Guest guest Posted October 31, 1999 Report Share Posted October 31, 1999 > Subject: Re: mercury fillings Hello everyone. I know of several instances of people having to have amalgam fillings replaced because it caused them to have severe headaches. This was done as a last resort, as it was the last thing on the 'predisposing causes' list. Each time it proved to be the problem. Another unfortunate person had to have the wiring in his mouth changed, as his teeth kept buzzing when near a loud radio source, giving him no peace. Anything 'Alien' to the human body has a chance to be an upset to the bodies system, especially if that person is hypersensitive. Mercury has been used a lot in medical history. It is a poison to the system, and there are alternatives to be used instead. Don't let this put you off going to the Dentist, there is nothing like your own teeth! Smile, and be happy...... :-)=) --------------------------------------------------------------------------- Jan 1 2000 - Stardate 0001.01 Let the voyage begin..... Rayesi@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 2, 1999 Report Share Posted November 2, 1999 JEWL,I have been thinking about you.How are you doing?We got married on Sat. the 30th and it was a beautiful day.Let me hear from you soon.Hugs.....Barb >From: " Rayesi " <rayesi@...> >Reply- onelist >< onelist> >Subject: RE: [ ] Digest Number 34 >Date: Sun, 31 Oct 1999 16:59:41 -0000 > > > Subject: Re: mercury fillings > > >Hello everyone. >I know of several instances of people having to have amalgam fillings >replaced because it caused them to have severe headaches. This was done as >a >last resort, as it was the last thing on the 'predisposing causes' list. >Each time it proved to be the problem. Another unfortunate person had to >have the wiring in his mouth changed, as his teeth kept buzzing when near a >loud radio source, giving him no peace. >Anything 'Alien' to the human body has a chance to be an upset to the >bodies >system, especially if that person is hypersensitive. >Mercury has been used a lot in medical history. It is a poison to the >system, and there are alternatives to be used instead. >Don't let this put you off going to the Dentist, there is nothing like your >own teeth! >Smile, and be happy...... :-)=) >--------------------------------------------------------------------------- >Jan 1 2000 - Stardate 0001.01 Let the voyage begin..... >Rayesi@... > > >------------------------------------------------------------------------ >_ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 28, 1999 Report Share Posted December 28, 1999 In a message dated 12/28/99 1:57:41 PM Central Standard Time, onelist writes: << Any good recipes for laundry soap. The commercial stuff is just making me itch like crazy. I switch >> girlfriend, get " symphony " . i am allergic to everything under the sun. if you use this, you won't need softener and IT WORKS FOR ME. if you can't find it locally on your grocer's shelf, let me know and i'll give you the addy of a local chem co. who reps it. LISA MITCHELL/COZY MOON Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2000 Report Share Posted February 2, 2000 Donnna- Don't be skeptical on the vaccines. I allready did that for you. Another virus could caus liver failure and luckily by the grace of God I survived it. I don't wish that on anyone. - " ...I dream then ask why not " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2000 Report Share Posted February 2, 2000 Donnna- Don't be skeptical on the vaccines. I allready did that for you. Another virus could caus liver failure and luckily by the grace of God I survived it. I don't wish that on anyone. - " ...I dream then ask why not " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 2, 2000 Report Share Posted February 2, 2000 I find it so strange that mot people are never told about hep a and b. I know years ago, think hep a was considered a gay mans disease, because supposedly they had unsafe sex, and were diganosed with it alot. I have knowa alot of people who have had hep b. I know hep b is extremley easy to catch. I am lucky for working at a hospital in 1989 to1995. I was so aware of diseases and viruses because I worked with patients. we had some thing called " universal precautions " where u assume every patient as something that can be spread through blood or body fluids, including stool. i worked with tb ( sputum ) patients, hiv, hep a, b, and c. I feel it is unfortunate that alot of doctors wil just assume the general public is knowledgeable of whatthe medical world knows. The comment about vaccines by somone. I have had the Hep B vac, and was told it was good for life, than read in a medical book it is only good for 3 to 5 years. I am anxous to be vaccinated for hep a and b, but cautious about maybe down the line having something awful happen because of it. I dont trust the medical comunity, especially after working in it. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2000 Report Share Posted February 3, 2000 Peggy, Don't be surprised if your skin where you inject gets blotchy/reddish and itches. Keep lots of moisturizer on your skin. Combo made me dry out. If you live in one of the 7 states where it's legal, I'd ask your doc about medical cannabis for the nausea and headaches. I hated treatment, but at least it was some treatment. Now that I'm a non-responder, it's really hard for me to not do anything (other than milk thistle, licithin, water, water, water). I go back for a 6-month checkup in March to see if the GI's going to let me try one of the new treatments. I had to stop combo after 6 months due to anemia & thyroid problems. Good luck and hang in there. It will get easier with each shot. I pray you're one of the 40% that clears the virus. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2000 Report Share Posted February 3, 2000 Peggy, Don't be surprised if your skin where you inject gets blotchy/reddish and itches. Keep lots of moisturizer on your skin. Combo made me dry out. If you live in one of the 7 states where it's legal, I'd ask your doc about medical cannabis for the nausea and headaches. I hated treatment, but at least it was some treatment. Now that I'm a non-responder, it's really hard for me to not do anything (other than milk thistle, licithin, water, water, water). I go back for a 6-month checkup in March to see if the GI's going to let me try one of the new treatments. I had to stop combo after 6 months due to anemia & thyroid problems. Good luck and hang in there. It will get easier with each shot. I pray you're one of the 40% that clears the virus. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2000 Report Share Posted February 15, 2000 Hey you guys, this is so weird, reading all of these stories! I can't believe that I've been on this list for almost a year and this is the very first that this issue about pica has come up- and it is so prevalent, it seems. We haven't had this issue with Ben at all, except for a litle licking when he was around 3 or 4 which lasted for a few months. He is a kid who can't use his tongue to swipe the food out of the sides of his mouth and down the chute to swallow, so to speak. He also doesn't use his tongue to lick anything. I tried to get him to lick the last bit of banana with meds off of a spoon. Nothing. He brought a sucker to me (Valentine's Candy) and said " candy " and wanted me to unwrap it. I unwrapped it and he just wanted to feel it. I kept putting it in his mouth and when he wouldn't lick it and couldn't bite off a chunk, he wanted to just feel it being nice and sticky. I showed him how to lick it and he just wasn't interested. So weird. He does chew on his fingers- they're all calloused, and from the sounds of the regular DS list, this seems pretty prevalent. We've had OT's give him rubber tubing but he won't chew on it- he just flips it. It fact, the tubing is his all-time favorite flippy. So I save them until he's either done something really great or he is in need of a real " boost " . Chewing gum is unreliable- don't know where the gum will end up, either. He also craves textures on his palms and on his feet. He'll take brushes or my fingernails to rub on his hands. A small sticky ball is often helpful in public- he gets the texture and it's discreet. So far as contortionism, well, he of course can get his feet up around his neck like most of our kids. The funniest time was when he was walking by the teacher who was seated next to a child at the child's desk and he stopped and casully flung HIS foot up on her shoulder for a moment. I still laugh thinking about it. Well, you gotta love em! Beth, Mum to Ben, 9 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2000 Report Share Posted February 15, 2000 Gail: I couldn't believe your comments about rather having your child eat and/or lick crap than losing a night's sleep due to restless kids.........well, I, for one, would rather stay up ALL NIGHT than have my child subjected to eating crap full of bacteria and God knows what other germs he may pick up. I can't believe your doctor thinks this is harmless.......would YOU want to be operated on by him if HE was a pica person and he didn't wash his hands first?? Would you eat at his house if he was the chef???? Sorry for the soapbox, but that comment just killed me......... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2000 Report Share Posted February 15, 2000 in reference to the pica vs sleepless child......... i think i would much rather stay up endless nights without ANY SLEEP than have ashton doodooing and eating it.......... and plaster and cement and grass and bark,,,,,,,,,, i have grown accustomed to no sleep..... we have a routine., ashton goes to bed around 9pm and wakes around 1-3 am and then i get up and study while she does school work or watches her movies........sounds strange but i sorta of look forward to her allnighters because it gives me and her mommy time....daddy and cameron are sleeping, so ITS A GIRLS NIGHT OUT........heheh if that were only realisticly true........ no wine involved here........just books and the puter and an adorable little angel who i would put my butt in front of a bus to save....... But.......... all of us on this list have special children or are involved with them somehow and are caring loving people...... all of these kids have their own querks and perks and little problems............ i am sure gail didnt choose to have a poop eating son on purpose nor did i intentionally wish for a child who is sleepless and sings LOUDLY at night and has pdd.......... but the fact is we all have something wrong and we have to deal with what is on our plate as best we can and sometimes the only way to do that is to LAUGH AND JOKE ABOUT IT TO KEEP SAIN..........so i think when we do no harm is meant to any others.....we are just trying to keep sanity in our souls for the sake of our children......... okay i am shutting up now..........have a good day to all......leah Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2000 Report Share Posted February 16, 2000 , you bet I'd choose poop eating over night after night of no sleep! Not that I like it, but it's what Seth does. I can handle anything if I get my sleep. Seth has the most beautiful smile (when his mouth is clean) and he's the happiest, cutest little guy on this earth who just happens to eat weird, disgusting things! Maybe it's that we all get used to all the weird things our kids do and they don't seem so bad. Endless, sleepless nights seem like the very worst thing to me. I have had my share with occasional all nighters between the 5 kids, but night after night? Not something I could handle. Oh, I would also choose that my husband be healthier, my daughter never touch alcohol again and 1,000 other things if I could. I'll take what I've got and choose to laugh instead of cry. gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2000 Report Share Posted February 16, 2000 In a message dated 2/15/0 3:43:51 PM, paul.3@... writes: << The funniest time was when he was walking by the teacher who was seated next to a child at the child's desk and he stopped and casully flung HIS foot up on her shoulder for a moment. I still laugh thinking about it. >> Beth, That is the best story, I can't stop laughing----hope the teacher had a sense of humor. Pam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 2002 Report Share Posted July 23, 2002 Very good points- especially when one considers the existence of 'beeswax absolute'- I suspect that the rich undertone to which you refer is thus to be obtained au natural in this case. The point on the frac coco- I had bought 3 batches of this. First had a definite 'off-tone'. I had wondered if it somehow had absorbed something from the plastic material of the bottle itself. 2nd batch was better. By the time I bought the 3 and larger batch it went straight into my fridge. Now I see your note on the alteration with heat, I am glad I went the way I did. I think I had a chance to share with Roseanne the scent of a bit of 'propolis absolute' I had made. It is truly exquisite, and I must find the time to work on this some more. The summer is so full of activity, that the bees are just getting to exist and fertilize without any intervention from me- hence no honey, but I hope this hive will continue to survive despite the mites. This is their 3rd year. I think they swarmed a while ago, and if so I hope I am seeding the environment with newly resistant bees. I do see (as has been reported by others) increasing evidence of wild bees doing well. There were several this year with sufficiently different coloration from my hive bees (and yet clearly they were honeybees) that I am sure there are wild hives around. I am watching the corn tassels to see what population will be working them. The wild bees were working multiflora rose and rosa canina. Now here's an OT note ...I made 'May wine' this spring with sweet woodruff and some Australian white. 'Twas interesting...so a few days ago I had picked a sprig of basil to avoid the plant going to seed- thought about putting it in tea- did put it in a cold cuppa, but not effectually. So THEN- I was having a bit of sake and I dropped the sprig in there. Well, HMMM...very quickly diffused into the wine. Quite nice. So of course tonight I tried it with a small bit of blossom of clary sage...this is very interesting indeed. What would you call this method? I see the possibility of a lot of the culinary herbs. I am quite familiar with herb vinegars- but herb wines? Almost along the line of the old medicinal cordials. I guess it's like a tincture, but very short term and not as harsh.I did hawthorn flower tincture this spring and will follow with hawthorne berry tincture- but what about hawthorne flower wine as a mild medicinal? I wonder. -- L Wakefield, owner and operator of the beastly truck heretik, that refuses to stay between the lines when parking -- Message: 2 Date: Sun, 21 Jul 2002 06:55:43 EDT From: scentart@... Subject: Bases I like for solids I have used beeswax, a combo of beeswax and shea butter and for liquid oils I have used jojoba, and fractionated coconut. I prefer beeswax. It holds the scent, augments it a bit with