Guest guest Posted August 11, 2000 Report Share Posted August 11, 2000 Hi Jada ! I am not sure if this helps...but your weight is already pre-existing...you did not become overweight overnight...you've had this problem, and they will see this when you give them the copies of your medical records...so it may not be a problem. I dont know..cuz i'm not an expert there..but I was just thinking maybe you might not have a problem, because, it would be like if you were pregnant and went to the doctor and then changed insurance companies...this is quite different. > >Reply-To: MiniGastricBypass (AT) egroups (DOT) com >To: <MiniGastricBypass (AT) egroups (DOT) com> >Subject: HELP >Date: Fri, 11 Aug 2000 18:11:51 -0400 > >Hey everybody, > > My name is Jada Munn and I have been a member of this site for almost >a week. I am hoping to have the MGB soon but I am having some trouble. I >have ran into a problem with my insurance company MAMSI. They have denied >me twice and in the exclusions of my policy it clearly states that it does >not pay for morbid obesity treatment. I have already gone to my clinic >appointment and I am beginning to think that was a bad mistake. If I >change insurance companies I will have to tell them of the visit with Dr. R >and that will be a pre-existing condition. If I don't tell them then when >I ask for approval for the MGB they will look at my past medical >appointments and find that visit. Then I will have insurance fraud on my >hands! I don't want to wait the pre-existing time period with a new >insurance co. because I am in school now and I will not miss any work if I >had it done over one of my breaks. Also, I want to have it soon so I can >be experiencing the wonderful things most of you already are. (not to >mention my health) Should I try to get a lawyer like Dr. R suggested even >though it clearly states in my policy? Does anyone know a lawyer who would >represent this case? I have considered being a self pay but I am afraid of >complications that may arise. Please someone offer me some advice!! > >Jada >BMI 52 >25 years old >Goldsboro, NC > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2000 Report Share Posted August 11, 2000 In a message dated 8/11/00 5:33:03 PM Central Daylight Time, dmalony@... writes: << I thought there was a new law about no longer being able to deny people for pre-existing conditions. I do not claim to up on politics and law. Maybe it has just been proposed, but I know I have heard about it. >> I am not sure if it is law, but I do know that my insurance (BCBS) doesn't not have a clause about pre-existing conditions. I have asthma, and I have gotten my asthma medicine paid for from the day I got the insurance, no questions asked. (Actually, the same was true for Prudential and Travelers that we've had in the past... I think that most group insurance will pay, maybe private policies won't) Hope this helps! Deb in IL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2000 Report Share Posted August 11, 2000 > Hey everybody, > If I change insurance companies I will have to tell them of the visit with Dr. R and that will be a pre-existing condition. If I don't tell them then when I ask for approval for the MGB they will look at my past medical appointments and find that visit. I never thought of this as a pre-existing condition. I have been denied by Cigna and will probably have to change when my insurance elections come up in November. If this is considered a pre-existing condition, does that mean even if I change I still won't be able to get this surgery? I feel so helpless I am getting more depressed over this by the day. Thanks for anyone's input. Did anyone else have to change insurance? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2000 Report Share Posted August 11, 2000 I thought there was a new law about no longer being able to deny people for pre-existing conditions. I do not claim to up on politics and law. Maybe it has just been proposed, but I know I have heard about it. Anyone else- Laurie in Ohio Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2000 Report Share Posted August 12, 2000 Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2000 Report Share Posted August 12, 2000 http://www.clos.net/preop_meds.htm kadbsn@... wrote: > > Hi everyone...I am trying to finish up my packet and was trying to > find a > complete list of pre-op meds ...can anyone tell me where I could find > this at > > Thanks Kendra in WV > ---------------------------------------------------------------------- > > ---------------------------------------------------------------------- > This message is from the Mini-Gastric Bypass Mailing List at > Onelist.com > Please visit our web site at http://clos.net > Get the Patient Manual at http://clos.net/get_patient_manual.htm > > To Unsubscribe Send and Email to: > MiniGastricBypass-unsubscribe (AT) egroups (DOT) com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2000 Report Share Posted August 23, 2000 The ladies at the office prefer you to use Federal Express. That way if it is lost they can track it. With Love, Lara M. Akin (BMI 61) Getting my weight down to do the dance with Dr. Rutledge. 