Guest guest Posted October 30, 2008 Report Share Posted October 30, 2008 Thanks Dianne, I seem to be getting mixed responses, most of them positive but a few negative (although some for sleeves). One of them said that when blood was taken before surgery gloves were not used, they didn't see any toxic waste bins for blood etc. My worst fear would be to go with Mexico and come away with a successful band but also an infection that i cant get rid of. My mom has scared me off a bit now, hence why i am trying to feel more confident after speaking to people who have been there and done that From: Dianne <diladirn@...> Sent: Wednesday, October 29, 2008 5:15:29 PMSubject: Re: help >> I have been trying for some time now to find a surgeon for WLS, costs within the US are so expensive that i think the only step is to go to Mexico. I have spoken to several surgical companies and think i feel confident in what i have heard about Dr Aceves, however to give myself piece of mind i wanted to speak to people who had experienced this surgery both by Dr Aceves and going to Mexico.> > Is Mexcio really that bad? what are the facilities really like? How do i know that the surgery wont go bad or me get an infection from the hosptal? Did anyone else have the same concerns?> > Please help andput my fears to bed>I was banded by Dr Aceves on Oct 20 and i have nothing but good things to say about the whole experience. Being a nurse and having been in many American hospitals-I hate to say that the hospital in Mexicali put ours to shame. Everyone was so nice. The hospital was cleaner than any I've ever seen. I would highly recommend the doctor and hospital . I was well taken care of. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2008 Report Share Posted October 30, 2008 There are safe cities in Mexico and some " not so safe " cities just like in every country. Mexicali is one of the safer cities.On Thu, Oct 30, 2008 at 5:46 AM, Hulmes <laurenhulmes@...> wrote: Thanks for that, unfortunately I'm all the way in Pennsylvania so is costly for me to go and check it out. I have looked at pictures on the Internet and they seem clean enough but you never know until you experience for yourself. I had not previously heard about the horror stories of Mexico until i mentioned it to my mom (who wants to also have surgery). What was the area like where the hospital is located? My husband feels happy about the location etc but i got myself scared after my mom talked about Mexico. Will you keep me posted about your experience, i would be interested to find out how you got on From: Wells <wbcasagrande33@...> Sent: Wednesday, October 29, 2008 10:13:50 PMSubject: Re: help I go for my band on 11/7, I had the same questions that you have. What really helped me is that in September I went and seen for myself, (I live in Arizona 3 hours away). I took a friend that has family from the area, my hubby and mother. We was all amazed of the hospital, it put our hospital to shame here. I also was able to be there when a group was coming in for there fills, to be able to see someone ask questions and to hear their stories was the best. I think that it helped my husband as well about the surgery. So if you get a chance and are close enough check it out for yourself. From: Hulmes <laurenhulmes> @groups. com Sent: Wednesday, October 29, 2008 11:43:08 AMSubject: [Dr-Aceves-bandster s] help I have been trying for some time now to find a surgeon for WLS, costs within the US are so expensive that i think the only step is to go to Mexico. I have spoken to several surgical companies and think i feel confident in what i have heard about Dr Aceves, however to give myself piece of mind i wanted to speak to people who had experienced this surgery both by Dr Aceves and going to Mexico. Is Mexcio really that bad? what are the facilities really like? How do i know that the surgery wont go bad or me get an infection from the hosptal? Did anyone else have the same concerns? Please help andput my fears to bed Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2008 Report Share Posted October 30, 2008 When staff take blood and use gloves that is to protect the staff member, not the patient. It is your blood that is an issue, the idea behind gloves during blood draws is to protect the person drawing your blood. The only danger for you during a blood draw is that you are exposed to your own blood, the staff wearing gloves isn't going to prevent that and it's not a danger to be exposed to your own blood anyway. ;o) Sure there are appropriate containers for blood and sharps containers for needles. They are in every single patient room and each place in the hospital. The person telling you this information simply didn't know what they were talking about. The sharps containers are bolted to the walls and red bag containers are in each area of the hospital where they are needed. It is exactly the same as in the US. It is not a matter of the containers were not there when this person was there, they are BOLTED to the walls of each patient room and major area of the hospital. I think the person who gave you this information simply does not know what they are talking about. If the information you were given was true people would be coming home with infections left and right and that simply isn't accurate. As for Mexico many people seem to get their education about Mexico through urban legends and that's too bad. On Thu, Oct 30, 2008 at 6:05 AM, Hulmes <laurenhulmes@...> wrote: Thanks Dianne, I seem to be getting mixed responses, most of them positive but a few negative (although some for sleeves). One of them said that when blood was taken before surgery gloves were not used, they didn't see any toxic waste bins for blood etc. My worst fear would be to go with Mexico and come away with a successful band but also an infection that i cant get rid of. My mom has scared me off a bit now, hence why i am trying to feel more confident after speaking to people who have been there and done that From: Dianne <diladirn@...> Sent: Wednesday, October 29, 2008 5:15:29 PMSubject: Re: help > > I have been trying for some time now to find a surgeon for WLS, costs within the US are so expensive that i think the only step is to go to Mexico. I have spoken to several surgical companies and think i feel confident in what i have heard about Dr Aceves, however to give myself piece of mind i wanted to speak to people who had experienced this surgery both by Dr Aceves and going to Mexico.> > Is Mexcio really that bad? what are the facilities really like? How do i know that the surgery wont go bad or me get an infection from the hosptal? Did anyone else have the same concerns?> > Please help andput my fears to bed>I was banded by Dr Aceves on Oct 20 and i have nothing but good things to say about the whole experience. Being a nurse and having been in many American hospitals-I hate to say that the hospital in Mexicali put ours to shame. Everyone was so nice. The hospital was cleaner than any I've ever seen. I would highly recommend the doctor and hospital . I was well taken care of. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2008 Report Share Posted October 30, 2008 I can vouch that latex gloves were used for each procedure and there were toxic waste boxes at shoulder height in each patient room that I was in. I am a public health nurse and I look for things like that. I checked there infection control records and they did not have any history of infectious communicable diseases...unlike the US hospitals where MRSA runs rapid. I think you are getting mis-information from someone. Why don't you go and visit and you can check it out in person. From: Hulmes <laurenhulmes@...>Subject: Re: Re: help Date: Thursday, October 30, 2008, 6:05 AM Thanks Dianne, I seem to be getting mixed responses, most of them positive but a few negative (although some for sleeves). One of them said that when blood was taken before surgery gloves were not used, they didn't see any toxic waste bins for blood etc. My worst fear would be to go with Mexico and come away with a successful band but also an infection that i cant get rid of. My mom has scared me off a bit now, hence why i am trying to feel more confident after speaking to people who have been there and done that From: Dianne <diladirnsbcglobal (DOT) net> @groups. comSent: Wednesday, October 29, 2008 5:15:29 PMSubject: [Dr-Aceves-bandster s] Re: help >> I have been trying for some time now to find a surgeon for WLS, costs within the US are so expensive that i think the only step is to go to Mexico. I have spoken to several surgical companies and think i feel confident in what i have heard about Dr Aceves, however to give myself piece of mind i wanted to speak to people who had experienced this surgery both by Dr Aceves and going to Mexico.> > Is Mexcio really that bad? what are the facilities really like? How do i know that the surgery wont go bad or me get an infection from the hosptal? Did anyone else have the same concerns?> > Please help andput my fears to bed>I was banded by Dr Aceves on Oct 20 and i have nothing but good things to say about the whole experience. Being a nurse and having been in many American hospitals-I hate to say that the hospital in Mexicali put ours to shame. Everyone was so nice. The hospital was cleaner than any I've ever seen. I would highly recommend the doctor and hospital . I was well taken care of. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2008 Report Share Posted October 30, 2008 I will be a nurse in 2 months. The wqoman who took my blood was wearing gloves, there were toxic waste bins in basically EVERY room, including my personal room.....That is some serious misinformation...I ws just there 5 days ago and had the sleeve done. That hospital is cleaner than the one I work at here in California! Helena From: Hulmes <laurenhulmes>Subject: Re: Re: help @groups. comDate: Thursday, October 30, 2008, 6:05 AM Thanks Dianne, I seem to be getting mixed responses, most of them positive but a few negative (although some for sleeves). One of them said that when blood was taken before surgery gloves were not used, they didn't see any toxic waste bins for blood etc. My worst fear would be to go with Mexico and come away with a successful band but also an infection that i cant get rid of. My mom has scared me off a bit now, hence why i am trying to feel more confident after speaking to people who have been there and done that From: Dianne <diladirnsbcglobal (DOT) net> @groups. comSent: Wednesday, October 29, 2008 5:15:29 PMSubject: [Dr-Aceves-bandster s] Re: help >> I have been trying for some time now to find a surgeon for WLS, costs within the US are so expensive that i think the only step is to go to Mexico. I have spoken to several surgical companies and think i feel confident in what i have heard about Dr Aceves, however to give myself piece of mind i wanted to speak to people who had experienced this surgery both by Dr Aceves and going to Mexico.> > Is Mexcio really that bad? what are the facilities really like? How do i know that the surgery wont go bad or me get an infection from the hosptal? Did anyone else have the same concerns?> > Please help andput my fears to bed>I was banded by Dr Aceves on Oct 20 and i have nothing but good things to say about the whole experience. Being a nurse and having been in many American hospitals-I hate to say that the hospital in Mexicali put ours to shame. Everyone was so nice. The hospital was cleaner than any I've ever seen. I would highly recommend the doctor and hospital . I was well taken care of. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2008 Report Share Posted October 30, 2008 WOW - 6 pounds in nine days? Did you ever imaginbe that you would find something that would allow you to lose 6 pounds in 9 days? woo hoo!! Keep it up. I am on my 3rd day of vlcd and I have lost 4 pounds. We are on a roll! > > According to the average weight loss for women, you are doing GREAT! Men > lose a average of 1 pound a day and women lose a average of ½ pound a day. I > did the shots through my menses and they were a little heaver then usual, > and I didn't have as good of a weight loss, but I didn't notice any other > difference. –Sounds like you are doing GREAT! > > > > From: [mailto: ] On > Behalf Of jamie_fstt > Sent: 2008-10-28 4:48 PM > > Subject: Help > > > > So I'm new to the HCG.. I'm on day 9.. I've only lost 6 lbs... I'm > starting to feel discouraged. I've been very very strict on the diet > and have not cheated. My question is.. I started mensus today. I'm > doing this on my own and the pounds and inches book says that I should > not give myself shots at all during this time.. but I've heard > elsewhere that its just supposed to be no shot for the first three > days.. Anyone have an opinion on this? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 30, 2008 Report Share Posted October 30, 2008 - , I have been a nurse for more then 30 years. i would never lead anyone falsely. As for wearing gloves when drawing blood there is danger only to the person drawing the blood not to you. Yes there were gloves. The nurses used them when removing my IV. As for surgery without gloves-there is no way this would be done because every one who has ever had surgery would have severe infections and or be dead from major infections. My experience is that there are many patients will find fault with the littlest things. Some people start with negative attitudes and look for things to go wrong. As for red bags-I don't care if there were red bags or not. Red bags have nothing to do with good or bad care. My daughter was banded there also . I saw the doctors there more than i have ever seen any doctor at hospitals here. there was no rushing etc. They all came in before I was discharged shook my hand and thanked me for using them. My room was cleaned several times a day but the smell didn't bother me. Some people may be more sensitive to smells. As for blood down the sink- yes it would have been better put into the toilet but oh well so long as it was rinsed good. As for the language barrier -almost everyone I saw spoke enough english to get my needs met. One time in recovery the nurse could not understand me and she went and got someone who did. you are given a list of spanish phrases and if needed you can use it. I never had to. The doctors all spoke very good english and everyone of them and the nurses were all great. I have never gotten such personalized care in my entire life. I had no problem getting pain meds and promptly. My call light was answered immediately. Not to say that this person who wrote negatively did not experience what he wrote-but sometimes our attitudes can make an experience bad. If i had to do it again,I would do it in a heartbeat. Think about the fact that there have been thousands of positives comments compared to this one neg. Don't let one person stop you from starting a new life. Keep researching and keep using this site because it is very helpful. God bless you. Dianne -- In , Hulmes <laurenhulmes@...> wrote: > > Thanks Dianne, > > I seem to be getting mixed responses, most of them positive but a few negative (although some for sleeves). One of them said that when blood was taken before surgery gloves were not used, they didn't see any toxic waste bins for blood etc. My worst fear would be to go with Mexico and come away with a successful band but also an infection that i cant get rid of. > > My mom has scared me off a bit now, hence why i am trying to feel more confident after speaking to people who have been there and done that > > > > > > ________________________________ > From: Dianne <diladirn@...> > > Sent: Wednesday, October 29, 2008 5:15:29 PM > Subject: Re: help > > > > > > > I have been trying for some time now to find a surgeon for WLS, > costs within the US are so expensive that i think the only step is to > go to Mexico. I have spoken to several surgical companies and think > i feel confident in what i have heard about Dr Aceves, however to > give myself piece of mind i wanted to speak to people who had > experienced this surgery both by Dr Aceves and going to Mexico. > > > > Is Mexcio really that bad? what are the facilities really like? > How do i know that the surgery wont go bad or me get an infection > from the hosptal? Did anyone else have the same concerns? > > > > Please help andput my fears to bed > > > > I was banded by Dr Aceves on Oct 20 and i have nothing but good > things to say about the whole experience. Being a nurse and having > been in many American hospitals-I hate to say that the hospital in > Mexicali put ours to shame. Everyone was so nice. The hospital was > cleaner than any I've ever seen. I would highly recommend the doctor > and hospital . I was well taken care of. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2008 Report Share Posted October 31, 2008 Thanks Dianne, I certainly havnt allowed for this one comment to change my outlook. The majority i have read have all been very positive, and am now in a potition where i will be scheduling with Dr A, im just trying to find reasonable priced flights before i confirm a date. This chat room has been a very helpful tool to me, just to see the worries others went thought, just the same as i am, before they had surgery. Thanks From: Dianne <diladirn@...> Sent: Thursday, October 30, 2008 11:33:31 PMSubject: Re: help -,I have been a nurse for more then 30 years. i would never lead anyone falsely. As for wearing gloves when drawing blood there is danger only to the person drawing the blood not to you. Yes there were gloves. The nurses used them when removing my IV. As for surgery without gloves-there is no way this would be done because every one who has ever had surgery would have severe infections and or be dead from major infections. My experience is that there are many patients will find fault with the littlest things. Some people start with negative attitudes and look for things to go wrong. As for red bags-I don't care if there were red bags or not. Red bags have nothing to do with good or bad care. My daughter was banded there also . I saw the doctors there more than i have ever seen any doctor at hospitals here. there was no rushing etc. They all came in before I was discharged shook my hand and thanked me for using them. My room was cleaned several times a day but the smell didn't bother me. Some people may be more sensitive to smells. As for blood down the sink-yes it would have been better put into the toilet but oh well so long as it was rinsed good. As for the language barrier -almost everyone I saw spoke enough english to get my needs met. One time in recovery the nurse could not understand me and she went and got someone who did. you are given a list of spanish phrases and if needed you can use it. I never had to. The doctors all spoke very good english and everyone of them and the nurses were all great. I have never gotten such personalized care in my entire life. I had no problem getting pain meds and promptly. My call light was answered immediately. Not to say that this person who wrote negatively did not experience what he wrote-but sometimes our attitudes can make an experience bad. If i had to do it again,I would do it in a heartbeat. Think about the fact that there have been thousands of positives comments compared to this one neg. Don't let one person stop you from starting a new life. Keep researching and keep using this site because it is very helpful. God bless you.Dianne-- In @groups. com, Hulmes <laurenhulmes@ ...> wrote:>> Thanks Dianne,> > I seem to be getting mixed responses, most of them positive but a few negative (although some for sleeves). One of them said that when blood was taken before surgery gloves were not used, they didn't see any toxic waste bins for blood etc. My worst fear would be to go with Mexico and come away with a successful band but also an infection that i cant get rid of.> > My mom has scared me off a bit now, hence why i am trying to feel more confident after speaking to people who have been there and done that> > > > > > ____________ _________ _________ __> From: Dianne <diladirn@.. .>> @groups. com> Sent: Wednesday, October 29, 2008 5:15:29 PM> Subject: [Dr-Aceves-bandster s] Re: help> > > > >> > I have been trying for some time now to find a surgeon for WLS, > costs within the US are so expensive that i think the only step is to > go to Mexico. I have spoken to several surgical companies and think > i feel confident in what i have heard about Dr Aceves, however to > give myself piece of mind i wanted to speak to people who had > experienced this surgery both by Dr Aceves and going to Mexico.