Guest guest Posted October 6, 2003 Report Share Posted October 6, 2003 Hi, Coyote, I am so glad you have a CPAP machine! One of my best friends has been on one for years. It really made a difference in his life, too. He was kind of upset about having the machine at first. He is a single man and was worried about how unattractive the machine would be to a girlfriend. He thought it was kind of like sleeping with Darth Vader! I told him that was a whole lot more attractive that waking up next to a dead person! Hugs, Piper Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2003 Report Share Posted October 6, 2003 Hi, Coyote, I am so glad you have a CPAP machine! One of my best friends has been on one for years. It really made a difference in his life, too. He was kind of upset about having the machine at first. He is a single man and was worried about how unattractive the machine would be to a girlfriend. He thought it was kind of like sleeping with Darth Vader! I told him that was a whole lot more attractive that waking up next to a dead person! Hugs, Piper Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2003 Report Share Posted October 6, 2003 Hi, SEPJ, I thimk lol means " laugh out loud " It has taken me a while to get the " lingo " down! Hope you are having a good day! Hugs, Piper Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2003 Report Share Posted October 6, 2003 Hi, SEPJ, I thimk lol means " laugh out loud " It has taken me a while to get the " lingo " down! Hope you are having a good day! Hugs, Piper Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2003 Report Share Posted October 10, 2003 Hi Deb, My Dad was just dx'ed a week or so ago by Dr. as well. I'm very sorry to here about your troubles, I bet we're probably going through some of the same emotions right now. I feel pretty comfortable with DR. so far, I'd be interested in your opinion. I just found this group this week myself, these folks seem very nice and the support level here seems great. Welcome to the group Deb, I sure hope you post again. If there is anything I can help with, please do not hesitate to ask. Regards, > Hello, > My dad was diagnosed with PD two years ago. The end of July he started seeing > people. Ended up in the hospital for seven days and things have not been the > same since. Doctors thought it was the meds. Sent him home. Then in September > he became so aggitated mom had to call the paramedics per the doctor. He ended > up in the hospital again for five days. Two weeks again he was diagnosed > Dementia with Lewy Body. Mom is home on family leave, but that runs out shortly. > We have to get her back to work, she is only 63 and needs her insurance. > The hardest part right now is the fact that dad rarely recognizes my mom. He > thinks that she is taking care of him and asks where mom is all the time. > First he thought there was one caregiver and now he sees three. All are actually > mom. She took him out to the store the other day, went for a walk at the park > and then to lunch. They went home, he did a few things around the house and > walked back into the room and asked mom when she got home from work. He then told > mom all about his day with the other lady while she was at work. He had been > with mom all day. Dad seems to know eveyone else, but has the hardest time > with mom. Has anyone else had this problem? He can be looking at a recent photo > of the two of them and still not recognize my mom holding the photo. > This is my first post and probably not my last. > Hi to . We just saw Dr. for the first time last week. Like you we > have so many questions? > Deb > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 14, 2003 Report Share Posted October 14, 2003 Deb, the short answer is yes, LBD can be rapid at times. It has stages and within those stages are cycles; your LO may appear to be doing great and then without warning and when you least expect it they seem to go into a downward spiral only to come back again. There may be time(as there have been for some of us) when you think the end is near only for them to rally again and all the while your emotions are being taken on a rollercoater ride. Try to hang in there and come to us at any time for whatever reason, we're always here for you. .x (no subject) I'm dealing with the same thing. My dad was diagnosed with PD about two years ago, and was actually doing very well. Two and a half months ago he started hallucinating, went into the hospital for a week and has never been the same. Mom's been home on family leave and has to go back to work. We have found someone to stay with him during the day. He can not stay home alone. Does not know who my mom is. I can go on and on. We seem to loose a little more of him each day. Does LBD usually happen so quickly? Thank you for all wonderful welcomes. Deb Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 