Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 In a message dated 8/1/2003 1:13:07 PM Central Daylight Time, dfreels@... writes: > The difference(s) between the IHA and IHMA was a frequent source of > controversy, confusion, and tension during the symposium. Some people > joined the IHA believing they were joining the IHMA. There may have been > others who joined the IHMA when they believed they were actually joining > the IHA. At one point IHMA membership applications and literature was found > on the IHA table. > you are totaly wrong. I was at the IHA both most of the symposium. Everyone was explained the difference between the two. They asked which one to join and they were told both. I can't believe anyone would even say that there was confusion there it was made perfectly clear to all those that joined that the IHA and IHMA were different organizations. Moving in the same direction in a scenes. The membership information that you claimed was found on the IHA table Now I don't think that happened but if you remember correctly the IHA was the only booth serving refreshments and people came in the both making coffee and getting refreshments could have left something on the table it was not intentional if that happened. But if someone filled out an application they was explained what they were joining and that the two were not the same. Who are these others that you are speaking of that thought they were joining instead of the other I don't no of one person on the list that thought they were joining one organization instead of the other. Now that is totally off base here. But IM not gripping IM just explaining Hopefully no one takes offense to this email. Darin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 In a message dated 8/1/2003 2:58:59 PM Central Standard Time, Bry8825@... writes: > The difference(s) between the IHA and IHMA was a frequent source of > >controversy, confusion, and tension during the symposium. Some people > >joined the IHA believing they were joining the IHMA. There may have been > >others who joined the IHMA when they believed they were actually joining > >the IHA. At one point IHMA membership applications and literature was found > >on the IHA table. > > , This is NOT true. I can't believe that professional people would stoop to this. I was in that booth for most of the conference and it was made clear that there are two organizations....and which one the booth was for. I guess the big sign could have been their first clue. This kind of behavior within the hbo community is the reason HBO for BI isn't taken seriously. Who would take anyone seriously when they fight their battles with these type of tactics. Show the proof or stop the lies. ette Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 In a message dated 8/1/2003 4:26:44 PM Central Daylight Time, dfreels@... writes: > Broader issue #1, Darin, we need to get some sort of documentation from > Wisconsin Medicaid so Lynn can take that into her August 12th hearing. Have > you heard anything else from ? I have not. > > Yes, . I have spoken with she is very busy im Meetings. They are working on that issue as we speak. My fax still did not go through to you. But all is well I want to wait till I get the documentation in had before I have anyone call the guy from Washington I have ben speaking with. If and when he sends this document it will be good for all of us. , > This is NOT true. I can't believe that professional people would stoop to >this. I was in that booth for most of the conference and it was made clear >that >there are two organizations....and which one the booth was for. I guess the >big sign could have been their first clue. This kind of behavior within >the hbo >community is the reason HBO for BI isn't taken seriously. Who would take >anyone seriously when they fight their battles with these type of tactics. >Show the >proof or stop the lies. >ette ett I commend you highly for standing up. You are correct and IM glad you told what really happened. Cause you were at the booth more than I was. Hearing it from two voices makes a greater statement. I don't know what the alternative motive was behind that statement meant but the ones that made it do. They know I know alot more than I say. I know what they are expecting to happen. Darin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 >, >Your comments about e are also uninformed. You need to >actually talk to e. I saw e at the 3rd symposium but did not get much of an opportunity to actually speak to her. The first night there she had a cellophane-wrapped package containing some sort of blue button thing that she attempted to open numerous times but was unable. She did ask me if I was " still mad at her. " I've never been mad at her, just curious. A while back she was invited to join the IHMA a few times and declined, stating she was going to sit on the fence and not join any group. I later learned that she had joined the UHMS, and at the 3rd symposium I was shown an IHA business card with e's name on it--but no title. I've since heard (at the symposium) and read (here or on hbotforcp) that e is the Executive Director of the IHA. The difference(s) between the IHA and IHMA was a frequent source of controversy, confusion, and tension during the symposium. Some people joined the IHA believing they were joining the IHMA. There may have been others who joined the IHMA when they believed they were actually joining the IHA. At one point IHMA membership applications and literature was found on the IHA table. Does any of this mean the IHA is a bad organization? No. e Creacy has done an awful lot to bring public awareness to Hyperbaric Oxygen Therapy. She has accomplished this in ways that no one else can do. She has tremendous gifts and tremendous talents for getting in to see the right people at the right time. She is to be commended, and I am often in awe of her. She can orchestrate things that the rest of us can't even imagine. She's incredible. There's another talented and gifted individual who has carried the brunt of the first two years of the IHMA's existence, often at great personal expense and sacrifice. His name is Ken Locklear, and he too has been a tremendous player in the achievements of the last two years. Ken too, is a strong personality, and sometimes I have suspected there has been occasional tension between Ken and e. Ironically, they are both quite complementary (just like the IHA and IHMA), and I have wondered if many of the tensions between the IHA and IHMA are not manifestations of the strengths of these two gifted and talented people. Now nearly two weeks post-symposium, I've been sitting back and mulling a lot of this over. I'll admit I've made a crack or two about e's UHMS membership, but seeing and watching in person many of the movers and shakers in this " movement " , I've come to the conclusion that we all definitely need to cease the potshots and backbiting. We are on the verge of making Hyperbaric Oxygen Therapy widely accepted and illegal to deny. We are at a moment in medical history that is without precedent. The power and stranglehold on this medicine, so long held in captivity by the UHMS, is about to be broken. Forever. Now I'm not saying that we shouldn't have (or won't have) any more differences; we will still have differences. What I am saying is that let's be civil in voicing, sharing, and settling our differences. This will not be an easy thing to accomplish and won't occur overnight. This will take patience, but I think we can get there if we keep our eyes on the prize. It always helps to meet people in person that we don't always agree with, and I was overjoyed to finally meet Hartsoe in person. What a guy. However, , next time you hand me the microphone to publicly ask Murray Goldstein a question or two--don't tell him who I am before I ask the question(s). (Not that he was going to give a candid answer.) Anyway, let's keep together on this thing. Join the IHA and join the IHMA. Support both. They are both good groups. >And tell me when did others who are free- >standing clinic operators that frequent this list turn in their UHMS >membership? Don't make this a war inside the war. This is another >instance of someone making statements based on half-truths and it >reveals some colors that are not pretty. By the way, I've left many >messages for you on your machine wanting to talk to you personally >about these issues. You've become very selective with your time out >of necessity, but you need to hear the rest of the story. I've been busy following up on a few things I discovered at the symposium, which I hope to share with other list members soon. >Medicaid >for hbot not apply to my daughter for 1 1/2 yrs. which by the way, is >enough time for me to prepare my case. Even though she is a mediCal >recipient, we cannot use it in our hospital. Our military hospital >is the only one in our area that has a Hyperbaric Chamber. It is not >open to the public, unless it is a declared