Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Sondra I still have periods after having that procedure done. They are much lighter now then before. I was very sore for about a week after. It was not to bad to deal with. Pennie Abby's mom **************A Good Credit Score is 700 or Above. See yours in just 2 easy steps! (http://pr.atwola.com/promoclk/100126575x1218822736x1201267884/aol?redir=http://\ www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=fe bemailfooterNO62) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Sondra I still have periods after having that procedure done. They are much lighter now then before. I was very sore for about a week after. It was not to bad to deal with. Pennie Abby's mom **************A Good Credit Score is 700 or Above. See yours in just 2 easy steps! (http://pr.atwola.com/promoclk/100126575x1218822736x1201267884/aol?redir=http://\ www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=fe bemailfooterNO62) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 there was of words here on a procedure that is of for females of the uterine but forget of the words of it but this day my medical shared he wanted to do this option for me and once he shared of its name to me it caused me to have of memory of here on this same things. abilations things? he to say to me it is of advancing and is of more safe and such than doing of a hystorectomy due to the many female issues i to have. He to also shared he felt i to had of a yeast issues and also fungus issues, because of the need to wear of pads so much it builded of moisture in a bad way which allowed of fungus to be of to develop there and thus the reason for so much itching there. so now have of to take of medicine to get rid of that. but on the abilation things did any have of it done and how painful was of it, he wants of to put me in to the outpatient to have of it done in a facility due to the my multiple health issues and sedate of me to do it so to minimize of the painful issues it might cause of me. but was of wondering if any had of it and how long you were of to hurt afterwards? sondra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Debi I think when I had it done it was a fairly new procedure. My OB said it was something that he had been doing for a short while. I had never heard of it before he mentioned it. Pennie Abby's Mom **************A Good Credit Score is 700 or Above. See yours in just 2 easy steps! (http://pr.atwola.com/promoclk/100126575x1218822736x1201267884/aol?redir=http://\ www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=fe bemailfooterNO62) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Debi I think when I had it done it was a fairly new procedure. My OB said it was something that he had been doing for a short while. I had never heard of it before he mentioned it. Pennie Abby's Mom **************A Good Credit Score is 700 or Above. See yours in just 2 easy steps! (http://pr.atwola.com/promoclk/100126575x1218822736x1201267884/aol?redir=http://\ www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=fe bemailfooterNO62) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Debi I never had any problems with my periods till I went on birth control pills. Sure my period was regular but I was sick all the time on those stupid things. There is not enough money in the world to get me to go on those things again. Pennie **************A Good Credit Score is 700 or Above. See yours in just 2 easy steps! (http://pr.atwola.com/promoclk/100126575x1218822736x1201267884/aol?redir=http://\ www.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=fe bemailfooterNO62) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Sondra, I see answered about the ablation thing. I have not had it done, my doctor wants me to get it done. So I cannot say on the pain issue. The brochure he gave me shows the balloon method which is smaller than the palm of my hand. It probably gets bigger once the solution is added. With all your issues, you might be a very good candidate for it. Debi - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 I'm thinking about trying hormones. It scares me though because of my being almost 38, having high bp, and being all around nasty when on the pill before. But that was about 15 yrs ago, I'm hoping the pills he just gave me will be better. Last time I had this problem I was a young adult with no health insurance, I went on the pill for about 1 1/2 yrs, it helped reduce my periods for years. About time they started getting bad again I had kids. That helped tremendously but over time it's been getting worse. Since my surgery it's significantly escalated, don't know why. I have gotten off my metformin schedule, that may be part of it. It's always something. Debi - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 I'm thinking about trying hormones. It scares me though because of my being almost 38, having high bp, and being all around nasty when on the pill before. But that was about 15 yrs ago, I'm hoping the pills he just gave me will be better. Last time I had this problem I was a young adult with no health insurance, I went on the pill for about 1 1/2 yrs, it helped reduce my periods for years. About time they started getting bad again I had kids. That helped tremendously but over time it's been getting worse. Since