14, 2003 Report Share Posted October 14, 2003 Deb, the short answer is yes, LBD can be rapid at times. It has stages and within those stages are cycles; your LO may appear to be doing great and then without warning and when you least expect it they seem to go into a downward spiral only to come back again. There may be time(as there have been for some of us) when you think the end is near only for them to rally again and all the while your emotions are being taken on a rollercoater ride. Try to hang in there and come to us at any time for whatever reason, we're always here for you. .x (no subject) I'm dealing with the same thing. My dad was diagnosed with PD about two years ago, and was actually doing very well. Two and a half months ago he started hallucinating, went into the hospital for a week and has never been the same. Mom's been home on family leave and has to go back to work. We have found someone to stay with him during the day. He can not stay home alone. Does not know who my mom is. I can go on and on. We seem to loose a little more of him each day. Does LBD usually happen so quickly? Thank you for all wonderful welcomes. Deb Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 7, 2003 Report Share Posted November 7, 2003 Both. Hard to say. Someone in the earlier stages the body would probably have more chance of making use of the added nutrition. The researchers originally got excited when aids patients where sending back letters saying their symptoms had gone. Research was then done in a pathology labs at a hospital and the results where so astounding that they could predict who would get results and who wouldnt. As far as I understand those with more advanced Aids it didnt help so much, whereas those in the early stages had better results. However, there have been people hours away from death ( one case of toxic shock syndrome for instance) who have had their lives saved after adding glyconutrients into their feeding tube. So who knows. If we were to trial it with a person in an advanced stage I would suggest it would need to be a large dosage and that would be a bigger cost, but we could work on that. And you would probably at least be able to see quicker if there is some change or not. Ilse Begin forwarded message: > > Date: Sat Nov 8, 2003 6:11:49 AM Australia/Melbourne > To: <LBDcaregivers > > Subject: Re: (no subject) > Reply-To: LBDcaregivers > > Ilse, I think it would be great if someone here could try the gluco's > without worrying about cost. My next question would be should the > LO's be > in the mild stage or should we try this on someone who is more > advanced in > the disease? > Courage > > (no subject) >>> Reply-To: LBDcaregivers >>> >>> IIse, >>> My reason would be the cost, I know we should not let that be a >>> factor, but >>> one must have money. I realize that precription drugs cost money, but >>> now there >>> is help from many of the drug companies that will issue a precription >>> card >>> for certain meds for a flat rate of 15 dollars or less per med. I >>> have >>> researched some of the natural stuff and it runs much more. It would >>> be great if we >>> could get help for preventive medicine but it doesn't work that way >>> here. >>> I do believe there are other choices but the cost is always a big >>> factor and >>> medicare doesn't help with precription drugs and certainly not >>> natural >>> stuff. >>> I read all your post and visit the web sites you sent, but when one >>> is >>> on >>> medicare with limited income it would make a difference in what they >>> choose as >>> their avenue of health care. >>> Please continue to give us the information, who knows, maybe a ship >>> will sail >>> into our port and then we could try your way. >>> >>> Thanks, >>> Jayn in S GA >>> >>> >>> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 2, 2008 Report Share Posted April 2, 2008 I agree- you need to get to a specialist who can develop a maintenance program for you. I am new to this group but am finding it to be a comforting and fantastic source of information. Currently I am under the care of an allergist who is also an asthmatic himself. We have tried 4 different daily steroid inhalers over the past year and now have one that I am using with some success. I was diagnosed 13 years ago but it was under control and only required the occasional use of an Albuterol inhaler 4 or 5 times a year. Last July this all changed. I started on Singulair then as well and have been one of those to experience the side effect of extremem depression. The lesson I am learning is that doctors are well trained and knoweldgeable but you know your body and mind best. Adhere to their advice but let them know when you think something is wrong. I am now off Singulair and feeling some better already. Hudifiers make me worse in the summer and