Guest guest Posted January 18, 2001 Report Share Posted January 18, 2001 do not send again please. MOM CURES SON BY ELIMINATING MILK > > --------------------------------------------- > MOM CURES SON BY ELIMINATING MILK > An article recently appeared in a Manchester, New Hampshire newspaper > (Derry News, December 22, 2000, p. 19) > Jill McIntosh (603-437-3375) had found a cure for her son's autism: > Eliminating all milk and dairy products and wheat from the child's diet. > She has allowed for her telephone number to be included in this article. > Jill links autism to a " milk allergy. " > SCIENTIFIC PROOF: MILK CAUSES AUTISM & ADD > Florida researcher, Cade, M.D., and his colleagues have identified a > milk protein, casomorphin, as the probable cause of attention deficit > disorder and autism. They found Beta-casomorphin-7 in high concentrations > of the blood and urine of patients with either schizophrenia or autism. > (AUTISM, 1999, 3) > Eighty percent of cow's milk protein is casein. It has been documented that > casein breaks down the stomach to produce a peptide casomorphine, an opiate. > Another researcher observed that casomorphin aggravated the symptoms of > autism. (Panksepp, J. Trends in Neuroscience, 1979, 2) > A third scientist produced evidence of elevated levels of endorphin-like > substances in the cerebro-spinal fluid of people with autism. (Gillberg, C. > (1988) Aspects of Autism: Biological Research Gaskell: London, pp. 31-37) > The Autism Research Unit, School of Health Sciences includes the following > information their website: > " The quantities of these compounds, as found in the urine, are much too > large to be of central nervous system origin. The quantities are such that > they can only have been derived from the incomplete breakdown of certain > foods. " > http://osiris.sunderland.ac.uk/autism/ > PARENT'S MAGAZINE REPORTS MILK LINK TO AUTISM > Search the Internet and you'll find many anecdotal stories from parents > blaming their childern's autism on milk and dairy products. One such story > appeared in the February 2000 issue of " Parent's Magazine. " > http://www.lingsensibly.org/autism.html > For children with autism, milk may very well be the major factor. One out > of five American children have been diagnosed with attention deficit > disorder. One out of five American children are made to take Ritalin. An > alternative therapy? NOTMILK! > For Jill, NOTMILK has made all the difference > --------------------------------------------- > I hope this article helps to educate you about the dangers of milk. > Thank you, > Ron Radstrom, > Founder > Health Freedom Resources > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 19, 2001 Report Share Posted January 19, 2001 To whomever is sending this message: " Rossetti Electronics Col., Ltd " wrote: > > do not send again please. > DO NOT send this message to us! You did not get on this list by accident! Someone with access to your computer signed you up for this list! Follow the directions below to unsubscribe! You have to do it yourself! jim oxyplus moderator > > You can unsubscribe via e-mail by sending A NEW e-mail to the following address - NOT TO THE OXYPLUS LIST! - > > DO NOT USE REPLY BUTTON & DO NOT PUT THIS IN THE SUBJECT LINE or BODY of > the message! : > > > > oxyplus-unsubscribeegroups > > ----- carpe diem, carpe pecunia, carpe femina. -- Jim Lambert jlambert@... http://www.entrance.to/madscience http://www.entrance.to/poetry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 13, 2002 Report Share Posted January 13, 2002 In a message dated 1/13/02 6:38:09 AM, writes: << I am interested in anyone whos school uses an adapted report cards for our kids. I brought it up to 's school and we would like to take a look at some to get some ideas on developing our own. Are they indivualized, grade appropiate, performance based, etc. or are they generic and can be just used to measure progress? If you can scan me a few I'd appreciate it or if a copy can be sent via snail mail, email me back and I'll send my addy. >> , FWIW, Holly gets the same report card as everyone else, BUT the WORK is adapted for her. She is in middle school and they give out letter grades. She always makes the honor roll, because she works so hard. I have teachers that do a fabulous job of modifiying materials, so I am very blessed. M. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2004 Report Share Posted January 1, 2004 Dear - from Kathleen, Twisted Sister in NJ 1998 flatbacker revision oldie.... first everyone under rates the healing time and adjustments our bodies do under go. first stop falling , will ya girl!!! THAT was one of my beginning disasters falling in my own bedroom just simple and enough to permanently have caused spinal cord injury. My surgery was Oct 1998 my posture was perfect and I finally stopped falling over in 2001. Are you using a cane all of the time. you should be...i made many mistakes and i hope people will learn from them. Falling is the most dangerous thing we can do..ever....for the rest of our lives. recently i had a bout of unsteadiness due to leg pain si joint pain and i now again am keeping my cane next to my bed and another in my van. USE the cane.. some of my falls also were the result of severe muscle twitching spasms enough to throw me onto the floor or lift me completely off a chair. since docs don't see this in action they doubt the severity of the muscle twitching but it can be as hazardous as falling as you never expect them. I find now that I am 5.5 years revision post-op I would say that NOW I think I am finally healed as much as i will ever be. Getting out as much of the hardware and hardware that may be moving certainly is a good idea but the risks are great. My posterior 2000 hardwarre removal was easy and easy recovery and lessened pain. My may 2003 anterior high risk hardwarre removal only partial success as I still have a screw into the spinal nerve and the f* & ^%$g plate I can feel still in as complications arose after the 3 other plate screws were removed. I almost died as my ilia vena cava vein (?) whatever the big one down in the groin tore open when it was gently retracted off the remaining screw head, attempted.... This gave me new pain in my left groin that was beyond excruciating but has subsided greatly as dr errico said it would get better but needs time and allot of time. especially those three screws spent 4.8 years irritating my spinal nerves as I complained to everyone of the pain....in the end I was right they were in a bad place..but that is the way the cookie crumbled so to speak. There is a chance that you can be worse off after this surgery and quite frankly your body hasn't recovered from the last one....have you just thought about hardware removal only posterior and heal from and see where you are in a year?? yes my posture changed and I did notice i lean a smidgen forward and when it first happened i was very aware I was forward and occassionally i can catch myself tilting a little and straighten up for the moment and I am sure I go back to wherever my body posture was... For your falling.. have you had balance retraining therapy? That is one of the most important tasks to be relearned. Reteaching your brain where your feet are.. That did not happen until this may when i insisted I go to rehab hospital after my hardware removal. I can't say enough good things about Rusk Institute connected with NYU Med Center Tisch Hospital. The p.t. Mark subspecializes in spinal and he had managed to get me moving and doing things I thought I'd never move. He manually manipulated my limbs since with fusion you lose the ability to stretch certain ways. he really drummed into me how imp[ortant it is to find someone who can manually help exercise your body with you. He did allot of work on my si region and managed to loosen up quite a bit of muscle spasms that were permanent so I thought... the biggest help though was the balance retraining. and getting in their pol for pt was a big plus. I hope that whichever surgery you do that you make sure you go for a spine rehab place inpatient from surgery. There was allot i learned about the wrong way I was doing and moving and just how the small wrong movements over time create pain and misalignment. besides Ondra have you gotten two other opinions about your condition, not including Rand....it sounds like you are going for a very drastic surgery and quite frankly sounds very scary that you will be re-revised with more osteotomies..none of this will ever help if you can't stop falling. if you need a walker, use one or a cane. But I honestly believe recovery from the initial revision was a 5 year project combatting various pains and problems and getting hardware removed helped immensely but acceptance of being in chronic pain is not easy to swallow and I fight it constantly but finally am allowing myself to accept this is my lot in life. Have you been checked to see if you have developed arachnoiditis. each time they go back near that spine the risks of developing arachnoiditis increase dramatically. I HAVE IT .. its not something i wish on anybody , scar tissue grows around the spinal cord and nerves, nice huh and its caused directly by surgery and resulting trauma, plain and simple its scar tissue and they wont remove it as it grows back,, I now have made explaining all of these various conditions, ailments simplified by just