Guest guest Posted February 22, 2011 Report Share Posted February 22, 2011 Hi , I am okay, are you enjoying yourself? did you go to the Hoover Dan or Golden Nugget?... thank you. Love, Live, and Laugh ________________________________ From: <fr_dxb@...> cures for AIDS Sent: Tue, February 22, 2011 3:41:08 PM Subject: Re: hello Hi dear Eva , how are you , I'm in Vegas now ... Sent from my BlackBerry® smartphone from du hello Is anyone here.? Love, Live, and Laugh Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2011 Report Share Posted February 22, 2011 I'm here...just busy as hell. Hope everyone is doing well. I'm in the middle of a candida cleanse, which is going great. Hopefully, I will get my toenail back...lol. From: Eva V <ev204@...> Subject: Re: hello cures for AIDS Date: Tuesday, February 22, 2011, 4:20 PM  Hi , I am okay, are you enjoying yourself? did you go to the Hoover Dan or Golden Nugget?... thank you.  Love, Live, and Laugh ________________________________ From: <fr_dxb@...> cures for AIDS Sent: Tue, February 22, 2011 3:41:08 PM Subject: Re: hello Hi dear Eva , how are you , I'm in Vegas now ... Sent from my BlackBerry® smartphone from du hello Is anyone here.?  Love, Live, and Laugh    Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 22, 2011 Report Share Posted February 22, 2011 LOL! I'm here, just been super busy lately. Nothing new with me although I might share my story with a radio show soon. If so I will post the link on here. From: Eva V <ev204@...> Subject: hello cures for AIDS Date: Tuesday, February 22, 2011, 2:14 PM  Is anyone here.?  Love, Live, and Laugh Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2011 Report Share Posted March 21, 2011 Hi Janna I am impressed that you have found out how " NOT NOT NOT " to have surgery. MY A started about 5 years ago. I am the same way, waiting for a better solution than a cut e, I know this works great for most people. http://en.wikipedia.org/wiki/Alkaline_diet " famous proponents of the alkaline diet is Young, who has come under scrutiny from the National Council Against Health Fraud.[1] " I am not sure about the Alkaline diet, however if it works, use it. Could you tell just what you eat for the Alkaline diet, I see many books are available. After doing years of research, I find out what works for me Butter,English Muffins toasted WELL with lots of holes for the butter to sink in, Coke with CO2, Magnesium two 250mg a day, chocolate, Hot coffee, Macoroni and cheese with butter mixed in, Pasta and mixed with butter, Bushes brown beans with some water and butter mixed in, ice cream, milk shakes and Lactaid 4% milk with cerial. Butter makes it slip down, you must use real butter for the fat content. Just have your Cholesterol checked out, I am on Crestor 10 mg. Foods Decrease LES Pressure from Medical Report on GERD, just don't eat the late in the day or you might get indigestion at night. Chocolate Coffee Ethanol Fat=butter Peppermint Spearmint High fiber diet Ray CA OC old as hell 80 doing great!!!!!!!!!!!!!!!!! > > I was diagnosed with A about 5 years ago and have worked to avoid surgery. I have followed several regimens for managing this situation which I understand are considered to be " alternative " but for me they have done a good job. I do not know if they would help anyone else. I rarely see these things mentioned on Achalasia sites. First, when I was diagnosed, I went on a 10 day fast. I consumed nothing but Spirulina, yogurt and a little fruit juice. Then I moved on to an alkaline diet, there are many books out there on the subject. I have tried to grasp an understanding through these books as to the foods that are acid producing. I also study yoga and was introduced to some routines called " bandhas " which include breathing practices that influence relaxation & digestion. Since that time I have also gotten my " green card " through the thcfn.org since my state has made it legal to use hemp oil in my food. This has helped a lot with digestion problems, acid reflux and achalasia. My own journeys with this situation have shown me a variety of alternatives to surgery. I do not know if they would work for others. I only know I am much happier and experience much fewer episodes. I can say that what I eat really influences the existence of inflammation and spasms in the esophagus, hence the use of anti-inflammatory foods which seem to follow the alkaline diet scheme. I sincerely hope this information is of help to you and that you are not offended by it. > > Sincerely, > > Janna > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 14, 2011 Report Share Posted July 14, 2011 HelloFYI Ellen Ellen Garber Bronfeld egskb@... Hello " Let's do together what we can't do alone! " From The Desk of Shirley A. Executive Director Family Support Network Is this email not displaying correctly? View it in your browser. Hello Family Support Network Members and Friends, I would like to take this opportunity to say thank you. Your telephone calls, emails and words of encouragement have truly inspired me! I am excited about our new partnership in advocacy and I look forward to working with each of you. As a parent of an adult with a developmental disability, I understand first-hand our daily struggles. I embrace the challenge of continuing the GREAT work of Charlotte Cronin, but I can’t do it without your support! Sincerely, Shirley A. ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~\ ~~~~~ Please find my Contact Information: The Family Support Network of Illinois 651 E. 159th Place South Holland, IL 60473 Telephone: 708-331-7370 ~ Fax: 708-339-5423 ~ Email: ShirleyFSN@... Website: www.familysupportnetwork.org ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~\ ~~~~~~ Help support the work of the Family Support Network and The Arc of Illinois in these difficult times. Please become a member! Here’s a link to our membership brochure. We NEED you. http://www.familysupportnetwork.org/miscellaneous%20pdfs/2009%20Membership%20Bro\ chure.pdf The mission of the Family Support Network is to unify individuals with disabilities and their families to advocate for funding, services, and community resources that strengthen and support the individual and the family directly by responding to their individual needs and empowering them to live in their own homes. The Family Support Network further seeks to ensure the continuation of all individual supports throughout the life span of the individual. follow on Twitter | friend on Facebook | forward to a friend Copyright © *|2011|* *|Family Support Network Illinois|*, All rights reserved. You are receiving this email because you signed up to be a part of our network. Thank you for your continued support! Our mailing address is: *ShirleyFSN@..._HTML|**|END:IF|* unsubscribe from this list | update subscription preferences Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 12, 2011 Report Share Posted October 12, 2011 Hi, I've just joined this group. I have the symptoms of an underactive thyroid, but my blood results suggest an overactive thyroid! Do you think I may benifit from t3? Going to make an appointment to see my GP to see if he's willing to test my T3, or to refer me to an endocrineologist. Any help and advice will be gratefully recieved. Judith Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 7, 2012 Report Share Posted May 7, 2012 I had that surgery and of you would like to talk more in depth I am willing to. I will be home around 6 tonight if you would like to call and talk and ask questions. in Georgia Sent from my iPhone On May 7, 2012, at 9:15, " amandatroff " <amandatroff@...> wrote: > Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. > > My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. > > Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) > > They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. > > > > > TODAY(Beta) • Powered by > New company tops Fortune 500 list > Privacy Policy > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 7, 2012 Report Share Posted May 7, 2012 Hi Yes I had the same problem on my second Barium swallow 3-4 years ago, when I was real real bad. The Doctor gave me barium, then said spit it out NOW, no opening, dont want it to get in the lungs.!Then had a manometry test and confirmed classic A. If the LES is really closed I should have suggested Nifedipine 10 mg which helps to open the LES. I used it a bit, crack in teeth but it worked for me. Just let a bit of it go down, 10 mg might give a headache. Still have the prescription June 2008, my god 4 years of suffering, maybe 6 years!. http://www.ncbi.nlm.nih.gov/pubmed/2679048 Ray CA OC > > > > But first of all you have to get some nourishment. If you cant get water down means you have food stuck in the LES, regurgitate the e using a lot of water or several COLD COKES. Just dont get it in the lungs. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 The National Institute of Health Study posted only indicated a 26% reduction in LES pressure while the Opioid Hypersensitivity in Achalasia study reported an average 46% drop in LES pressure among achalasians with administration of morphine. Google achalasia and morphine and read the whole pdf. Study parameters were similar with double blind/placebo and a control/test group, although the Opioid hypersensitivity study included a " healthy " group which was markedly less sensitive to LES relaxation than the achalasia group. I certainly wouldn't want Nifedipine's severe headache side effects and limited efficacy. Steve > > > > > > > But first of all you have to get some nourishment. If you cant get water down means you have food stuck in the LES, regurgitate the e using a lot of water or several COLD COKES. Just dont get it in the lungs. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 Hi. I had what we at the group called an oesophagectomy or an " ectomy " for short back in October 2004. I went on to require 8 dilatations within the 1st year post-op but it soon settled down and i went on to live a normal life. My eating remained fairly poor so the doctors decided to put in a Jejunostomy feeding tube for me to use overnight and have used it now for over 6 years in total, the recent one was only changed a few months ago after the previous one being in situ for over 2 years. Don't get me wrong i still eat but not enough to put any weight on so i use the jejunal feeding tube to give me that little bit extra of nutrients while i don't have to worry about eating during the day. I enjoy 3 snacks a day but not enough to maintain my weight. With my stomach up in my chest (it was made into a new tube) there is less room for food but i get by. I had to have my oesophagus removed as it had enlarged so big it was pushing my lungs to either side and pressing on my heart (it was as big as an average sized football). If i had to go through with the operation again i would as i believe it saved my life. from the UK ________________________________ From: amandatroff <amandatroff@...> achalasia Sent: Monday, May 7, 2012 2:15 PM Subject: Hello  Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 I had the surgery when I was 29, I am now 34 and doing well. As has said, I too am willing to talk more in depth. I'm a silent member, mainly read since I had surgery. Just shout. in WV Connected by DROID on Verizon Wireless Re: Hello I had that surgery and of you would like to talk more in depth I am willing to. I will be home around 6 tonight if you would like to call and talk and ask questions. in Georgia Sent from my iPhone On May 7, 2012, at 9:15, " amandatroff " <amandatroff@...> wrote: > Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. > > My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. > > Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) > > They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. > > > > > TODAY(Beta) • Powered by > New company tops Fortune 500 list > Privacy Policy > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 Thanks . I appreciate your reply. It is helpful to hear about other's experiences. I'm trying to calm myself down. Are you able to work and have a decent quality of life? My best to you. Faith Sent from my iPod On May 8, 2012, at 3:19, Hulmes <christine.hulmes@...> wrote: > Hi. > I had what we at the group called an oesophagectomy or an " ectomy " for short back in October 2004. I went on to require 8 dilatations within the 1st year post-op but it soon settled down and i went on to live a normal life. My eating remained fairly poor so the doctors decided to put in a Jejunostomy feeding tube for me to use overnight and have used it now for over 6 years in total, the recent one was only changed a few months ago after the previous one being in situ for over 2 years. Don't get me wrong i still eat but not enough to put any weight on so i use the jejunal feeding tube to give me that little bit extra of nutrients while i don't have to worry about eating during the day. I enjoy 3 snacks a day but not enough to maintain my weight. With my stomach up in my chest (it was made into a new tube) there is less room for food but i get by. I had to have my oesophagus removed as it had enlarged so big it was pushing my lungs to either side and > pressing on my heart (it was as big as an average sized football). If i had to go through with the operation again i would as i believe it saved my life. > from the UK > > > ________________________________ > From: amandatroff <amandatroff@...> > achalasia > Sent: Monday, May 7, 2012 2:15 PM > Subject: Hello > > > > > Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. > > My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. > > Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) > > They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 Hi Faith My quality of life is as best as i can have considering that i have had the surgery but i try and eat what i can and again i can have my off days where i am lucky to be able to eat one snack. But never mind as i don't worry because i have the jejunal feed to fall back on so i don't " starve " as some would say. On a good day i can eat 3 sometimes 4 small snacks! Try not to worry. What wil be wil be. If you're meant to have the operation then you'll have it. There are plenty of others who both contribute and offer good advice here so don't just take my advice, read other posts before deciding on the ectomy as it is a life changing operation and no turning back once you have it. Please ask me some more questions if you think i can help. Take care. from the UK ________________________________ From: Faith Weiss <weissf@...> " achalasia " <achalasia > Sent: Tuesday, May 8, 2012 12:14 PM Subject: Re: Hello  Thanks . I appreciate your reply. It is helpful to hear about other's experiences. I'm trying to calm myself down. Are you able to work and have a decent quality of life? My best to you. Faith Sent from my iPod On May 8, 2012, at 3:19, Hulmes <christine.hulmes@...