Guest guest Posted April 7, 2001 Report Share Posted April 7, 2001 In a message dated 4/6/01 11:06:13 PM, duodenalswitch writes: << The DS absolutely can be done laprascopically. In fact mine was. Mine took 7-1/2 hours though mine was the third or fourth that my surgeon did lap so that probably is lots longer than most. I think about 5 hours is the norm, barring complications. >> It can be less that five hours... my lap BPD/DS (with gallbladder removal) was done laparoscopically by Dr. Michel Gagner/Mt. Sinai/NYC in three hours. I think that he usually does a three hour + laparoscopic BPD/DS with him as the surgeon (barring any kind of complications), but then again he is one of the most experienced in the field having pioneered the lap BPD/DS procedure (or, one of the forms of it - he doesn't do proportional limbs, etc.). Now, there weren't any complications and I hadn't had any previous abdominal surgeries. I've known others who had more complicated situations having the lap surgery in five hours or so. All the best, laparoscopic BPD/DS with gallbladder removal Dr. Gagner/Dr. Quinn assisting/Mt. Sinai/NYC January 25, 2001 76 days post-op and still feelin' fab! pre-op: 307 lbs/bmi 45 (5'9 " ) now: 269.5/bmi 40 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2001 Report Share Posted April 7, 2001 In a message dated 4/6/01 11:06:13 PM, duodenalswitch writes: << The DS absolutely can be done laprascopically. In fact mine was. Mine took 7-1/2 hours though mine was the third or fourth that my surgeon did lap so that probably is lots longer than most. I think about 5 hours is the norm, barring complications. >> It can be less that five hours... my lap BPD/DS (with gallbladder removal) was done laparoscopically by Dr. Michel Gagner/Mt. Sinai/NYC in three hours. I think that he usually does a three hour + laparoscopic BPD/DS with him as the surgeon (barring any kind of complications), but then again he is one of the most experienced in the field having pioneered the lap BPD/DS procedure (or, one of the forms of it - he doesn't do proportional limbs, etc.). Now, there weren't any complications and I hadn't had any previous abdominal surgeries. I've known others who had more complicated situations having the lap surgery in five hours or so. All the best, laparoscopic BPD/DS with gallbladder removal Dr. Gagner/Dr. Quinn assisting/Mt. Sinai/NYC January 25, 2001 76 days post-op and still feelin' fab! pre-op: 307 lbs/bmi 45 (5'9 " ) now: 269.5/bmi 40 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2001 Report Share Posted May 17, 2001 Hi Genell, You will learn alot here! It is a very friendly, informitive group. Best of luck in your research. One place to start is www.duodenalswitch.com It is a great site and will answer many of your questions. Sorry I can't help you with the Dr you're asking about as I'm from Ohio. There are many good surgeons out there, you'll find them posted on that site I was talking about. Good luck and hope to hear from you again. Angel --- Genell Pridgen rainbow@...> wrote: > Hi. My name is Genell Pridgen. I am 32 years old > and the mother to two > absolutely beautiful and precious children, Hardy(4) > and Alena(3). I live > in eastern North Carolina. I am just in the > beginning stages of researching > wls. I am 5'1 " and weigh 292 lbs. I have been > large and getting larger all > my life. I have been gaining at about the rate of > 9-10 lbs a year. Doesn't > matter what I do. I have tried many diets. > Physician's weight loss, lost > about 20 lbs there but they had to get me down to > 600 calories a day to get > me to lose anything. The best diet that I ever > tried was Carbo Addict's. I > lost about 40 lbs but then plateaued. I didn't > cheat at all and still > stayed plateaued for nearly one year. I had to get > off of it when I went to > Ukraine in 1999. My husband and I were there 21 > days and only eating 3 > meals a day with no snacks in between I gained 14 > lbs. It was so very > disheartening. I suffer with PCOS and consequently > genetics and the weight > has caused me to not ovulate. So, you wonder how I > ended up with two > children. They are both adopted from Ukraine and > the light of my life. I > am at the heaviest that I have ever been with a BMI > of 51. My feet are > holding fluid now. I am scared. My children have > already been orphans one > time, they deserve better than to lose their mama. > I need them and they > need me. I looked at wls about 10 months ago, but > was concerned what long > term malabsorption issues would do to my body even > if I take vitamins and > minerals. I also didn't like the fact that I might > lose some more hair as > my hair is already too thin on top right now from > the PCO. So, I pushed the > surgery out of my mind. But I know that I can't do > this with a diet and I > am scared that I won't even live 4 more years much > less be around to raise > my children and possibly see grandchildren. > > I have been reviewing some of the old posts and I > was particularly > interested in the person(excuse me, I can't remember > her name) that used Dr. > Dennis at the Obesity Surgery Center in > Georgia. I had hoped to get > the surgery done in NC. There is a surgeon in > Greenville, NC who does wls > surgery, but I don't think that he does lap BD/DS. > I have seen some of the > pictures of people who had open surgery and their > scars and staples. My > mother had colon cancer about 14 years ago and she > had to be cut like that. > I just really didn't want to be cut on that much. > Just a personal feeling. > Could the person who used Dr. Dennis please > write to me privately? I > have many questions for you. > > I am so glad that there is an e-mail list like this > one. I hope to learn a > lot here. > > Genell Pridgen > > > > ---------------------------------------------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2001 Report Share Posted May 17, 2001 Hi Genell, You will learn alot here! It is a very friendly, informitive group. Best of luck in your research. One place to start is www.duodenalswitch.com It is a great site and will answer many of your questions. Sorry I can't help you with the Dr you're asking about as I'm from Ohio. There are many good surgeons out there, you'll find them posted on that site I was talking about. Good luck and hope to hear from you again. Angel --- Genell Pridgen rainbow@...