disaster. They do not >take MediCal or Medicaire payments for anything. >In our case, the IHMA leadership has not done the very things they've >promised to do, because it is not on their agenda. As far as I'm >concerned they can claim all they want that they've helped. I only >know that when they claim they've helped me or my daughter, it is >just talk, and false. I have not found the penney in the pudding >yet. Not one has done what they've promised to do. Why? Because it >is not their agenda. I'm not angry, so much, about that. I >understand agenda's. What I am angry with, is that they use my >daughter as a shining example of what they have done. What has been >done for my daughter is not because of the IHMA leadership or anybody >that has worked in concert with them in TX, FL or CA. My daughter is >not better because of anything the UHMS has done. The UHMS >leadership wants my daughter to stay in the condition she is in. They >want things to stay the way they are which means more money for them >individually. My daughter is better than she was because of Mitch >Hoggard and his staff at Chico Hyperbarics. Dr.'s Lane , >Ignacio Fogjel and Gunnar Heuser who have spent time with me talking >about my daughters individual issues and have led me in her >treatment. The last group I am indebted to is the very organization >that has sponsored, backed up with the lions share, the last two >symposiums in FL. Everybody seems to be willing to take their money, >but nobody wants to give them credit for being the most influential >people in the cause. This group is OxyHealth Corp. The Dr's and >professionals assoc. with the mild chambers have formed the IHA. >Whomever is part of this org. has my undying gratitude. >The closest hospital chamber to us is Stanford. They only use their >chamber for animal studies. My only recourse, which is the same as >most of us who continue to watch their children over the years get >older and older waiting for it to happen for them, is to raise funds >and go to a free-standing clinic. It is that, or purchase my own >hard chamber for $30,000 so I can service others as well which as >well does not fit my situation. Or it is to purchase my own mild >chamber, learn the science involved and do treatments at 1.3 ATA's on >my own daughter every day which fits me to a t despite the >fearmongering of people who don't believe we parents are intelligent >enough to understand it all. We do miracles everyday by using >medical equipment in our homes in ways the equipment was never meant >to be used. Marlena--what an example your story is of what is wrong with the system and what a bright and resourceful parent will do to get what her child most needs. I do hope you've kept the documentation of all this. >Darin, >This is the reason why many just stop helping the cause. There is >always someone in the forefront who gets kicked in the pants on a >daily basis for their efforts. Then there are those who parse their >words very carefully to continue their subversive efforts. You have >to meet everyone. You have to sit down with them and get to know >their hearts. 98% of the people on this list care and are willing to >move heaven or hell to get HBOT as a first choice medical treatment. >Many of them also have a monetary interest, which could be construed >as other than honest, but I don't believe that. I believe that if >you don't invest your money into something you believe in, it really >proves you don't believe in it. Money can be used only as legal >tender or it can be where we put our treasure. I for one have decided >to put my money where my treasure is...my loved ones. Which is the >same decision we all have made to one certain extent or another. >What would happen if we pooled our intelligence, talents and >resources together, as parents? Can we do that? Would we do it? >Will we? Shall we? > >With Much respect, >Marlena Orndorff Amen, Marlena. Thank you for your insightful wisdom. ``````````````````````````````````````````````````````` Freels 2948 Windfield Circle Tucker, GA 30084-6714 770/491-6776 (phone and fax) 720/269-5289 (efax, sends fax as email attachment) mailto:dfreels@... http://www.freelanceforum.org/df Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 >In a message dated 8/1/2003 2:58:59 PM Central Standard Time, Bry8825@... >writes: > >> The difference(s) between the IHA and IHMA was a frequent source of >> >controversy, confusion, and tension during the symposium. Some people >> >joined the IHA believing they were joining the IHMA. There may have been >> >others who joined the IHMA when they believed they were actually joining >> >the IHA. At one point IHMA membership applications and literature was found >> >on the IHA table. >> > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 >In a message dated 8/1/2003 1:13:07 PM Central Daylight Time, >dfreels@... writes: > >> The difference(s) between the IHA and IHMA was a frequent source of >> controversy, confusion, and tension during the symposium. Some people >> joined the IHA believing they were joining the IHMA. There may have been >> others who joined the IHMA when they believed they were actually joining >> the IHA. At one point IHMA membership applications and literature was found >> on the IHA table. >> > > you are totaly wrong. I was at the IHA both most of the symposium. >Everyone was explained the difference between the two. They asked which >one to >join and they were told both. I can't believe anyone would even say that >there >was confusion there it was made perfectly clear to all those that joined that >the IHA and IHMA were different organizations. Moving in the same >direction in a >scenes. The membership information that you claimed was found on the IHA >table Now I don't think that happened but if you remember correctly the >IHA was >the only booth serving refreshments and people came in the both making coffee >and getting refreshments could have left something on the table it was not >intentional if that happened. But if someone filled out an application >they was >explained what they were joining and that the two were not the same. Who are >these others that you are speaking of that thought they were joining >instead of >the other I don't no of one person on the list that thought they were joining >one organization instead of the other. Now that is totally off base here. >But IM >not gripping IM just explaining Hopefully no one takes offense to this email. > > >, > This is NOT true. I can't believe that professional people would stoop to >this. I was in that booth for most of the conference and it was made clear >that >there are two organizations....and which one the booth was for. I guess the >big sign could have been their first clue. This kind of behavior within >the hbo >community is the reason HBO for BI isn't taken seriously. Who would take >anyone seriously when they fight their battles with these type of tactics. >Show the >proof or stop the lies. >ette > Okay. Time out. If I could whistle with my fingers, I'd whistle with my fingers. If you say that this was not going on, then I believe you; however, I do know of at least one person who did join the IHA who thought they were joining the IHMA. I don't know the specific circumstances around that sign-up, and at this point it really doesn't matter, as they wound up joining the IHMA too--as we all should. If you say this didn't happen, I believe you both because I know you both. Both of these groups are invaluable. Both of them. The IHA has a large, grass-roots membership base which is critical to pushing this thing forward; the IHMA has a large amount of credibility with the FDA, CMS, and the US Congress--credibility which is crucial to reaching universal acceptance and reimbursement. I believe it's essential for both groups to work together, side by side. We do have a common nemesis in the UHMS--whose historic failure necessitated the creation of BOTH the IHA and the IHMA. I'm glad to know nothing underhanded was going on. ette, you're right, we can't be taken seriously if there's infighting going on. So I apologize for suggesting there was anything going on at the IHA table and if I hear discussion of this in the future I will set the record straight based on what you both have said and a private email I received from e. I guess the point I'm trying to make here is that we have some very talented and gifted people on our side in all this. Yes, there have been differences in the past, and most likely there will be differences in the future, but we have to keep ourselves together by what binds us together. This is not an either/or situation; this is a both situation. You know, we're a bunch of big people here. We're grown-ups. We are taking care of loved ones with brain-injury. That's a tough job. It's difficult. We also have learned through experience that the main road we're advised to travel doesn't have many answers; in fact, it has no answers. That's why we're here. Because we've found part of the answer, and