my surgery it's significantly escalated, don't know why. I have gotten off my metformin schedule, that may be part of it. It's always something. Debi - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 pennie i to feel the same about the pill they maked of me so very very sick within the first 24 hours would begin of the vomitting and would be to do this for hours and hours and be of so weak and not able to sit or do anythings for days from it. Often end to hospital for dehydrations from it. sondra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 HERE HERE Pennie!! LOL I was so ill all the time when I was on BC, granted it was nearly 18 years ago that I last tried any and I know they claim to have advanced, but it was too bad for me. I had the Noraplant put in when I was 16 after having a early start on kids and they actually ended up removing it during an ER visit I was so sick. Theresa > > Debi I never had any problems with my periods till I went on birth > control > pills. Sure my period was regular but I was sick all the time on those > stupid > things. There is not enough money in the world to get me to go on those > things > again. > > Pennie > **************A Good Credit Score is 700 or Above. See yours in just 2 easy > > steps! > ( > http://pr.atwola.com/promoclk/100126575x1218822736x1201267884/aol?redir=http://w\ ww.freecreditreport.com/pm/default.aspx?sc=668072%26hmpgID=62%26bcd=fe > bemailfooterNO62) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Exactly the same experience for me. Horrific! It makes me wonder how many lies are told by the pharmaceutical companys who ignore how sick they make us feel. We are only a few women here and yet agree that we have had this reaction. They sure must liberally alter their statistics. . -- Re: debi pennie i to feel the same about the pill they maked of me so very very sick within the first 24 hours would begin of the vomitting and would be to do this for hours and hours and be of so weak and not able to sit or do anythings for days from it. Often end to hospital for dehydrations from it. sondra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 My primary problem was, for lack of a better word, extreme bitchiness. Hubby used to say he'd rather have 10 kids than live with me on BC pills. That and my heart seemed to flutter quite a bit. They made my periods far lighter, though. I guess compared with irregular periods, not bad side effects, huh? Maybe since I'm so grumpy these days they will make me nice? Lol, Debi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 One of my best friends got noraplant on medicaid after her son was born. She bled every day for the entire 5 years. Since that was her only form of insurance they refused to remove it, but she didn't complain to the doctors much. I would have been in the office every day til they got it out. She used to say it worked as BC because it made her so gross (from the bleeding) no man would want her. Lol. Debi - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 One of my best friends got noraplant on medicaid after her son was born. She bled every day for the entire 5 years. Since that was her only form of insurance they refused to remove it, but she didn't complain to the doctors much. I would have been in the office every day til they got it out. She used to say it worked as BC because it made her so gross (from the bleeding) no man would want her. Lol. Debi - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Debi the sad is that many of you here can describe of the issues and such but many with spectrum cannot so this is of why so much fear to subject of our kids to medications as they cant say things like it makes of my heart do strange things, it maked me feel as if it were of flip flopping inside of me, but back then did not have of words for it but the sensation caused of me to feel intense anxiety and panic in me because it was overwhelming to have of that sensation and because had no words to say of it I to reacted in SIB sorts of things. I ot use of to bite of my hand much by my wrist and thumb area or the outside of my thumb and palm areas not sure of exactly how to describe of it. I to bit of self for years and not once did I to say to my thinking bite self ... it just came as a reaction or response impulsively. that would also be on one of the reports as an adult person when read of a file of me under mental health. I to use to bite until some of the areas of my thumb area was of bruised and sort of thick there. now it is of rare for me to bite to self but if in much distress and then will have interventions to me for this reaction. the one that is of still prevelant to me much is of the hitting of self and pinching of self and self scratching. but anyways back to topic , I to be of just so much worry over the use of some things for children of autism and or those with no verbal or low verbal to be on so much as they cant say what is of affecting them or how. it has to be of much scary to them to feel things and not have ways to communicate of it. another things is ever since little often have of low blood sugar drops but did not know of the words to that and did not know what was happening to me as my body just suddenly felt like it was of having earth quakes inside of me. and the sensation of hunger was not related