> wrote: > Hi. My name is Genell Pridgen. I am 32 years old > and the mother to two > absolutely beautiful and precious children, Hardy(4) > and Alena(3). I live > in eastern North Carolina. I am just in the > beginning stages of researching > wls. I am 5'1 " and weigh 292 lbs. I have been > large and getting larger all > my life. I have been gaining at about the rate of > 9-10 lbs a year. Doesn't > matter what I do. I have tried many diets. > Physician's weight loss, lost > about 20 lbs there but they had to get me down to > 600 calories a day to get > me to lose anything. The best diet that I ever > tried was Carbo Addict's. I > lost about 40 lbs but then plateaued. I didn't > cheat at all and still > stayed plateaued for nearly one year. I had to get > off of it when I went to > Ukraine in 1999. My husband and I were there 21 > days and only eating 3 > meals a day with no snacks in between I gained 14 > lbs. It was so very > disheartening. I suffer with PCOS and consequently > genetics and the weight > has caused me to not ovulate. So, you wonder how I > ended up with two > children. They are both adopted from Ukraine and > the light of my life. I > am at the heaviest that I have ever been with a BMI > of 51. My feet are > holding fluid now. I am scared. My children have > already been orphans one > time, they deserve better than to lose their mama. > I need them and they > need me. I looked at wls about 10 months ago, but > was concerned what long > term malabsorption issues would do to my body even > if I take vitamins and > minerals. I also didn't like the fact that I might > lose some more hair as > my hair is already too thin on top right now from > the PCO. So, I pushed the > surgery out of my mind. But I know that I can't do > this with a diet and I > am scared that I won't even live 4 more years much > less be around to raise > my children and possibly see grandchildren. > > I have been reviewing some of the old posts and I > was particularly > interested in the person(excuse me, I can't remember > her name) that used Dr. > Dennis at the Obesity Surgery Center in > Georgia. I had hoped to get > the surgery done in NC. There is a surgeon in > Greenville, NC who does wls > surgery, but I don't think that he does lap BD/DS. > I have seen some of the > pictures of people who had open surgery and their > scars and staples. My > mother had colon cancer about 14 years ago and she > had to be cut like that. > I just really didn't want to be cut on that much. > Just a personal feeling. > Could the person who used Dr. Dennis please > write to me privately? I > have many questions for you. > > I am so glad that there is an e-mail list like this > one. I hope to learn a > lot here. > > Genell Pridgen > > > > ---------------------------------------------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2001 Report Share Posted May 17, 2001 Hi Genell, You will learn alot here! It is a very friendly, informitive group. Best of luck in your research. One place to start is www.duodenalswitch.com It is a great site and will answer many of your questions. Sorry I can't help you with the Dr you're asking about as I'm from Ohio. There are many good surgeons out there, you'll find them posted on that site I was talking about. Good luck and hope to hear from you again. Angel --- Genell Pridgen rainbow@...> wrote: > Hi. My name is Genell Pridgen. I am 32 years old > and the mother to two > absolutely beautiful and precious children, Hardy(4) > and Alena(3). I live > in eastern North Carolina. I am just in the > beginning stages of researching > wls. I am 5'1 " and weigh 292 lbs. I have been > large and getting larger all > my life. I have been gaining at about the rate of > 9-10 lbs a year. Doesn't > matter what I do. I have tried many diets. > Physician's weight loss, lost > about 20 lbs there but they had to get me down to > 600 calories a day to get > me to lose anything. The best diet that I ever > tried was Carbo Addict's. I > lost about 40 lbs but then plateaued. I didn't > cheat at all and still > stayed plateaued for nearly one year. I had to get > off of it when I went to > Ukraine in 1999. My husband and I were there 21 > days and only eating 3 > meals a day with no snacks in between I gained 14 > lbs. It was so very > disheartening. I suffer with PCOS and consequently > genetics and the weight > has caused me to not ovulate. So, you wonder how I > ended up with two > children. They are both adopted from Ukraine and > the light of my life. I > am at the heaviest that I have ever been with a BMI > of 51. My feet are > holding fluid now. I am scared. My children have > already been orphans one > time, they deserve better than to lose their mama. > I need them and they > need me. I looked at wls about 10 months ago, but > was concerned what long > term malabsorption issues would do to my body even > if I take vitamins and > minerals. I also didn't like the fact