Guest guest Posted March 25, 2001 Report Share Posted March 25, 2001 Hey! (I used to live down south, too, and know this is the preferred version of " hi " !) I don't know any surgeons in the Austin area with qualifications in performing myotomy, but I wanted to chime in on the part of your message concerning length of time you could " safely " postpone surgery. While I wouldn't delay because, really, what's the point if you're only going to have the surgery anyhow, waiting six months probably won't make much difference. You've only been recently diagnosed, a point which is in your favor since, presumably, there hasn't been as much stress and damage done to your esophagus and LES muscle as is the case with folks who have suffered for years. The more trauma we put those body parts through, the weaker they are and the more distorted they can become. Good luck and take care - Carol New Patient > Hi, > > My name is Murali and have been diagnosed with Achalasia very recently > (Just last week). A year back, I started having heartburn, I started > taking Zantac and then, slowly, it got worse. Meaning I had excessive > belching, started having diffficulty swallowing. My > Gastroenterologist did an endoscopy ( in mid-february) and suspected > Achalasia right away, because of the fact that he had to force the > tube through my LES. It was very tight. He dilated it to 20mm. He > also put me on ISODRIL, a vasodilator(given to heart patients, to > dilate blood vessels), so that I can eat properly and regularly. It > works wonders. Then, he asked me to go for a barium swallow and a > manometry test. Manometry Test proved that I am a Classic example for > Achalasia. My Gastroenterologist has asked me to see a surgeon and > discuss/schedule myotomy(laproscopic one). My question to y'all: > Please recommend me some good surgeons in Austin, Texas who can do > this surgery. The surgeon I have been referred to is Dr. Fass. > Also, how long can I postpone (say 6 months) my surgery. Any help I > can get from y'all is greatly appreciated. > > Thank You very much. > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 4, 2001 Report Share Posted April 4, 2001 Howdy, Thanks for the information and support. Did you also have a myotomy, if yes when and how are you feeling now. Do let me know. Bye, Murali > Hey! (I used to live down south, too, and know this is the preferred version > of " hi " !) > I don't know any surgeons in the Austin area with qualifications in > performing myotomy, but I wanted to chime in on the part of your message > concerning length of time you could " safely " postpone surgery. While I > wouldn't delay because, really, what's the point if you're only going to > have the surgery anyhow, waiting six months probably won't make much > difference. You've only been recently diagnosed, a point which is in your > favor since, presumably, there hasn't been as much stress and damage done to > your esophagus and LES muscle as is the case with folks who have suffered > for years. The more trauma we put those body parts through, the weaker they > are and the more distorted they can become. > > Good luck and take care - > Carol > > New Patient > > > > Hi, > > > > My name is Murali and have been diagnosed with Achalasia very recently > > (Just last week). A year back, I started having heartburn, I started > > taking Zantac and then, slowly, it got worse. Meaning I had excessive > > belching, started having diffficulty swallowing. My > > Gastroenterologist did an endoscopy ( in mid-february) and suspected > > Achalasia right away, because of the fact that he had to force the > > tube through my LES. It was very tight. He dilated it to 20mm. He > > also put me on ISODRIL, a vasodilator(given to heart patients, to > > dilate blood vessels), so that I can eat properly and regularly. It > > works wonders. Then, he asked me to go for a barium swallow and a > > manometry test. Manometry Test proved that I am a Classic example for > > Achalasia. My Gastroenterologist has asked me to see a surgeon and > > discuss/schedule myotomy(laproscopic one). My question to y'all: > > Please recommend me some good surgeons in Austin, Texas who can do > > this surgery. The surgeon I have been referred to is Dr. Fass. > > Also, how long can I postpone (say 6 months) my surgery. Any help I > > can get from y'all is greatly appreciated. > > > > Thank You very much. > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2006 Report Share Posted March 4, 2006 CPT defines a new patient as someone you have not seen before, or someone you have not seen within the last three years. The premise is that you should have recent history and past medical history available. Also understand that your threshold for a higher level of service with an establish patient procedure code is easier to reach since you are only required to meet two of the three main parameters. Thus a detailed established patient evaluation could be submitted with 