Guest guest Posted February 16, 2004 Report Share Posted February 16, 2004 Its so much easier to simply find another doctor, one who won't PUSH the issue..... Perhaps we could start somekind of referal list to doctors who don't push vaccines ? ? ? Chelly Re: RE: another question At 10:04 AM 02/16/2004 -0600, you wrote: ><< But you will be in over your head if you think you can explain this >to the doctor.>> > >I so agree with this statement! I can't believe what a wimpy idiot I >become when my son's doctor starts in on me about vaccines. YOu are not alone . Even those of us who are nurses are bowled over by them, even with as much as I know. I don't even try anymore. They will only wake up when one of their own is damaged and not even then sometimes due to the denial I have so >admired her care of my older two kids (she is very reluctant to use >antibiotics or do invasive things) yet she has used every trick, and I >do mean " trick " , in the book to jab this baby. The GUILT they induce is >enormous. > Exactly Sheri -------------------------------------------------------- Sheri Nakken, R.N., MA, Classical Homeopath Vaccination Information & Choice Network, Nevada City CA & Wales UK $$ Donations to help in the work - accepted by Paypal account vaccineinfo@... voicemail US 530-740-0561 (go to http://www.paypal.com) or by mail Vaccines - http://www.nccn.net/~wwithin/vaccine.htm Vaccine Dangers On-Line course - http://www.nccn.net/~wwithin/vaccineclass.htm Homeopathy On-Line course - http://www.nccn.net/~wwithin/homeo.htm ANY INFO OBTAINED HERE NOT TO BE CONSTRUED AS MEDICAL OR LEGAL ADVICE. THE DECISION TO VACCINATE IS YOURS AND YOURS ALONE. ****** " Just look at us. Everything is backwards; everything is upside down. Doctors destroy health, lawyers destroy justice, universities destroy knowledge, governments destroy freedom, the major media destroy information and religions destroy spirituality " .... Ellner Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2004 Report Share Posted February 16, 2004 At 11:03 AM 02/16/2004 -0800, you wrote: >Its so much easier to simply find another doctor, one who won't PUSH the issue..... >Perhaps we could start somekind of referal list to doctors who don't push vaccines ? ? ? >Chelly Yes, it is easier to find another doctor, but we don't want a 'list' as they can become targets if there is such a list. So we do it discreetly Sheri -------------------------------------------------------- Sheri Nakken, R.N., MA, Classical Homeopath Vaccination Information & Choice Network, Nevada City CA & Wales UK $$ Donations to help in the work - accepted by Paypal account vaccineinfo@... voicemail US 530-740-0561 (go to http://www.paypal.com) or by mail Vaccines - http://www.nccn.net/~wwithin/vaccine.htm Vaccine Dangers On-Line course - http://www.nccn.net/~wwithin/vaccineclass.htm Homeopathy On-Line course - http://www.nccn.net/~wwithin/homeo.htm ANY INFO OBTAINED HERE NOT TO BE CONSTRUED AS MEDICAL OR LEGAL ADVICE. THE DECISION TO VACCINATE IS YOURS AND YOURS ALONE. ****** " Just look at us. Everything is backwards; everything is upside down. Doctors destroy health, lawyers destroy justice, universities destroy knowledge, governments destroy freedom, the major media destroy information and religions destroy spirituality " .... Ellner Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2004 Report Share Posted February 16, 2004 Dear , Just the thought that your Isaiah may be diagnosed autistic (vaccine injured children is my definition) is enough to sound the ALARM. I have an autistic son and when he was diagnosed it wasn't long after my husband and I suspected vaccines even before we knew what we know today. I stopped vaccinating ALL my children in 98 not long after I received the news about my son. If your daughter is healthy, SKIP the check up. More than likely your doc wants her there in the hopes of making money by vaccinating her with a poison that about 80% of most docs don't do to their own children! When I get those little reminders in the mail for my infant, I tear them up and in the garbage they go. The doc I have now though knows that if he even mentions vaccines, I'll pull my whole family out. Why take your healthy baby to be exposed to those that may be sick (flu, etc.) only to be pressured into what I would consider a barbaric practice--vaccination. (BTW-all vaccines are poisonous--if it isn't anti-freeze, formaldehyde, etc., its aluminum or mercury ) My baby is 10 months old and has only been to ONE check up and she didn't need that one. She is completely unvaxed, NO vit. K shot, breastfeed, organic food as much as possible, have a homeopath if needed. etc. She is developing at