that I might > lose some more hair as > my hair is already too thin on top right now from > the PCO. So, I pushed the > surgery out of my mind. But I know that I can't do > this with a diet and I > am scared that I won't even live 4 more years much > less be around to raise > my children and possibly see grandchildren. > > I have been reviewing some of the old posts and I > was particularly > interested in the person(excuse me, I can't remember > her name) that used Dr. > Dennis at the Obesity Surgery Center in > Georgia. I had hoped to get > the surgery done in NC. There is a surgeon in > Greenville, NC who does wls > surgery, but I don't think that he does lap BD/DS. > I have seen some of the > pictures of people who had open surgery and their > scars and staples. My > mother had colon cancer about 14 years ago and she > had to be cut like that. > I just really didn't want to be cut on that much. > Just a personal feeling. > Could the person who used Dr. Dennis please > write to me privately? I > have many questions for you. > > I am so glad that there is an e-mail list like this > one. I hope to learn a > lot here. > > Genell Pridgen > > > > ---------------------------------------------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2002 Report Share Posted April 22, 2002 > At 11:16 AM 04/22/2002 -0500, wrote: Hey -- Nice to see a familiar face, although I wouldn't wish this FM thing on anyone except maybe my worst enemy. Enjoy the list -- it's a great place. Best, Em ~~~~~~~~~~~~~ " I can't deal with cleaning up. Let's sell the house. " I'll sing for my supper, but I won't audition. ~~~~~~~~~~~~~ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2002 Report Share Posted April 22, 2002 > At 11:16 AM 04/22/2002 -0500, wrote: Hey -- Nice to see a familiar face, although I wouldn't wish this FM thing on anyone except maybe my worst enemy. Enjoy the list -- it's a great place. Best, Em ~~~~~~~~~~~~~ " I can't deal with cleaning up. Let's sell the house. " I'll sing for my supper, but I won't audition. ~~~~~~~~~~~~~ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2002 Report Share Posted April 22, 2002 Welcome, , to our list. It is, in my opinion, a very good list. Very supportive, caring and loving. If you have any questions, please ask, someone will be sure to have an answer. Please let us know more about you. Again, welcome. Take care, Irene Books may well be the only true magic Alice Hoffman. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2002 Report Share Posted April 22, 2002 Welcome, , to our list. It is, in my opinion, a very good list. Very supportive, caring and loving. If you have any questions, please ask, someone will be sure to have an answer. Please let us know more about you. Again, welcome. Take care, Irene Books may well be the only true magic Alice Hoffman. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2002 Report Share Posted August 7, 2002 Hello, Bec...not that I've got a lotta advice about dealing with CF...I'm new to the dx and to the group as well...but I'll tell ya, humor is what gets us all through the day...here's one for ya.....(my EX=hubby told me this one the other day...) Osama Bin Laden strode up to the pearly gates and was met by seventy politicians. To this he threw his hands up and swore, " WHAT is THIS? I thought I was supposed to receive seventy Virgins!! " and they all replied, " It's 'seventy Virginians' you idiot! " heehee...(and I'm not being anti-Islamic...I happen to be Muslim, myself) I just thought it was hilarious. Hope it made ya smile. love and hugs from Deranda, Mom of daughter with suspected CF and two other children with multiple handicaps. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2002 Report Share Posted August 7, 2002 Welcome Bec. I too am new to the group and am finding it nice to hear of similar experiences, etc. Hope that we can share a laugh or two. Deb New To List Hello All! I have been reading the list digest for the last week or so and thought it time I introduced myself and my ladies. I am the Mum of twin daughters with CF, they are now 10 months old and despite the usual run of colds etc they have been really well. I guess what I am looking for from this group is some advice, information and hopefully some humour about dealing with children with CF. Not that it is a humourous business, believe me, but I think we all need to stop every now and then and have a bit of a laugh. Hope to hear from some of you soon! Stay well Bec Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2002 Report Share Posted August 7, 2002 Welcome Bec. I too am new to the group and am finding it nice to hear of similar experiences, etc. Hope that we can share a laugh or two. Deb New To List Hello All! I have been reading the list digest for the last week or so and thought it time I introduced myself and my ladies. I am the Mum of twin daughters with CF, they are now 10 months old and despite the usual run of colds etc they have been really well. I guess what I am looking for from this group is some advice, information and hopefully some humour about dealing with children with CF. Not that it is a humourous business, believe me, but I think we all need to stop every now and then and have a bit of a laugh. Hope to hear from some of you soon! Stay well Bec Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2002 Report Share Posted August 7, 2002 Welcome Bec. I too am new to the group and am finding it nice to hear of similar experiences, etc. Hope that we can share a laugh or two. Deb New To List Hello All! I have been reading the list digest for the last week or so and thought it time I introduced myself