusions of Remicade has he had? How long after the first infusion did he notice the symptoms? Not an MD I'll tell you where to go! Mayo Clinic in Rochester http://www.mayoclinic.org/rochester s Hopkins Medicine http://www.hopkinsmedicine.org [ ] new member > My name is Vera and I have joined your wonderful group. > > > My husband has had RA since he was 27 and is now 71. His medications > stopped working so his Rheumatoligist suggested Remicade. After the first > infusion of Remicade he began having pain in his lower back then both legs > and the front of one thigh have become numb. He's been x-rayed and back > problems are ruled out. So the thinking is his problem is a side effect > of > the Remicade. Any problems such as he's having are listed as possible > side > effects in the litature. > > Have any of you experienced such side effects after you were given > Remicade?? Did it clear up over time?? > > Thank you, > Vera/Central Florida Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 2005 Report Share Posted June 17, 2005 Welcome to the group, Vera and ! You will find wonderful information, and meet lots of great people. I have never taken Remicade, but sure you will get some answers from other members. Hugs, Tawny --- In , " and Vera Penick " <vppp@c...> wrote: > My name is Vera and I have joined your wonderful group. > > > My husband has had RA since he was 27 and is now 71. His medications > stopped working so his Rheumatoligist suggested Remicade. After the first > infusion of Remicade he began having pain in his lower back then both legs > and the front of one thigh have become numb. He's been x-rayed and back > problems are ruled out. So the thinking is his problem is a side effect of > the Remicade. Any problems such as he's having are listed as possible side > effects in the litature. > > Have any of you experienced such side effects after you were given > Remicade?? Did it clear up over time?? > > Thank you, > Vera/Central Florida > > > > -- > No virus found in this outgoing message. > Checked by AVG Anti-Virus. > Version: 7.0.323 / Virus Database: 267.7.5/18 - Release Date: 6/15/2005 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2005 Report Share Posted June 20, 2005 Dear new member, Making the descion to have my implants removed was one of the hardest things I have ever had to do. But my Children and my family are way more important than my apperiences. I was so sick that my 16 year old son had to care for me as if I were an invalid. He also had to take on taking care of my 9 year old daughter who was struggling with dyslexia and trying to learn to read. My life consisted of going from the bed to the bathroom with help. If I pushed myself too hard I would end up on the floor and unable to get up. I had my implants for about 5 years. From the begining I was fatigued and just became sicker and sicker to the point that had become convinced that I was dying. My daughter told me today that she likes me "this way". When I asked her what she ment she explained that she liked that I was playing with her and not sleeping. Good luck to you with this difficult descion. lots of hugs and support, Toni__________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2005 Report Share Posted June 20, 2005 LADIES......PLEASE!!! Sports Rekindle the Rivalries. Sign up for Fantasy Football Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2005 Report Share Posted June 21, 2005 Hi new member, I just joined today. I understand how your feeling. Im finally starting to realize that i will probably have to take the implants out. Over the last two years i have done blood work to try and figure out what is wrong with me. My naturopath physician believes its the implants but i would just love for him to find somthing else wrong with me so we can just fix it. But all we can come up with is i am having immune system disorders, among other things. I dont know if you have already tried doctors but maybe ruling some other things out first will help you realize what you need to do. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 22, 2005 Report Share Posted June 22, 2005 - Hi Diane and welcome to our group. Your rheumy isn't much different from most of the doctors who spout the same party line--implants don't cause autoimmune disease. Undoubtedly they do, and the amount of women who come to this site who were well until they got implants is staggering. Also, when these women get explanted they tend to get better. There are plastic surgeons who believe that implants cause women to get sick--among them Dr. Feng, Dr. Melmed and Dr. Kolb. They do alot of explants on women from this group and they do an excellent job. Please feel free to ask any questions you might have and we will help you in anyway we can. Hugs, kathy -- In , " fantasyworld_31501 " <taco@w...