an unbeleivable rate and has been very healthy since birth. If your daughter is healthy and growing and developing normally, you might benefit by canceling the appointment and/or reschedule at a later date in order for you and your husband to research the issue more with out being pressured by your doc. If you choose not to vax, you may get pressured. That is why I sought out a physician (our family doc.) and gave him an all or nothing. I went to his office and layed out my terms, not his, and he accepted. We are rarely at his office though because we don't vax! (And we use preventative med. ) Lynda ERIN CORN wrote: >I hope I do not aggravate you ladies to much but someone mentioned that baby shots have anti freeze and formaldehyde in them can someone tell me which ones. > >Right now I am at a very difficult cross road. is 11 months old today. Before all the things surfaced that Isaiah may have autism we are currently going through the testing I blindly let both of my children receive every vaccination that the doctor said they should have. We will be going in for her 12 months check up in 1 month I have to decide in now what I want to do. I told my husband I did not know if I would let get the vaccinations or not and he wanted to know why. So I told him of some of the things I have been learning. I want to be armed with as much knowledge as possible when we go in for that visit. Any suggestions are appreciated. Thank you for listening. I just hope I did not allow my children to be damaged by something I thought was good for them. > >May God bless you and yours. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2004 Report Share Posted March 23, 2004 Pam, I have been following your thread with Dr Grim and I just had a couple of comments. I am not sure where you are at but there is one lab in the USA that can differentiate the spironolactone from the aldosterone and it may be worth your doctors looking into. That was a major issue with my daughter because each time we tried to back down the Spironolactone in anticipation of the vein sampling her BP would skyrocket and it took some investigative work by ther endo to find the lab. Sorry I don't know the name of it though. Secondly they can do the dexamethesone suppression test while they wait for the results from Dr Lifton's lab at Yale. You should be able to get an idea it will work or not in 5-6 days although my daughters nephrology team was dead set on the fact that she had GRA when she did not that they tried it for 9 months. Additionally there is an additional type of familial aldostronism. It is reffered to as Familial aldostronism Type II. My daughter and I had this and it is not dexamethesone supressible. It also has a charteristically higher or more severe BP. It is much more difficult to control. If you go to the pubmed website and type in aldostrone then you should pull up some articles refrencing GRA and those same articles will generally also outline the type II. Unfortunaltly there is no DNA testing as yet for type two and it is generally discovered by the eliminatin method. Good luck, W Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2004 Report Share Posted March 23, 2004 In a message dated 3/23/04 11:42:58, tn_weldys@... writes: Pam, I have been following your thread with DR Grim and I just had a couple of comments.  I am not sure where you are at but there is one lab in the USA that can differentiate the spironolactone from the aldosterone and it may be worth your doctors looking into. That was a major issue with my daughter because each time we tried to back down the Spironolactone in anticipation of the vein sampling her BP would skyrocket and it took some investigative work by ther endo to find the lab. Sorry I don't know the name of it though. Secondly they can do the dexdexamethasone suppression test while they wait for the results from Dr Lifton's lab at Yale. You should be able to get an idea it will work or not in 5-6 days although my daughters nephrology team was dead set on the fact that she had GRA when she did not that they tried it for 9 months. Additionally there is an additional type of familial aldostronism. It is reffered to as Familial aldostronism Type II. My daughter and I had this and it is not dexamethesone supressible. It also has a charteristically higher or more severe BP. It is much more difficult to control. If you go to the pubmed website and type in aldostrone then you should pull up some articles refrencing GRA and those same articles will generally also outline the type II. Unfortunaltly there is no DNA testing as yet for type two and it is generally discovered by the eliminatin method. Good luck, W We have published