as hunger so did not know to fix this sensation was of to eat it just shut of me down more and more until so weak and sick to my tummy I to just lay of there staring off , they just thinked maybe " thank goodness she is of quiet and being still " lol so them it was of maybe a brief time of respite for the family LOL but they had of no clue to what was really going on. the same way when my colitis was of really flaring up much... I to forget of what caused of the family of me to take of me to the medical for the tummy but was of around the age of 13 or so , around the same time as the more pronounced crisis levels of SIB was happening so maybe that triggered the doctor to do medical testing. not sure though. but anyways so much physical pains and such as a kid and not the words to tell of it and then when in that crisis time they tended to not know and actually were of overdosing me over and over on many things. Espeically the thoriazine was of a much bad drug things for me. it sadated of me greatly but then it caused surges of panic and agitations. the only thing that was of right about the one mental ward was on is you had to go to the nurse door and stand of there to get of the medications and she would be of to say the names of the medications as she gave each one to you. this is of how I to learned of the names of them. but the thorazine was of a liquid things to me and also I to think was of what was injected by shot into me when escalated.this I to not knwo for sure but somethings in my memory tells me this. so how can we know when we try of things that the medical say is of okay , it might be of okay for NS/NT females who can speak but what about us with autism who have very different biomedical wiring as well as different brain wirings, and may not have of the words to say of how the medications are of affecting us. scary indeed. this is of not just for medications but even for me some supplements and things and or vitamins or minerals have caused of me issues such as cant take any iron of any level or fashions. also some of them put me into much severe mental fogs and jumbles up my words. so it is for the life of me is just because seem to be of doing well at times does not indicate of the truth, and just because in the begin I to not seem to be of doing well on a new things does not mean it is of wrong for me so this is of the complexities of autism. it is of always a guessing game. one things though is of the best things one of my past mental health people shared to me was of power naps. it is of the best medicine for me... it gives my brain and internal states a break and down time for a recover time. the key is not to rest or sleep more than an hour, but best for only 30 minutes or so. if I to sleep more than an hour it will have of a negative affect and cause of me to be of loopy and agitated because now want to rest longer because the rest was of too long and now the body of me wants to sleep longer because make of self too rested inside. sondra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Debi the sad is that many of you here can describe of the issues and such but many with spectrum cannot so this is of why so much fear to subject of our kids to medications as they cant say things like it makes of my heart do strange things, it maked me feel as if it were of flip flopping inside of me, but back then did not have of words for it but the sensation caused of me to feel intense anxiety and panic in me because it was overwhelming to have of that sensation and because had no words to say of it I to reacted in SIB sorts of things. I ot use of to bite of my hand much by my wrist and thumb area or the outside of my thumb and palm areas not sure of exactly how to describe of it. I to bit of self for years and not once did I to say to my thinking bite self ... it just came as a reaction or response impulsively. that would also be on one of the reports as an adult person when read of a file of me under mental health. I to use to bite until some of the areas of my thumb area was of bruised and sort of thick there. now it is of rare for me to bite to self but if in much distress and then will have interventions to me for this reaction. the one that is of still prevelant to me much is of the hitting of self and pinching of self and self scratching. but anyways back to topic , I to be of just so much worry over the use of some things for children of autism and or those with no verbal or low verbal to be on so much as they cant say what is of affecting them or how. it has to be of much scary to them to feel things and not have ways to communicate of it. another things is ever since little often have of low blood sugar drops but did not know of the words to that and did not know what was happening to me as my body just suddenly felt like it was of having earth quakes inside of me. and the sensation of hunger was not related as hunger so did not know to fix this sensation was of to eat it just shut of me down more and more until so weak and sick to my tummy I to just lay of there staring off , they just thinked maybe " thank goodness she is of quiet and being still " lol so them it was of maybe a brief time of respite for the family LOL but they had of no clue to what was really going on. the same way when my colitis was of really flaring up