99214. The same exam, history, clinical decision making would be consistent with 99203 as a new patient. The Relative Value Units between the two are close (2.56 vs 2.18). Tom Freedland Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2006 Report Share Posted March 4, 2006 leary353@... wrote: > docs; > I know this has been dealt with before, but, when an existing patient is involved in a new MVA, the mechanism of injury is different, new body parts involved and new exam necessary, shouldn't we be billing for a new patient exam? got one kicked back denied because they were an existing patient. > > any thoughts, > Don Leary, Dc > West Salem > > IMHO, most certainly YES.....New injury requires new exam....It is necessary to determine whether the old treatment plan or diagnosis were adequate for the new post-injury status. I think the denial is bogus. Document your findings, list what is new and different, and what treatment arises from the new injury. Keep notes that reflect which care/diagnosis is related to which condition. With the proper documentation and the proper attorney, you will help your patient's legal case too, as he is entitled to certain standard of care, including diagnostic exams. Good luck. Keep us posted. J. Pedersen DC > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2006 Report Share Posted March 4, 2006 Hi Don, It would be my opinion that since this is an established patient you are performing a " new exam " new area, due to a new injury, nonetheless they are an established patient in your clinic. Consequently you would need to use one of the established patient exam codes. Vern Saboe, DC Albany new patient > docs; > I know this has been dealt with before, but, when an existing patient is involved in a new MVA, the mechanism of injury is different, new body parts involved and new exam necessary, shouldn't we be billing for a new patient exam? got one kicked back denied because they were an existing patient. > > any thoughts, > Don Leary, Dc > West Salem > > > > OregonDCs rules: > 1. Keep correspondence professional; the purpose of the listserve is to foster communication and collegiality. No personal attacks on listserve members will be tolerated. > 2. Always sign your e-mails with your first and last name. > 3. The listserve is not secure; your e-mail could end up anywhere. However, it is against the rules of the listserve to copy, print, forward, or otherwise distribute correspondence written by another member without his or her consent, unless all personal identifiers have been removed. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2006 Report Share Posted March 4, 2006 Don, I agree with Tom and Vern. You've seen the pt. before but it requires a new exam so it''s an established pt. exam. To be accurate and to work in the best interest of truth and your patients, you need to keep your treatments separate and keep your records carefully separated. (Within reason.) In the future when you reexamine the pt. you need to do two separate exams for the different injuries. It would be reasonable to downcode to a lower level exam for each but unreasonable to pretend they were not more complicated than examining the whole patient. You must anticipate being asked to demarcate all sorts of weird conclusions such as the affect of one injury on the recovery of the other. For that hassle, you get to separate your work and get paid for it. To further the argument, if there were 2 separate insurers, it would be dishonest to make one of them pay for care for the other's covered injuries. On the other hand, some things overlap. (A hospital stay for 2 conditions would necessarily be 1/2 the cost of 2 consecutive stays.) I have had reasonable adjusters agree to share the cost of certain services. It is reasonable and defensible. If either case went to trial, the judge would probably instruct the attorneys to avoid discussing why some things were charged differently. Important to add that if your name is Leary, then it once was O'leary and if so you already know that something that is Irish and sits out in the rain is termed... Patio Furniture! (Top of the evenin’ to ya!) ( E. Abrahamson, D.C.) Chiropractic physician Lake Oswego Chiropractic Clinic 315 Second Street Lake Oswego, OR 97034 503-635-6246 Website: http://www.lakeoswegochiro.com > From: " leary353@... " <leary353@...> > Date: Sat, 4 Mar 2006 21:42:12 GMT > < > > Subject: new patient > > docs; > I know this has been dealt with before, but, when an existing patient is > involved in a new MVA, the mechanism of injury is different, new body parts > involved and new exam necessary, shouldn't we be billing for a new patient > exam? got one kicked back denied because they were an existing patient. > > any thoughts, > Don Leary, Dc > West Salem > > > > OregonDCs rules: > 1. Keep correspondence professional; the purpose of the listserve is to foster > communication and collegiality. No personal attacks on listserve members will > be tolerated. > 2. Always sign your e-mails with your first and last name. > 3. The listserve is not secure; your e-mail could end up anywhere. However, it > is against the rules of the listserve to copy, print, forward, or otherwise > distribute correspondence written by another member without his or her > consent, unless all personal identifiers have been removed. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2006 Report Share Posted March 4, 2006 Hi Don, We had a billing on a new patient kicked back without payment for the initial exam. They just paid for the treatment. The front desk asked me to call them. I asked how I was suppose to know what to do for the patient without an exam. The first responder told me that it was included in the treatment code. I asked to speak to her supervisor and repeated my question. The super said, " It's an obvious mistake; I'll take care of it. " And, it was.... Sears Portland On Mar 4, 2006, at 1:42 PM, leary353@... wrote: > docs; > I know this has been dealt with before, but, when an existing patient > is involved in a new MVA, the mechanism of injury is different, new > body parts involved and new exam necessary, shouldn't we be billing > for a new patient exam? got one kicked back denied because they were > an existing patient. > > any thoughts, > Don Leary, Dc > West Salem > > > > OregonDCs rules: > 1. Keep correspondence professional; the purpose of the listserve is > to foster communication and collegiality. No personal attacks on > listserve members will be tolerated. > 2. Always sign your e-mails with your first and last name. > 3. The listserve is not secure; your e-mail could end up anywhere. > However, it is against the rules of the listserve to copy, print, > forward, or otherwise distribute correspondence written by another > member without his or her consent, unless all personal identifiers > have been removed. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 20, 2008 Report Share Posted October 20, 2008 Mike and his mom  Welcome to our home and now your home also  Yes stress can do some strange things to us. For some it can make us worse and others it can bring on flairs. I have had this fun life of stills now for over 8 years and I was 41 when I was dx with it. I was married at the time and had two kids and a great Job. Well life threw me a few loops and some major changes but in the end stills gave me some gifts and a happier life and a great wife that replaced a none understanding one who divorced me because of stills.   One thing I can suggest that will help I believe you both and all of your family that live with Mike and care and love him as you his Mother I believe dose is go to concealing both for Mike as some things in life will change and it can help him change and adjust to life with a chronic illness and to the rest of the family as in dealing with some one in Mikes boat and how to best help them but not destroy there self worth. It is a learning process and it is always learning. Be it about stills or about your self. Life dose go one for some better then others but it go's on and how you deal with it will I feel depends on family, friends, and your doctors.  You have started in a good place as we try to pass info on and we have some fun also. So with that welcome and ask any thing you wish be it here or privately but I will worn you I am honest so do not ask if you do not want to really know. By the way I am a man who is now 50 had stills for almost 9 years now and had both bad and good changes from and because of it Best to ya the rednecks Marty & G. the redneck's my space http://www.myspace.com/martyg58   Stills ; An illness I know to well! To learn about Stills  http://www.stillsdisease.org/stills_info If you find yourself in a hole, the first thing to do is stop diggin'.  In the old days a man who saved money was a miser; nowadays he's a wonder. ~Author Unknown  " Taking my gun away because I might shoot someone is like cutting my tongue out because I might yell `Fire!' in a crowded theater. " -- Venetoklis  a government and its agents are under no general duty to provide public services, such as police protection, to any particular individual citizen... -- Warren v. District of Columbia, 444 A.2d 1 (D.C. App.181) __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 20, 2008 Report Share Posted October 20, 2008 Mike and his mom  Welcome to our home and now your home also  Yes stress can do some strange things to us. For some it can make us worse and others it can bring on flairs. I have had this fun life of stills now for over 8 years and I was 41 when I was dx with it. I was married at the time and had two kids and a great Job. Well life threw me a few loops and some major changes but in the end stills gave me some gifts and a happier life and a great wife that replaced a none understanding one who divorced me because of stills.   