we've seen the results of this extra-oxygen thing first hand. We know it works, and we're pretty passionate about it. We're very passionate about it, and if we can crack this nut this will create a floodgate of who knows what for our brain-injured children because we've got proof that things are not hopeless for them. There's something that can be done, and we want to know what else can be done. All I'm saying is that we don't need to get into a tit-for-tat thing between the IHA and the IHMA--so let's don't. Let's lay it down and focus on the broader issue. Broader issue #1, Darin, we need to get some sort of documentation from Wisconsin Medicaid so Lynn can take that into her August 12th hearing. Have you heard anything else from ? I have not. ``````````````````````````````````````````````````````` Freels 2948 Windfield Circle Tucker, GA 30084-6714 770/491-6776 (phone and fax) 720/269-5289 (efax, sends fax as email attachment) mailto:dfreels@... http://www.freelanceforum.org/df Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 In a message dated 8/1/2003 3:30:08 PM Central Daylight Time, knkeeney@... writes: > In a message dated 8/1/2003 2:58:59 PM Central Standard Time, > Bry8825@... > writes: > > >The difference(s) between the IHA and IHMA was a frequent source of > >>controversy, confusion, and tension during the symposium. Some people > >>joined the IHA believing they were joining the IHMA. There may have been > >>others who joined the IHMA when they believed they were actually joining > >>the IHA. At one point IHMA membership applications and literature was > found > >>on the IHA table. > >> > > , > This is NOT true. I can't believe that professional people would stoop to > this. I was in that booth for most of the conference and it was made clear > that > there are two organizations....and which one the booth was for. I guess the > big sign could have been their first clue. This kind of behavior within the > hbo > community is the reason HBO for BI isn't taken seriously. Who would take > anyone seriously when they fight their battles with these type of tactics. > Show the > proof or stop the lies. > ette > Let me chime in as someone who spent a lot of time at the IHA booth, no one was deceived into signing up for the unintended organization. Darin's explanation as to how literature from IHMA got to the booth (if in fact this is true) is very plausible. In addition many IHMA Board Members stopped by the booth and spent time talking (and I'm being very generous and respectful here) to e and others with literature in their hands. While the acronyms may be confusing the signs and representation at the booth were not. God Bless, Pat Mom to , 28 yrs old, 1/98 MVA/Near Drowning Come meet    <A HREF= " www.georgemelendez.org " >www.georgemelendez.org</A> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 >In a message dated 8/1/2003 4:26:44 PM Central Daylight Time, >dfreels@... writes: > >> Broader issue #1, Darin, we need to get some sort of documentation from >> Wisconsin Medicaid so Lynn can take that into her August 12th hearing. Have >> you heard anything else from ? I have not. >> >> > >Yes, . I have spoken with she is very busy im Meetings. They are >working on that issue as we speak. My fax still did not go through to you. >But all is well I want to wait till I get the documentation in had before >I have >anyone call the guy from Washington I have ben speaking with. If and when he >sends this document it will be good for all of us. Did you use 720/269-5289? I had to send something twice before it would go through. What's it doing when you send it? ``````````````````````````````````````````````````````` Freels 2948 Windfield Circle Tucker, GA 30084-6714 770/491-6776 (phone and fax) 720/269-5289 (efax, sends fax as email attachment) mailto:dfreels@... http://www.freelanceforum.org/df Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 In a message dated 8/1/2003 6:52:36 PM Central Daylight Time, rhartsoe@... writes: > , I just wanted to clarify a couple of things. First of all, I did > not > make the decision to join the IHA until the last day in the afternoon. I > was very observant of everything that went on. I want to make it clear that > e never once implied that the IHA was the IHMA nor gave anyone the > wrong impression. On one occasion, I heard someone ask about the IHMA and > why there was noone at the IHMA booth. e told them that there should > be literature at the booth and to try again later. She did not try to > recruit them into the IHA booth instead. This impressed me. > e told them that there should be literature at the booth and to try again later. She did not try to recruit them into the IHA booth instead. This impressed me. As far as that statement there that shows true leadership a organization we can trust to lead you in the right direction. e is one of the most encourageing people you can ever meet. She was placed in some ackward cituations at the symposium and held her composure. IM glad to be a part of the IHA. I will devote time inhelping in whatever needs the IHA has. Pat and ette where both correct they were there with e most of the time they were very helpfull to her during the symposium. Both of these lady's are incredible as well. We have some awesome people joined in the IHA and it will prove to be a wonderfull organization. Look at the recognition it has gained just since e has tooken over. I think we can call that progress headed in the right direction. once said who can lead us we will see it is looking good so far. Darin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 > The difference(s) between the IHA and IHMA was a frequent source of > controversy, confusion, and tension during the symposium. Some people > joined the IHA believing they were joining the IHMA. There may have been > others who joined the IHMA when they believed they were actually joining > the IHA. At one point IHMA membership applications and literature was found > on the IHA table. , I just wanted to clarify a couple of things. First of all, I did not make the decision to join the IHA until the last day in the afternoon. I was very observant of everything that went on. I want to make it clear that e never once implied that the IHA was the IHMA nor gave anyone the wrong impression. On one occasion, I heard someone ask about the IHMA and why there was noone at the IHMA booth. e told them that there should be literature at the booth and to try again later. She did not try to recruit them into the IHA booth instead. This impressed me. As far as membership applications and literature found on the IHA table? Dr. Harch left them there, probably by accident. I was there early one morning when Dr. Harch came to the booth to talk to e and had literature in his hand. When he left, the literature remained on the round table in the booth. I'm sure he just forgot it. The only reason I noticed these things is because the IHA booth was at the entrance and it was pretty common for people to stand in front of the booth to talk, myself included. I have not heard of a single person joining thinking they were joining the IHMA. The IHMA was not manned much of the time. The IHA booth was manned all the time. This probably resulted in a lot of people joining the IHA. As far as the confusion in the names, The IHA was formed before the IHMA. The only reason I am adding to your comments is because I heard some of the same comments and feel like it should be clarified as I know we both dislike rumors and misconceptions. Congratulations on being a new board member for the IHMA. They should have done this long ago. With you and on board, I feel like I can be more supportive and would encourage everyone to support both organizations. Let me know if I can ever be of help. By the way, I handed you the microphone because Murray Goldstein was trying to escape without answering our questions and I was trying to delay him until Dr. Harch could get inside. If I would have said anything else, I would have lost my temper and blew it which I did not want to do so I pitched it to you. I actually took the microphone away from another lady and ran up front because I thought Murray was going to " escape " without answering to some of the, shall we say " mistruths " , that I heard stated? 