saying i have spinal cord injury.... that seems to get their attention and they immediately understand the seriousness of my spinal health. Anything goes wrong with me and everyone loves to say gee you had so much done to your spine it must be your spine! even if its like kidney stone pain. I can empathize with your frustration and pain at this 2.5 year mark but you must realize every time you fall you have possibly reeinjured your spine and those spinal nerves. those spinal nerves are fragile creatures that need time , years in order to heal if at all possible. have you considered just hardware removal first and give that a year to see how you feel?. if you want to talk on the phone write me off list at kulina@... and i'll give you my tele#, I also have verizon cell too. If it is any consolation my life sucked big time at 2-3 years post-op and I saw no light at the end of the tunnel, I was in the tunnel forever I thought...... wishing you many peaceful moments TwistedSister in NJ 1982 Scoliosis Harrington fusion, 1998 Revision A/P Surgery for Flatback Syndrome, 1998 Post Traumatic Stress Disorder, 1999 Degenrative SI Joints, 2000 Weight Loss Surgery, 2000 Spinal Hardware Removed, 2001 Cervical bulging discs, 2002 Arachnoiditis, 2002 GERD, 2002 Adhesions, 1993 Mitral Valve Prolapse, 1996 Fibromyalgia, 2001 Kidney Stones, 2003 Interstitial Cystitis, May 2003 Anterior spine hardware removal ** LIFE IS UNCERTAIN.............EAT DESSERT FIRST ** Harrington Rod scoliosis people and other post-op multiple spine surgery people may interested in the following website dedicated to Flatback Syndrome and revision/salvage spine surgery... " Salvaged Sisters of Scoliosis " website on Delphi Forums at: http://forums.delphiforums.com/adultscoliosis/messages Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Matt, Cudos to you for having the courage and the curiosity to ask a bunch of jade dissidents for anything. As long term survivor of 18 years, I still consult with the medical community even though I do not participate in chemotherapy. My health is fine as I have built a mountain home, earned 3 graduate degrees, studied in Paris, and so forth. You spend more time reading about this disease than I do and I have it. I hope you find the people you are looking for as I am sure they are out here. The earlier comment that this may not be the best group (or friendliest) for you to contact, thank you for your professional commitment to keep asking the hard questions. One day at a time... and best of luck! ________________________________________________________________________ > > Message: 1 > Date: Sun, 08 Feb 2004 05:48:22 -0000 > From: " Ketterling " <mattk470@...> > Subject: I'm courious > > As a HIV researcher (Molecular Biologist/Virologist) > at University I > tend to read several HIV related science journals a > day, along with > my own research I've conducted so I'm fairly > knowledgable about the > HIV virus and it's interactions. I like to think > outside the box > when it comes to my research/views and I'd like to > talk to a couple > people who strongly believe in the alternative > approaches. I would > like them to be either a MD with exposure in AIDS > treatments or a > Molecular biologist/Virologist. My goal is to talk > to someone that > knows the molecular " workings " of the HIV virus yet > believes in > alternative approaches. My goal is not to attempt > to change anyones > view just to enlighten me on your own. > > thanks, > ---Matt > > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 2 > Date: Sun, 8 Feb 2004 22:54:36 -0700 > From: " caerfree@... " <caerfree@...> > Subject: Re: I'm courious > > , You are soooo in the wrong group. I know > you believe that you're doing > good work and if you're truly open minded, then I > hope you will find the following > sites useful: > [http://www.aliveandwell.org]www.aliveandwell.org > [http://www.duesberg.com]www.duesberg.com > [http://www.aidsrc.org]www.aidsrc.org > [http://www.virusmyth.com]www.virusmyth.com > Most of us in this community do not believe that > the HIV virus has anything to > do with AIDS, if it even exists at all. The > majority of us are dissidents. We > have spent much of our time researching HIV and find > it to be a giant machine for > getting drug money and that's it. You will find > that the sites listed above have > a plethorah of research and analysis conducted by > mainstream and dissident scientists. > If you're patient and truly open minded as you say, > I think you'll find the information > interesting and informative. > If you think we're all crazy, you might consider > the fact that the majority of > us are HIV postive people who are healthy and have > been healthy