Guest guest Posted April 22, 2003 Report Share Posted April 22, 2003 Welcome, Libby. This is a wonderful place to find support and laughter. I'm glad you found the group. Maggie ________________________________________________________________ The best thing to hit the internet in years - Juno SpeedBand! Surf the web up to FIVE TIMES FASTER! Only $14.95/ month - visit www.juno.com to sign up today! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2003 Report Share Posted April 23, 2003 > Hi , and thank you for your kind words. > I live in central Ohio. My kids go to a school here that is for kids with ASD. The classes, are for the most part, half ASD and half > typical. The school is naturalistic ABA. Ohio has an ASD school?? REALLY?? Sorry, just in a bit of shock there. But what can I say? I live in one of the 2 counties in Ohio that doesn't even have a hospital.... Oh wait... I think the other county built one last year. : / Tina *in Southwest Ohio* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2008 Report Share Posted September 16, 2008 In frequent-dose-chelation sarahpetersonus wrote: Hello everyone!!! I am new to the group. ----------Hello and welcome.------------Jackie I have Cutler's copyright 1999 book. Is there an supplemental information published or is there a new edition that I do not know about? Thank you in advance for any information. ----------There is not a new edition of Amalgam Illness, but Cutler did publish a second book in 2004, titled " Hair Test Interpretation: Finding Hidden Toxicities " , which is also available at his website. http://www.noamalgam.com/hairtestbook.html This covers how to read a hair test and to look for mercury toxicity, and other toxicities too, and it also has updated information about what he suggests for chelation dosages, etc. Andy has also posted numerous times to various chelation groups over the past number of years, and we often link to those old posts, and you can search archives for his comments, which would be more up to date than the book. The search engine we use is onibasu, and the groups we search are Autism-Mercury, Adult-Metal-Chelation, and this group, Frequent Dose Chelation. Here's the link. http://www.onibasu.com A collection of some of his posts can be found here: http://www.onibasu.com/wiki http://home.earthlink.net/~moriam/ANDY_INDEX.html Jackie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2009 Report Share Posted August 27, 2009 To all you with partners...be thankful you have been blessed with someone to lean on...I live alone with my dog and cat, good sounding boards and huggers...but that's about it! C Familial IPF 5/09 > > > > > > > > Hi everyone, my name is and I appreciate being a member of > > your > > > > group. I was diagnosed just about 2 years ago now and went to > > rehab > > > > and am continuing with what the hospital calls phase 3 where you > > have > > > > a director, but take your own stats and write them into a sheet. > > It's > > > > a nice group with people with different forms of COPD, > > unfortunately > > > > I'm the only one with IPF so they don't feel like I do. After > > reading > > > > some of the posts on this site I see others having the same > > problems > > > > and feelings that I have so I can relate with them. I live in > > New > > > > Hampshire in a mobile home in a park, it's a coop park and there > > are > > > > many nice people here. I was the operations manager doing > > everything > > > > for everyone, but now I can't do the physical stuff for them or > > > > myself. It's hard seeing my wife trying to do a lot of the > > physical > > > > things I used to do. Well just a little to introduce myself. > > > > > > > > God be with you all, > > > > HCarson, sawman23us@... <mailto:sawman23us%40yahoo.com> > > > > hey , I was told I had IPF in 2005 and we all on here know > > what u are going through.I don't get on here to much but I still > > read a lot of the post on here,I say a specal > > prayer every night for our group,just don't feel you are alone in > > this because there are a lot of good people on here that you can > > talk to and a lot of friends.I knowq what you mean when you said > > your wife does the things you use to do because my wife does that > > also. > > > > > > > > > > > > > > >------------------------------------------------------------------------ > > > >No virus found in this incoming message. > >Checked by AVG Free Edition. > >Version: 7.5.467 / Virus Database: 269.6.4/790 - Release Date: 5/5/2007 10:34 AM > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 29, 2009 Report Share Posted August 29, 2009 , Thank you, but the headache turned into a very bad illness. Today is the first day I've been able to get on the computer. I have 100 e-mail. I don't know if I;ll be able to get through them all today. I'm still weak and shaky, Thank you for thinking about me. I think about you too.Beverley Joy,71, UIP,NSIP 1-09,Diabetes,Sjogren's,Fibromyalgia Idaho From: dovaltman <dovaltman (AT) yahoo (DOT) com>Subject: New to the groupTo: Breathe-Support@ yahoogroups. comDate: Tuesday, August 25, 2009, 10:40 PM Hi all, I just joined the group today. I was diagnosed with idiopathic familial pulmonary fibrosis 4 years ago and I had a lung biopsy 3 years ago to confirm the diagnosis. Up until 2 weeks ago, it seemed to be dormant with no changes in my pulmonary functions. The only problem I seemed to have was my chronic dry cough. Then 2 weeks ago, after a routine pulmonary function test, we found that my lung capacity had decreased significantly and my CT scan shows that the fibrosis has increased. My doctor has now referred me to the transplant team. My doctor also put me on prednisone after being reluctant to do so. The prednisone took away my cough and did improve my breathing, however, it spiked my blood sugar to levels that sent me into the emergency room and 15 units of insulin. I was told that I was borderline diabetic, but I was always able to keep my sugar levels low through diet. So now, I am caught between a rock and a hard place, if I continue to take the prednisone, I am going to have to take regular insulin injections and follow a strict diabetic lifestyle. If I stop, then I go back to the cough and shortness of breath while I wait for my condition to deteriorate until I need the transplant.Needless to say, I am little bummed out about this. I am looking forward to hearing from others in the group and learning more about what I can do to live with this.ThanksDov start: 0000-00-00 end: 0000-00-00 start: 0000-00-00 end: 0000-00-00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 29, 2009 Report Share Posted August 29, 2009 Thank you. Tomorrow I have to start getting ready for my trip to the boat. We are leaving Wednesday. I may have to get Bob to help tomorrow because after that he will have to go home and get ready too.Beverley Joy,71, UIP,NSIP 1-09,Diabetes,Sjogren's,Fibromyalgia Idaho From: dovaltman <dovaltman (AT) yahoo (DOT) com>Subject: New to the groupTo: Breathe-Support@ yahoogroups. comDate: Tuesday, August 25, 2009, 10:40 PM Hi all, I just joined the group today. I was diagnosed with idiopathic familial pulmonary fibrosis 4 years ago and I had a lung biopsy 3 years ago to confirm the diagnosis. Up until 2 weeks ago, it seemed to be dormant with no changes in my pulmonary functions. The only problem I seemed to have was my chronic dry cough. Then 2 weeks ago, after a routine pulmonary function test, we found that my lung capacity had decreased significantly and my CT scan shows that the fibrosis has increased. My doctor has now referred me to the transplant team. My doctor also put me on prednisone after being reluctant to do so. The prednisone took away my cough and did improve my breathing, however, it spiked my blood sugar to levels that sent me into the emergency room and 15 units of insulin. I was told that I was borderline diabetic, but I was always able to keep my sugar levels low through diet. So now, I am caught between a rock and a hard place, if I continue to take the prednisone, I am going to have to take regular insulin injections and follow a strict diabetic lifestyle. If I stop, then I go back to the cough and shortness of breath while I wait for my condition to deteriorate until I need the transplant.Needless to say, I am little bummed out about this. I am looking forward to hearing from others in the group and learning more about what I can do to live with this.ThanksDovstart: 0000-00-00 end: 0000-00-00 start: 0000-00-00 end: 0000-00-00 Quote Link to comment Share on other sites More sharing options...
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