that the Dex test can be done overnight. Give 2 mg at midnight and check aldo and cortisol thenex am. Aldo will be donw to nearly zero. The BP effect takes longer but is usually there in a couple of weeks. The Australian Group (Tom Stowasser) thought they had a geneitc test for type 2 but I havent seen anything lately. Dr. Lfiton's lab does the testing for free or GRA May your pressure be low! Clarence E. Grim, BS, MS, MD, FACP, FACC Professor of Medicine and Epidemiology Board Certified in Internal Medicine, Geriatrics and Hypertension Focusing on difficult to control high blood pressure and high cholesterol especially in the African Diaspora Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2004 Report Share Posted March 23, 2004 The reasons to suspect GRA in your son are: 1. You have PA and it may be GRA. 2. Your son has enough HTN to get LVH and so is a good candidate.' 3. The "normal" aldo is seen many times and it is the renin you need to index the aldo with to get the ratio. So ask what the renin was. Aldo alone is almost useless. Thanks for helping us train more Drs. to know what this is and how to diagnose it. May your pressure be low! Clarence E. Grim, BS, MS, MD, FACP, FACC Professor of Medicine and Epidemiology Board Certified in Internal Medicine, Geriatrics and Hypertension Focusing on difficult to control high blood pressure and high cholesterol especially in the African Diaspora Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2004 Report Share Posted March 23, 2004 In a message dated 3/22/04 17:48:18, spirlhelix@... writes: I just realized that when I came up with that "normal" aldosterone-renin test, it was only three weeks before my diagnosis with congestive heart failure. I wonder how the usual increase in aldosterone secondary to heart failure might have affected my test results? Depends on what was causing your heart failure. I dont know what levels to expect in CHF but this is usually secondary aldosteronism where the aldo is high becasure the renin is high. Also blood sodium tends to be low not high as it is in PA. What did the think caused your CHF and what were the Sx you were having? May your pressure be low! Clarence E. Grim, BS, MS, MD, FACP, FACC Professor of Medicine and Epidemiology Board Certified in Internal Medicine, Geriatrics and Hypertension Focusing on difficult to control high blood pressure and high cholesterol especially in the African Diaspora Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2004 Report Share Posted March 23, 2004 In a message dated 3/23/04 19:42:43, leslie@... writes: A couple other questions from what I've read... Is there a relationship between pyelonephritis and hyperaldosteronism? Also, can long term low K cause permanent muscle damage? Yes-Pyleo can cause seconday aldo Low K can damage kidneys Some pyleo become K losers and some Na losers. Severe low K will cause enought muscle weakness that people become paralyzed all over and can diet from not being aboe to breathe. Severe low K will increase muscle damamge and can be reflected by very high CPKs. May your pressure be low! Clarence E. Grim, BS, MS, MD, FACP, FACC Professor of Medicine and Epidemiology Board Certified in Internal Medicine, Geriatrics and Hypertension Focusing on difficult to control high blood pressure and high cholesterol especially in the African Diaspora Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2004 Report Share Posted March 23, 2004 Hi, I've been reading several threads with much interest and learning a lot, but I'm a bit lost on some of the acronyms. Could someone please list the most commonly used ones and what they mean? The below message is a good example. A couple other questions from what I've read... Is there a relationship between pyelonephritis and hyperaldosteronism? Also, can long term low K cause permanent muscle damage? Thanks! PS - I'm collecting records from my previous physicians. Dr. Grim, when your clinic is up and running in Milwaukee, I'd like to schedule a visit. Re: Re: Another Question The reasons to suspect GRA in your son are:1. You have PA and it may be GRA.2. Your son has enough HTN to get LVH and so is a good candidate.'3. The "normal" aldo is seen many times and it is the renin you need to index the aldo with to get the ratio. So ask what the renin was. Aldo alone is almost useless.Thanks for helping us train more Drs. to know what this is and how to diagnose it. May your pressure be low!Clarence E. Grim, BS, MS, MD, FACP, FACCProfessor of Medicine and EpidemiologyBoard Certified in Internal Medicine, Geriatrics and HypertensionFocusing on difficult to control high blood pressure and high cholesterol especially in the African