> wrote: > Hi. > I had what we at the group called an oesophagectomy or an " ectomy " for short back in October 2004. I went on to require 8 dilatations within the 1st year post-op but it soon settled down and i went on to live a normal life. My eating remained fairly poor so the doctors decided to put in a Jejunostomy feeding tube for me to use overnight and have used it now for over 6 years in total, the recent one was only changed a few months ago after the previous one being in situ for over 2 years. Don't get me wrong i still eat but not enough to put any weight on so i use the jejunal feeding tube to give me that little bit extra of nutrients while i don't have to worry about eating during the day. I enjoy 3 snacks a day but not enough to maintain my weight. With my stomach up in my chest (it was made into a new tube) there is less room for food but i get by. I had to have my oesophagus removed as it had enlarged so big it was pushing my lungs to either side and > pressing on my heart (it was as big as an average sized football). If i had to go through with the operation again i would as i believe it saved my life. > from the UK > > > ________________________________ > From: amandatroff <amandatroff@...> > achalasia > Sent: Monday, May 7, 2012 2:15 PM > Subject: Hello > > > > > Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. > > My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. > > Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) > > They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 That might work, Ray, except that I'm *very* allergic to it (ALL calcium channel blockers) -- and wasn't long before I discovered that it was the *only* drug my GIs considered suitable for Achalasia. Beyond that, they had *zip* to offer. They seemed terrified of nitro compounds. I'm lucky I stumbled on the GERD list on my own, or I might not have made it TO the Heller. The GIs seemed quite content to say: " Ensure, " and let me starve. xox > > > > > > > But first of all you have to get some nourishment. If you cant get water down means you have food stuck in the LES, regurgitate the e using a lot of water or several COLD COKES. Just dont get it in the lungs. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 Oh my gosh -that is terrible at such a young age. And a very drastic step. There are a few here I believe who have experience in that category.  Best of luck to you!@  Kim A Wi ________________________________ From: amandatroff <amandatroff@...> achalasia Sent: Monday, May 7, 2012 7:15 AM Subject: Hello  Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 8, 2012 Report Share Posted May 8, 2012 Ethanol? Isn't that in gasoline? ________________________________ From: mer <ray_me_99@...> achalasia Sent: Monday, May 7, 2012 1:07 PM Subject: Re: Hello  Hi I have posted this before, from a GERD medical report. Also in my case I would try Magnesium Oxide 250 mg fron the drug store, believe it seems to open the LES, in my case. It dissolves quickly in the e. I use two a day and makes a great BM, if you get some fiber down. Also butter add a teaspoon to the water, fat or butter does two things, opens the LES and relaxes it. Or olive oil also works. Foods Decrease LES Pressure Chocolate Coffee Ethanol Fat Peppermint Spearmint High fiber diet Foods Increase LES Pressure Protien I try to get foods with a high fiber content. Clearing out the e after every meal and especially at night will prevent the large e, this is how I manage the A. I hope that if you clear out the e the large e MIGHT retreat, will take some time, have not seen a study on this, it is worth a try. But first of all you have to get some nourishment. If you cant get water down means you have food stuck in the LES, regurgitate the e using a lot of water or several COLD COKES. Just dont get it in the lungs. I wish you well!! Let us know of your progress. I hope will respond to your question. Ray CA OC 81 old as hell and no HM. > > Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. > > My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. > > Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) > > They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2012 Report Share Posted May 9, 2012 For those of us who work full time and have to drive long distances to work, I cannot perceive taking morphine to control A. It just isn't realistic for everyone. ________________________________ From: nailheader <stevenakamichi@...> achalasia Sent: Tuesday, May 8, 2012 12:39 AM Subject: Re: Hello  The National Institute of Health Study posted only indicated a 26% reduction in LES pressure while the Opioid Hypersensitivity in Achalasia study reported an average 46% drop in LES pressure among achalasians with administration of morphine. Google achalasia and morphine and read the whole pdf. Study parameters were similar with double blind/placebo and a control/test group, although the Opioid hypersensitivity study included a " healthy " group which was markedly less sensitive to LES relaxation than the achalasia group. I certainly wouldn't want Nifedipine's severe headache side effects and limited efficacy. Steve > > > > > > > But first of all you have to get some nourishment. If you cant get water down means you have food stuck in the LES, regurgitate the e using a lot of water or several COLD COKES. Just dont get it in the lungs. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2012 Report Share Posted May 10, 2012 Lol to Ray " old as hell but still no hm " ... Too funny! California Sent from my iPhone On May 8, 2012, at 6:15 PM, Kim Abrams <xploring37@...> wrote: > Ethanol? Isn't that in gasoline? > > ________________________________ > From: mer <ray_me_99@...> > achalasia > Sent: Monday, May 7, 2012 1:07 PM > Subject: Re: Hello > > > > > Hi I have posted this before, from a GERD medical report. > Also in my case I would try Magnesium Oxide 250 mg fron the drug > store, believe it seems to open the LES, in my case. It dissolves quickly in the e. I use two a day and makes a great BM, if you get some fiber down. > > Also butter add a teaspoon to the water, fat or butter does two things, opens the LES and relaxes it. Or olive oil also works. > > Foods Decrease LES Pressure > Chocolate > Coffee > Ethanol > Fat > Peppermint > Spearmint > High fiber diet > > Foods Increase LES Pressure > Protien > > I try to get foods with a high fiber content. > > Clearing out the e after every meal and especially at night will prevent the large e, this is how I manage the A. I hope that if you clear out the e the large e MIGHT retreat, will take some time, have not seen a study on this, it is worth a try. > > But first of all you have to get some nourishment. If you cant get water down means you have food stuck in the LES, regurgitate the e using a lot of water or several COLD COKES. Just dont get it in the lungs. > > I wish you well!! Let us know of your progress. > > I hope will respond to your question. > > Ray CA OC 81 old as hell and no HM. > > > > > > Good Morning everyone. I joined this group a few weeks back, and wow, I finally feel like I am not alone with this horrible disease. > > > > My issues started as a young child (I can remember eating and throwing up regularly as young as 5). When I was 25 my lungs were 3/4 full of food and finally a Dr. figured out I was throwing up and it was going into my lungs. I went to Mayo in Rochester where I had a few different surgeries, I think that HM you all talk about and they cut the muscle into my stomach, made me a new flapper to keep stomach acids down etc. > > > > Now 6 years later I started having food stick so I went back for testing (barium, EDG etc.) and they found that my esophogus is so stretched and worn out it is now deforming and looks like a sink drain. So it goes down then makes a sharp 90 degree corner then has another length to go before emptying into my stomach. (My esophogus measures at 8 mm, the average is 2 mm) > > > > They told me my only option is to have my esophogus removed and to move my stomach up into it's place!?! Anybody know anything about this? I might agree to such a major body transformation at 80 but I am only 32 and scared. Looking for advice. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2012 Report Share Posted May 11, 2012 Hello, I concede this may be a fear reaction, and the treatment may not be suitable for everyone. (like for me, I can't possibly fathom why people drink alcohol, smoke tobacco or let their docs choose meds with overly adverse side-effect profiles). However, if a properly managed pain regimen is slowly titrated to effect, it can greatly ameliorate A symptoms, without causing sedation or loss of functionality. During pain management was the first time I gained any meaningful weight while also working a professional career, doing a lot of driving and road trips, engaging in hobbies and activities, exercising and socializing - many things that aren't possible for me now without any medical care. Also my attitude was much better than the bitter one expressed on this forum. This is just an option for people to consider. The Peligrani study showed a 46% drop in achalasia LES pressure, which seems to show more promising results with less risks and incisiveness compared to mechanical manipulation. Steve > > > > > > > > > > But first of all you have to get some nourishment. If you cant get water down means you have food stuck in the LES, regurgitate the e using a lot of water or several COLD COKES. Just dont get it in the lungs. > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2012 Report Share Posted May 26, 2012 wrote: > > ... For some of us, some times, it *isn't* a matter of a food bolus > holding things up, it is simply a matter of *nothing* is going to get > through. ... > Right. When I had my manometry the person doing the test told me that with the pressure my LES was making (well over 100 mmhg) it was impossible to get anything past it. He could not understand how I was surviving and yet unlike many I did not loose any weight. I suspect that my progression was so slow that my body learned to use the longitudinal muscles in a way to compensate for the problems with the circular muscles. But, it was getting worse and I was at a point that I didn't want to see how bad it could get and decided to have the surgery. notan Quote Link to comment Share on other sites More sharing options...
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