only help me in the winter. Read as much information on asthma as you can and be as well informed as is possible. This group is a great place to start!! > > I have allergies and was diagnosed with asthma less than one year ago. > Over the past couple of weeks my allergies have become less managable > as the weather changes and, as a result, I have been having trouble > with my asthma. I am waking up in the night either coughing a very > dry cough that only gets better when I use my Albuterol inhaler or I > wake up feeling like I am gasping for air. I am also having trouble > during the day feeling short of breath and a lot of wheezing. Today I > called my doctor's office and was told by the doctor to use my rescue > inhaler at scheduled times twice a day and to come in for an > appointment next Monday. Does this sound right? I am so new to all > of this and want to feel better so badly I will try anything. > Thanks everyone. > a > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2008 Report Share Posted May 24, 2008 Hi Kathy, I understand all too well what you, your sister and your family is going through.? We went through it with my daughter, Alyssa.? I hate to say it but your lives will never be the same...not that they are going to be bad by any means, just different.? Adjusting to having a child with special needs is hard, we have come a long way in my daughter four and a half years but we have a long way to continue to go too.? Take things one step at a time, one hour or one day at a time.? Make lists, document what the doctors and nurses are saying?and your thoughts about how the babies are doing, what problems they are having and what progress they are making.? You will be surprised how it will all that will come in handy for many years to come. Yes, ask for a second opinion and maybe even a third.? Ask and ask until you find a doctor that you feel right with, one that has hope for the children.? There is a doctor in Chicago, Dr. Dobyns, who specializes in migrational abnormalities, which is polymicrogyria and lissencephaly.? Many MRIs are read wrong, due to the inexperience of the radiologists and neurologist that read the films.? Dobyns reads MRIs like this daily and can tell slight variations that make a big difference!? Those slight variations cannot be seen by your regular radiologists and neurologist because they just dont see enough MRIs from children with these brain abnormalities.? Get in touch with the pediatric geneticist at the hospital the babies are in and that office can get in touch with Dr. Dobyns.? I will give you his contact information too though, for you to follow up yourself if you like.? Be aware, that he is very busy, so it may take some time for the films to be read.? We had a good turn around time, I believe it was due to going through our local geneticist for the referral.? You can send the films into Dobyns yourself too, I have heard that you get a quicker response by giving a donation to his research. There are lots of horror stories out there but you cannot let them affect you, too much that is.? Yes they are sad, and yes we pray the they dont happen to our loved one or anyone else for that matter, but you have to keep moving forward, thinking positive and doing whatever it is that you can for those babies that need you and your family to rally around them.? There is hope!? Remember that and please share it with your sister.? Remember that the doctors will tell you the worse case scenerio and its up to you to fight for more for?the children.? My daughter was almost totally non responsive when we brought her home from the hospital after her first seizures.? The ones?that took her almost completely away from us.? She was a blob of baby, literally, she didnt move or babble, just breathed.? She is doing well now, over four years later.? She does have major issues though, she doesnt walk, only says a few words and is developmentally delayed.? She has spastic quad CP, all four limbs are involved and she has a weak trunk, so its hard for her to hold herself up.? She has seizures and they are pretty well controlled by medication.? Its amazing that the doctors wrote her off at first.? If I would have listened to them I dont know what she would be like now, certainly not as well as she is.? She is a fighter and has been in therapy and Early Intervention since she was five months old.? Of course I wish she could do more but she is doing more than I have let myself dream she would be doing, since before we knew of her issues.? And she is a determined girl so I know that she will continue fighting and I will continue to, taking her to all of her therapies and school, etc. It will take some time, a week or two for the babies bodies to get acclimates to the medications, the phenobarb.? So they may be groggy for a time but let the medication work its