and my ladies. I am the Mum of twin daughters with CF, they are now 10 months old and despite the usual run of colds etc they have been really well. I guess what I am looking for from this group is some advice, information and hopefully some humour about dealing with children with CF. Not that it is a humourous business, believe me, but I think we all need to stop every now and then and have a bit of a laugh. Hope to hear from some of you soon! Stay well Bec Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2002 Report Share Posted August 7, 2002 WELCOME....Enjoy all here. It is a great list LOVE & HUGS, GrandmomBEV New To List Hello All! I have been reading the list digest for the last week or so and thought it time I introduced myself and my ladies. I am the Mum of twin daughters with CF, they are now 10 months old and despite the usual run of colds etc they have been really well. I guess what I am looking for from this group is some advice, information and hopefully some humour about dealing with children with CF. Not that it is a humourous business, believe me, but I think we all need to stop every now and then and have a bit of a laugh. Hope to hear from some of you soon! Stay well Bec PLEASE do not post religious emails to the list. ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. -------------------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2002 Report Share Posted August 7, 2002 WELCOME....Enjoy all here. It is a great list LOVE & HUGS, GrandmomBEV New To List Hello All! I have been reading the list digest for the last week or so and thought it time I introduced myself and my ladies. I am the Mum of twin daughters with CF, they are now 10 months old and despite the usual run of colds etc they have been really well. I guess what I am looking for from this group is some advice, information and hopefully some humour about dealing with children with CF. Not that it is a humourous business, believe me, but I think we all need to stop every now and then and have a bit of a laugh. Hope to hear from some of you soon! Stay well Bec PLEASE do not post religious emails to the list. ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. -------------------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 7, 2002 Report Share Posted August 7, 2002 WELCOME....Enjoy all here. It is a great list LOVE & HUGS, GrandmomBEV New To List Hello All! I have been reading the list digest for the last week or so and thought it time I introduced myself and my ladies. I am the Mum of twin daughters with CF, they are now 10 months old and despite the usual run of colds etc they have been really well. I guess what I am looking for from this group is some advice, information and hopefully some humour about dealing with children with CF. Not that it is a humourous business, believe me, but I think we all need to stop every now and then and have a bit of a laugh. Hope to hear from some of you soon! Stay well Bec PLEASE do not post religious emails to the list. ------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. -------------------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 8, 2002 Report Share Posted August 8, 2002 Hi Bec, welcome to the list! You're right, a good portion of humour helps to handle the whole situation. Maureen McIssac, one of our funniest members is offline at the moment. But here is one of her masterpieces to let you know where you are at. Peace Torsten, dad of Fiona 5wcf e-mail: torstenkrafft@... POSITION: Mom JOB DESCRIPTION: Long term team players needed for challenging permanent work in an often chaotic environment. Candidates must possess excellent communication and organizational skills and be willing to work variable hours, which will include evenings and weekends and frequent 24 hour shifts on call. Some overnight travel required, including trips to primitive camping sites on rainy weekends and endless sports tournaments in faraway cities. Travel expenses not reimbursed. Extensive courier duties also required. RESPONSIBILITIES: Must provide on-the-site training in basic life skills, such as nose blowing. Must have strong skills in negotiating,conflict resolution and crisis management. Ability to suture flesh wounds a plus. Must be able to think out of the box but not lose track of the box, because you most likely will need it for a school project. Must reconcile petty cash disbursements and be proficient in managing budgets and resources fairly, unless you want to hear, " He got more than me! " for the rest of your life. Also, must be able to drive motor vehicles safely under loud and adverse conditions while simultaneously practicing above mentioned skills in conflict resolution. Must be able to choose your battles and stick to your guns. Must be able to withstand criticism, such as " You don't know anything. " Must be willing to be hated at least temporarily, until someone needs $5 to go skating. Must be willing to bite tongue repeatedly. Also, must possess the physical stamina of a pack mule and be able to go from zero to 60 mph in three seconds flat in case, this time, the screams from the backyard are not someone just crying wolf. Must be willing to face stimulating technical challenges, such as small gadget repair, mysteriously sluggish toilets and stuck zippers. Must screen phone calls, maintain calendars and coordinate production of multiple homework projects. Must have ability to plan and organize social gatherings for clients of all ages and mental outlooks. Must be willing to be indispensable one minute, an embarrassment the next. Must handle assembly and product safety testing of a half million cheap, plastic toys