> > > > Is Mexcio really that bad? what are the facilities really like? > How do i know that the surgery wont go bad or me get an infection > from the hosptal? Did anyone else have the same concerns?> > > > Please help andput my fears to bed> >> > I was banded by Dr Aceves on Oct 20 and i have nothing but good > things to say about the whole experience. Being a nurse and having > been in many American hospitals-I hate to say that the hospital in > Mexicali put ours to shame. Everyone was so nice. The hospital was > cleaner than any I've ever seen. I would highly recommend the doctor > and hospital . I was well taken care of.> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2008 Report Share Posted October 31, 2008 ---Good for you. Keep a positive attitude and pray. I've been doing a lot of that. You will be fine and you know you have a lot of friends to help you through you. Dianne In , Hulmes <laurenhulmes@...> wrote: > > Thanks Dianne, > > I certainly havnt allowed for this one comment to change my outlook. The majority i have read have all been very positive, and am now in a potition where i will be scheduling with Dr A, im just trying to find reasonable priced flights before i confirm a date. > > This chat room has been a very helpful tool to me, just to see the worries others went thought, just the same as i am, before they had surgery. > > Thanks > > > > > > ________________________________ > From: Dianne <diladirn@...> > > Sent: Thursday, October 30, 2008 11:33:31 PM > Subject: Re: help > > > - > > , > I have been a nurse for more then 30 years. i would never lead anyone > falsely. As for wearing gloves when drawing blood there is danger > only to the person drawing the blood not to you. Yes there were > gloves. The nurses used them when removing my IV. As for surgery > without gloves-there is no way this would be done because every one > who has ever had surgery would have severe infections and or be dead > from major infections. My experience is that there are many patients > will find fault with the littlest things. Some people start with > negative attitudes and look for things to go wrong. As for red bags- I > don't care if there were red bags or not. Red bags have nothing to do > with good or bad care.. My daughter was banded there also . I saw the > doctors there more than i have ever seen any doctor at hospitals > here. there was no rushing etc. They all came in before I was > discharged shook my hand and thanked me for using them. My room was > cleaned several times a day but the smell didn't bother me. Some > people may be more sensitive to smells. As for blood down the sink- > yes it would have been better put into the toilet but oh well so long > as it was rinsed good. As for the language barrier -almost everyone I > saw spoke enough english to get my needs met. One time in recovery > the nurse could not understand me and she went and got someone who > did. you are given a list of spanish phrases and if needed you can > use it. I never had to. The doctors all spoke very good english and > everyone of them and the nurses were all great. I have never gotten > such personalized care in my entire life. I had no problem getting > pain meds and promptly. My call light was answered immediately. Not > to say that this person who wrote negatively did not experience what > he wrote-but sometimes our attitudes can make an experience bad. If > i had to do it again,I would do it in a heartbeat. Think about the > fact that there have been thousands of positives comments compared to > this one neg. Don't let one person stop you from starting a new life. > Keep researching and keep using this site because it is very helpful. > God bless you. > Dianne > > -- In @groups. com, Hulmes > <laurenhulmes@ ...> wrote: > > > > Thanks Dianne, > > > > I seem to be getting mixed responses, most of them positive but a > few negative (although some for sleeves). One of them said that when > blood was taken before surgery gloves were not used, they didn't see > any toxic waste bins for blood etc. My worst fear would be to go > with Mexico and come away with a successful band but also an > infection that i cant get rid of. > > > > My mom has scared me off a bit now, hence why i am trying to feel > more confident after speaking to people who have been there and done > that > > > > > > > > > > > > ____________ _________ _________ __ > > From: Dianne <diladirn@ .> > > @groups. com > > Sent: Wednesday, October 29, 2008 5:15:29 PM > > Subject: [Dr-Aceves-bandster s] Re: help > > > > > > > > > > > > I have been trying for some time now to find a surgeon for WLS, > > costs within the US are so expensive that i think the only step is > to > > go to Mexico. I have spoken to several surgical companies and > think > > i feel confident in what i have heard about Dr Aceves, however to > > give myself piece of mind i wanted to speak to people who had > > experienced this surgery both by Dr Aceves and going to Mexico. > > > > > > Is Mexcio really that bad? what are the facilities really like? > > How do i know that the surgery wont go bad or me get an infection > > from the hosptal? Did anyone else have the same concerns? > > > > > > Please help andput my fears to bed > > > > > > > I was banded by Dr Aceves on Oct 20 and i have nothing but good > > things to say about the whole experience. Being a nurse and having > > been in many American hospitals-I hate to say that the hospital in > > Mexicali put ours to shame. Everyone was so nice. The hospital was > > cleaner than any I've ever seen. I would highly recommend the > doctor > > and hospital . I was well taken care of. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2008 Report Share Posted December 11, 2008 what parasite/fungus do you have that is not in humans? the tincutre is the best way to get black walnut into blood stream and is high in iodine. the alcohol is miniscule and necessary for parasitic treatment. you also need to do a bowel/kidney cleanse first by your reaction to the med. dandelion root tea is effective for both along with something to clean your bowel. hth, thx, linda rn help Excuse me if I have posted this in the past, but I am desperate for help, which I have not been able to get from my doctor. I had several tests done one being a DNA stool test that showed parasites and yeast unknown in humans. My doctor gave me Vermox, which I later found out is full of sugar. Just what someone needs that has yeast. Well it did not help my symptoms. Not sure how to treat something that is not know in humans. I am assuming that I got this from my dog or travel to Mexico. I tried wormwood and it really made everything a lot worse (eyes crusting and oozing with a white liquid and itching, rectal itching, ear itching, chronic constipation, pain behind eyes, increased coated tongue). I can't do 's parasite protocol as the tincture is in alcohol. That would make the yeast worse. I feel like I am caught between a rock and a hard place. I would appreciate anyone that could help me. ThanksDeb Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2008 Report Share Posted December 11, 2008 Diatomaceous earth is where I would start. It's cheap -- http://www.internet-grocer.net/diatome.htm and immediately effective. Don't over do it with this product. 