423/417/413 Waist 51/46 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2000 Report Share Posted August 23, 2000 Thanks Lara for the information Kendra in WV Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2000 Report Share Posted August 23, 2000 You are most welcome With Love, Lara M. Akin (BMI 61) Getting my weight down to do the dance with Dr. Rutledge. 423/417/413 Waist 51/46 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2000 Report Share Posted August 23, 2000 > Today is my third week anniversary post-op. I am doing really well > as far as no nausea, pain, or any discomfort at all. However, I am > not losing. I haven't lost an ounce in over a week and 1/2. My > typical diet is maybe 1/2 banana on my way to work, 1/3 cup of yogurt > around 10:00, 1/2 cup soup or mac and cheese at lunch, and maybe a > handfull of oyster crackers in the afternoon, and yogurt or 1/2 baked > potato at dinner. Am I eating too much? Yesterday, I had a meeting > after work and didn't have anything to eat, so I ate 4 bites of a > happy meal burger. Is this bad? What is everyone else eating? > What's wrong with me? > Kay Hi Kay, You didn't say how much you had lost already, but my advice is don't let what is on the scales control your life. You don't have to diet, the weight will come off. Don't put yourself back in that prison. It's hard to break out of that old diet mentality but just concentrate on eating healthy. My goal after surgery was to get back to eating as normally as possible and if it takes 1 year or 2 years to lose this weight, that's okay, as long as I'm heading in the right direction. Nothing is wrong with you. Each of us are individuals and we will all have different experiences and varying results. Throw the scales out and concentrate on life. Best of luck to you and hang in there. Suzanne MGB 7/17/00 25 lbs gone forever Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2002 Report Share Posted March 3, 2002 Dear Jo, grocery stores sometimes have candy but I usually get mine from the drug store. They have a great suletion, even chocolate. Granted they don't taste as good as the " old " ones but after awile you forget that the old ones tasted like....Sue M Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2002 Report Share Posted March 3, 2002 thanks, much Re: help >Dear Jo, grocery stores sometimes have candy but I usually get mine from the >drug store. They have a great suletion, even chocolate. Granted they don't >taste as good as the " old " ones but after awile you forget that the old ones >tasted like....Sue M > > >DISCLAIMER!! >WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 29, 2002 Report Share Posted March 29, 2002 Susiecue, You will be in my thought on Monday. You will probably be on of the fortunate ones who just breezes through it. I hope the swelling goes down quickly. Please let us know how you are doing. I hope you are getting this post. LOL Hope I signed you back up and everything is okay. Have a wonderful Easter. hugs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2004 Report Share Posted February 26, 2004 HI Jen! I too have pancreas divisum: was diagnosed last fall after having problems since july 2000. What triggered my pancreatitis is a surgery that I had that month. Most people with PD usually do not have any problem with it. But there is a small percentage of us that do. This diagnosis is very controversial as many physicians think that the divisum is just an interesting anatomical anomaly, but does not cause disease. But it is obvious from what you describe that you fall into that category of symptomatic PD, like me! As far as treatment: if you get to a very experience endoscopist he / she will most likely be able to access your duct. They may opt to do a papillotomy first (cuts the opening of the duct) and then put the stent in after doing an ERP to check for signs of chronic pancreatitis. That is what they did for me - my papilla was so small and tight that he had to cut it first to do any of the diagnostics, then he did the stent (the smallest that they had). I also had endoscopic ultrasound done too, which theoretically is more sensitive than the ERP to find changes of CP. Some docs will want to do a series of stents - have you go in for a new stent every 6 weeks or so for a total of 3 stents. Again, theoretically this is suppose to stretch the duct enough to give you pain relief. Unfortunately, it doesn't always work that way - if you do not get much relief from the first stent, they are reluctant to go on, thinking that they are not treating the right thing. It is also important to understand that stenting is also very controversial as some doctors absolutely believe that the stent causes more harm than good. But when I had to make the decision I realized that I was not able to go on as I was and that it was worth the risk to