One thing I can suggest that will help I believe you both and all of your family that live with Mike and care and love him as you his Mother I believe dose is go to concealing both for Mike as some things in life will change and it can help him change and adjust to life with a chronic illness and to the rest of the family as in dealing with some one in Mikes boat and how to best help them but not destroy there self worth. It is a learning process and it is always learning. Be it about stills or about your self. Life dose go one for some better then others but it go's on and how you deal with it will I feel depends on family, friends, and your doctors.  You have started in a good place as we try to pass info on and we have some fun also. So with that welcome and ask any thing you wish be it here or privately but I will worn you I am honest so do not ask if you do not want to really know. By the way I am a man who is now 50 had stills for almost 9 years now and had both bad and good changes from and because of it Best to ya the rednecks Marty & G. the redneck's my space http://www.myspace.com/martyg58   Stills ; An illness I know to well! To learn about Stills  http://www.stillsdisease.org/stills_info If you find yourself in a hole, the first thing to do is stop diggin'.  In the old days a man who saved money was a miser; nowadays he's a wonder. ~Author Unknown  " Taking my gun away because I might shoot someone is like cutting my tongue out because I might yell `Fire!' in a crowded theater. " -- Venetoklis  a government and its agents are under no general duty to provide public services, such as police protection, to any particular individual citizen... -- Warren v. District of Columbia, 444 A.2d 1 (D.C. App.181) __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2008 Report Share Posted October 21, 2008 Good morning and welcome to your new home. I'm glad you've found us, sorry you had to but glad you're here. Now, let's talk. Yes, stress is a factor much as it is for everyone else in the world; just for us it triggers " other " things. Learning how to handle stress is an important part of our lives. Remember, your son now has an added bonus of incredibly painful joints, that in itself is stressful. OK, so what do you do? Talk with the doctor of course. Everyone is different in general and we're no exception with Still's disease. personally, I've learned to breathe through some stresses, others I just have to relax completely and still other times I rough house with my dogs (as much as i can). If your son is taking prednisone he might have extra energy so an outlet of somesort isn't out of line but again, talk with the doctor first. We're here for all of you. You'll see my email address at the top of this posting. You're more than welcome to email me personally if you wish. Take care and be well. ellen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2008 Report Share Posted October 21, 2008 Good morning and welcome to your new home. I'm glad you've found us, sorry you had to but glad you're here. Now, let's talk. Yes, stress is a factor much as it is for everyone else in the world; just for us it triggers " other " things. Learning how to handle stress is an important part of our lives. Remember, your son now has an added bonus of incredibly painful joints, that in itself is stressful. OK, so what do you do? Talk with the doctor of course. Everyone is different in general and we're no exception with Still's disease. personally, I've learned to breathe through some stresses, others I just have to relax completely and still other times I rough house with my dogs (as much as i can). If your son is taking prednisone he might have extra energy so an outlet of somesort isn't out of line but again, talk with the doctor first. We're here for all of you. You'll see my email address at the top of this posting. You're more than welcome to email me personally if you wish. Take care and be well. ellen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2008 Report Share Posted October 21, 2008 Good morning and welcome to your new home. I'm glad you've found us, sorry you had to but glad you're here. Now, let's talk. Yes, stress is a factor much as it is for everyone else in the world; just for us it triggers " other " things. Learning how to handle stress is an important part of our lives. Remember, your son now has an added bonus of incredibly painful joints, that in itself is stressful. OK, so what do you do? Talk with the doctor of course. Everyone is different in general and we're no exception with Still's disease. personally, I've learned to breathe through some stresses, others I just have to relax completely and still other times I rough house with my dogs (as much as i can). If your son is taking prednisone he might have extra energy so an outlet of somesort isn't out of line but again, talk with the doctor first. We're here for all of you. You'll see my email address at the top of this posting. You're more than welcome to email me personally if you