Diaspora Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 24, 2004 Report Share Posted March 24, 2004 Having suffered with PA bi lateral adrenal hyperplasia for over 7 years now with relatively low K, I developed hypokalaemic myopathy which led to some permanent muscle damage in hands and legs. My professors game plan is to try and keep my K level around 4.0 - but hasn't yet achieved it. I hover around 3.5 and below. Kind Regards, Grahamlowerbp2@... wrote: In a message dated 3/23/04 19:42:43, leslie@... writes: A couple other questions from what I've read... Is there a relationship between pyelonephritis and hyperaldosteronism? Also, can long term low K cause permanent muscle damage?Yes-Pyleo can cause seconday aldoLow K can damage kidneys Some pyleo become K losers and some Na losers.Severe low K will cause enought muscle weakness that people become paralyzed all over and can diet from not being aboe to breathe. Severe low K will increase muscle damamge and can be reflected by very high CPKs. May your pressure be low!Clarence E. Grim, BS, MS, MD, FACP, FACCProfessor of Medicine and EpidemiologyBoard Certified in Internal Medicine, Geriatrics and HypertensionFocusing on difficult to control high blood pressure and high cholesterol especially in the African Diaspora Messenger - Communicate instantly..."Ping" your friends today! Download Messenger Now Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 24, 2004 Report Share Posted March 24, 2004 Pam, there are differing levels of the sevarity of the disease. My daughter was aparently much more severe than I was. Her BP has been recorded at 237/123 while in the hospital, asleep when she was only 15 months old. THis was confirmed by a very stressed doc by every mechanical BP machine he could get his hands on and by manual BP . Thankfully they have many more medicines with which to control BP mow than back when I had my diagnosis. Nearly thirty years ago had my BP been that high I have been told that I most likley would not have made it long enough to have the surgery. I wish you luck in your search, W. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 25, 2004 Report Share Posted March 25, 2004 In a message dated 3/25/04 5:14:27, spirlhelix@... writes: > stressed doc by every > mechanical BP machine he could get his hands on and > by manual BP . > Thankfully they have many more medicines with which > to control BP mow > than back when I had my diagnosis. Nearly thirty > years ago had my BP > been that high I have been told that I most likley > would not have > made it long enough to have the surgery. I wish you > luck in your > search, W. that is the reason even today to do BP the real way. Not machine beats a trained human. May your pressure be low! Clarence E. Grim, BS, MS, MD, FACP, FACC Professor of Medicine and Epidemiology Board Certified in Internal Medicine, Geriatrics and Hypertension Focusing on difficult to control high blood pressure and high cholesterol especially in the African Diaspora Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2004 Report Share Posted May 10, 2004 Not sure. I've been on 10 mg for a couple months, but if your situation is different, maybe it's not too fast. Thea another question > also my doctor started me right out at 10mg of lexapro and then > wanted me to go up to 20mg in a couple of weeks was this too fast???? > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 7, 2004 Report Share Posted December 7, 2004 Hi Dawn, The only way to tell if your oesophagus is getting bigger is to compare barium x-rays a couple of years apart. I can't say with certainty if there are more or less symptoms before and after but there is more collected food sitting there to ferment and cause acid and burping. Joan another question how do you know if you have end stage achalasia??? and can you tell if your esoph is getting bigger?? are there symptoms?dawn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 9, 2004 Report Share Posted December 9, 2004 The endoscopy or camera inserted into your esop. You will have to have several tests to make a comparison but a trained doctor can tell if it is enlarged. another question how do you know if you have end stage achalasia??? and can you tell if your esoph is getting bigger?? are there symptoms?dawn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2004 Report Share Posted December 22, 2004 > My question is about the DS community. Are you all involving yourselves > in the DS community such as the buddy walks and picnics etc... and making > that part of his/her life or are you informing yourselves but raising your > childeren solely in the typical society. << i am raising Fiona with as much contact to