go in. Happily it cured the immediate problem but has not cured the ongoing one (the chronic pancreatitis). In my case, I was proably obstructed too long before I was diagnosed so my pancreas has been damaged permenantly. But the good news is if it is found early enough (which in your case sounds like it!) this can be very successfully treated! Don't give up - go to the second opinion guy, ask questions do research, talk to us and if you go through with it realize that the first procedure is the worst and it gets easier after that (hopefully, I am being optimistic here). But that it may take a few weeks to recover completely from each stent placement. So if you do not feel well at first, don't think that it didn't work! Also be persistent and be clear about the pain being interferring with your life! Also ask about getting referred to a pain clinic and what the long term outlook will be - that is, if stents are not an option, or they end up not helping you, make sure that you ask what happens then. Is there a plan " B " . Anyways, as you can see I have strong opinions about this disease and lots of recent relevant experience. If you would like to talk to me more feel free to email me at goutbuster@.... It will be my way of passing on the kindness that I received from this group since I first joined. Laurie (I also have about a 80 references big database on almost everything you want to know about pancreas divisum,. pain control, acute pancreatitis and chronic pancreatitis. I am happy to share any of these with you - Just ask ! she has been inundated with my attachments! my philosophy is that knowledge is power!) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2006 Report Share Posted July 29, 2006 > Date: Sat, 29 Jul 2006 6:43:34 -0700 > From: > To: Pecanbread@... > Subject: Help > > > I have ordered the almond flour all ground up from the net and am finding that I have to throw out batches due to the inside not cooking. The consistency of the batter is different and I need to make adjustments from the recipe in the book. > Has anyone else had this problem and how did you adjust the batter? Thanks. > Rainlady's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2006 Report Share Posted July 29, 2006 > Date: Sat, 29 Jul 2006 6:43:34 -0700 > From: > To: Pecanbread@... > Subject: Help > > > I have ordered the almond flour all ground up from the net and am finding that I have to throw out batches due to the inside not cooking. The consistency of the batter is different and I need to make adjustments from the recipe in the book. > Has anyone else had this problem and how did you adjust the batter? Thanks. > Rainlady's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 31, 2006 Report Share Posted July 31, 2006 Hi Rainladys' mom, I get eggs from a friend's hens so the size varies, which in turn makes some batters wetter. If the batter is wetter than normal I add a little more nut flour. Sheila, SCD 2/01, UC 22yrs mom of and > > > I have ordered the almond flour all ground up from the net and am finding that I have to throw out batches due to the inside not cooking. The consistency of the batter is different and I need to make adjustments from the recipe in the book. > Has anyone else had this problem and how did you adjust the batter? Thanks. > Rainlady's mom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 14, 2006 Report Share Posted August 14, 2006 > > hi new here. going to start our family on this new diet. two older > boys, 7 and 3 have autism. we have a baby too that has an ear > infection, but I refuse to use antibiotics. anyways, the only thing > that bothers me is the no milk thing. they drink rice milk right now > or Vance's potato based milk. these are both a big fat NO right? and > almond milk cannot be used right away? Also, what brand of almond milk > could be used? I notice the ones I have seen have rice syrup in them. > is there a list like they have for a GFCF diet of everyday products > that can be used? Like brands. Like we can use Prego spag. sauce-it is > GFCF. I'm sure they add sugar so it would be illegal, but I was just > using that for an example. ANy help as far as how to get started would > be helpful-A > Commercial nut milks cannot be used. We make our own. Here is the recipe: NUT MILK by Marjan 100 grams of whole blanched hazelnuts, almonds or pecans (gives brownish milk) 1 litre of water a small pinch of salt optional: 1 tbsp of clear honey Put ingredients in blender and spin for about 10 minutes. Pour through a fine sieve. Squeeze out residue with the back of a spoon or squeeze out in a tea towel. Freeze residue (this is in fact very fine nut flour) and use for baking purposes. Store in the fridge. Use withing 2-3 days. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 14, 2006 Report Share Posted August 14, 2006 You're not going to have a whole lot of choices for the intro diet. Someone else may have some other suggestions, but I have not found that there are prepared foods that are scd legal. You can find a " legal " list of foods on the Breaking the Vicious Cycle web site. Be prepared that you're going to need to make your own apple or pear sauce for the diet, your own tomato sauce, ect. It can be overwhelming at first, but it's well worth the work of figuring it all out. Many people do introduce dairy a good month or long after beginning, but most use goat milk for their yogurt and goat cheeses. Personally, we switched from goat to cow for our son, and we've seen no problems. We're 3 1/2 months into the diet now. We have lots of frozen carrots for cooking, bananas, applesauce, chicken, and ground beef on hand. Especially in the first month. You'll also want to have the green beans around...my son just doesn't like them. Also, Welch's 100% grape juice is legal. Just make sure to dilute it. As I said, just keep at it even when you begin to feel overwhelmed. This group is a great help. Meleah scd 05/06 iel 3yrs., asd Ethan 5yrs., Mark 1yr. help > hi new here. going to start our family on this new diet. two older > boys, 7 and 3 have autism. we have a baby too that has an ear > infection, but I refuse to use antibiotics. anyways, the only thing > that bothers me is the no milk thing. they drink rice milk right now > or Vance's potato based milk. these are both a big fat NO right? and > almond milk cannot be used right away? Also, what brand of almond milk > could be used? I notice the ones I have seen have rice syrup in them. > is there a list like they have for a GFCF diet of everyday products > that can be used? Like brands. Like we can use Prego spag. sauce-it is > GFCF. I'm sure they add sugar so it would be illegal, but I was just > using that for an example. ANy help as far as how to get started would > be helpful-A > > > > > > > > For information on the Specific Carbohydrate Diet, please read the book > _Breaking the Vicious Cycle_ by Elaine Gottschall and read the following > websites: > http://www.breakingtheviciouscycle.info > and > http://www.pecanbread.com > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 14, 2006 Report Share Posted August 14, 2006 You're not going to have a whole lot of choices for the intro diet. Someone else may have some other suggestions, but I have not found that there are prepared foods that are scd legal. You can find a " legal " list of foods on the Breaking the Vicious Cycle web site. Be prepared that you're going to need to make your own apple or pear sauce for the diet, your own tomato sauce, ect. It can be overwhelming at first, but it's well worth the work of figuring it all out. Many people do introduce dairy a good month or long after beginning, but most use goat milk for their yogurt and goat cheeses. Personally, we switched from goat to cow for our son, and we've seen no problems. We're 3 1/2 months into the diet now. We have lots of frozen carrots for cooking, bananas, applesauce, chicken, and ground beef on hand. Especially in the first month. You'll also want to have the green beans around...my son just doesn't like them. Also, Welch's 100% grape juice is legal. Just make sure to dilute it. As I said, just keep at it even when you begin to feel overwhelmed. This group is a great help. Meleah scd 05/06 iel 3yrs., asd Ethan 5yrs., Mark 1yr. help > hi new here. going to start our family on this new diet. two older > boys, 7 and 3 have autism. we have a baby too that has an ear > infection, but I refuse to use antibiotics. anyways, the only thing > that bothers me is the no milk thing. they drink rice milk right now > or Vance's potato based milk. these are both a big fat NO right? and > almond milk cannot be used right away? Also, what brand of almond milk > could be used? I notice the ones I have seen have rice syrup in them. > is there a list like they have for a GFCF diet of everyday products > that can be used? Like brands. Like we can use Prego spag. sauce-it is > GFCF. I'm sure they add sugar so it would be illegal, but I was just > using that for an example. ANy help as far as how to get started would > be helpful-A > > > > > > > > For information on the Specific Carbohydrate Diet, please read the book > _Breaking the Vicious Cycle_ by Elaine Gottschall and read the following > websites: > http://www.breakingtheviciouscycle.info > and > http://www.pecanbread.com > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2009 Report Share Posted June 27, 2009 I am a Lurker,have been for a year and a half, sorry I don't post but I do read almost everyday. I have learned a lot from all of you. I used to have a oximeter (my Granddaughters bit off the button to turn it on) I have UIP I am not on 02 yet. I used to check my sats and I have told my Pulmodude about my sats dropping into the 80s when walking or doing things around house. He didn't believe me because my 6mw test is in the low 90s. Well I finially got my Dr to perscribe Pulminary Rehab. My question for all of you is this, I have been going to PR for 3 weeks already, this week I did 15 min on treadmill the whole time