4 pounds should last a year. Http://nowfoods.com make a powded compination of wormwood, black wallnut and cloves that is inexpensive and effective and your right on with the no alcohol it is a myotoxin and should never be injested in any form. Are you familiar with Doug Kaufmanns broadcasts at -- Http://know-the-cause.com ---. awareness-investigation-knowledge-potential-motivation-action-patience-results Duke Dallas - Texas info@... iodine From: deborah.harper@...Date: Thu, 11 Dec 2008 13:22:03 +0000Subject: help Excuse me if I have posted this in the past, but I am desperate for help, which I have not been able to get from my doctor. I had several tests done one being a DNA stool test that showed parasites and yeast unknown in humans. My doctor gave me Vermox, which I later found out is full of sugar. Just what someone needs that has yeast. Well it did not help my symptoms. Not sure how to treat something that is not know in humans. I am assuming that I got this from my dog or travel to Mexico. I tried wormwood and it really made everything a lot worse (eyes crusting and oozing with a white liquid and itching, rectal itching, ear itching, chronic constipation, pain behind eyes, increased coated tongue). I can't do 's parasite protocol as the tincture is in alcohol. That would make the yeast worse. I feel like I am caught between a rock and a hard place. I would appreciate anyone that could help me. ThanksDeb Suspicious message? There’s an alert for that. Get your Hotmail® account now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2008 Report Share Posted December 11, 2008 > > > Diatomaceous earth is where I would start. It's cheap -- http://www.internet-grocer.net/diatome.htm and immediately effective. Don't over do it with this product. 4 pounds should last a year. > > Http://nowfoods.com make a powded compination of wormwood, black wallnut and cloves that is inexpensive and effective and your right on with the no alcohol it is a myotoxin and should never be injested in any form. > Are you familiar with Doug Kaufmanns broadcasts at -- Http://know-the-cause.com ---. > Hope that the above-recommended herbs will help you. Sounds awful what you've got! I wanted to go off topic slightly - Duke Stone wrote, above, that " alcohol is a myotoxin and should never be ingested in any form " . I myself don't drink, except maybe a bit at a wedding, but I was wondering about the claims that red wine (organically grown grapes) is excellent for one's health; also, that people who do not drink alcohol at all, ever, are less healthy than those who do take some. I don't know what to think, now... - Mrs. B. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2008 Report Share Posted December 11, 2008 Deb... Check out http://humaworm.com They have a very thorough wormer. You can also use Hulda 's ia which is just wormwood, clove and green black walnut hulls. Hulda has devoted her entire career in eradicating parasites. She has developed a " zapper " that runs on a simple 9v battery (think smoke detector size battery) that runs a very low current of electricity (you probably won't even feel it) through your skin that kills the parasites. One of her more pricey models has programmable frequencies that you can dial in to attack specific fungi and parasites as well as bacteria. Google hulda clark clarkia and Hulda clark zappers for more info. Lorie > > what parasite/fungus do you have that is not in humans? the tincutre is the best way to get black walnut into blood stream and is high in iodine. the alcohol is miniscule and necessary for parasitic treatment. you also need to do a bowel/kidney cleanse first by your reaction to the med. dandelion root tea is effective for both along with something to clean your bowel. hth, thx, linda rn > help > > > Excuse me if I have posted this in the past, but I am desperate for > help, which I have not been able to get from my doctor. I had > several tests done one being a DNA stool test that showed parasites > and yeast unknown in humans. My doctor gave me Vermox, which I > later found out is full of sugar. Just what someone needs that has > yeast. Well it did not help my symptoms. Not sure how to treat > something that is not know in humans. I am assuming that I got this > from my dog or travel to Mexico. I tried wormwood and it really > made everything a lot worse (eyes crusting and oozing with a white > liquid and itching, rectal itching, ear itching, chronic > constipation, pain behind eyes, increased coated tongue). I can't > do 's parasite protocol as the tincture is in alcohol. That > would make the yeast worse. I feel like I am caught between a rock > and a hard place. I would appreciate anyone that could help me. > Thanks > Deb > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 11, 2008 Report Share Posted December 11, 2008 Deb.. For the clarkia... if you put your drops in warm water, and let it sit for a little bit -- few minutes, the alcohol will evaporate. Go to Dr. ia's site and see if there is a contact email that you can ask about the alcohol. The humaworm, btw is in capsules -- no alcohol, so that might be your best bet.... Lorie > > > > what parasite/fungus do you have that is not in humans? the > tincutre is the best way to get black walnut into blood stream and is > high in iodine. the alcohol is miniscule and necessary for parasitic > treatment. you also need to do a bowel/kidney cleanse first by your > reaction to the med. dandelion root tea is effective for both along > with something to clean your bowel. hth, thx, linda rn > > help > > > > > > Excuse me if I have posted this in the past, but I am desperate for > > help, which I have not been able to get from my doctor. I had > > several tests done one being a DNA stool test that showed parasites > > and yeast unknown in humans. My doctor gave me Vermox, which I > > later found out is full of sugar. Just what someone needs that has > > yeast. Well it did not help my symptoms. Not sure how to treat > > something that is not know in humans. I am assuming that I got this > > from my dog or travel to Mexico. I tried wormwood and it really > > made everything a lot worse (eyes crusting and oozing with a white > > liquid and itching, rectal itching, ear itching, chronic > > constipation, pain behind eyes, increased coated tongue). I can't > > do 's parasite protocol as the tincture is in alcohol. That > > would make the yeast worse. I feel like I am caught between a rock > > and a hard place. I would appreciate anyone that could help me. > > Thanks > > Deb > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 