Guest guest Posted February 2, 2001 Report Share Posted February 2, 2001 > Temera > who is trying to figure out how many calories to eat a day, and if 1650 is > too high for me to lose weight. Although I cannot go below!!! Temera, I don't think that 1650 is too low for you. If you have 120 lbs to lose, you should actually be eating more calories. I'm not sure exactly how much more, but I do know that with WW, the more you weigh, the more you are allowed to eat and as you lose weight, the number of points (or calories) you are allowed to eat goes down! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2001 Report Share Posted February 3, 2001 Thanks , that helps!! Temera Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2001 Report Share Posted November 8, 2001 , Have you made any changes to your workouts or food intake or are you doing everything the same? I would suggest, if things are the same, to change them slightly. Hope this helps. LB fl > Hello my friends, > > If you are a very slow loser, and I don't mean pouting , but weight comes > off in minute tiny teeny pieces instead of layers, how long is it before you > start to see results. I've been faithfully exercising for the last 4 weeks. > Haven't overdone my cardio like the last time, have increased my weights and > or reps each wt workout, and have eaten fairly clean with the exception of a > few falls. > > But I'm not seeing anything yet? Am I expecting too much? I lost it so fast > the first time around, it's like my body knows what's happening and is > hanging on to the fat because it lost it awhile back and doesn't want to > give it up (especially with winter upon us). > > I think I'm going to re-read the book this weekend and try to re- focus > again. I also think I'm going to add a carb choice into my meals and see if > that gives me more energy. I will go by the book rather than what my > nutritionist recommended. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 Be sure and ask about progress on IEP goals and the lack of progress. If there is a lack of progress find the source of the cause. If there is no progress, it could be behavior or teaching methods. Try to pin them down, and if it is behavior it is never too early to ask for a behavior intervention plan. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 Hi Anne, I was a teacher before my children were born, and there are many books( see amazon for a sample listing) you can use and many old back to school issues of parenting magazines give great tips for both n/t kids and special needs kids as well. I remember Parents and Child both had a few good issues- maybe you can view them online. Some things that stands out is to have a list as you are doing and to try to be a good listener and absorb what is being said, ask all your questions before you leave and last of all- take notes. This site : www.psparents.net/parent-teacher.htm I hope I have it correct- is a great resource for parents in dealing with public school personnel, and parent/teacher connections. Click on the learning disabilities section as well and if you view it, you can get a general list of questions. Also, below the parent/ teacher conference area there is an article called " Is your child falling through the cracks? " that is pretty good. Yes, it's pre-k, but if you look at the goals of the iep and what n/t pre-k children do, you can get a feel for where your son has gained and where he needs to continue working on present goals, and if a BIP is necessary. All the Best, Fran Anne wrote: I have a parent-teacher conference coming up for my son in Pre-K. I'm never sure what to ask at these things, even for my NT child. My son has a diagnosis of PDD-NOS. Any suggestions would be great. I'm making a list. Anne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2006 Report Share Posted February 23, 2006 Hi . The process is called chelation therapy. It is a process that should be done on a protocol basis. No matter which one you choose, stick with it. I do not know of any ASD families that are using IV, because of the obvious difficulties involving ASD kids and needles...or ANY kid for that matter. There are DAN doctors available in different cities that can help you, but chelation is only one part of the equation. Proper diet and supplementation are huge in this stuff. If you know what part of the state you are moving to, several on here can help you locate a provider that can and will help. Jeff Cunningham, DC Sulphur Springs, TX Question Hi! There was some info posted the other day about different products that remove metals from the body. (Specifically mercury from vaccinations)I am just curious if anyone has ever tried these products and if you did, what were your results? Thanks! from Washington, who is going to be moving to the great state of Texas : ) Texas Autism Advocacy www.TexasAutismAdvocacy.org Texas Disability Network Calendar of Events www.TexasAutismAdvocacy.org Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2006 Report Share Posted February 23, 2006 We did an IV EDTA push. Probably one of the easiest procedures we have done yet... Try and figure these kids out????? Big smiles. Liz > Hi . The process is called chelation therapy. It is a > process that should be done on a protocol basis. No matter which > one you choose, stick with it. I do not know of any ASD families > that are using IV, because of the obvious difficulties involving > ASD kids and needles...or ANY kid for that matter. There are DAN > doctors available in different cities that can help you, but > chelation is only one part of the equation. Proper diet and > supplementation are huge in this stuff. If you know what part of > the state you are moving to, several on here can help you locate a > provider that can and will help. > > > Jeff Cunningham, DC > Sulphur Springs, TX > Question > > > Hi! > There was some info