for many years. > We have done nothing except take care of ourselves. > No toxic medications. No stupid > Viral Load tests or CD4 counts. Just plain living > well. Good luck. Caer > > > > I'm courious > As a HIV researcher (Molecular Biologist/Virologist) > at University I > tend to read several HIV related science journals a > day, along with > my own research I've conducted so I'm fairly > knowledgable about the > HIV virus and it's interactions. I like to think > outside the box > when it comes to my research/views and I'd like to > talk to a couple > people who strongly believe in the alternative > approaches. I would > like them to be either a MD with exposure in AIDS > treatments or a > Molecular biologist/Virologist. My goal is to talk > to someone that > knows the molecular " workings " of the HIV virus yet > believes in > alternative approaches. My goal is not to attempt to > change anyones > view just to enlighten me on your own. > > > thanks, > > ---Matt > > > > > > Read AIDS-Cured Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2004 Report Share Posted November 8, 2004 Dear Feistys, The Discovery Channel IS NOT The Discovery Health Channel. I believe that is why so many of you could not find it. Ask your cabel company if you get The Discovery Health Channel before it airs again on Dec 6th. Love, Di Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2004 Report Share Posted November 8, 2004 Hmmmm, I only get the Discovery channel, and I saw part of the scoliosis show. Maybe they are just repeating it on the Health Channel, which I do not get? We only got a few cable channels for quite awhile, because we live in an older area of Oakland. Took forever to get digital cable. Finally we got it last year, and, of course, got a raise in our bill. But we still don't have very many that are shown in our area. (Cable Oakland was taken over by TCI, then AT & T.) in Oakland At 07:45 AM 11/08/2004 -0500, Diane1B@... wrote: >Dear Feistys, The Discovery Channel IS NOT The Discovery Health >Channel. I believe that is why so many of you could not find it. Ask >your cabel company if you get The Discovery Health Channel before it >airs again on Dec 6th. >Love, >Di > > > > >Support for scoliosis-surgery veterans with Harrington Rod Malalignment >Syndrome. Not medical advice. Group does not control ads or endorse any >advertised products. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2004 Report Share Posted November 9, 2004 Hmmmmm, I still have not been able to find the TV show about 's Surgery. I get quite a few cable channels, including Discovery, and got up at 6:30 a.m. to be sure it was taping, but there was something else on. I plan to try again, but I do know it is not listed in my guides. Just my two cents' worth. Carole M. (the elder) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2004 Report Share Posted November 9, 2004 Thank you, Loriann. It has been a " puzzlement " ! Carole M. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2004 Report Share Posted November 9, 2004 Carole M, I don't know about all areas, but I think in at least some areas Discovery Health is only available if you have a satellite service, rather than a cable service that would typically have the regular Discovery Channel. I don't have either, and am just going by what someone else told me, so please forgive me if this is wrong information. loriann > Hmmmmm, I still have not been able to find the TV show about 's > Surgery. I get quite a few cable channels, including Discovery, and got up at 6:30 > a.m. to be sure it was taping, but there was something else on. I plan to > try again, but I do know it is not listed in my guides. Just my two cents' > worth. > > Carole M. (the elder) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 9, 2004 Report Share Posted November 9, 2004 Carole, I have Charter Cable and on the menu it lists the Discovery Health Channel as: D-HC. I just figured out what that meant today. Now I have to wait till Dec. to watch it, if I don't forget. I hope you are doing well. I keep up with you through your posts. Joyce Re: Digest Number 886 Hmmmmm, I still have not been able to find the TV show about 's Surgery. I get quite a few cable channels, including Discovery, and got up at 6:30 a.m. to be sure it was taping, but there was something else on. I plan to try again, but I do know it is not listed in my guides. Just my two cents' worth. Carole M. (the elder) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 17, 2005 Report Share Posted November 17, 2005 Thanks for all the responses about gas pains. It seems to be getting progressively worse so I don't thinks its IBS. She did recently have a hernia repair and does wear tight