course and see how they are in two or so weeks before you decide if?they are tolerating the medication well and not being to sleepy.? You dont want to have them be sleepy/groggy all the time, so that is important too.? Its a lot of give and take and waiting.? Tons of waiting... Have you guys been told about Early Intervention through your local school district?? Get in touch with them and get the babies into therapy.? At this young of an age the therapists will come to your house to treat the babies.? Also think about outpatient physical, occupational and eventually speech therapy, along with feeding therapy.? It is never to early to get them started, it gives them a better chance to get them started asap!? And you need a Physiatrist (Physical Medicine and Rehabilition Doctor) to evaluate, treat and follow the babies progress.? That doctor will follow the therapy progress, the babies development and per scribe any medications for spasticity, if needed, like Baclofen and/or Botox injections.? Also you should find your closest Neurodevelopmental Pediatrician, not a regular pediatrician, but you need one of those too that has experience with special needs children.? Another therapy to look up is Conductive Education.? We are involved in a full time school called the Conductive Learning Center that has made all of the difference with my daughter.? They start kids as young as possible, so it would be somethign you could look into now. Where are you and your family located?? My daughter and I live in Grand Rapids, MI. Take care, and Alyssa Office Postal Address B. Dobyns, MD University of Chicago Department of Human Genetics 5841 S. land Avenue Room L151, MC 0077 Chicago, IL 60637 Email wbd@... Office Phone Office Fax ? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2008 Report Share Posted June 19, 2008 shelley, I was reading yoru letter to kathy and felt we could relate to eachother as our girls are almost the same age! ( will be 5 on june 27th) I was interested in the school and docs you mentioned, could you give me more detailed info. I have never heard of any of them. I was curious what therapies and meds your daughter is taking too. was diagnosed at 5 months and came home from ther hospital (after developing almost totally normal till that point) liek a lump on a log too. She now has a g-tube but we only use it for meds and when she is sick and she eats/drinks from a sippy cup periasure. She just started accepting bits of food about 2 months ago, she learned to sit up last year and is no longer floppy (we attribute this mainly to a suppliment we give her called Reliv) she scoots around on her back to get around and does not talk but is very verbal. She was seizure free for the first time in oct-march but stated having them again after being very ill. She had infantile spasms but now is having drop and tonic seizures. She is taking Vigabitrin/Sabril and ativan. I live in Sacramento, Ca and several of us special needs mom's get together monthly to hang out. We feel normal in oneanothers company, but all but 2 have boys and I have never met anyone else that has a child like our . SO just wanted to say hi adn I would be interested in staying in touch (= ~carrie > > Hi Kathy, > I understand all too well what you, your sister and your family is going through.? We went through it with my daughter, Alyssa.? I hate to say it but your lives will never be the same...not that they are going to be bad by any means, just different.? Adjusting to having a child with special needs is hard, we have come a long way in my daughter four and a half years but we have a long way to continue to go too.? Take things one step at a time, one hour or one day at a time.? Make lists, document what the doctors and nurses are saying?and your thoughts about how the babies are doing, what problems they are having and what progress they are making.? You will be surprised how it will all that will come in handy for many years to come. > > Yes, ask for a second opinion and maybe even a third.? Ask and ask until you find a doctor that you feel right with, one that has hope for the children.? There is a doctor in Chicago, Dr. Dobyns, who specializes in migrational abnormalities, which is polymicrogyria and lissencephaly.? Many MRIs are read wrong, due to the inexperience of the radiologists and neurologist that read the films.? Dobyns reads MRIs like this daily and can tell slight variations that make a big difference!? Those slight variations cannot be seen by your regular radiologists and neurologist because they just dont see enough MRIs from children with these brain abnormalities.? Get in touch with the pediatric geneticist at the hospital the babies are in and that office can get in touch with Dr. Dobyns.? I will give you his contact information too though, for you to follow up yourself if you like.? Be