posted the other day about different products > that > remove metals from the body. (Specifically mercury from > vaccinations)I > am just curious if anyone has ever tried these products and if you > did, what were your results? > Thanks! > from Washington, who is going to be moving to the great > state of Texas : ) > > > > > > Texas Autism Advocacy > www.TexasAutismAdvocacy.org > > Texas Disability Network > Calendar of Events > www.TexasAutismAdvocacy.org > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2009 Report Share Posted January 19, 2009 I was wondering if your AST, ALT, and GGT go back to normal after treatment and you remain undetectable. I don't know if they keep track of most people's GGT, but they do with me since I had a transplant. I will be doing my 8th shot tomorrow night, have genotype 1a, and I have been undetectable since the sixth day of treatment. The treatment has been pretty easy for me so far. My blood cell counts have been dropping. My hemoglobin is now 10.5, my hematocrit, 30.5, my RBC is 3.35, and my white blood cell count is 3.9. I am supposed to start the Procrit shots once my hemoglobin goes below 11, which it is now, but haven't heard from my post transplant coordinator about it yet. I've never thought to ask the question about the AST, ALT, and GGT to my coordinator yet, and was wondering if people who are SVR, if those liver enzymes went back to normal. Mine are like a yo yo going all over the place since my transplant, and since being on treatment too. Thanks. Penny Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2009 Report Share Posted January 19, 2009 Penny, my alt/ast went back into the normal level within the first couple of weeks of treatment and have remained there ever since. Subject: QuestionTo: Hepatitis_C_Central Date: Monday, January 19, 2009, 3:42 PM I was wondering if your AST, ALT, and GGT go back to normal after treatment and you remain undetectable. I don't know if they keep track of most people's GGT, but they do with me since I had a transplant. I will be doing my 8th shot tomorrow night, have genotype 1a, and I have been undetectable since the sixth day of treatment. The treatment has been pretty easy for me so far. My blood cell counts have been dropping. My hemoglobin is now 10.5, my hematocrit, 30.5, my RBC is 3.35, and my white blood cell count is 3.9. I am supposed to start the Procrit shots once my hemoglobin goes below 11, which it is now, but haven't heard from my post transplant coordinator about it yet.I've never thought to ask the question about the AST, ALT, and GGT to my coordinator yet, and was wondering if people who are SVR, if those liver enzymes went back to normal. Mine are like a yo yo going all over the place since my transplant, and since being on treatment too.Thanks.Penny Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2009 Report Share Posted January 19, 2009 Thanks. Maybe I could be different since having a transplant, and having the anti rejection drugs in the mix too. Penny > > > > Subject: Question > To: Hepatitis_C_Central > Date: Monday, January 19, 2009, 3:42 PM > > > > > > > I was wondering if your AST, ALT, and GGT go back to normal after > treatment and you remain undetectable. I don't know if they keep track > of most people's GGT, but they do with me since I had a transplant. I > will be doing my 8th shot tomorrow night, have genotype 1a, and I have > been undetectable since the sixth day of treatment. The treatment has > been pretty easy for me so far. My blood cell counts have been > dropping. My hemoglobin is now 10.5, my hematocrit, 30.5, my RBC is > 3.35, and my white blood cell count is 3.9. I am supposed to start the > Procrit shots once my hemoglobin goes below 11, which it is now, but > haven't heard from my post transplant coordinator about it yet. > > I've never thought to ask the question about the AST, ALT, and GGT to > my coordinator yet, and was wondering if people who are SVR, if those > liver enzymes went back to normal. Mine are like a yo yo going all > over the place since my transplant, and since being on treatment too. > > Thanks. > Penny > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2009 Report Share Posted January 19, 2009 yep, maybe thats the difference, I dunno but once you kill this virus, all you need is a sliver of liver to work,, lol,, altho the more the better Subject: Re: QuestionTo: Hepatitis_C_Central Date: Monday, January 19, 2009, 8:37 PM Thanks. Maybe I could be different since having a transplant, and having the anti rejection drugs in the mix too. Penny > > > From: preciouspenny3 <preciouspenny3@ ...>> Subject: [Hepatitis_C_ Central] Question> To: Hepatitis_C_ Central@yahoogro ups.com> Date: Monday, January 19, 2009, 3:42 PM> > > > > > > I was wondering if your AST, ALT, and GGT go back to normal after > treatment and you remain undetectable. I don't know if they keep track > of most people's GGT, but they do with me since I had a transplant. I > will be doing my 8th shot tomorrow night, have genotype 1a, and I have > been undetectable since the sixth day of treatment. The treatment has > been pretty easy for me so far. My blood cell counts have been > dropping. My hemoglobin is now 10.5, my hematocrit, 30.5, my RBC is > 3.35, and my white blood cell count is 3.9. I am supposed to start the > Procrit shots once my hemoglobin goes below 11, which it is now, but > haven't heard from my post transplant coordinator about it yet.> > I've never thought to ask the question about the AST, ALT, and GGT to > my coordinator yet, and was wondering if people who are SVR, if those > liver enzymes went back to normal. Mine are like a yo yo going all > over the place since my transplant, and since being on treatment too.> > Thanks.> Penny> Quote Link to comment Share on other sites More sharing options...
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