and battery operated devices. Also, must have a highly energetic entrepreneurial spirit, because fund-raiser will be your middle name. Must have a diverse knowledge base, so as to answer questions such as " What makes the wind move? " or " Why can't they just go in and shoot Sadam Hussein? " on the fly. Must always hope for the best but be prepared for the worst. Must assume final, complete accountability for the quality of the end product. Responsibilities also include floor maintenance and janitorial work throughout the facility. POSSIBILITY FOR ADVANCEMENT AND PROMOTION: Virtually none. Your job is to remain in the same position for years, without complaining, constantly retraining and updating your skills, so that those in your charge can ultimately surpass you. PREVIOUS EXPERIENCE: None required, unfortunately. On-the-job training offered on a continually exhausting basis. WAGES AND COMPENSATION: You pay them, offering frequent raises and bonuses. A balloon payment is due when they turn 18 because of the assumption that college will help them become financially independent. When you die, you give them whatever is left. The oddest thing about this reverse-salary scheme is that you actually enjoy it and wish you could only do more. BENEFITS: While no health or dental insurance, no pension, no tuition reimbursement, no paid holidays and no stock options are offered, job supplies limitless opportunities for personal growth and free hugs for life if you play your cards right. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 9, 2002 Report Share Posted August 9, 2002 Welcome Bec, I am a mother of a bi-lateral lung transplantee wCF who is doing great. Have fun the rollercoaster life has a lot of hard knocks but wonderful love, laughter and general mischevious. Debi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 2, 2002 Report Share Posted September 2, 2002 Hi Dawn, Welcome... I had my RNY, 23 years ago, July 13, 1979. Are you on any perscriptioned Iron supplement? I have tried many different brands over the years (all perscriptioned) and have found Chromagen Forte to be the most absorbable..yet I still am anemic and yes, I also suffer with " low " blood sugar too (actually have since 1981). The best that my red blood count has been since surgery, was while taking a protein supplement (which brought my red count to around 12.0..but since the onset of abdominal intestinal fistulas from Colon resection surgery (January, 1999) I have been unable to take any protein supplement and have been very week and lack the vitality that I previously had... What liver count are you talking about, yo-yo up and down? Is it the fat content? I had a fat content rise to over 1500! This was during recovery from my second " unsuccessful " surgical procedure to repair my intestinal fistulas in April, 2000. I was put on TPN through a Pic line feed (12 hours/daily) till March, 2001. Since, being taken off of the TPN, my liver fat count has returned to normal. Bob new to list > Hello all. My name is Dawn and I am new to your group. I am not new to life after surgery as I had mine May 17, 1993. I have been looking for others who are long term post op to compare notes. There are not many resources past three yrs. post op. > > To tell you a little about my history, I weighed 256 lbs. prior to having RNY. I am 5 5 1/2. After 10 months, I had lost half my body weight, weighing 128 lbs. During the next year, I went down to 117 lbs. This was too thin for my bone structure. My surgeon advised me how to gain a little back. Now I go between 130 and 135 lbs and have for several years. I have taken my vitamins religiously, am very active, and watch what I eat, making sure to get plenty of what I need. I have had no major complications and have been very healthy. > > At this time, I am living in Denmark. I have a specialist who follows my health. The only drawback is that no one has had this type of surgery in over 20 years. Everything is based on earlier type surgeries. My surgeon always makes time for me if I call him but it is difficult being so far away. > > My current health is as follows...last year my blood glucose was below normal. This means my iron is low. I have been taking extra iron for the past year but feel it is still low. I will get my newest results within 2 weeks to know for sure. My calcium levels are a bit low. I was given a bone density test which showed that my mass is just below normal. This can be corrected with vitamin D injections. Also, for the past year, my liver counts have been very high but jump back to normal then rise again. My surgeon tells me that it is not normal. My doctor here tells me it is common with this surgery. A little confusing. > > Other than feeling tired, I feel great. I have never regretted having my surgery. I had the best surgeon anyone could ask for. As I said, after almost 10 years, he still takes time for me. My entire life changed for the better post op and probably saved my life...high blood pressure, risk of heart failure, etc. > > Is anyone out there several years post op? Thank you as I know this has gotten a bit long. > Dawn Conner-Jeppesen > http://www.geocities.com/frwhlngrl/ > http://community.webshots.com/user/frwhlngrl > > > --- > Outgoing mail is certified Virus Free. > Checked by AVG anti-virus system (http://www.grisoft.com). > Version: 6.0.384 / Virus Database: 216 - Release Date: 8/21/2002 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 2, 2002 Report Share Posted September 2, 2002 Hi Dawn, Welcome... I had my RNY, 23 years ago, July 13, 1979. Are you on any perscriptioned Iron supplement? I have tried many different brands