Guest guest Posted June 30, 2012 Report Share Posted June 30, 2012 You can have Achalasia of the Upper Esophageal Sphincter which is what i have these days after having had the ectomy in 2004! I have blockages high up in my htroat that they press on the windpipe and make me breathless! I am booked in for a dilatation of the upper sphincter this coming Wednesday. So what you say is that i don't have Achalasia! I have previously had Acalasia for the past13 years but in the early years it was confined to the lower sphincter and not the upper one. Having the ectomy was supposed to stop the Achalasia afecting the upper portion of my esophagus but the doctors differed so much about when to do the ectomy that i ended up being diagnosed at the end-stage of Achalasia and was warned to expect problems with the upper sphincter later in life. So these days i have to have regular dilatations of the upper sphincter to relieve my swallowing! from the UK ________________________________ From: bigbrillohead <imahockeymom@...> achalasia Sent: Friday, June 29, 2012 9:31 PM Subject: Achalasia on tv show -- Royal Pains  Does anyone watch the series Royal Pains on the USA network? This week's show really ticked me off.... there is a male who is " choking " on a soft bolus that won't dislodge with the Heimlich because it is too malleable. (The doctor ends up MacGyvering a sort of suction machine at the side of the road to " save " the guy's life.) Later on the same patient has chest pains that the doc chalks up to heartburn. Then at the end of the show the doc has a " lightbulb moment " and decides that the patient has achalasia and ends up tracking down the patient " choking " while running in a race, and the guy has coughed up a bunch of blood. The doc ends up " scoping " the guy at the side of the running trail (using only about 5 " of the scope tube) and then uses what looked to be tonsil forceps to remove the foreign body. The guy can now breathe, and he gets sent off to the hospital to be checked to see if he tore his esophagus. Now, being a nursing student, I'm known to scoff at medical shows from time to time (did y'all know that they DO NOT shock you with the defibrillator if you have a flat-line on the EKG? and yet EVERY medical show will show that time and time again... " Asystole, charge to 300! " ). Doctors don't really start IVs or take blood pressures, in spite of what you may see on tv, and I'll call 'em out on it every time I see it in a show. But this? Achalasia causing someone to choke and turn blue? Achalasia causing someone (who is such a new onset achalasian that this is only their second " stuckage " ever!) to bleed copious amounts of blood from a SOFT foreign body? And since when do our stuckages occur in the back of our mouth (able to be reached with tonsil forceps), instead of down lower in our esophagus? Oh man, I was SOOOOO pissed off watching that show. My 12yo son came in late in the show, and I paused the tv and looked at him and said, " The doctor thinks the guy has achalasia... have you EVER seen me look ANYTHING like that??? " I was diagnosed with achalasia four years before my son was even born -- his mom having achalasia is all he knows -- and even HE was scoffing at the inaccurate portrayal on the tv show. I know it's just Hollywood and they make things up for maximum entertainment value, but it REALLY ticks me off when they exploit our disease like that. Can you imagine some newly-diagnosed person seeing that, thinking they're going to just start choking and bleeding while they walk down the street? *sigh* Debbi in Michigan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2012 Report Share Posted July 1, 2012 I'd give the show a pass if not for the fact that the doc talked about it being the sphincter muscle at the top of the stomach.... kinda hard to pass that off as being the UES!!! > > You can have Achalasia of the Upper Esophageal Sphincter which is what i have these days after having had the ectomy in 2004! I have blockages high up in my htroat that they press on the windpipe and make me breathless! I am booked in for a dilatation of the upper sphincter this coming Wednesday. So what you say is that i don't have Achalasia! I have previously had Acalasia for the past13 years but in the early years it was confined to the lower sphincter and not the upper one. Having the ectomy was supposed to stop the Achalasia afecting the upper portion of my esophagus but the doctors differed so much about when to do the ectomy that i ended up being diagnosed at the end-stage of Achalasia and was warned to expect problems with the upper sphincter later in life. So these days i have to have regular dilatations of the upper sphincter to relieve my swallowing! > from the UK > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2012 Report Share Posted July 1, 2012 The upper sphincter that i am talking about is at the top of the esophagus not the stomach. My ectomy anastomosis in about 2 inches below the upper sphincter so that rules me out of further surgery for now and have to content myself with dilatations to help ease the strictures that i get in that area. from the UK ________________________________ From: bigbrillohead <imahockeymom@...> achalasia Sent: Sunday, July 1, 2012 9:48 AM Subject: Re: Achalasia on tv show -- Royal Pains  I'd give the show a pass if not for the fact that the doc talked about it being the sphincter muscle at the top of the stomach.... kinda hard to pass that off as being the UES!!! > > You can have Achalasia of the Upper Esophageal Sphincter which is what i have these days after having had the ectomy in 2004! I have blockages high up in my htroat that they press on the windpipe and make me breathless! I am booked in for a dilatation of the upper sphincter this coming Wednesday. So what you say is that i don't have Achalasia! I have previously had Acalasia for the past13 years but in the early years it was confined to the lower sphincter and not the upper one. Having the ectomy was supposed to stop the Achalasia afecting the upper portion of my esophagus but the doctors differed so much about when to do the ectomy that i ended up being diagnosed at the end-stage of Achalasia and was warned to expect problems with the upper sphincter later in life. So these days i have to have regular dilatations of the upper sphincter to relieve my swallowing! > from the UK > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2012 Report Share Posted July 1, 2012 Oh my! Best wishes,. Interesting that our ailment is on the telly (I think that's what you guys call it.) Dan Hulmes <christine.hulmes@...