I have the thing on my finger to check my sats and they were never over 89. Then I did 15min on the Nustep when I was done my sats were only 83, then I did the stair steps, I did 1min 40sec and dropped to 79. Should I call my Dr and tell him all of this or should I just wait until I am done with PR and have them send the report to my Dr. I would really like some help with this. Jo Ann 53, UIP 9/07 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2009 Report Share Posted June 27, 2009 joann have the PR send a report to the doc immediately and call him to let him know what is happening if you can get a copy of the report, hand deliver it to your doc my 6 min walk can be very decieving -- it is on a flat surface in a controlled environment put me on steps and watch the SAT drop-- there are no steps when i do the 6 min walk plus... i don't talk in the beginning, i couldn't walk and talk at the same time -- my sat would drop quickly this was before O2 Pink Joyce (IPF 3/06) IFA 5/09 Pennsylvania Donate Life Listed 1/09 Inactive 4/09 www.transplantfund.org--- Subject: HelpTo: Breathe-Support Date: Saturday, June 27, 2009, 7:34 AM I am a Lurker,have been for a year and a half, sorry I don't post but I do read almost everyday. I have learned a lot from all of you. I used to have a oximeter (my Granddaughters bit off the button to turn it on) I have UIP I am not on 02 yet. I used to check my sats and I have told my Pulmodude about my sats dropping into the 80s when walking or doing things around house. He didn't believe me because my 6mw test is in the low 90s. Well I finially got my Dr to perscribe Pulminary Rehab. My question for all of you is this, I have been going to PR for 3 weeks already, this week I did 15 min on treadmill the whole time I have the thing on my finger to check my sats and they were never over 89. Then I did 15min on the Nustep when I was done my sats were only 83, then I did the stair steps, I did 1min 40sec and dropped to 79. Should I call my Dr and tell him all of this or should I just wait until I am done with PR and have them send the report to my Dr. I would really like some help with this.Jo Ann 53, UIP 9/07 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 27, 2009 Report Share Posted June 27, 2009 Hi Jo Ann and welcome! I'm glad you decided to post. It must be immensely frustrating to have your pulmonologist not believe you when you tell him your sats are dropping. Why on earth would you make that up? Sometimes a 6MW is over valued by doctors. It's usefulness is limited because it doesn't give you any information about how your sats react when you do your normal daily activities. Walking up a flight of stairs, folding a load of laundry, taking a shower etc. When I went to rehab 3 years ago, if a patients sats dropped as you describe yours, the therpists would have put in a call to the physician to get an order for oxygen. I would assume that's not happening in your case. Have you asked anyone at rehab about whether they think you need oxygen? Sats dropping to 79 is cause for action on their part. And yes, if they are not calling your doctor, you most certainly should. He has to believe what's happening at rehab as it's documented by a third party. Have you given any thought to switching pulmonologists or to seeking a second opinion? I'm uncomfortable with what you are describing. You don't say where you are but if you haven't already done so I would strongly suggest you seek out a university medical center with specialists in interstitial lung disease. You can start here, www.ipfnet.org but there are others. As you know we have members all over the place so let us know where you are if you want suggestions. Please continue to post, I'm glad you are here! Beth Moderator Fibrotic NSIP 06/06 Dermatomyositis 11/08 To: Breathe-Support Sent: Saturday, June 27, 2009 7:34:01 AMSubject: Help I am a Lurker,have been for a year and a half, sorry I don't post but I do read almost everyday. I have learned a lot from all of you. I used to have a oximeter (my Granddaughters bit off the button to turn it on) I have UIP I am not on 02 yet. I used to check my sats and I have told my Pulmodude about my sats dropping into the 80s when walking or doing things around house. He didn't believe me because my 6mw test is in the low 90s. Well I finially got my Dr to perscribe Pulminary Rehab. My question for all of you is this, I have been going to PR for 3 weeks already, this week I did 15 min on treadmill the whole time I have the thing on my finger to check my sats and they were never over 89. Then I did 15min on the Nustep when I was done my sats were only 83, then I did the stair steps, I did 1min 40sec and dropped to 79. Should I call my Dr and tell him all of this or should I just wait until I am done with PR and have them send the report to my Dr. I would really like some help with this.Jo Ann 53, UIP 9/07 Quote Link to comment Share on other sites More sharing options...
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