5 will get you 10 that he will not show up at the next one if he knows you and I will be there. :-) Hartsoe > e Creacy has done an awful lot to bring public awareness to Hyperbaric > Oxygen Therapy. She has accomplished this in ways that no one else can do. > She has tremendous gifts and tremendous talents for getting in to see the > right people at the right time. She is to be commended, and I am often in > awe of her. She can orchestrate things that the rest of us can't even > imagine. She's incredible. > > There's another talented and gifted individual who has carried the brunt of > the first two years of the IHMA's existence, often at great personal > expense and sacrifice. His name is Ken Locklear, and he too has been a > tremendous player in the achievements of the last two years. Ken too, is a > strong personality, and sometimes I have suspected there has been > occasional tension between Ken and e. > > Ironically, they are both quite complementary (just like the IHA and IHMA), > and I have wondered if many of the tensions between the IHA and IHMA are > not manifestations of the strengths of these two gifted and talented people. > > Now nearly two weeks post-symposium, I've been sitting back and mulling a > lot of this over. I'll admit I've made a crack or two about e's UHMS > membership, but seeing and watching in person many of the movers and > shakers in this " movement " , I've come to the conclusion that we all > definitely need to cease the potshots and backbiting. > > We are on the verge of making Hyperbaric Oxygen Therapy widely accepted and > illegal to deny. We are at a moment in medical history that is without > precedent. The power and stranglehold on this medicine, so long held in > captivity by the UHMS, is about to be broken. Forever. > > Now I'm not saying that we shouldn't have (or won't have) any more > differences; we will still have differences. What I am saying is that let's > be civil in voicing, sharing, and settling our differences. This will not > be an easy thing to accomplish and won't occur overnight. This will take > patience, but I think we can get there if we keep our eyes on the prize. > > It always helps to meet people in person that we don't always agree with, > and I was overjoyed to finally meet Hartsoe in person. What a guy. > However, , next time you hand me the microphone to publicly ask > Murray Goldstein a question or two--don't tell him who I am before I ask > the question(s). > > (Not that he was going to give a candid answer.) > > Anyway, let's keep together on this thing. Join the IHA and join the IHMA. > Support both. They are both good groups. > > > >And tell me when did others who are free- > >standing clinic operators that frequent this list turn in their UHMS > >membership? Don't make this a war inside the war. This is another > >instance of someone making statements based on half-truths and it > >reveals some colors that are not pretty. By the way, I've left many > >messages for you on your machine wanting to talk to you personally > >about these issues. You've become very selective with your time out > >of necessity, but you need to hear the rest of the story. > > I've been busy following up on a few things I discovered at the symposium, > which I hope to share with other list members soon. > > > >Medicaid > >for hbot not apply to my daughter for 1 1/2 yrs. which by the way, is > >enough time for me to prepare my case. Even though she is a mediCal > >recipient, we cannot use it in our hospital. Our military hospital > >is the only one in our area that has a Hyperbaric Chamber. It is not > >open to the public, unless it is a declared disaster. They do not > >take MediCal or Medicaire payments for anything. > >In our case, the IHMA leadership has not done the very things they've > >promised to do, because it is not on their agenda. As far as I'm > >concerned they can claim all they want that they've helped. I only > >know that when they claim they've helped me or my daughter, it is > >just talk, and false. I have not found the penney in the pudding > >yet. Not one has done what they've promised to do. Why? Because it > >is not their agenda. I'm not angry, so much, about that. I > >understand agenda's. What I am angry with, is that they use my > >daughter as a shining example of what they have done. What has been > >done for my daughter is not because of the IHMA leadership or anybody > >that has worked in concert with them in TX, FL or CA. My daughter is > >not better because of anything the UHMS has done. The UHMS > >leadership wants my daughter to stay in the condition she is in. They > >want things to stay the way they are which means more money for them > >individually. My daughter is better than she was because of Mitch > >Hoggard and his staff at Chico Hyperbarics. Dr.'s Lane , > >Ignacio Fogjel and Gunnar Heuser who have spent time with me talking > >about my daughters individual issues and have led me in her > >treatment. The last group I am indebted to is the very organization > >that has sponsored, backed up with the lions share, the last two > >symposiums in FL. Everybody seems to be willing to take their money, > >but nobody wants to give them credit for being the most influential > >people in the cause. This group is OxyHealth Corp. The Dr's and > >professionals assoc. with the mild chambers have formed the IHA. > >Whomever is part of this org. has my undying gratitude. > >The closest hospital chamber to us is Stanford. They only use their > >chamber for animal studies. My only recourse, which is the same as > >most of us who continue to watch their children over the years get > >older and older waiting for it to happen for them, is to raise funds > >and go to a free-standing clinic. It is that, or purchase my own > >hard chamber for $30,000 so I can service others as well which as > >well does not fit my situation. Or it is to purchase my own mild > >chamber, learn the science involved and do treatments at 1.3 ATA's on > >my own daughter every day which fits me to a t despite the > >fearmongering of people who don't believe we parents are intelligent > >enough to understand it all. We do miracles everyday by using > >medical equipment in our homes in ways the equipment was never meant > >to be used. > > > Marlena--what an example your story is of what is wrong with the system and > what a bright and resourceful parent will do to get what her child most > needs. I do hope you've kept the documentation of all this. > > > >Darin, > >This is the reason why many just stop helping the cause. There is > >always someone in the forefront who gets kicked in the pants on a > >daily basis for their efforts. Then there are those who parse their > >words very carefully to continue their subversive efforts. You have > >to meet everyone. You have to sit down with them and get to know > >their hearts. 98% of the people on this list care and are willing to > >move heaven or hell to get HBOT as a first choice medical treatment. > >Many of them also have a monetary interest, which could be construed > >as other than honest, but I don't believe that. I believe that if > >you don't invest your money into something you believe in, it really > >proves you don't believe in it. Money can be used only as legal > >tender or it can be where we put our treasure. I for one have decided > >to put my money where my treasure is...my loved ones. Which is the > >same decision we all have made to one certain extent or another. > >What would happen if we pooled our intelligence, talents and > >resources together, as parents? Can we do that? Would we do it? > >Will we? Shall we? > > > >With Much respect, > >Marlena Orndorff > > > Amen, Marlena. > > Thank you for your insightful wisdom. > > > > > ``````````````````````````````````````````````````````` > > > Freels > 2948 Windfield Circle > Tucker, GA 30084-6714 > 770/491-6776 (phone and fax) > 720/269-5289 (efax, sends fax as email attachment) > mailto:dfreels@... > > http://www.freelanceforum.org/df > > > > > _._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._. > Join the International Hyperbaric Medical Association http://www.hyperbaricmedicalassociation.org/forms/Friends_of_IHMA_Join.pdf > > Unrestricted downloads of 50+ pdf files on HBOT efficacy medicaid/files/ , HDO-documentation/files/ and http://www.drneubauerhbo.com/papers.htm > > Download your state EPSDT program http://www.hcfa.gov/medicaid/stateplan/Map.asp by doing a search on the word " ameliorate " . State Medicaid websites http://www.medi-cal.ca.gov/RelSites_Oth_States.asp . Medicaid waiver programs: http://www.geocities.com/HotSprings/Villa/1029/medicaid.html > > Find a hyperbaric clinic http://www.netnet.net/mums/hbolist.htm > > HBOT can save billions of dollars and millions of heartaches. Subscribe to by sending a blank email to mailto:medicaid-subscribe > > Unsubscribe? Click here mailto:medicaid-unsubscribe .. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 I should have said Dr. Harch left IHMA literature on the table, I don't know about applications. Sorry about that. The reason I know is because I got a cup of coffee at the booth and set down at the table and saw it laying there. I was setting in the same chair as Dr. Harch. I hope this clears it up. Re: [MedicaidforHDOT] Regarding Medicaid and HBOT > > The difference(s) between the IHA and IHMA was a frequent source of > > controversy, confusion, and tension during the symposium. Some people > > joined the IHA believing they were joining the IHMA. There may have been > > others who joined the IHMA when they believed they were actually joining > > the IHA. At one point IHMA membership applications and literature was > found > > on the IHA table. > > , I just wanted to clarify a couple of things. First of all, I did not > make the decision to join the IHA until the last day in the afternoon. I > was very observant of everything that went on. I want to make it clear that > e never once implied that the IHA was the IHMA nor gave anyone the > wrong impression. On one occasion, I heard someone ask about the IHMA and > why there was noone at the IHMA booth. e told them that there should > be literature at the booth and to try again later. She did not try to > recruit them into the IHA booth instead. This impressed me. > > As far as membership applications and literature found on the IHA table? > Dr. Harch left them there, probably by accident. I was there early one > morning when Dr. Harch came to the booth to talk to e and had > literature in his hand. When he left, the literature remained on the round > table in the booth. I'm sure he just forgot it. The only reason I noticed > these things is because the IHA booth was at the entrance and it was pretty > common for people to stand in front of the booth to talk, myself included. > > I have not heard of a single person joining thinking they were joining the > IHMA. The IHMA was not manned much of the time. The IHA booth was > manned all the time. This probably resulted in a lot of people joining the > IHA. As far as the confusion in the names, The IHA was formed before the > IHMA. > > The only reason I am adding to your comments is because I heard some of the > same comments and feel like it should be clarified as I know we both dislike > rumors and misconceptions. Congratulations on being a new board member for > the IHMA. They should have done this long ago. With you and on > board, I feel like I can be more supportive and would encourage everyone to > support both organizations. Let me know if I can ever be of help. > > By the way, I handed you the microphone because Murray Goldstein was trying > to escape without answering our questions and I was trying to delay him > until Dr. Harch could get inside. If I would have said anything else, I > would have lost my temper and blew it which I did not want to do so I > pitched it to you. I actually took the microphone away from another lady > and ran up front because I thought Murray was going to " escape " without > answering to some of the, shall we say " mistruths " , that I heard stated? > 5 will get you 10 that he will not show up at the next one if he knows you > and I will be there. :-) > > Hartsoe > > > e Creacy has done an awful lot to bring public awareness to > Hyperbaric > > Oxygen Therapy. She has accomplished this in ways that no one else can do. > > She has tremendous gifts and tremendous talents for getting in to see the > > right people at the right time. She is to be commended, and I am often in > > awe of her. She can orchestrate things that the rest of us can't even > > imagine. She's incredible. > > > > There's another talented and gifted individual who has carried the brunt > of > > the first two years of the IHMA's existence, often at great personal > > expense and sacrifice. His name is Ken Locklear, and he too has been a > > tremendous player in the achievements of the last two years. Ken too, is a > > strong personality, and sometimes I have suspected there has been > > occasional tension between Ken and e. > > > > Ironically, they are both quite complementary (just like the IHA and > IHMA), > > and I have wondered if many of the tensions between the IHA and IHMA are > > not manifestations of the strengths of these two gifted and talented > people. > > > > Now nearly two weeks post-symposium, I've been sitting back and mulling a > > lot of this over. I'll admit I've made a crack or two about e's UHMS > > membership, but seeing and watching in person many of the movers and > > shakers in this " movement " , I've come to the conclusion that we all > > definitely need to cease the potshots and backbiting. > > > > We are on the verge of making Hyperbaric Oxygen Therapy widely accepted > and > > illegal to deny. We are at a moment in medical history that is without > > precedent. The power and stranglehold on this medicine, so long held in > > captivity by the UHMS, is about to be broken. Forever. > > > > Now I'm not saying that we shouldn't have (or won't have) any more > > differences; we will still have differences. What I am saying is that > let's > > be civil in voicing, sharing, and settling our differences. This will not > > be an easy thing to accomplish and won't occur overnight. This will take > > patience, but I think we can get there if we keep our eyes on the prize. > > > > It always helps to meet people in person that we don't always agree with, > > and I was overjoyed to finally meet Hartsoe in person. What a guy. > > However, , next time you hand me the microphone to publicly ask > > Murray Goldstein a question or two--don't tell him who I am before I ask > > the question(s). > > > > (Not that he was going to give a candid answer.) > > > > Anyway, let's keep together on this thing. Join the IHA and join the IHMA. > > Support both. They are both good groups. > > > > > > >And tell me when did others who are free- > > >standing clinic operators that frequent this list turn in their UHMS > > >membership? Don't make this a war inside the war. This is another > > >instance of someone making statements based on half-truths and it > > >reveals some colors that are not pretty. By the way, I've left many > > >messages for you on your machine wanting to talk to you personally > > >about these issues. You've become very selective with your time out > > >of necessity, but you need to hear the rest of the story. > > > > I've been busy following up on a few things I discovered at the symposium, > > which I hope to share with other list members soon. > > > > > > >Medicaid > > >for hbot not apply to my daughter for 1 1/2 yrs. which by the way, is > > >enough time for me to prepare my case. Even though she is a mediCal > > >recipient, we cannot use it in our hospital. Our military hospital > > >is the only one in our area that has a Hyperbaric Chamber. It is not > > >open to the public, unless it is a declared disaster. They do not > > >take MediCal or Medicaire payments for anything. > > >In our case, the IHMA leadership has not done the very things they've > > >promised to do, because it is not on their agenda. As far as I'm > > >concerned they can claim all they want that they've helped. I only > > >know that when they claim they've helped me or my daughter, it is > > >just talk, and false. I have not found the penney in the pudding > > >yet. Not one has done what they've promised to do. Why? Because it > > >is not their agenda. I'm not angry, so much, about that. I > > >understand agenda's. What I am angry with, is that they use my > > >daughter as a shining example of what they have done. What has been > > >done for my daughter is not because of the IHMA leadership or anybody > > >that has worked in concert with them in TX, FL or CA. My daughter is > > >not better because of anything the UHMS has done. The UHMS > > >leadership wants my daughter to stay in the condition she is in. They > > >want things to stay the way they are which means more money for them > > >individually. My daughter is better than she was because of Mitch > > >Hoggard and his staff at Chico Hyperbarics. Dr.'s Lane , > > >Ignacio Fogjel and Gunnar Heuser who have spent time with me talking > > >about my daughters individual issues and have led me in her > > >treatment. The last group I am indebted to is the very organization > > >that has sponsored, backed up with the lions share, the last two > > >symposiums in FL. Everybody seems to be willing to take their money, > > >but nobody wants to give them credit for being the most influential > > >people in the cause. This group is OxyHealth Corp. The Dr's and > > >professionals assoc. with the mild chambers have formed the IHA. > > >Whomever is part of this org. has my undying gratitude. > > >The closest hospital chamber to us is Stanford. They only use their > > >chamber for animal studies. My only recourse, which is the same as > > >most of us who continue to watch their children over the years get > > >older and older waiting for it to happen for them, is to raise funds > > >and go to a free-standing clinic. It is that, or purchase my own > > >hard chamber for $30,000 so I can service others as well which as > > >well does not fit my situation. Or it is to purchase my own mild > > >chamber, learn the science involved and do treatments at 1.3 ATA's on > > >my own daughter every day which fits me to a t despite the > > >fearmongering of people who don't believe we parents are intelligent > > >enough to understand it all. We do miracles everyday by using > > >medical equipment in our homes in ways the equipment was never meant > > >to be used. > > > > > > Marlena--what an example your story is of what is wrong with the system > and > > what a bright and resourceful parent will do to get what her child most > > needs. I do hope you've kept the documentation of all this. > > > > > > >Darin, > > >This is the reason why many just stop helping the cause. There is > > >always someone in the forefront who gets kicked in the pants on a > > >daily basis for their efforts. Then there are those who parse their > > >words very carefully to continue their subversive efforts. You have > > >to meet everyone. You have to sit down with them and get to know > > >their hearts. 