aware, that he is very busy, so it may take some time for the films to be read.? We had a good turn around time, I believe it was due to going through our local geneticist for the referral.? You can send the films into Dobyns yourself too, I have heard that you get a quicker response by giving a donation to his research. > > There are lots of horror stories out there but you cannot let them affect you, too much that is.? Yes they are sad, and yes we pray the they dont happen to our loved one or anyone else for that matter, but you have to keep moving forward, thinking positive and doing whatever it is that you can for those babies that need you and your family to rally around them.? There is hope!? Remember that and please share it with your sister.? Remember that the doctors will tell you the worse case scenerio and its up to you to fight for more for?the children.? My daughter was almost totally non responsive when we brought her home from the hospital after her first seizures.? The ones?that took her almost completely away from us.? She was a blob of baby, literally, she didnt move or babble, just breathed.? She is doing well now, over four years later.? She does have major issues though, she doesnt walk, only says a few words and is developmentally delayed.? She has spastic quad CP, all four limbs are involved and she has a weak trunk, so its hard for her to hold herself up.? She has seizures and they are pretty well controlled by medication.? Its amazing that the doctors wrote her off at first.? If I would have listened to them I dont know what she would be like now, certainly not as well as she is.? She is a fighter and has been in therapy and Early Intervention since she was five months old.? Of course I wish she could do more but she is doing more than I have let myself dream she would be doing, since before we knew of her issues.? And she is a determined girl so I know that she will continue fighting and I will continue to, taking her to all of her therapies and school, etc. > > It will take some time, a week or two for the babies bodies to get acclimates to the medications, the phenobarb.? So they may be groggy for a time but let the medication work its course and see how they are in two or so weeks before you decide if?they are tolerating the medication well and not being to sleepy.? You dont want to have them be sleepy/groggy all the time, so that is important too.? Its a lot of give and take and waiting.? Tons of waiting... > > Have you guys been told about Early Intervention through your local school district?? Get in touch with them and get the babies into therapy.? At this young of an age the therapists will come to your house to treat the babies.? Also think about outpatient physical, occupational and eventually speech therapy, along with feeding therapy.? It is never to early to get them started, it gives them a better chance to get them started asap!? And you need a Physiatrist (Physical Medicine and Rehabilition Doctor) to evaluate, treat and follow the babies progress.? That doctor will follow the therapy progress, the babies development and per scribe any medications for spasticity, if needed, like Baclofen and/or Botox injections.? > > Also you should find your closest Neurodevelopmental Pediatrician, not a regular pediatrician, but you need one of those too that has experience with special needs children.? Another therapy to look up is Conductive Education.? We are involved in a full time school called the Conductive Learning Center that has made all of the difference with my daughter.? They start kids as young as possible, so it would be somethign you could look into now. > > Where are you and your family located?? My daughter and I live in Grand Rapids, MI. > > Take care, > and Alyssa > > > > Office Postal Address > > B. Dobyns, MD > University of Chicago > Department of Human Genetics > 5841 S. land Avenue > Room L151, MC 0077 > Chicago, IL 60637 > > > Email > > wbd@... > > Office Phone > > > > Office Fax > > > > ? > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2008 Report Share Posted June 19, 2008 -- You mention a supplement that has affected your 's tone-- Reliv? Would you tell me more? Thanks, ;o) mom to 5 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 27, 2009 Report Share Posted January 27, 2009 Hi, Carol: I've been using the same silver wire for years and I've made well over 100 quarts using the original wire. My hot tub holds about 4000 lbs of water. I purify it using 10 quarts. That's just a " guesstimate, " but it's worked. It will depend on the size of your hot tub. I thoroughly cleaned a saline solution spray bottle rinsing it many times and again cleaning it with CSW. Then I filled it with double strength (6 hours of preparing the CSW instead of the normal three hours) CSW to use it to spray directly into my nose. I tilt my head