much... I to forget of what caused of the family of me to take of me to the medical for the tummy but was of around the age of 13 or so , around the same time as the more pronounced crisis levels of SIB was happening so maybe that triggered the doctor to do medical testing. not sure though. but anyways so much physical pains and such as a kid and not the words to tell of it and then when in that crisis time they tended to not know and actually were of overdosing me over and over on many things. Espeically the thoriazine was of a much bad drug things for me. it sadated of me greatly but then it caused surges of panic and agitations. the only thing that was of right about the one mental ward was on is you had to go to the nurse door and stand of there to get of the medications and she would be of to say the names of the medications as she gave each one to you. this is of how I to learned of the names of them. but the thorazine was of a liquid things to me and also I to think was of what was injected by shot into me when escalated.this I to not knwo for sure but somethings in my memory tells me this. so how can we know when we try of things that the medical say is of okay , it might be of okay for NS/NT females who can speak but what about us with autism who have very different biomedical wiring as well as different brain wirings, and may not have of the words to say of how the medications are of affecting us. scary indeed. this is of not just for medications but even for me some supplements and things and or vitamins or minerals have caused of me issues such as cant take any iron of any level or fashions. also some of them put me into much severe mental fogs and jumbles up my words. so it is for the life of me is just because seem to be of doing well at times does not indicate of the truth, and just because in the begin I to not seem to be of doing well on a new things does not mean it is of wrong for me so this is of the complexities of autism. it is of always a guessing game. one things though is of the best things one of my past mental health people shared to me was of power naps. it is of the best medicine for me... it gives my brain and internal states a break and down time for a recover time. the key is not to rest or sleep more than an hour, but best for only 30 minutes or so. if I to sleep more than an hour it will have of a negative affect and cause of me to be of loopy and agitated because now want to rest longer because the rest was of too long and now the body of me wants to sleep longer because make of self too rested inside. sondra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 I think what you describe is why we parents have to be so very careful to monitor our kids when ever we give them something. It's definitely not always easy. I don't know how you can find communicative ways of expressing how something is making you feel. To me the good/bad, better/worse might be good. But like with Allie & her food stuff I would question whether the med is making her feel good/bad or if she doesn't like the taste of something. That's another hard thing to overcome. With biting & hitting, have you ever tried to replace the behavior? Like having some chew tubes/bracelet to wear so when you feel the urge to bite instead of doing it to self you do it to the bracelet. That way you still get the benefit if the bite, but without the harm. Same with hitting, maybe find some simple something you could hook to your clothes so you could slap it instead. I'm thinking immediately a tambourine, but that wouldn't be to socially appropriate in public. I have experienced the same thing with low glucose & with power naps. I used to feel really shaky & start cramming down food but I never knew why. Since I struggled with weight in middle/high school I figured I was a freak. Now I realize I probably had borderline diabetes for many of those years. But what scares me now is that when I start having a low I get almost rage-like without knowing it's the sugar. It really scares me sometimes how ugly I can be with hubby and sometimes even the kids, I start yelling at them about silly stuff. To make it worse, they can see a low before me & tell me I'm having a low, then I'm so angry I get angry at them for saying that to me because I'm not being rational. Once we figured it all out I've worked really hard to maintain my sugar 'cause it's sure not fair to kids for their mamma to be yelling at them because I've so poorly planned/cared for my body's needs. I keep those glucose liquid drinks and tablets on hand. It's difficult to because I'm trying so hard to lose weight and when I get a low I want to eat and eat things I shouldn't and then it makes the weight loss even more difficult. with the glucose drink/tablets I can take a couple, count them as a point on my Weight Watchers, and they work much, much faster than regular food. I can doze off for 15-30 minutes & feel so refreshed but if I sleep much longer I'm so ill the rest of the day. I don't know what that is, perhaps it messes up our brain waves somehow? Debi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 I think what you describe is why we parents have to be so very careful to monitor our kids when ever we give them something. It's definitely not always easy. I don't know how you can find communicative ways of