98% of the people on this list care and are willing to > > >move heaven or hell to get HBOT as a first choice medical treatment. > > >Many of them also have a monetary interest, which could be construed > > >as other than honest, but I don't believe that. I believe that if > > >you don't invest your money into something you believe in, it really > > >proves you don't believe in it. Money can be used only as legal > > >tender or it can be where we put our treasure. I for one have decided > > >to put my money where my treasure is...my loved ones. Which is the > > >same decision we all have made to one certain extent or another. > > >What would happen if we pooled our intelligence, talents and > > >resources together, as parents? Can we do that? Would we do it? > > >Will we? Shall we? > > > > > >With Much respect, > > >Marlena Orndorff > > > > > > Amen, Marlena. > > > > Thank you for your insightful wisdom. > > > > > > > > > > ``````````````````````````````````````````````````````` > > > > > > Freels > > 2948 Windfield Circle > > Tucker, GA 30084-6714 > > 770/491-6776 (phone and fax) > > 720/269-5289 (efax, sends fax as email attachment) > > mailto:dfreels@... > > > > http://www.freelanceforum.org/df > > > > > > > > > > _._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._._. > > Join the International Hyperbaric Medical Association > http://www.hyperbaricmedicalassociation.org/forms/Friends_of_IHMA_Join.pdf > > > > Unrestricted downloads of 50+ pdf files on HBOT efficacy > medicaid/files/ , > HDO-documentation/files/ and > http://www.drneubauerhbo.com/papers.htm > > > > Download your state EPSDT program > http://www.hcfa.gov/medicaid/stateplan/Map.asp by doing a search on the word > " ameliorate " . State Medicaid websites > http://www.medi-cal.ca.gov/RelSites_Oth_States.asp . Medicaid waiver > programs: http://www.geocities.com/HotSprings/Villa/1029/medicaid.html > > > > Find a hyperbaric clinic http://www.netnet.net/mums/hbolist.htm > > > > HBOT can save billions of dollars and millions of heartaches. Subscribe to > by sending a blank email to > mailto:medicaid-subscribe > > > > Unsubscribe? Click here mailto:medicaid-unsubscribe > . > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 Guys, I spoke with and she explained to me that her victory was based on Medicaid's non-compliance. They did not provide the necessary notification of rejection and were forced to pay for HBOT for her child because of it. That is hardly a ringing endorsement for HBOT - it is a victory won on a technicality. I know, I know, it is still a victory but I don't know that it will help me with my insurance company. I say this for two reasons: 1) Winning on a technicality will only allow my insurance company the opportunity to say that it doesn't prove HBOT works, only that Medicaid screwed up and 2) if my insurance company thinks that Medicaid may be forced to pay down the line, I believe that will make my insurance company less likely to pay now - they can just sit back and wait until Medicaid gets forced to pay and it is no skin off their nose and, more importantly, no money out of their pocket. They have taken this stance with therapy for my son - they know we have an excellent Birth to 3 program funded by the state that will cover my son's therapeutic needs and, therefore, they can get away without reimbursing Birth to 3 for any of the therapeutic services they provide my son.  Lynn you are correct. I can't argue with you there. That is what i have said in the past. Me and david talked about this. That is why Medicaid waited to process the claim so they could say they paid out of non compliance. That has been my whole issue. Medicaid has not willingly paid in any case they have been forced to all along. But I still think you got a good chance. At least it does finally show that Medicaid did pay out of Medicaid funding for HBOT. Now do we all see here while back what I was talking about when I said a state may pay but it wont pay again cause it was forced to. There has been no precidence set yet. In some states you may think so but dig deeper int o what got them to pay and how they did it. Plus what Lynn just said they were forced to. Not willingly forced big difference. Darin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2003 Report Share Posted August 1, 2003 > Broader issue #1, Darin, we need to get some sort of documentation from Wisconsin Medicaid so Lynn can take that into her August 12th hearing. Have you heard anything else from ? I have not. < Guys, I spoke with and she explained to me that her victory was based on Medicaid's non-compliance. They did not provide the necessary notification of rejection and were forced to pay for HBOT for her child because of it. That is hardly a ringing endorsement for HBOT - it is a victory won on a technicality. I know, I know, it is still a victory but I don't know that it will help me with my insurance company. I say this for two reasons: 1) Winning on a technicality will only allow my insurance company the opportunity to say that it doesn't prove HBOT works, only that Medicaid screwed up and 2) if my insurance company thinks that Medicaid may be forced to pay down the line, I believe that will make my insurance company less likely to pay now - they can just sit back and wait until Medicaid gets forced to pay and it is no skin off their nose and, more importantly, no money out of their pocket. They have taken this stance with therapy for my son - they know we have an excellent Birth to 3 program funded by the state that will cover my son's therapeutic needs and, therefore, they can get away without reimbursing Birth to 3 for any of the therapeutic services they provide my son. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2003 Report Share Posted August 2, 2003 In a message dated 8/2/2003 10:19:28 AM Central Daylight Time, dfreels@... writes: > The fact that they > are paying is the only important issue. In WI, there are two local news > reporters who are waiting to pounce on this story as soon as that check > comes in. > IT is an important issue you are correct. But the fact still remains we have to change the system. We cannot do that till we fight this correctly. On a national level instead of one case at a time. When receives that check it will help. But only and Only if there is proper Media Coverage to support what is happening. We have a reporter coming out within the next two weeks' here to do a story on what is happening to us here in Texas I don't have a lot of time to elaborate on that but it is for the greater good of Texas. we are on the right track yes. But please understand what is taking place with Medicaid is good right now. But it is not going to change until the public gets wend of what is going on and there is a national outcry for help. You would not believe the changes that are taking place with the Katy Beckett Waiver the MDCP waiver and the Texas Chip program are any of you aware of the new Changes that are taking affect. Katy Beckeet used to be regardless of Parents income from what I understand now they are going to start looking at Parents Resources. Darin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2003 Report Share Posted August 2, 2003 > > >> Broader issue #1, Darin, we need to get some sort of documentation >from Wisconsin Medicaid so Lynn can take that into her August 12th >hearing. Have you heard anything else from ? I have not. < > >Guys, I spoke with and she explained to me that her victory >was based on Medicaid's non-compliance. They did not provide the >necessary notification of rejection and were forced to pay for HBOT >for her child because of it. That is hardly a ringing endorsement >for HBOT - it is a victory won on a technicality. I know, I know, it >is still a victory but I don't know that it will help me with my >insurance company. I say this for two reasons: 1) Winning on a >technicality will only allow my insurance company the opportunity to >say that it doesn't prove HBOT works, only that Medicaid screwed up >and 2) if my insurance company thinks that Medicaid may be forced to >pay down the line, I believe that will make my insurance company less >likely to pay now - they can just sit back and wait until Medicaid >gets forced to pay and it is no skin off their nose and, more >importantly, no money out of their pocket. They have taken this >stance with therapy for my son - they know we have an excellent Birth >to 3 program funded by the state that will cover my son's therapeutic >needs