way back over the edge of my bed and let it drain deeply into the sinus cavities. It may burn a little as it kills the infection but that passes. I think you'll be surprised on how well it works and in a short time your sinus cavities will be clean again and you'll be able to breathe much easier. It should also work on your fungus infection. Hulda R. (drclark.com or drclark.net - one is the info web site, the other her store) has a great liver flush. Oberdorf at NSW Publishing in Brooklyn also has a great liver flush that I've used three or four times. His flush uses a concentrate of phosphorus, choline and inositol. It's called Super Phos 30. You can reach him at . Just follow the instructions that come with the solution. Which are: 90 drops of Super Phos in each of three unsweetened quarts of apple juice, or orange juice or apple cider (the pectin in the apple drinks helps to cleanse the liver, too). You drink one quart over the course of a day for three days straight. On the evening of the third day, you mix one cup of extra virgin olive oil (organic if you wish), one cup of classic coke (not diet) which " kills: " the taste, and the juice of one freshly squeezed lemon. Stir it, and drink it all down. It will still taste terrible. Then go and lay on your bed in a fetal position for an hour. This will push the mixture through your liver. Then, if you wish and feel like it, you can get up and do what you wish. Or sleep. The next morning with your first bowel movement you will see hundreds of green colored cholesterol balls (the green is from the bile). You'll be amazed at how many come out. It's not painful - it's just cleansing the liver. These little and sometimes larger green balls of cholesterol have been fushed out of the ducts of your liver. After this flush you'll feel an abundance of energy. A teapoon of olive oil daily after that will keep your liver clean. I've gotta' dash - I'll adress the other concerns in a while. Take care. On Mon, Jan 26, 2009 at 9:06 PM, Maple Springs Farm wrote: > oooo hot tub.... cool! i was looking for something besides chlorine for > that... > i had tried the food grade hydrogen peroxide and on my third time in had a > really really bad reaction to it. > i haven't been in the hot tub much since because i don't like all the > chorine and thought i tried everything else under the sun.. > what concentration and doseage do you use for the hottub please? > > i'm also looking forward to trying it on my sinuses... i used to work at a > company that made tile about 20 years ago... > was there 4 1/2 years... i breathed in a lot of tile dust and my > kineseologist says some is still stuck in there... > nothing is attached so it still has a chance of coming out but between that > and the lyme and i guess co infections... > my sinuses used to feel like glue... now it's like of moved up to my eyes > so i think it's coming out and moving up. > > she also says i have a problem with fungus... which i'm gonna try the cs > for... > my liver is my weakest organ.. if that was healthier this would move along > faster. > > idk if i needed it but i ordered the 5 foot of the cs with the micro > particle csw maker.. > when you use the 6 inches is it just good for one batch or can you reuse > it? > and once you make the csw, how much do you start out drinking? > my kineseologist is against cs because she says it's still a metal but hey > i'm gonna try it anyway... > i've been 10 years once a week with her and while i'm much much better than > when i first walked in > (i now have full time plus 2 part time jobs) but i want to feel great not > just ok. > > thanks > carol > > > E. s wrote: > > Hi, Carol: > > Thanks for you vote of confidence in what I've been talking about. I > appreciate it. Apologies for getting ticked off at Larson, but he gets on > my case too often and I lost it for a moment. > > You'll get a lot out of your Micro-particle CSW maker - I guarantee it. I > spray the counters, use it in the second rinse of a wash to purify the > clothes, use it in my hot tub instead of chlorine, spray it on wounds - > cuts, drain into - or spray into the nose and let it drain deeply into the > sinus cavities for sinus infections, no sore throats (gargle and swallow), > helps with skin cancer and other cancers in conjunction with other things, > treats eye infection (me or my felines), etc.,. My 94 year old Aunt controls > her asthma with an ounce a day - more if her asthma kicks up. One lady, > Nadine Wooley who was in a wheel chair with MS, drank 16 ounces (the most > I've ever heard of) daily for two years and is out of her wheel chair > walking with a cane. No side effects. That was her experience - I would > never recommend taking that much - but she did. She wrote a book about her > experience. You'll find that it's a miracle in a bottle with no side > effects. > > I