expressing how something is making you feel. To me the good/bad, better/worse might be good. But like with Allie & her food stuff I would question whether the med is making her feel good/bad or if she doesn't like the taste of something. That's another hard thing to overcome. With biting & hitting, have you ever tried to replace the behavior? Like having some chew tubes/bracelet to wear so when you feel the urge to bite instead of doing it to self you do it to the bracelet. That way you still get the benefit if the bite, but without the harm. Same with hitting, maybe find some simple something you could hook to your clothes so you could slap it instead. I'm thinking immediately a tambourine, but that wouldn't be to socially appropriate in public. I have experienced the same thing with low glucose & with power naps. I used to feel really shaky & start cramming down food but I never knew why. Since I struggled with weight in middle/high school I figured I was a freak. Now I realize I probably had borderline diabetes for many of those years. But what scares me now is that when I start having a low I get almost rage-like without knowing it's the sugar. It really scares me sometimes how ugly I can be with hubby and sometimes even the kids, I start yelling at them about silly stuff. To make it worse, they can see a low before me & tell me I'm having a low, then I'm so angry I get angry at them for saying that to me because I'm not being rational. Once we figured it all out I've worked really hard to maintain my sugar 'cause it's sure not fair to kids for their mamma to be yelling at them because I've so poorly planned/cared for my body's needs. I keep those glucose liquid drinks and tablets on hand. It's difficult to because I'm trying so hard to lose weight and when I get a low I want to eat and eat things I shouldn't and then it makes the weight loss even more difficult. with the glucose drink/tablets I can take a couple, count them as a point on my Weight Watchers, and they work much, much faster than regular food. I can doze off for 15-30 minutes & feel so refreshed but if I sleep much longer I'm so ill the rest of the day. I don't know what that is, perhaps it messes up our brain waves somehow? Debi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Debi while aware i to do them not have ability to think when they emerge to stop of them always and so the reaction is of just pure impulsive like some people when suddenly feared so much they jump and and jump and sort of flap about in the air and cant seem to get of the sceam out. or some if they are of angry scream and or slam of doors and or hit like men do is they are of threatened and or challenged might hit another. or those who are of so overly happy shake and cant seem to think and the words get of jumbled , none of them think on it they just respond or react .. that is of that way for me too but I do it towards self. usually now if i to bit I to be of overly and prolonged frustrated and usually in great distress, but when able to can now sit on the hands or twist of them into my clothings or find self finger twisting and flicking it is for me like crossing the two first digits hard and them flicking them to be uncrossed and repeating. it provides a deep pressure sort of things or have found when the need is of there will chew on the shirt collar, this one was of a new stim things triggered by lexapro in the last 3-4 years but is of not often. I to find self grinding teeth over the shirt collar and stimming off the sensation and sounds of it. for hitting head that one is of not a choice but is of most commonly seen from me when feared and or overloaded and not processing clear and or when agitated with self. If a person is of near me and a sudden noise happens they will get of grabbed or hit or it will turn to self but either way some one is of going to get of hit. it is of a strong response to fear in me. not know of how to redirect that one for self. because it happens so fast cant stop and think of do this instead mindsets. I to be of share these things not for pity but because if we only focus and share on the good and our gifts and talents and strengths then we lose out on those understanding the cores of the challenges and negatives to living with autism. most see of their kids as parents see of them and they love that kid they see but they want to help the side they do to understand , and hurts and confuses that is of why the focus for me is of sharing so much of the whole of me. some only want of to share the positives of it all, that leaves it unbalanced to me. so for me I to share it as it is of for me and not be hide of self but in my sharing am of true to self and hope to be of reflect the whole of me in the process. some days hate of autism and some days embrace of it and some days hate of being sondra and other days okay and coping of who I to be in this life. well it is of past the 12:34 time and so now need of to go to the bed because it is of past my need for sleep sondra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 17, 2009 Report Share Posted February 17, 2009 Debi while aware i to do them not have ability to think when they emerge to stop of them always and so the reaction is of just pure impulsive like some people when suddenly feared so much they jump and and jump and