and, therefore, they can get away without reimbursing Birth to >3 for any of the therapeutic services they provide my son. > >Lynn > Lynn, Excellent points. However, your son needs HDOT now, right now--that is what is most important. WI Medicaid has chosen the non-compliance route just so no precedent would be set. You can present the evidence in 's case in conjunction with all the other decisions so that the judge can " see " what's going on here and what WI Medicaid has done. Remember, Paragraph 5 is not enforcible unless the treatment works. When you present the court decisions--starting with Virginia, Colorado, Georgia, Pennsylvania, Maine, etc. you can establish a clear pattern that is creating a domino effect. Medicaid won't pay for something unless it works. Insurance companies follow what Medicaid does, and historically, until now, Medicaid has followed Medicare policy. You can present the Medicare reimbursement policy--also found at medicaid/files/ --and show where state Medicaid plans are following this policy--even though they are NOT required to do so. Medicare has 13 " covered " uses and I think 20 " non-covered " uses. There is evidence in the medical literature that HDOT is effective on the " non-covered " uses. Medicare is not saying HDOT is not effective for those 20 " non-covered " uses, they're just saying they're not going to pay for them. In addition, since your insurance company has stated they follow Blue Cross/Blue Shield as a model, download the Blue Cross/Blue Shield policy on HBOT at medicaid/files/ . In that document, BC/BS states that they follow Undersea and Hyperbaric Medical Society guidelines on HBOT reimbursement and concede that of the 13 approved indications (the same as Medicare's 13), there is only clinical trial evidence to support the approval of 4 of the 13 indications--which means deciding what will or won't be a covered indication is a completely arbitrary decision. The UHMS has conceded this point in their Ethics Committee report, which can be downloaded at HDO-documentation/files/ .. Historically, the UHMS has been against the use of HBOT for brain-injury. There are also letters from the UHMS at HDO-documentation/files/ which document this. Get these too. Also, and this is the kicker, there's is more evidence to support the use of HBOT for brain-injury than all the other indications--combined. All of this is so ludicrous, and you must present this: Also on medicaid/files/ is a pdf of nearly all the papers that have been published using HBOT for brain-injury (through 2001). Just the titles and references are 35 pages long. ``````````````````````````````````````````````````````` Freels 2948 Windfield Circle Tucker, GA 30084-6714 770/491-6776 (phone and fax) 720/269-5289 (efax, sends fax as email attachment) mailto:dfreels@... http://www.freelanceforum.org/df Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2003 Report Share Posted August 2, 2003 >Guys, I spoke with and she explained to me that her victory >was based on Medicaid's non-compliance. They did not provide the >necessary notification of rejection and were forced to pay for HBOT >for her child because of it. That is hardly a ringing endorsement >for HBOT - it is a victory won on a technicality. I know, I know, it >is still a victory but I don't know that it will help me with my >insurance company. I say this for two reasons: 1) Winning on a >technicality will only allow my insurance company the opportunity to >say that it doesn't prove HBOT works, only that Medicaid screwed up >and 2) if my insurance company thinks that Medicaid may be forced to >pay down the line, I believe that will make my insurance company less >likely to pay now - they can just sit back and wait until Medicaid >gets forced to pay and it is no skin off their nose and, more >importantly, no money out of their pocket. They have taken this >stance with therapy for my son - they know we have an excellent Birth >to 3 program funded by the state that will cover my son's therapeutic >needs and, therefore, they can get away without reimbursing Birth to >3 for any of the therapeutic services they provide my son. > >Lynn you are correct. I can't argue with you there. That is what i have said >in the past. Me and david talked about this. That is why Medicaid waited to >process the claim so they could say they paid out of non compliance. That has >been my whole issue. Medicaid has not willingly paid in any case they have >been >forced to all along. But I still think you got a good chance. At least it >does >finally show that Medicaid did pay out of Medicaid funding for HBOT. Now do >we all see here while back what I was talking about when I said a state >may pay >but it wont pay again cause it was forced to. There has been no precidence >set yet. In some states you may think so but dig deeper int o what got >them to >pay and how they did it. Plus what Lynn just said they were forced to. Not >willingly forced big difference. > >Darin > Darin, Nearly every state has been forced. A few have willingly paid--Virginia, Missouri--even Maine. Pennsylvania is paying for it will the state agency is appealing. Whether forced or willing is irrelevant. The fact that they are paying is the only important issue. In WI, there are two local news reporters who are waiting to pounce on this story as soon as that check comes in. Once the public undertands the BS that's going on, the court of public opinion will bring pressure to create justice. It's important to remember that Lynn's insurance company has no idea why they are saying " no " ; they do not understand why it's their policy to not reimburse HBOT; all they know is that they just don't. This is the time and the opportunity to educate them. ``````````````````````````````````````````````````````` Freels 2948 Windfield Circle Tucker, GA 30084-6714 770/491-6776 (phone and fax) 720/269-5289 (efax, sends fax as email attachment) mailto:dfreels@... http://www.freelanceforum.org/df Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2003 Report Share Posted August 2, 2003 > In WI, there are two local news reporters who are waiting to pounce on this story as soon as that check comes in. < I'd be curious to speak to these individuals. Can you provide me with their names off list? Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2003 Report Share Posted August 2, 2003 >In a message dated 8/2/2003 10:19:28 AM Central Daylight Time, >dfreels@... writes: > >> The fact that they >> are paying is the only important issue. In WI, there are two local news >> reporters who are waiting to pounce on this story as soon as that check >> comes in. >> > >IT is an important issue you are correct. But the fact still remains we have >to change the system. We cannot do that till we fight this correctly. On a >national level instead of one case at a time. When receives that >check it >will help. But only and Only if there is proper Media Coverage to support >what is happening. We have a reporter coming out within the next two >weeks' here >to do a story on what is happening to us here in Texas I don't have a lot of >time to elaborate on that but it is for the greater good of Texas. >we are >on the right track yes. But please understand what is taking place with >Medicaid is good right now. But it is not going to change until the public >gets >wend of what is going on and there is a national outcry for help. You >would not >believe the changes that are taking place with the Katy Beckett Waiver the >MDCP >waiver and the Texas Chip program are any of you aware of the new Changes >that are taking affect. Katy Beckeet used to be regardless of Parents >income from >what I understand now they are going to start looking at Parents Resources. > >Darin > Darin--this fight is now being fought correctly with the tools we have been given, and right now there is no better way to fight this than one case at a time, one building block at a time--and it is being fought on a national level. There are parents here from all across the US, and many parents too from around the world. While I do appreciate your point, this fight is about to step up another notch when we go to Washington in March. If you'll remember Darin, this was your first your idea, and now many people agree with what you've been saying. There are three branches of government, and we will be speaking to one of those three branches and bringing with us evidence of how the other two branches are interpreting the collected data on Hyperbaric Oxygen Therapy for brain-injury. The Executive Branch, via the FDA and the Department of Health and Human Services by way of the Centers for Medicare and Medicaid Services (HCFA/CMS), has a long and deficient record of stifling access to HBOT, primarily through the influence of the UHMS. On the other hand, case by case, building block by building block, there are cases going to court and the patients (and parents) are winning--because the law and the science is on our side; the truth is on our side. Now, most