over the years (all perscriptioned) and have found Chromagen Forte to be the most absorbable..yet I still am anemic and yes, I also suffer with " low " blood sugar too (actually have since 1981). The best that my red blood count has been since surgery, was while taking a protein supplement (which brought my red count to around 12.0..but since the onset of abdominal intestinal fistulas from Colon resection surgery (January, 1999) I have been unable to take any protein supplement and have been very week and lack the vitality that I previously had... What liver count are you talking about, yo-yo up and down? Is it the fat content? I had a fat content rise to over 1500! This was during recovery from my second " unsuccessful " surgical procedure to repair my intestinal fistulas in April, 2000. I was put on TPN through a Pic line feed (12 hours/daily) till March, 2001. Since, being taken off of the TPN, my liver fat count has returned to normal. Bob new to list > Hello all. My name is Dawn and I am new to your group. I am not new to life after surgery as I had mine May 17, 1993. I have been looking for others who are long term post op to compare notes. There are not many resources past three yrs. post op. > > To tell you a little about my history, I weighed 256 lbs. prior to having RNY. I am 5 5 1/2. After 10 months, I had lost half my body weight, weighing 128 lbs. During the next year, I went down to 117 lbs. This was too thin for my bone structure. My surgeon advised me how to gain a little back. Now I go between 130 and 135 lbs and have for several years. I have taken my vitamins religiously, am very active, and watch what I eat, making sure to get plenty of what I need. I have had no major complications and have been very healthy. > > At this time, I am living in Denmark. I have a specialist who follows my health. The only drawback is that no one has had this type of surgery in over 20 years. Everything is based on earlier type surgeries. My surgeon always makes time for me if I call him but it is difficult being so far away. > > My current health is as follows...last year my blood glucose was below normal. This means my iron is low. I have been taking extra iron for the past year but feel it is still low. I will get my newest results within 2 weeks to know for sure. My calcium levels are a bit low. I was given a bone density test which showed that my mass is just below normal. This can be corrected with vitamin D injections. Also, for the past year, my liver counts have been very high but jump back to normal then rise again. My surgeon tells me that it is not normal. My doctor here tells me it is common with this surgery. A little confusing. > > Other than feeling tired, I feel great. I have never regretted having my surgery. I had the best surgeon anyone could ask for. As I said, after almost 10 years, he still takes time for me. My entire life changed for the better post op and probably saved my life...high blood pressure, risk of heart failure, etc. > > Is anyone out there several years post op? Thank you as I know this has gotten a bit long. > Dawn Conner-Jeppesen > http://www.geocities.com/frwhlngrl/ > http://community.webshots.com/user/frwhlngrl > > > --- > Outgoing mail is certified Virus Free. > Checked by AVG anti-virus system (http://www.grisoft.com). > Version: 6.0.384 / Virus Database: 216 - Release Date: 8/21/2002 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 2, 2002 Report Share Posted September 2, 2002 In a message dated 09/02/2002 8:28:54 PM Eastern Daylight Time, vitalady@... writes: > Have you had a dexascan to see where your bones are? Hey , I have a dexascan in the early am.. will let you know how this year compares to last year as soon as I get the results../ Hugs, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 2, 2002 Report Share Posted September 2, 2002 I'm 8 yrs post-op, RNY distal. What kind of iron are you taking? What kind & how much calcium? Have you had a dexascan to see where your bones are? Is your RNY proximal? Distal? new to list > Hello all. My name is Dawn and I am new to your group. I am not new to life after surgery as I had mine May 17, 1993. I have been looking for others who are long term post op to compare notes. There are not many resources past three yrs. post op. > > To tell you a little about my history, I weighed 256 lbs. prior to having RNY. I am 5 5 1/2. After 10 months, I had lost half my body weight, weighing 128 lbs. During the next year, I went down to 117 lbs. This was too thin for my bone structure. My surgeon advised me how to gain a little back. Now I go between 130 and 135 lbs and have for several years. I have taken my vitamins religiously, am very active, and watch what I eat, making sure to get plenty of what I need. I have had no major complications and have been very healthy. > > At this time, I am living in Denmark. I have a specialist who follows my health. The only drawback is that no one has had this type of surgery in over 20 years. Everything is based on earlier type surgeries. My surgeon always makes time for me if I call him but it is difficult being so far away. > > My current health is as follows...last year my blood glucose was below normal. This means my iron is low. I have been taking extra iron for the past year but feel it is still low. I will get my newest results within 2 weeks to know for sure. My calcium levels are a bit low. I was given a bone density test which showed that my mass is just below normal. This can be corrected with vitamin D injections. Also, for the past year, my liver counts have been very high but jump back to normal then rise again. My surgeon tells me