sort of flap about in the air and cant seem to get of the sceam out. or some if they are of angry scream and or slam of doors and or hit like men do is they are of threatened and or challenged might hit another. or those who are of so overly happy shake and cant seem to think and the words get of jumbled , none of them think on it they just respond or react .. that is of that way for me too but I do it towards self. usually now if i to bit I to be of overly and prolonged frustrated and usually in great distress, but when able to can now sit on the hands or twist of them into my clothings or find self finger twisting and flicking it is for me like crossing the two first digits hard and them flicking them to be uncrossed and repeating. it provides a deep pressure sort of things or have found when the need is of there will chew on the shirt collar, this one was of a new stim things triggered by lexapro in the last 3-4 years but is of not often. I to find self grinding teeth over the shirt collar and stimming off the sensation and sounds of it. for hitting head that one is of not a choice but is of most commonly seen from me when feared and or overloaded and not processing clear and or when agitated with self. If a person is of near me and a sudden noise happens they will get of grabbed or hit or it will turn to self but either way some one is of going to get of hit. it is of a strong response to fear in me. not know of how to redirect that one for self. because it happens so fast cant stop and think of do this instead mindsets. I to be of share these things not for pity but because if we only focus and share on the good and our gifts and talents and strengths then we lose out on those understanding the cores of the challenges and negatives to living with autism. most see of their kids as parents see of them and they love that kid they see but they want to help the side they do to understand , and hurts and confuses that is of why the focus for me is of sharing so much of the whole of me. some only want of to share the positives of it all, that leaves it unbalanced to me. so for me I to share it as it is of for me and not be hide of self but in my sharing am of true to self and hope to be of reflect the whole of me in the process. some days hate of autism and some days embrace of it and some days hate of being sondra and other days okay and coping of who I to be in this life. well it is of past the 12:34 time and so now need of to go to the bed because it is of past my need for sleep sondra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 18, 2009 Report Share Posted February 18, 2009 LOL on the way she said it worked! I was on Medicaid too, but they didn't have much of a choice to remove mine, no matter how much hydration they gave me as soon as they stopped it I would get dehydrated again from being so ill, and they came to the conclusion that it was the Noraplant causing it. I think I had it in for just over a month, but didn't bleed at all. A friend of mine went with me and got hers the same day I did, she never had any trouble with it and had it in for the full 5 years. She did bleed more often than she did before but not all the time.... man would that suck! I would have been complaining big time! LOL A dr later told me that I just can't have any BC that uses hormones. After Tiffanie I had an IUD in for a little more than a year before we removed it to start trying for . Theresa > > One of my best friends got noraplant on medicaid after her son was > born. She bled every day for the entire 5 years. Since that was her > only form of insurance they refused to remove it, but she didn't > complain to the doctors much. I would have been in the office every > day til they got it out. She used to say it worked as BC because it > made her so gross (from the bleeding) no man would want her. Lol. > > Debi > > - > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 18, 2009 Report Share Posted February 18, 2009 LOL on the way she said it worked! I was on Medicaid too, but they didn't have much of a choice to remove mine, no matter how much hydration they gave me as soon as they stopped it I would get dehydrated again from being so ill, and they came to the conclusion that it was the Noraplant causing it. I think I had it in for just over a month, but didn't bleed at all. A friend of mine went with me and got hers the same day I did, she never had any trouble with it and had it in for the full 5 years. She did bleed more often than she did before but not all the time.... man would that suck! I would have been complaining big time! LOL A dr later told me that I just can't have any BC that uses hormones. After Tiffanie I had an IUD in for a little more than a year before we removed it to start trying for . Theresa > > One of my best friends got noraplant on medicaid after her son was > born. She bled every day for the entire 5 years. Since that was her > only form of insurance they refused to remove it, but she didn't > complain to the doctors much. I would have been in the office every > day til they got it out. She used to say it worked as BC because it > made her so gross (from the bleeding) no man would want her. Lol. > > Debi > > - > > > Quote Link to comment Share on other sites More sharing options...
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