> wrote: The upper sphincter that i am talking about is at the top of the esophagus not the stomach. My ectomy anastomosis in about 2 inches below the upper sphincter so that rules me out of further surgery for now and have to content myself with dilatations to help ease the strictures that i get in that area. from the UK ________________________________ From: bigbrillohead <imahockeymom@...> achalasia Sent: Sunday, July 1, 2012 9:48 AM Subject: Re: Achalasia on tv show -- Royal Pains  I'd give the show a pass if not for the fact that the doc talked about it being the sphincter muscle at the top of the stomach.... kinda hard to pass that off as being the UES!!! > > You can have Achalasia of the Upper Esophageal Sphincter which is what i have these days after having had the ectomy in 2004! I have blockages high up in my htroat that they press on the windpipe and make me breathless! I am booked in for a dilatation of the upper sphincter this coming Wednesday. So what you say is that i don't have Achalasia! I have previously had Acalasia for the past13 years but in the early years it was confined to the lower sphincter and not the upper one. Having the ectomy was supposed to stop the Achalasia afecting the upper portion of my esophagus but the doctors differed so much about when to do the ectomy that i ended up being diagnosed at the end-stage of Achalasia and was warned to expect problems with the upper sphincter later in life. So these days i have to have regular dilatations of the upper sphincter to relieve my swallowing! > from the UK > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2012 Report Share Posted July 1, 2012 I have also had problems with my upper sphincter - didn't know of anyone else until this post! Glad to know that I can get the upper sphincter dilated! Although I haven't choked yet, I do often feel food get stuck up there. This didn't show up on me until I had my HM last summer. I drink a magnesium drink (highly recommend ionic fizz magnesium drink - it tastes like pink lemonade) every day which helps. Also avoiding stress, coffee, alchohol helps. Thanks for the info! This post is not to say that the tv show is justified, at least it's getting some national coverage. Gunn > > You can have Achalasia of the Upper Esophageal Sphincter which is what i have these days after having had the ectomy in 2004! I have blockages high up in my htroat that they press on the windpipe and make me breathless! I am booked in for a dilatation of the upper sphincter this coming Wednesday. So what you say is that i don't have Achalasia! I have previously had Acalasia for the past13 years but in the early years it was confined to the lower sphincter and not the upper one. Having the ectomy was supposed to stop the Achalasia afecting the upper portion of my esophagus but the doctors differed so much about when to do the ectomy that i ended up being diagnosed at the end-stage of Achalasia and was warned to expect problems with the upper sphincter later in life. So these days i have to have regular dilatations of the upper sphincter to relieve my swallowing! > from the UK > > > ________________________________ > From: bigbrillohead <imahockeymom@...> > achalasia > Sent: Friday, June 29, 2012 9:31 PM > Subject: Achalasia on tv show -- Royal Pains > > > Â > > Does anyone watch the series Royal Pains on the USA network? > > This week's show really ticked me off.... there is a male who is " choking " on a soft bolus that won't dislodge with the Heimlich because it is too malleable. (The doctor ends up MacGyvering a sort of suction machine at the side of the road to " save " the guy's life.) Later on the same patient has chest pains that the doc chalks up to heartburn. > > Then at the end of the show the doc has a " lightbulb moment " and decides that the patient has achalasia and ends up tracking down the patient " choking " while running in a race, and the guy has coughed up a bunch of blood. The doc ends up " scoping " the guy at the side of the running trail (using only about 5 " of the scope tube) and then uses what looked to be tonsil forceps to remove the foreign body. The guy can now breathe, and he gets sent off to the hospital to be checked to see if he tore his esophagus. > > Now, being a nursing student, I'm known to scoff at medical shows from time to time (did y'all know that they DO NOT shock you with the defibrillator if you have a flat-line on the EKG? and yet EVERY medical show will show that time and time again... " Asystole, charge to 300! " ). Doctors don't really start IVs or take blood pressures, in spite of what you may see on tv, and I'll call 'em out on it every time I see it in a show. > > But this? Achalasia causing someone to choke and turn blue? Achalasia causing someone (who is such a new onset achalasian that this is only their second " stuckage " ever!) to bleed copious amounts of blood from a SOFT foreign body? And since when do our stuckages occur in the back of our mouth (able to be reached with tonsil forceps), instead of down lower in our esophagus? Oh man, I was SOOOOO pissed off watching that show. > > My 12yo son came in late in the show, and I paused the tv and looked at him and said, " The doctor thinks the guy has achalasia... have you EVER seen me look ANYTHING like that??? " I was diagnosed with achalasia four years before my son was even born -- his mom having achalasia is all he knows -- and even HE was scoffing at the inaccurate portrayal on the tv show. > > I know it's just Hollywood and they make things up for maximum entertainment value, but it REALLY ticks me off when they exploit our disease like that. Can you imagine some newly-diagnosed person seeing that, thinking they're going to just start choking and bleeding while they walk down the street? > > *sigh* > > Debbi in Michigan > > > > > Quote Link to comment Share on other sites More sharing options...
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