> wrote: > hello, > my name is diane and i saline implants after taking out the silicone. > i have been having problems with my health since getting the implants > in my late 20's. i have fibromyalgia, cfs, arthritis, immune problems, > and much more. i worked 20 years as a nurse in a busy emergency room. i > am now totally disabled at the age of 49..the sad thing about being > sick is remembering when i was well..my rheu. dr. says there is no > connection with the implants and these diseases, but i disagree. i > never ever had any problem my whole life until i got the implants..but > hey guys so glad to meet all of you and join this group.i am from ga > where its hot hot hot and the godzilla skeeters live.. > diane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 24, 2005 Report Share Posted June 24, 2005 Hello Shirley and welcome, You have come to a place where many people can show you a spirit of courage you won't believe. My hat is off to them and my heart goes out to them. I am one of the lucky ones. Got RA at 58 and so far have a mild case. Are there doctors who specialize in pain management in your area? Perhaps if so, one of them might be able to make you somewhat more comfortable. Kathy in Ct [ ] NEW MEMBER HELLO EVERYBODY AND KK, I JUST WANTED TO SAY HELLO. I DONT HAVE RA(I DONT THINK) BUT KIM SAID I SHOULD JOIN YOUR GROUP. SO HERE GOES.. I AM 49, MARRIED, AND AT 47 YRS HAD MY WHOLE LIFE AHEAD OF ME.. I MEAN I HAD IT ALL. MY HUSBAND AND I HAD OUR OWN SEMI TRUCK, MAKING A VERY COMFORTABLE LIVING, 175K PLUS, WERE TOGHETHER 24/7, GETTING PAID TO BE ON VACATION YEAR ROUND, THE WHITE HOUSE, MISSING THE PICKET FENCE, TWO DOGS TO REPLACE THE CHILDREN I COULD NOT HAVE...ECT...ECT... ON MAY 5, 2003 LIFE AS WE KNEW IT HIT THE FAN. WE WERE DELIVERING A LOAD OF HOUSEHOLD GOOD (MOVING IN A GREAT MILITARY FAMILY) WHEN I BENT OVER TO UNWRAP A PIECE OF FURNITURE, WHEN SOMETHING IN MY BACK SNAPPED, INSTANT AND SEVER PAIN. TO MAKE THIS VERY LONG STORY SHORT, I HAD HERNIATED L4-L5 (DOUBLE HERNIATION, WHICH MEANS I BLEW OUT BOTH SIDES OF THE SAME DISC). I WAS SEEN @ OUR GREAT ER HERE(HA!HA!) AND THE DR TOLD ME NOTHING WAS BROKEN AND TO RETURN TO WORK THE FOLLOWING DAY. I WENT TO SEE MY FAMILY DR, WHO ACTED AS IF I JUST WANTED SOME TIME- OFF ON WC. THIS WAS ON A TUESDAY. HE SET UP PT AND HAD ME RETURN ON FRIDAY, AS HE WAS GOING ON VACATION!! PT WAS CAUSING EVEN MORE PAIN, AND I JUST HURT ALL THE TIME. ON FRIDAY HE SET UP AN MRI AND SAID TO COME BACK A WEEK FROM MONDAY, BUT CONTINUE PT!!! MRI THE FOLLOWING TUESDAY REVEALED THE HERINATED DISC. WAS CALLED FROM DR'S OFC TO TELL ME TO DO NOTHING, NOT EVEN SNEEZE IF AVOIDABLE AS I COULD PARALIZE MYSELF AND THEY WERE SETTING UP APPT WITH NEUR SURGEON. I WAITED TIL SAW MY DR THE FOLLOWING MONDAY, AT WICH TIME HIS ATTITUDE TOWARDS ME HAD CHANGED. COMPLETE 360... SAW NEUR SURGEON ON WED, OF THE SAME WEEK, HAD SURGERY ON THURS. FOR ABOUT 3-4 MOS I WAS DOING GREAT. LIFE WAS GOOD!! THEN MY WORLD CRASHED AGAIN. I STARTED HAVING SEVERE PAIN SHOOTING DOWN MY LEGS AND SEVERE PAIN IN MY TAILBONE, ESPECIALLY WHEN HAVING BM. WENT BACK TO NEUR DR AND HAD SECOND MRI,WICH REVEALED DISC DESICCATION AT L3-4, L4-5, AND L5-S1, AND LUMBAR SPINAL STENOSIS. AT THIS TIME HE SET UP FCA AND SPINAL EPIDURAL STERIOD INJECTION, WHICH WERE DONE TWICE WITH LITTLE COMFORT. AFTER THE FCA I SAW THE NEUR SERGEON AND WAS TOLD THAT THERE WAS NOTHING THAT COULD BE DONE, AT WHICH TIME I ASKED FOR A SECOND OPINION, ALSO TURNED OUT TO BE A JOKE, BUT I WENT TO WICHITA,KS TO SEE ANOTHER NEUR DR WHO BASICALLY TOLD ME HE COULD OPERATE AGAING, BUT WAS 50/50 BE PARALIZED AND ONLY 25% DO ANYTHING FOR MY PAIN, AND OH YEAH, 2YR RECOVERY TIME AND MUST QUIT SMOKING FIRST. NOT VERY GOOD ODDS. IN FEB 04 I WAS RELEASED BY NUER SERGEON, TOLD I WAS TOTALLY DISABLED, AND GO HOME AND LEARN TO LIVE WITH THIS PAIN. I AM CURRENTLY TAKING SOMA 350MG(3X DAILY), 1 OR 2 LORTAB 10/500MG. I TRIED NEURONTIN, BUT SIDE EFFECTS WERE TERRIBLE. I AM IN SEVERE PAIN ALL THE TIME, I CANNOT SIT OR STAND FOR ANY LENGTH OF TIME WITHOUT VERY SEVERE PAIN. HOW DOES A PERSON COPE WITH THIS? ANY AND ALL COMENTS WILL BE GREATLY APRECIATED!!! OH, AT THIS TIME I HAVE APPLIED FOR SSD, HUSBAND MAKES TOO MUCH MONEY FOR SSID, EVEN THOUGH WE HAVE LOST OUR TRUCK AND HAD TO FILE BANKRUPTCY!!! I AM VERY DEPRESSE MOST DAYS. PLEASE HELP ME!!!!!!!!! Quote Link to comment Share on other sites More sharing options...
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