mainstream kids and to ds kids as possible. i am trying to get in " the best of both worlds " . as much as i see the benefits of her learning from other kids and being a part of the " normal " everyday world, her chances of a partnership later on or of lasting friendships will be among her " own kind " , among kids or young adults who understand each other, know what the other is going thru, someone who is really tuned in. this is true for every young person looking for a partner or a friend. you look for someone on your wave-length, someone who will understand you, someone who shares your interests, someone who laughs and cries about the same things you do. for a person with down syndrom (or any other special person for that matter) this holds true too. so the chances of finding someone for a lasting friendship will be greater the more kids they know who share their interests and their way of experiencing life. this means i do a lot of networking within the down syndrom community, trying to build up many many contacts and relationships. just think of how many people an average person gets to know before they pick their soul-mate. how much more limited is the choice our special kids have. i am trying to make the choice options as large as possible. my daughter hopefully won't pick someone just because there is no other choice. that never is a good reason for a relationship, with ds or without. gundula Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 22, 2004 Report Share Posted December 22, 2004 On one thing. We haven't seen Santa at a mall the last few years but it hasn't been long. He will be 40 next month. One year he " asked " Santa for an electric beard trimmer and the next year when we went back it was the same guy and he remembered and the beard trimmer. I don't imagine Santa gets too many requests for those. of course hasn't " believed " for years but we still have a lot of fun with it. I believe tho. Jessie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2004 Report Share Posted December 23, 2004 Hi And like Jessie, I believe too. And I have more fun with my Santa Claus suit than just about anything I own. I was Santa at 's party yesterday. and were elves who helped me give out presents to the kids. This year we went to see both Santa and the Fairy Princess in Kansas City. I plan to take them to see Santa as long as they want to go, regardless of how old they are. Same goes for other holiday stuff. Make glad the hearts of childhood. says I am just a big kid too. I think that is one of the nicest things she's called me (and she only calls me nice things). I can hardly wait to our nieces move here from California. They are younger than our four here and still into all this stuff 100 percent. Dad to , Kristi, (all three Down syndrome ages 12-13-14) and Cri du chat (age 7) Husband to C. in Mo. Uncle Daddy to and in Calif. (Down syndrome) Re: another question > > On one thing. We haven't seen Santa at a mall the last few years > but it hasn't been long. He will be 40 next month. One year he " asked " Santa > for an electric beard trimmer and the next year when we went back it was the > same guy and he remembered and the beard trimmer. I don't imagine > Santa gets too many requests for those. of course hasn't " believed " for > years but we still have a lot of fun with it. I believe tho. Jessie > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2004 Report Share Posted December 23, 2004 Quite a few years ago, at Easter had said he didn't want a stuffed bunny that year so I hadn't got one. When the time came my husband was in the hospital and decided he wanted a bunny after all. I couldn't leave him alone to shop so I asked a friend to find one for us. I knew he'd enjoy shopping for one. But he said something like, " are you telling me the Easter bunny isn't real? " He acted so shocked. And I said, " you mean I asked the wrong person? " Of course he found a great bunny for . This guy was about 40 at the time. So it's not just our kids. It's our friends too. or mine anyway. Jessie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 23, 2004 Report Share Posted December 23, 2004 Quite a few years ago, at Easter had said he didn't want a stuffed bunny that year so I hadn't got one. When the time came my husband was in the hospital and decided he wanted a bunny after all. I couldn't leave him alone to shop so I asked a friend to find one for us. I knew he'd enjoy shopping for one. But he said something like, " are you telling me the Easter bunny isn't real? " He acted so shocked. And I said, " you mean I asked the wrong person? " Of course he found a great bunny for . This guy was about 40 at the time. So it's not just our kids. It's our friends too. or mine anyway. Jessie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2005 Report Share Posted February 8, 2005 Hope Bri had a GREAT birthday. Oh my goodness. One more year and you'll have a TEENAGER!!!!! 