that it is not normal. My doctor here tells me it is common with this surgery. A little confusing. > > Other than feeling tired, I feel great. I have never regretted having my surgery. I had the best surgeon anyone could ask for. As I said, after almost 10 years, he still takes time for me. My entire life changed for the better post op and probably saved my life...high blood pressure, risk of heart failure, etc. > > Is anyone out there several years post op? Thank you as I know this has gotten a bit long. > Dawn Conner-Jeppesen > http://www.geocities.com/frwhlngrl/ > http://community.webshots.com/user/frwhlngrl > > > --- > Outgoing mail is certified Virus Free. > Checked by AVG anti-virus system (http://www.grisoft.com). > Version: 6.0.384 / Virus Database: 216 - Release Date: 8/21/2002 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2002 Report Share Posted September 4, 2002 Hi there everyone. My name is Cathie. I was diagnosed with fms/cfs several years ago. I have been trying to learn to live a full life with the limitations this has given me. I am anxious to talk to others and get some support with this as well as give what I have to offer. Take Care Cathie Re: What I gain from having Fibro Hello , I have CFS. I can really relate to your bit about the childhood abuse. I always wanted to make everyone happy too. Or try to save people (like my mother) from alcoholism. In my case I often wonder if my health problems, especially my asthma, stem from the environment I grew up in. My mother drank and smoked when she was pregnant with me. As a child I was exposed to cigarrette smoke and marijuanna smoke. I often wonder if I'd be healthy if my mother didn't treat her body bad when she was carrying me. Well even if I knew the answer I can't change the past and I guess I'm lucky I'm more or less normal as there are worse things that can happen to people who's mothers drank while they were pregnant. I suffer from the suicidality sometimes. I don't think about it daily like I used to, but when I have a really bad day the thoughts creep into my mind. How did you manage to give up your suicidality? ~Jen I thought the post about what people have to gain from their sickness is very interesting. I'll give 2 examples how I've felt this impact in my life. Last summer, I was going through a very dark period in my life and was in and out of suicidality. My psychiatrist and I had several discussions about what I gained from being suicidal. What I gained was having that " quick fix. " As a recovering bulemic and alcoholic who was clean/abstinent for the first time since I was 8 - I knew the answer. Suicidality had become my drug of choice. As I gave up my suicidality, I was forced to learn how to deal with day to day life without any easy outs. I am also a survivor of childhood sexual abuse. My *theory* about why I (and no one else) have fibro is that it is a result of all the physical and emotional trauma held in my body. As an ultimate people pleaser, I kept running myself into the ground. I could never make room to heal. I could not say " no " to people - especially those I loved. Having fibro has taught me to say " no " and it has opened up the doors for me to allow others to take care of me (I was always the caretaker.) As I find ways to manage my fibro, I risk other people beginning to expect more of me. My personal challenge is learning to say " no " simply b/c I want to and not b/c I'm too tired, too achy, etc. Does this mean fibro is all in my head? Well, in my view, yes (kind of.) I'm a firm believer that body, mind and spirit cannot be seperated. How we think about ourselves - how we love - or don't love - ourselves influences how we feel in our physical bodies. As I'm learning to love myself and heal from old wounds, I find my fibro is more easily managed. As I get sucked into vortices of stress, I find my fibro worsens. I want to make sure to qualify the above my saying it is *my opinion* -- it is what works for *me*. Take what you want and leave the rest. There are as many paths to healing as there are people on the journey. Thanks for " listening " , --------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2002 Report Share Posted September 4, 2002 Hi there everyone. My name is Cathie. I was diagnosed with fms/cfs several years ago. I have been trying to learn to live a full life with the limitations this has given me. I am anxious to talk to others and get some support with this as well as give what I have to offer. Take Care Cathie Re: What I gain from having Fibro Hello , I have CFS. I can really relate to your bit about the childhood abuse. I always wanted to make everyone happy too. Or try to save people (like my mother) from alcoholism. In my case I often wonder if my health problems, especially my asthma, stem from the environment I grew up in. My mother drank and smoked when she was pregnant with me. As a child I was exposed to cigarrette smoke and marijuanna smoke. I often wonder if I'd be healthy if my mother didn't treat her body bad when she was carrying me. Well even if I knew the answer I can't change the past and I guess I'm lucky I'm more or less normal as there are worse things that can happen to people who's mothers drank while they were pregnant. I suffer from the suicidality sometimes. I don't think about it daily like I used to, but when I have a really bad day the thoughts creep into my mind. How did you manage to give up your suicidality? ~Jen I thought the post about what people have to gain from their sickness is very interesting. I'll give 2 examples how I've felt this impact in my life. Last summer, I was going through a very dark period