hope you don't mind me forwarding this to Rife. I want the moderator to > view what you and I have said. > > I'd be glad to address any health issue you may be concerned with - if I > have the knowledge, I'd be glad to share it. If I don't, I'll tell you > straight out. Take care. In good health. > > > > On Mon, Jan 26, 2009 at 2:03 PM, maple springs farm <info@... > > wrote: > >> hey please don't stop talking just because of one jerk... >> i do enjoy your posts and actually did order one of those cs gerators >> from that company you said this morning... >> carol >> >> >> > Whooppee ding you big jerk... >> > >> > On Mon, Jan 26, 2009 at 10:25 AM, bob Larson wrote: >> > >> > > ..this is the reply sent directly to me, which i feel obliged to >> post to >> > > the group where it belongs. >> > > >> > > You're some piece of work. I don't work for them in any way or >> fashion. >> > > Hey, I'm trying to help folks through these messages. If you don't >> like it >> > > stick it. If Rife doesn't like my help they can stick it, too. I'd >> like to >> > > meet you face to face and tell you exactly where to go. I'm tired of >> your >> > > crap - I may be 67 but I'm in damn good health and ready to kick your >> butt >> > > down the road. You think you know so damn much about CS generators - >> > > wonderful. HOW do you know this one isn't better than anything you've >> ever >> > > tried? I've used a number of CS generators that couldn't stack up to >> it. >> > > If you knew anything about this one - you shut your face! I mention >> the one >> > > I mention because it's damn good. Whether you like it or not. >> > > >> > > On Sun, Jan 25, 2009 at 8:31 PM, bob Larson <bobList@...<bobList% >> 40cablespeed.com>> >> > > wrote: >> > > >> > > your relentless marketing of this CS generator leads me to believe >> that >> > > you >> > > are at the least part of that enterprise. >> > > again, that machine is overpriced with no particular advantage over >> others >> > > costing substantially less. >> > > so how about please stopping your salesmanship here? how about our >> list >> > > owner putting a stop to it if needbe??? how about limiting yourself to >> > > recommending CS in generic but specific terms if you like, but never >> ever >> > > mentioning this particular manufacturer and model again???? >> > > if you are forbidden to continue it, it'd be interesting to see just >> how >> > > your overall presence here might change... my guess is you'd drift off >> > > after >> > > not long. >> > > >> > > > Re: MSRA Staph Infections, treatable with Rife ? >> > > > >> > > > >> > > > I don't treat this with RIFE. It's very treatable (both) with >> colloidal >> > > > silver water. Make your own with a Micro-Particle Colloidal Silver >> Water >> > > > maker from silveredgehealth.com. You can make it as strong as you >> wish >> > > by >> > > > increasing the time. You can make it for about 40 cents a quart. >> Health >> > > > Food Store will charge you about $140.00 a quart. Why is a >> > > micro-particle >> > > > machine better? Because the smaller particles get into the smallest >> > > > capillaries, kills the infection, and leaves the body faster than >> > > > commercial >> > > > brands. Check it out on line. Then after curing this, build the >> immune >> > > > system up so you'll never get it again. >> > > > >> > > > >> > > > >> > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2012 Report Share Posted March 23, 2012 This post does not belong on this website Sent from my Verizon Wireless BlackBerry (no subject) Making m0ney fr0m h0me has never been s0 easy! http://prof-congress.hu/knmpoe.php?aqyrranknumber=486 Fri, 23 Mar 2012 13:28:10 _____________________ " There was four or five men cavorting around on their horses in the openplace before the log store, cussing and yelling, and trying to get at acouple of young chaps that was behind the wood-rank alongside of thesteamboat landing; but they couldnt come it. " © lourdes aelfdene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 6, 2012 Report Share Posted August 6, 2012 I am feeling so much anxiety in regards to food right now.  I am afraid nothing will ever be enough, that if I start eating I may never quit.  Realistically I am afraid I will eat and purge.  You know you are messed up with food when you say to yourself if you just eat this healthy portion right now on Saturday you can eat a jar of peanut butter and purge.  How crazy is that?  Anyway I am trying to just let this crawling anxiety be and not act out with food to numb it away.  I thought maybe just putting my intent out there to not restrict, not binge, not purge, not over exercise might give me some strength in this moment. Sent from my Samsung Epic™ 4G Touch Quote Link to comment Share on other sites More sharing options...
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