garments around her waist b/c of the hernia repair. I will mention some of these ideas to her during our next appt. For now she is popping 7-8 tums per day. She is hoping to meet with a gastroenterologist. I suspect there is a medical problem...ulcer? Mogg --- wrote: > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 17, 2006 Report Share Posted January 17, 2006 In the coconut farm of my father-in-law, they don't spray with fungicide and pesticides because: (a) the trees are so tall it is impossible to be reached by a sprayer; ( the cost of the chemicals, even those applied to the ground, are just too costly that it would not be augmented by the cheap sale of the nuts. The " fresh " coconuts shipped to mainland US are irradiated before shipping. --- Coconut Oil wrote: > There are 4 messages in this issue. > > Topics in this digest: > > 1. Re: Ben and Jerry's coconut oil > connection!! > From: " Bob and " > <flowerpowerpetalpusher@...> > 2. Re: VCO side effect > From: " k8teeth " <stonesigns@...> > 3. Re: Re: VCO side effect > From: Alobar <Alobar@...> > 4. Re: VCO > From: lexus lexi > <lexus_lexi2002@...> > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 1 > Date: Sat, 14 Jan 2006 17:42:14 -0000 > From: " Bob and " > <flowerpowerpetalpusher@...> > Subject: Re: Ben and Jerry's coconut oil > connection!! > > It would also be interesting to know the name of the > fungicide used. > If someone could please find out that would help. I > have wondered if > coconuts shipped to the USA or other places could be > contaminated in > any way? I had a reaction to fresh coconut in the > shell. It is > apparent that some of the producers here do not > really want to say > what goes on with the coconut process for fear of > being found out on > what actually takes place in process. It really is > too bad, that they > could help. It is also important that the organic > aspect is truly > organic. It is one thing to say virgin and organic > but some of us > need to know if pesticides or fungicides effect what > we are eating or > if there is an allergic reaction to a product. Good > information helps > us make informed decisions on who we can buy from > that will meet our > individual needs. > > > Bob > > > > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 2 > Date: Sat, 14 Jan 2006 21:30:35 -0000 > From: " k8teeth " <stonesigns@...> > Subject: Re: VCO side effect > > I think its amasing how there are so many with > differant sleep effects > from VCO. > Im one who when I first started to eat it,couldnt > figure out why I > couldnt get to sleep if I ate it after 5pm or even > earlier. > So when a few sites mentioned that some cant sleep > because of VCO,I > stopped taking in the afternoon,and now i sleep just > fine. > But the first couple of nights I couldnt get to > sleep till way past 2AM! > > > > > > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 3 > Date: Sat, 14 Jan 2006 16:53:43 -0600 > From: Alobar <Alobar@...> > Subject: Re: Re: VCO side effect > > On 1/14/06, k8teeth <stonesigns@...> wrote: > > I think its amasing how there are so many with > differant sleep effects > > from VCO. > > Im one who when I first started to eat it,couldnt > figure out why I > > couldnt get to sleep if I ate it after 5pm or even > earlier. > > So when a few sites mentioned that some cant sleep > because of VCO,I > > stopped taking in the afternoon,and now i sleep > just fine. > > But the first couple of nights I couldnt get to > sleep till way past 2AM! > > > > > > > I wonder if me having a normal bedtime of 3-4 AM > might explain why > if did not impact me with loss of sleep? > > Alobar > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 4 > Date: Sun, 15 Jan 2006 06:36:00 -0800 (PST) > From: lexus lexi <lexus_lexi2002@...> > Subject: Re: VCO > > just continue takin your VCO and in the long run > your blood pressure will normalize, I also have that > problem like yours before, but now I am very much > OK. Take 1 tbsp in the morning, 1 at lunch time & 1 > before dinner time. > > Jane Hyde <gizmopippy@...> wrote: Hi, I am a > new member, I have high blood pressure, I'm on three > different meds, and they still can't get it under > control. I would like to purchase VCO, I have look > everywhere, where can I do that? Thanks, Jane > > > --------------------------------- > Photos > Got holiday prints? See all the ways to get quality > prints in your hands ASAP. > > [Non-text portions of this message have been > removed] > > > > > > --------------------------------- > ! GROUPS LINKS > > > Visit your group " Coconut Oil " on the > web. > > Quote Link to comment Share on other sites More sharing options...
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