in my life and was in and out of suicidality. My psychiatrist and I had several discussions about what I gained from being suicidal. What I gained was having that " quick fix. " As a recovering bulemic and alcoholic who was clean/abstinent for the first time since I was 8 - I knew the answer. Suicidality had become my drug of choice. As I gave up my suicidality, I was forced to learn how to deal with day to day life without any easy outs. I am also a survivor of childhood sexual abuse. My *theory* about why I (and no one else) have fibro is that it is a result of all the physical and emotional trauma held in my body. As an ultimate people pleaser, I kept running myself into the ground. I could never make room to heal. I could not say " no " to people - especially those I loved. Having fibro has taught me to say " no " and it has opened up the doors for me to allow others to take care of me (I was always the caretaker.) As I find ways to manage my fibro, I risk other people beginning to expect more of me. My personal challenge is learning to say " no " simply b/c I want to and not b/c I'm too tired, too achy, etc. Does this mean fibro is all in my head? Well, in my view, yes (kind of.) I'm a firm believer that body, mind and spirit cannot be seperated. How we think about ourselves - how we love - or don't love - ourselves influences how we feel in our physical bodies. As I'm learning to love myself and heal from old wounds, I find my fibro is more easily managed. As I get sucked into vortices of stress, I find my fibro worsens. I want to make sure to qualify the above my saying it is *my opinion* -- it is what works for *me*. Take what you want and leave the rest. There are as many paths to healing as there are people on the journey. Thanks for " listening " , --------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 5, 2002 Report Share Posted September 5, 2002 Can you tell me the difference in proximal or distal? I can tell you mine was Roux-y Gastric Bypass and Cholecystectomy. I know exactly what was done but am not familiar with the two terms. I am taking iron with vitamin C. Each pill contains 330mg iron and 60mg vitamin C. I take two a day as recommended by the doctor here. The calcium I take has 400mg calcium and 10mg vitamin D. I take 3 of these a day. These seem the best vitamins I can get here in Denmark. Another thing, I get plenty of calcium in my diet. I love cheese! The problem is I'm not getting enough vitamin D. Nothing here is fortified with it like our milk is. I really don't understand why. As for my bone density scan, it was not terribly low but below what it should be. I don't know the exact numbers. The graph put me in the middle between normal and osteoporoses. I was at the high end being closer to normal. Does this tell you anything? What should I do? I am getting my newest blood results next week. I plan on getting a copy and sending to my surgeon to see what he says. The doctor here seems to take a wait and see attitude. Dawn new to list > > > > Hello all. My name is Dawn and I am new to your group. I am not new to > life after surgery as I had mine May 17, 1993. I have been looking for > others who are long term post op to compare notes. There are not many > resources past three yrs. post op. > > > > To tell you a little about my history, I weighed 256 lbs. prior to having > RNY. I am 5 5 1/2. After 10 months, I had lost half my body weight, weighing > 128 lbs. During the next year, I went down to 117 lbs. This was too thin for > my bone structure. My surgeon advised me how to gain a little back. Now I go > between 130 and 135 lbs and have for several years. I have taken my vitamins > religiously, am very active, and watch what I eat, making sure to get plenty > of what I need. I have had no major complications and have been very > healthy. > > > > At this time, I am living in Denmark. I have a specialist who follows my > health. The only drawback is that no one has had this type of surgery in > over 20 years. Everything is based on earlier type surgeries. My surgeon > always makes time for me if I call him but it is difficult being so far > away. > > > > My current health is as follows...last year my blood glucose was below > normal. This means my iron is low. I have been taking extra iron for the > past year but feel it is still low. I will get my newest results within 2 > weeks to know for sure. My calcium levels are a bit low. I was given a bone > density test which showed that my mass is just below normal. This can be > corrected with vitamin D injections. Also, for the past year, my liver > counts have been very high but jump back to normal then rise again. My > surgeon tells me that it is not normal. My doctor here tells me it is common > with this surgery. A little confusing. > > > > Other than feeling tired, I feel great. I have never regretted having my > surgery. I had the best surgeon anyone could ask for. As I said, after > almost 10 years, he still takes time for me. My entire life changed for the > better post op and probably saved my life...high blood pressure, risk of > heart failure, etc. > > > > Is anyone out there several years post op? Thank you as I know this has > gotten a bit long. > > Dawn Conner-Jeppesen > > http://www.geocities.com/frwhlngrl/ > > http://community.webshots.com/user/frwhlngrl > > > > > > --- > > Outgoing mail is certified Virus Free. > > Checked by AVG anti-virus system (http://www.grisoft.com). > > Version: 6.0.384 / Virus Database: 216 - Release Date: 8/21/2002 > > > > > > Quote Link to comment Share on other sites More sharing options...
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