I'm sorry for what you are going through and hope you can get on top of it. I've read Extra Virgin Coconut Oil is good for parasites. It won't have any alcohol or sugar (I don't think it would anyway). It might be a milder treatment than what you wanted but it would also support your body in many ways. http://www.coconut-connections.com/parasites.htm http://www.shokos.com/extra_virgin_coconut_oil_myths_and_facts.html http://www.coconut-oil-central.com/coconut-oil-parasites.html Tara Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 12, 2008 Report Share Posted December 12, 2008 I have been taking coconut oil for 3 years. I no longer have Rheumatoid Arthritis, my gums healed up instead of seeing periodontist saved like $800 on that, haven't had a cold, flu or pink eye in 3 years. When my adult son and I got food poisoning- mine lasted half day and his lasted 6 days and I ate 3 times as much of the suspicious item at the restaurant. I now seem to be able to maintain my immune system with just adding coconut milk to my coffee in the morning and cooking with coconut milk or oil when the opportunity appears. It really seems to help get the health back. Pam On Fri, Dec 12, 2008 at 12:04 PM, Grant and Tara <grant.tara@...> wrote: > I'm sorry for what you are going through and hope you can get on top of > it. I've read Extra Virgin Coconut Oil is good for parasites. It won't > have any alcohol or sugar (I don't think it would anyway). It might be a > milder treatment than what you wanted but it would also support your > body in many ways. > > http://www.coconut-connections.com/parasites.htm > http://www.shokos.com/extra_virgin_coconut_oil_myths_and_facts.html > http://www.coconut-oil-central.com/coconut-oil-parasites.html > > Tara > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2009 Report Share Posted January 7, 2009 When I was doing it, I continued the shots on my menses. I was hungrier and I did not lose weight as quickly. I really needed my protein shake at that time ( I used Ultra Lean by BioGenesis, I also added a TBS of MCT oil) and I really needed steak, chicken did not seem like enough. Also, needed more water. I was told only to eat fruit with meals and if not losing as quickly to cut fruit(including tomatoes) from dinner and if still not losing to cut fruit out lunch, too. Also, did you count your loading days in your 9 days? I gained 3 pounds on my loading days, but it averaged out afterwards. > From: jamie_fstt <jamie_fstt@...> > Subject: Help > > Date: Tuesday, October 28, 2008, 3:48 PM > So I'm new to the HCG.. I'm on day 9.. I've only > lost 6 lbs... I'm > starting to feel discouraged. I've been very very > strict on the diet > and have not cheated. My question is.. I started mensus > today. I'm > doing this on my own and the pounds and inches book says > that I should > not give myself shots at all during this time.. but > I've heard > elsewhere that its just supposed to be no shot for the > first three > days.. Anyone have an opinion on this? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2009 Report Share Posted February 13, 2009 Dave, Welcome to the group. I sent you out an invitation to our chat group and science group but I have had notification of non delivery because "this account has been disabled or discontinued". Could you please check that you have given us a working email address. Lilian Moderator Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2009 Report Share Posted February 13, 2009 Hi Lilian, Thank toy for getting back to me so soon - try dcrump@... - this is my usual e-mail addy. Not sure why the ayhoo addy is not working, but it is the first time I have used this addy, and joined a group. Dave > > Dave, > > Welcome to the group. > > I sent you out an invitation to our chat group and science group but I have had notification of non delivery because " this account has been disabled or discontinued " . > > Could you please check that you have given us a working email address. > > Lilian > Moderator > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2009 Report Share Posted February 13, 2009 Hi Dave and welcome to our forum where I hope you get the support you need. Yes, some people do OK on levothyroxine but there is a large minority who do not. This is because thyroxine (T4) is only one hormone, and this hormone is mainly inactive anyway and must convert to the active hormone triiodothyronine (T3) in the liver, kidneys and other thyroid receptor sites. T3 is needed by every cell in your body and brain to make it function. Can you get hold of your last thyroid function tests and post the results here together with the reference range for each of the tests. Many doctors don't really know how to interpret them and laboratories just write " normal " against the result if the are within the reference range - and this leads to confusion. You might be very low in the range, slap bang in the middle of the range or at the top of the range. TSH are Thyroid Stimulating Hormone (TSH), Free thyroxine (FT4), Free Triiodothyronine (FT3) and have you ever been tested to see if you have antibodies to your thyroid. If this tested positive, it means the antibodies see your thyroid tissue as public enemy number one and set about its gradual destruction over time, so eventually, your thyroid will not be able to put out the thyroid hormones your body needs. If your doctor cannot get your Free T3 tested through your local laboratory, then ask if he will write on a separate blood form (without anything else) " Free T3 - ? Hyperthyroidism), and that way, they should test it. They refuse to test it if it is requested as a full TFT, because laboratories are trying to save money and believe that if your TSH and FT4 are within range, there is no need to check FT3. Ask your GP for some further blood tests. The following are needed to see whether any of them are low. Ferritin (stored iron), B12, Vitamin D, Magnesium, Copper and Zinc. If any of these are low, they will stop your thyroid hormones from being absorbed, as will low adrenal fatigue and Candida. The last two you can get tested privately through Genova Diagnostics www.gdx.uk.net .. The first is a 24 hour salivary test that will tell you where your cortisol and DHEA lie at four specific times during the day. Many sufferers of hypothyroidism suffer with this, and it MUST be treated with adrenal glandulars (or even HC) so your thyroid hormone replacement will work, and once treated, you will feel so much better. Another problem NHS doctors don't know exists. They only know about the two extremes, 's disease and Cushing's syndrome. If you are not converting, you may need the addition of synthetic Liothyronine (T3) or you might need the natural thyroid extract (Armour Thyroid,USP). Go to our web site and learn about the conditions that can stop your thyroid hormone replacement from working. Click on 'Hypothyroidism' in the Menu and