likely there are a few congressional members who might feel the pain of a family dealing with a brain-injury, but by and large they will be most concerned with (a) abusive and/or inefficiencies in government programs, and ( the cost of those abuses and/or inefficiencies, and © what needs to be done to amend/correct the mechanisms in " the system " to make sure these abuses and/or inefficiencies don't re-occur in the future. While you and I and everybody else on this list can shout to the world that HBOT works, and we can trot out as many presenters as we can find from the 1st, 2nd, and 3rd Symposiums as we can find, what will get their attention most are the one-by-one court victories--because a steady stream of court decisions aren't based on opinion--but on fact. These court decisions mean that we're not blowing smoke. They are the proof that HBOT works, and the Congress will want to know why it's not being utilized since it will obviously create a tremendous cost savings. Secondly, as for your anxieties about the proposed changes to the CHIPS and Katy Beckett program, the fastest way to guarantee the continued existence of those programs is to keep doing exactly what we are all doing on this list. See ( above. The parents of brain-injured children are about to prove to the US government that the most cost-efficient treatment for brain-injury discovered in the last 2000 years was not discovered by the NIH or Harvard or s Hopkins or Yale or the CDC or whoever--it was discovered and fought for by the parents. We're the Research and Development Department. Once our worth is proven, they're not going to shut us down. Are you crazy? This is the government we're talking about. If anything they'll start throwing money at us. ``````````````````````````````````````````````````````` Freels 2948 Windfield Circle Tucker, GA 30084-6714 770/491-6776 (phone and fax) 720/269-5289 (efax, sends fax as email attachment) mailto:dfreels@... http://www.freelanceforum.org/df Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2003 Report Share Posted August 3, 2003 To All, RE: UHMS members.... I think everyone knows how I feel about the UHMA and the damage they have wrecked on children like my daughter, , with their " voodoo research " positions (sic Kindwalls support of HBOT for cyanide poisoning verse HBOT for brain injuries; or Dr. Hart's failed arguments against PED Neurol. HBOT at the Congress debates OCt, 2002.). But, we all have to note that there are many, many good members of the UHMS. Because people are trying to change it and help it doesn't mean they have gone to the " dark side " of HBOT. Dr. Mitch Hoggart is one good example. He runs a great clinic in chico and helps a lot of ped. neurol.s. (our kids) and has done so for years. Further, because someone support the IHA verses the IHMA, doesn't mean any less of them either. We all have to calculate out our view point and do what we feel is correct and support our kids needs going forward. Also, while I was not at the symposium, I have heard enough reports to understand some of the friction that existed. Things happen, whether by accident, or on purpose. We don't know all that was going on. I think we have to move forward, possibly with some healthy skepticism, but, we have to keep moving forward. Thus, I hope that while there are different camps, we can all agree on going forward together top help our kids. Let's all search our souls to do what is right and necessary for the benefit of our kids. (FYI for full disclosure, I am an IHMA Member) Best Regards, Ed Nemeth At 11:25 AM 8/1/2003, you wrote: >In a message dated 8/1/2003 1:13:07 PM Central Daylight Time, >dfreels@... writes: > > > Now nearly two weeks post-symposium, I've been sitting back and mulling a > > lot of this over. I'll admit I've made a crack or two about e's UHMS > > membership, but seeing and watching in person many of the movers and > > shakers in this " movement " , I've come to the conclusion that we all > > definitely need to cease the potshots and backbiting. > > > > > >I have no Idea why someone wouuld make a pop shot about her being a UHMS >member. e has the abilty to be a member and still remain in the feild >for >Neurological indications. Most of us take POP shot's at the UHMS instead of >trying to keep all imformation open and joined together. e Knows what >she is >doing and many of us question how she does what she does. Stop Step back and >wacth her. You will see the things she does and Make pop shots not realizing >she is gaining ground while some of us are still trying to get on the >field. See >you have to stay open and that is what she does. She doe's not throw punches >learns walks away if she has to till she can regroup. But she is never left >standing in the end alone. I admire this lady she is my best friend int he >world >right now and I love her with all my heart. What she has done for me no one >can ever take away. She has stopped what she was doing to help me when no one >else would. Yes, She even went to Austin with me to fight my case when others >were supposed to said they would and never did. But however we wont go there. >If you guy's only knew how hard she worked. Ive talked to her at 5:00 am and >then again at 1:00 am the next morning and she is still working for the >cause of >HBOT. Could we all give credit where credit is due? >Darin > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2003 Report Share Posted August 6, 2003 Greetings, I don't think any one is down on UHMS member that are presently providing Baromed Therapy on the Brain Injured or for any other off label indication. The reality is the hardliners who show up at all the trade shows peddling their $500,000 fees for making sure clinics are FDA and safety approved. That's the going rate folks. That's how these crooks make their money. They have no more understanding of the medical benefits of this therapy than you or I. They only know the technical end and they continue to use their scare tactics to keep parents from trying to help their kiddos. Knowledge is power, and they know it. They only except those who play the game the way they want it played which makes them no better than the AMA and other Medical trade orgs who exist soley to make you think that they are th only ones who know anything. Oh, it's not the ones who have existing clinics, however, very few are in the fight to get third party payment. They have their own reasons, one of which is that they don't need to. They have plenty of patients willing to pay out of pocket. There are those who are giving cost breaks and extended billings to help the parents. Bravos to you all. If you go on the UHMS website, you will find nothing about off-lable usage, but many are prescribing for it, but the official position is that it is not approved, and there is no movement to study it. I'm willing to admit that I can be wrong and I am wrong many times during my day, but these people can't see the science, or won't. I ask the question again, Why? With Much Respect, Marlena Orndorff > >In a message dated 8/1/2003 1:13:07 PM Central Daylight Time, > >dfreels@m... writes: > > > > > Now nearly two weeks post-symposium, I've been sitting back and mulling a > > > lot of this over. I'll admit I've made a crack or two about e's UHMS > > > membership, but seeing and watching in person many of the movers and > > > shakers in this " movement " , I've come to the conclusion that we all > > > definitely need to cease the potshots and backbiting. > > > > > > > > > >I have no Idea why someone wouuld make a pop shot about her being a UHMS > >member. e has the abilty to be a member and still remain in the feild > >for > >Neurological indications. Most of us take POP shot's at the UHMS instead of > >trying to keep all imformation open and joined together. e Knows what > >she is > >doing and many of us question how she does what she does. Stop Step back and > >wacth her. You will see the things she does and Make pop shots not realizing > >she is gaining ground while some of us are still trying to get on the > >field. See > >you have to stay open and that is what she does. She doe's not throw punches > >learns walks away if she has to till she can regroup. But she is never left > >standing in the end alone. I admire this lady she is my best friend int he > >world > >right now and I love her with all my heart. What she has done for me no one > >can ever take away. She has stopped what she was doing to help me when no one > >else would. Yes, She even went to Austin with me to fight my case when others > >were supposed to said they would and never did. But however we wont go there. > >If you guy's only knew how hard she worked. Ive talked to her at 5:00 am and > >then again at 1:00 am the next morning and she is still working for the > >cause of > >HBOT. Could we all give credit where credit is due? > >Darin > > > > > > Quote Link to comment Share on other sites More sharing options...
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