8-) Following site is St Jude's take on CVID http://www.stjude.org/disease-summaries/0,2557,449_2164_6532,00.html This is from Lucile Packard's Children's Hospital at Stanford http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/allergy/cvid.html But I really have to snicker at this quote found at http://www.utoronto.ca/kids/Hypogam.htm " Hypogammaglobulinemia (Common Variable Immunodeficiency) " But I really didn't have time to look at what it was saying in context..... I just put " CVID " and " Hypogammaglobulinemia " in a Google search. Love the info highway! Wenoka Another Question Hi Everyone, has Ig1 subclass deficiency and Polysaccharide antibody deficiency. Is this technically CVID?? His Immuno is telling me that CVID is only referring to patients who also have t-cell issues. He did diagnose him with Hypogammaglobulinemia. Sandi, Mom to , age 12. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 9, 2005 Report Share Posted February 9, 2005 Sandi: Don't quote me but I think I recall the doc saying CVID was a combination of more than one Ig deficit, like low IgG AND low IgA? Then alot of times you'll see the combination of a subclass def and an IgA def but they don't call that CVID? I don't think it has to have a t-cell component. (mom to , age 6, dairy intolerant-related GERD -- currently has polysaccharide antibody def, previously had transient IgG, IgA, t-cell & other defs... and also to Kate, age 2, more dairy intolerant but very healthy!) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 9, 2005 Report Share Posted February 9, 2005 Sandi: Don't quote me but I think I recall the doc saying CVID was a combination of more than one Ig deficit, like low IgG AND low IgA? Then alot of times you'll see the combination of a subclass def and an IgA def but they don't call that CVID? I don't think it has to have a t-cell component. (mom to , age 6, dairy intolerant-related GERD -- currently has polysaccharide antibody def, previously had transient IgG, IgA, t-cell & other defs... and also to Kate, age 2, more dairy intolerant but very healthy!) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 9, 2005 Report Share Posted February 9, 2005 has the dx of CVID but has normal levels of all his IgG, IgA, IgM. He had no response to the intra-dermal testing, and if I remember right there was something wrong with his b cells? I can't remember now. other than that it was just his titers that showed no immunity. When I called the IDF to question the dx they said that CVID used to be IgG, IgA and or IgM but now it is being used to encompass a larger group of things. I then questioned the immuno and he said that when Nick was first tested he had low everything and then he gained all his IgG, IgA, IgM. but since he still wasn't making antibodies to the titers they were like shooting blanks. Amy, mom to , 2 years old, CVID, asthma, GERD, on prophalatic abx (rotating Septra and Amoxicillin) and IVIG (Carimune NF) every 4 weeks, flovent, xopenex, albuterol and claritin. Allergic to latex.. among other things. Visit Nick's Caringbridge site at http://www3.caringbridge.org/ne/nicholasb/ Re: Another Question > > Sandi: > > Don't quote me but I think I recall the doc saying CVID was a combination > of > more than one Ig deficit, like low IgG AND low IgA? > > Then alot of times you'll see the combination of a subclass def and an IgA > def but they don't call that CVID? > > I don't think it has to have a t-cell component. > > (mom to , age 6, dairy intolerant-related GERD -- currently has > polysaccharide antibody def, previously had transient IgG, IgA, t-cell & > other > defs... and also to Kate, age 2, more dairy intolerant but very healthy!) > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 9, 2005 Report Share Posted February 9, 2005 In a message dated 2/8/2005 10:13:16 PM Pacific Standard Time, yhwhworship@... writes: http://www.lpch.org/DiseaseHealthInfo/HealthLibrary/allergy/cvid.html Wenoka, Thank you for the links...this is exactly what I thought!! I have no idea where this Immuno is coming from most of the time. Sandi, Mom to , age 12. Polysaccharide deficiency, IgG1 subclass deficiency, Tetrology of Fallot, Pulmonary valve transplant (2003), Mitral valve stenosis, COPD, asthma, Carnitine deficiency, GERD, suspected Velocardiofacial syndrome. Quote Link to comment Share on other sites More sharing options...
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