in the drop down Menu, click on ' Associated Conditions' and on the window that opens, click on each of the conditions shown and read all about them. This will help you understand what is happening (or not) to you. Any questions, just ask and somebody will hopefully come along to try to answer them. Read all the information in the FILES on this forum website and also have a look at the many LINKS to good information too. Luv - Sheila I am so glad I found this website and forum as I feel that alot of my original symptoms are now re-occuring, and I just feel so ill, tired and now depressed, all the time. Please help as I feel I'm going mad. Everyone seems to think that because I now take Levothyroxine, all should be OK now, but it is not - far from it ! _,_._,___ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2009 Report Share Posted February 14, 2009 Hi Dave, For a man 125 mcg thyroxine ( T4) isn't a big dose- dosage is affected by weight. What were you last blood tests Can you please show then with ranges- I bet T3 wasn't done which is a pity as it is the active hormone that the body should convert from T4, but after a while of T4 only meds the conversion mechanism fails and symptoms recur. Docs are often happy with any TSH in range whereas over 90% of health folk have a TSh of around 1.0 -which any good doc should aim for. T3 is the thyroid fraction that has the strongest bearing on mood- I remember clearly the 5th day after starting T3 containing meds- it was like the sun coming out after years of winter- magic stuff! Subject: Help I have been diagnised as Hypothyroid for the past few years. I am currently on 125mg Levethyroxine a day.. I am currently off work, again, due to work related stress, IBS and, now, depression. My GP has been giving me anti-depressants to,initially, counteract the IBS symptoms. Dave ------------------------------------ TPA is not medically qualified. Consult with a qualified medical practitioner before changing medication. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2009 Report Share Posted February 14, 2009 Hello (do you have a name) - welcome to the forum and I hope you get the support you need. Many of us have been in almost exactly the same spot you have found yourself in and desperately seeking somebody who knows what they are doing. Sadly, the NHS produce few good doctors with a specialty in thyroid disease - and we are usually under the care of an endocrinologist who's specialty is diabetes - which really doesn't help us at all. Doesn't your GP realise that heart problems "flutters/palps" can be caused through untreated hypothyroidism, and from your numbers (and especially your symptoms) you do seem to be suffering with this. You could also be suffering with hypoadrenalism - but we will come to that later. You need to write to your GP and tell him you would like a referral to an endocrinologist. there is one in Glasgow who has been highly recommended to me and I am sending the name of this doctor to you privately. In the letter to your GP, list all of your symptoms and any 'signs' Check these against the list in our web site www.tpa-uk.org.uk . List also your basal temperature for 4/5 days. You take this before you get out of bed in a morning and before you have anything to eat or drink. Normal temperature is 98.6. If your's is 97.8 (and it could be much less), this is indicative that your metabolism is running too slow i.e. hypothyroidism. Ask in the letter for a full thyroid function test which should include TSH, Free T3 and Free T4. Ask also for him to test your ferritin level (stored iron) B12, Vitamin D, Magnesium, zinc and copper.If any of these are low your normal thyroid hormone will not be getting properly absorbed. Ask for your letter to be placed in your medical notes and send a copy to your Head of Practice. Ask specifically to be referred to the doctor I am sending you and tell him/her you do not wish to see anybody else. (I have heard the endocrinology specialty in that area is not particularly good, and follow the NHS mainstream protocol to the letter). Luv - Sheila > Last blood test taken came back with result of 5.5, but overall > thyroid antibody was 150 , and the normal level 50. I am awaiting a > result of other blood test...Dr Chan has now reneged on meds saying > now wants to see consistent rising. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2009 Report Share Posted February 14, 2009 Hi, Welcome to the forum. I'm really sorry to hear about how bad you are feeling. I have found there are lots of supportive people here so you have come to the right place. None of us are medically trained though, so it might be best to check all of the info you receive on the forum with your health professional. I'm assuming the test that was done that was 6 to start with, then 3. something, then around 10 and now at 5.5 was a TSH test. Could you please let me know if that is correct? If it was a TSH test, I had levels similar to yours and the doctor didn't do anything for me. I was very unwell, like you. I decided to find help through another doctor. The 'new' doctor tested me again, found my levels were rising higher (at one point to nearly 10) and started thyroid hormone replacement. Did your doctor do any blood tests to determine your Free T4 levels and your Free T3 levels? Here is some info about the tests I just mentioned. The free T3 test says that it is used to determine whether you have hyperthyroidism, however my doctor tested my levels and found they were below the normal reference range with my hypothyroidism. I've also provided a link to info about the free T4 test. The labtests online website is reputable and I refer to it alot. http://www.labtestsonline.org/understanding/analytes/t4/sample.html http://www.labtestsonline.org/understanding/analytes/t3/sample.html Just out of curiosity, when did you have your tests done? I always have my tests done as early as possible in the morning prior to taking my thyroid medication. I used to remember why it is important to have the tests early in the morning, but the reasons have fallen out of my brain and onto the floor at the moment, ie - I can't remember!!!! Re your heart palpitations. My doctor started me on a really low dose of thyroid replacement hormone (thyroxine in my case) because I was having palpitations from using it. He said that he had to start me on an 'old folks' dose, even though I was only just over 40 years old. He also said that I had to do something about my thyroid levels because I was so unwell. Perhaps this is something for your doctor to consider. Like you, I sometimes feel as though I am about 80, but thankfully I don't feel like that very often these days. You also mentioned that your doc tested for thyroid auto antibodies. What was the name of the test? Was it called Anti- microsomal antibody or Thyroid peroxidase antibody? This is usually used to help detect the