wish. Take care and be well. ellen Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2008 Report Share Posted October 21, 2008 , so glad you found us! I was just diagnosed this past summer... I'm 40, and over in NB, Canada. I hope Mike joins in with us and asks the thousands of questions he probably has... it's overwhelming at first, and this group was a godsend to me. I hope it is for you and Mike as well. The most frustrating thing about Stills is that sometimes there are no answers for the questions like " So, how am I going to feel in 6 months? " It's so different for everyone. I'm so lucky in that I'm slowly weaning off my medications, and the joint pain is very tolerable for me so far. Some people come bouncing back with very few symptoms, and some aren't so lucky. I'm one of those that believes your mindset is half of the battle... probably Mike's hardest struggle is going to be the next few weeks of trying to get everything all figured out. It's hard to be positive when you hurt! It's so great that you are actively helping him like this. Please keep us up-to-date on his progress until he can join in himself. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2008 Report Share Posted October 21, 2008 , so glad you found us! I was just diagnosed this past summer... I'm 40, and over in NB, Canada. I hope Mike joins in with us and asks the thousands of questions he probably has... it's overwhelming at first, and this group was a godsend to me. I hope it is for you and Mike as well. The most frustrating thing about Stills is that sometimes there are no answers for the questions like " So, how am I going to feel in 6 months? " It's so different for everyone. I'm so lucky in that I'm slowly weaning off my medications, and the joint pain is very tolerable for me so far. Some people come bouncing back with very few symptoms, and some aren't so lucky. I'm one of those that believes your mindset is half of the battle... probably Mike's hardest struggle is going to be the next few weeks of trying to get everything all figured out. It's hard to be positive when you hurt! It's so great that you are actively helping him like this. Please keep us up-to-date on his progress until he can join in himself. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2008 Report Share Posted October 21, 2008 Hi there. Thank you so much for your response. It is very helpful knowing there are others out there who are suffering with this crazy disease but are managing to get on top of things. I am passing this note on to Mike (via his excellent wife who he could never manage without!)... I hope they both join this group as I've gotten a number of e-mails today...all very informative. Thanks again and I hope you come off of your medications without too many problems!! Re: Re: New patient , so glad you found us! I was just diagnosed this past summer... I'm 40, and over in NB, Canada. I hope Mike joins in with us and asks the thousands of questions he probably has... it's overwhelming at first, and this group was a godsend to me. I hope it is for you and Mike as well. The most frustrating thing about Stills is that sometimes there are no answers for the questions like " So, how am I going to feel in 6 months? " It's so different for everyone. I'm so lucky in that I'm slowly weaning off my medications, and the joint pain is very tolerable for me so far. Some people come bouncing back with very few symptoms, and some aren't so lucky. I'm one of those that believes your mindset is half of the battle... probably Mike's hardest struggle is going to be the next few weeks of trying to get everything all figured out. It's hard to be positive when you hurt! It's so great that you are actively helping him like this. Please keep us up-to-date on his progress until he can join in himself. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 21, 2008 Report Share Posted October 21, 2008 Hi there. Thank you so much for your response. It is very helpful knowing there are others out there who are suffering with this crazy disease but are managing to get on top of things. I am passing this note on to Mike (via his excellent wife who he could never manage without!)... I hope they both join this group as I've gotten a number of e-mails today...all very informative. Thanks again and I hope you come off of your medications without too many problems!! Re: Re: New patient , so glad you found us! I was just diagnosed this past summer... I'm 40, and over in NB, Canada. I hope Mike joins in with us and asks the thousands of questions he probably has... it's overwhelming at first, and this group was a godsend to me. I hope it is for you and Mike as well. The most frustrating thing about Stills is that sometimes there are no answers for the questions like " So, how am I going to feel in 6 months? " It's so different for everyone. I'm so lucky in that I'm slowly weaning off my medications, and the joint pain is very tolerable for me so far. Some people come bouncing back with very few symptoms, and some aren't so lucky. I'm one of those that believes your mindset is half of the battle... probably Mike's hardest struggle is going to be the next few weeks of trying to get everything all figured out. It's hard to be positive when you hurt! It's so great that you are actively helping him like this. Please keep us up-to-date on his progress until he can join in himself. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2011 Report Share Posted October 5, 2011 I'm a 75 year old male who was diagnosed with CLL about 1 year ago. We took a wait & see approach which was necessitated in part by major surgery in Feb. of this year. The surgery happened to confirm the CLL. Blood tests in June, July & August, including the fact that 90% of the B- cells were ZAP-70 positive, confirmed the need for Chemo. My first cycle during August using FCR followed by a Neulasta injection went well, however, my WBC, RBC, HGB and PLT all dropped precipitously, necessitating a blood transfusion. Since then I have had 20 Neupogen injections and another blood transfusion. My WBC and PLT levels appeared to be increasing modestly, but were still far below normal. Finally, after a final week of Neupogen, my WPC and PLT again dropped precipitously. At this point, and now 8 weeks after my initial cycle, my Oncologist recommended that I only have Rituxan, but not FC. I had this yesterday, and I'm also on Prednisone, now at 25mg daily. Apparently my initial cycle of FCR seriously affected my bone marrow's ability to produce new cells and platelets, even with repeated Neupogen injections designed to stimulate the bone marrow into producing new white blood cells. Any comments or suggestions would be greatly appreciated. Jerry Rubin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2011 Report Share Posted October 5, 2011 Hi Jerry - here are some suggestions. * Go to http://www.cllinfogroup.org to see the booklet called " UNDERSTANDING CLL/SLL " http://tinyurl.com/3l9kevf This explains much of the CLL basics. You can read it online, download it or order it (90 plus pages). This excellent resource is co-sponsered by the CLL Information Group (CIG) which also is responsible for this wonderful discussion site tour on now. 1) IMPORTANT - Find a CLL expert (specialist) doctor as soon as possible. To insure you are receiving the best possible care & treatment a CLL expert (specialist) is the best answer. Local/general oncologists do not see many CLL patients (CLL is relatively rare) so they are not usually up to date on all the latest CLL research/findings. Since you having serious issues & concerns with your current treatment - I suggest you find & see a CLL expert doctor as soon as possible. See the following online resources to help find a CLL expert doctor close to where you live. http://www.cll.acor.org/DRdoctors http://www.cllfoundation.org/drdirectory 2) It's critical that your local hematologist/oncologist (H/O) is willing to work with your CLL expert doc - if your current local H/O is not open to this, find another one. Your primary care physician (PCP) can probably help with this. 3) Organize your team with 1 & 2 above - then be pro-active and take the necessary steps to get good care and advice. Here's more resource info - CLL Topics is at http://www.clltopics.org/PI/PrognosisatDiagnosis.htm and the article updates are at http://updates.clltopics.org/ Note: if you register for the updates@ clltopics.org you can then read and post to the comments section that's after each new article. Again, it's a lot of interesting information. Some of the notable posters here are Dr. Hamblin, from CLL Canada, and a few doctors (general practice) who themselves have CLL. Dwyer started the excellent http://cllcanada.ca/2010/index.htm -again more scientifically/medically oriented. is one of the best researchers and nicest people I have encountered on the lists. This is not a discussion group - it's a source of up to date information about all things related to CLL. is also is very active on this discussion group you're now on. /?yguid=190002089 It really helps me to make every possible effort to stay mentally, emotionally & spiritually fit. Enjoy life, spend time with family and loved ones. And good friends are priceless. Warm regards - Patti Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 5, 2011 Report Share Posted October 5, 2011 Expert doctors may be found at the ACOR Site at: http://cll.acor.org/DRdoctors.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2011 Report Share Posted October 6, 2011 Hi Guys - Here's a correction to the links for finding a CLL expert. These should get you to the CLL expert doctor listings. http://cll.acor.org/DRdoctors.html http://www.cllfoundation.org/drdirectory.aspx Regards - Patti Patti Kruse wrote: /message/16155 Quote Link to comment Share on other sites More sharing options...
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