presence of a thyroid autoimmune disease. You sound like you have many classic symptoms of hypothyroidism. I really think that it might be worthwhile seeing a different doctor for another opinion because I don't think you should have to suffer the way you are suffering at the moment. I didn't get any help until I sought the help of another doctor. Sheila (the person who looks after this forum) knows of a number of doctors, so perhaps she can suggest some to you. If you like, you could send her a private email to ask her about this. Sheila is really helpful. If you ever want any support, or want to ask a question (no matter how trivial you may think it is) please go ahead and post a message. Sometimes the messages get lost in the mountains of messages that come through the forum, so just give us all a reminder and re-post it again. Thought I'd mention that because the forum is getting more and more messages on it these days. Quite a number of us on the forum use supplements (such as zinc, b group vitamins, Vit D, selenium, iron, magnesium, etc) so if you are interested in this stuff, please ask. There are a number of blood tests that can be done to look for deficiencies in some of those things. Oh, and please check the files (see the LHS of your screen) because they contain lots of info about thyroid related illness. Bye for now. P xo Hi am new as of today and would welcome any advice as I am feeling very low indeed.......Dr.....has now reneged on meds saying now wants to see consistent rising.....I am so fed up , probably have low grade depression, have had endometriosis treatment, got IBS,Raynauds, dry skin,/hair, losing eyebrows, lashes, general cognitive impairment, feeling cold, night sweats,constant dry throat, choking fits, hoarse voice, lack of energy, inability to lose weight ( not gained much but working out regulary) the hole nine yards ( all symptoms have for over year if not longer) and had problems after my daughter was born in 2001 but seemed to regulate...it's how long I have to put up with this before they will bloody do anything to make me feel on the planet..... does anyone think should push to see one on NHS or go private..? ... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2009 Report Share Posted February 14, 2009 MODERATED TO DELETE MOST OF PREVIOUS MESSAGE. PLEASE DELETE THIS BEFORE SENDING TO THE FORUM. THANKS, SHEILA _________________________________________________________ Hi my name is Jill, sorry brain fog prevailing again..!! thank you so much for your considerate and informative reply. I normally find my GP quite sympathetic and diagnostically good, but when comes to this just treading water. I have managed to gain the help of a husband of friend who is a consultant Orthopeadic surgeon, who is willing to speak to the endo up at Inverclyde Royal, if don't gain any satisfcation from that route will definitley ask for referral to the one in Glasgow you are kindly providing. Further to symptoms and health issue have had ,both the anaesthetist that administered my epidural during may daughter's birth which was not good ( had high blood pressure ) and the chap that carried out my colon/endoscopy said had marked Raynaud's and I passed this onto my GP's at the time, one in Edinburgh, and the other to Dr Chan. I have not had a test carried out though. ( is it fingernail.??) Also when going through endometriosis treatment/consultations, last test showed low oestrogen. I just hate the feeling of lack of energy, don't know where to channel energy when I do have it , and the mental slowing which is ridiculous to the point, I have forgotten what was discussed a minute ago and repeat the question asked, and ineloquence, and lack of articulation, and by that I mean I completely forget people's names and proverbs, adverbs, nouns, adjectives, and don't know how to place them into the context of the subject I'm talking about, which maybe can be bypassed unless I've forgotten the thread of the conversation already!! If I'm really tired, I get words muddled up and replace letters at beginning of words. It's gotten to the point I avoid all spoken conversation with some people if having an off day, must think I'm a weirdo. At least my husband and I can laugh about it, he says it's like living with a pensioner of 85 with dementia...To be honest what I find hard to deal is the slow stripping of femininity, the hoarse voice, losing some of my eyebrows, and lashes and thinning of my hair in certain places, and my nails, hair and skin being really dry and brittle, and slow hair growth. I just want to feel me again.. Don't feel particularly confident due my appearance and brain fog.. Ask also for him to test your ferritin level (stored iron) B12, > Vitamin D, Magnesium, zinc and copper.If any of these are low your > normal thyroid hormone will not be getting properly absorbed. Ask for > your letter to be placed in your medical notes and send a copy to your > Head of Practice. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2009 Report Share Posted February 14, 2009 MODERATED TO REMOVE MESSAGES ALREADY READ. PLEASE DELETE THESE BEFORE CLICKING 'SEND'. THANKS. SHEILA _______________________________________________________ Hi I'm Jill ..thanks for listening have all tests done on TSH basis I think which is the norm, last one was full thyroid screening but not sure what antibody test was carried out. i am not sure has done the free T3 and free T4..Always have bloods done in the morning as soon as can and as patient schedule of duty priactice nurse will allow after dropping kids off at school. Not on any meds at all when TSH reached over 10 Dr was going to then I opened my big mouth and said was having some palps..Was then referred to cardio for ECG , was 2 minutes long and didn't show anything, quelle surpise..!! Then referred for heart monitoring for 24 hrs using strap on monitor..waiting on results of that currently ,didn't feel any when had it on, just like the thing. The palps have been less frequent and intense than previous, but I know that may change . Dr that was going to put me on meds has now decided against it saying he now wants to see a constant rise before doing so..??!! Wanted to do him bodily harm when I was told that, he is a nice person generally, but was so angry that previous medical history and presentation of classic symptoms, that I have dealt/ am dealing with, overlooked or not noted at all..ggggrrrrr > Re your heart palpitations. My doctor started me on a really low > dose of thyroid replacement hormone (thyroxine in my case) because I > was having palpitations from using it. He said that he had to start > me on an 'old folks' dose, even though I was only just over 40 years > old. He also said that I had to do something about my thyroid > levels because I was so unwell. Perhaps this is something for your > doctor to consider. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.