it's rich undertone, and I find the texture allows for longer life without somewhat dampening it as the shea butter has. This is a subtle difference, however, and shea butter allows for a richer creamier texture. eliminate 1/3 of however much beeswax you are using and substitute that amount w/shea butter. I have found that one has to be careful about heating frac. coconut btw. I infused some orris root in it, and gently heated it. It changed the frac. coconut and created a rancid quality. This has happened twice with infusions of jasmine, and infusions of the orris... I have gone back to jojoba. This is my all time favorite general purpose carrier. But all is personal and subjective (g) blessings, gail " She was wearing a French perfume so dark it was almost carbolic... " Fowles 'The Magus' Gail , Fragranceur L.Cos. www.gailadrian.com Custom-Blended Natural Artisan Perfumes T'arotmatics, Facials, Reiki, Energy Bodywork Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2004 Report Share Posted May 26, 2004 Excuse me A. Habok - I was merely asking a question! We're all in the same boat here (messed up spines & necks) and I was merely trying to learn something. I don't know what would be left to do after they cut out part of the boney structure. Where would they screw in the hardware if they cut out the back part of the vertebrae? These are the questions I have. I guess your problem is lumbar - while I have herniations, bone spurs, & stenosis in all three levels... my c-spine is the most severe right now. I'm sorry you misunderstood. And I don't know how you think I was " going on " . ________________________________________________________________________ ________________________________________________________________________ Message: 3 Date: Tue, 25 May 2004 17:53:39 -0400 From: " A. Habok " <northernstars@...> Subject: Re: Digest Number 33 I know a lot of people on other lists that have had fusions done. I know what hard ware is and I know all about what fusion is. It reduces the mobility of the spine and stabilizes it but puts more strain on the other levels that compensate. Well yes with a laminectomy they remove vertebrae but with many types of stenosis they have to mainly because of bone and osteophytes and/or discs (well duh!). In lumbar spine surgery depending on what needs to be done anything that has to do with discs either a laminotomy or laminectomy is performed. In my case I had such a huge centrally herniated disc that they HAD to do an open discectomy (and not a micro) in order to get all of the contents out of my canal and remove the bone overgrowth that occurred because of my DDD. Laminectomy is the norm with dealing with stenosis as it clears the way for the nerves. I don't need a fusion yet and I am so glad I never had one. I have other lumbar herniated discs what would be worse I'm sure. I doubt I'd ever fuse with the way I heal. If I had a fusion it would not be because of stenosis it would be because of the DDD. I am just curious how they manage to remove your bone spurs without either a laminectomy or a foramenotomy because I know fusions do not remove them. I was just trying to be helpful and nice. With the way you are going on then why should I bother? safegirl@... wrote: > Well with a fusion (I've already had one and many more to come) they > add hardware. > > With a laminectomy the cut out section of the vertebrae. Don't they? > ________________________________________________________________________ Message: 7 Date: Tue, 25 May 2004 22:36:36 -0400 From: " A. Habok " <northernstars@...> Subject: stenosis links I just wanted to add that a Laminectomy is NOT the removal of a vertebra as a whole. It is only the removal of the laminar (roof) area of the vertebra and usually they do not remove 100% of the lamina. In some cases a partial laminectomy can be done and they only remove what they have to in order to access the disc, make more room for the nerve roots, be able to get enough room to explore the thecal sac for disc fragments, etc. A Corpectomy is the removal/partial removal of a vertebral body. It is normally done when a vertebra is crushed by trauma, etc. I have only met one person to this day that has had one and it was only done because he/she were shot in the back and the bullet completely crushed the L3 vertebra. WHen this happens sometimes doctors use rib bone or whatever to try to rebuild a new vertebra in a sense. Fusion is mandatory in this situation because there is no stability when this happens. Remember we are all different and there are many types of spinal stenosis. I have added two links to the links page on the group home page which clarify how different they are from each other. I hope this clarifies some things for some of us. Have a nice day Ama Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2004 Report Share Posted May 26, 2004 PS - I also have DDD and fibromyalgia. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2004 Report Share Posted May 26, 2004 Well excuse me M. Hussli, actually you were coming across in your email as quite condescending and in return I was treating you the way you treated me when I asked you if a fusion is necessary at ALL those levels. The reason why I got so annoyed is your definition of " laminectomies being the be all end all of spine surgeries " . I know many people that would argue against that and most people would say that definition describes fusion and not a laminectomy. The only reason why I asked in the first place is because you told me you never fused so I was wondering if they had to fuse all those levels and could get away with other decompression. If you don't fuse at one level then you are bound to have the same problem with fusion at another level. A laminectomy is done frequently and yes they can fuse with a laminectomy. Heck I know someone who has been able to fuse after a corpectomy which is way more invasive than a laminectomy. When they do a fusion they to not attach hard ware to the lamina in the first place. Normally the instrumentation is put in and screws are put into the pediles to hold the instrumentation in place. If they can do successful fusion with a corpectomy which is a lot more invasive than a laminectomy it is possible. I've met many people who have had laminectomies in combination with a fusion and they have fused fine. BTW it is normally a laminectomy that removes bone spurs if you were wondering so what did the operation do to remove yours if you never had one? BTW I have DDD, lumbar herniated discs, Cauda Equina Syndrome, Stenosis, all in the lumbar spine plus I have spondylolysis (slippage) from C2 through C5. Yah know the simple fact that I haven't ended up in a wheelchair for life from the CES makes me feel extremely lucky to be alive. My life may be agony but with the right balance of pain meds I live life all I can and don't let my disabilities define who I am. Ok I want this subject dropped before this gets out of hand. I came to this group for support and to give advice not to have flame wars with members. I have made my point and will ignore any further emails on this thread. M. Hussli wrote: > Excuse me A. Habok - I was merely asking a question! We're all in the > same boat here (messed up spines & necks) and I was merely trying to > learn something. > > I don't know what would be left to do after they cut out part of the > boney structure. Where would they screw in the hardware if they cut > out the back part of the vertebrae? These are the questions I have. > > I guess your problem is lumbar - while I have herniations, bone spurs, & > stenosis in all three levels... my c-spine is the most severe right now. > > I'm sorry you misunderstood. And I don't know how you think I was > " going on " . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 29, 2004 Report Share Posted May 29, 2004 You know what? Why is it that I go and join a list hoping to find help, information, support and a shoulder to cry on cuz God knows my husband doesn't care how much pain I'm in or what my future looks like and yet everytime I'm fool enough to join one of these lists, everybody acts like know it alls and starts fighting and who is that helping? <sigh> I wish you all well...... Someone with Spinal Stenosis and a perorated disc who knows hardly anything about my condition except that it will get worse with age and that I'm in alot of pain already...... -- Re: Digest Number 34 Well excuse me M. Hussli, actually you were coming across in your email as quite condescending and in return I was treating you the way you treated me when I asked you if a fusion is necessary at ALL those levels. The reason why I got so annoyed is your definition of "laminectomies being the be all end all of spine surgeries". I know many people that would argue against that and most people would say that definition describes fusion and not a laminectomy. The only reason why I asked in the first place is because you told me you never fused so I was wondering if they had to fuse all those levels and could get away with other decompression. If you don't fuse at one level then you are bound to have the same problem with fusion at another level. A laminectomy is done frequently and yes they can fuse with a laminectomy. Heck I know someone who has been able to fuse after a corpectomy which is way more invasive than a laminectomy. When they do a fusion they to not attach hard ware to the lamina in the first place. Normally the instrumentation is put in and screws are put into the pediles to hold the instrumentation in place. If they can do successful fusion with a corpectomy which is a lot more invasive than a laminectomy it is possible. I've met many people who have had laminectomies in combination with a fusion and they have fused fine. BTW it is normally a laminectomy that removes bone spurs if you were wondering so what did the operation do to remove yours if you never had one? BTW I have DDD, lumbar herniated discs, Cauda Equina Syndrome, Stenosis, all in the lumbar spine plus I have spondylolysis (slippage) from C2 through C5. Yah know the simple fact that I haven't ended up in a wheelchair for life from the CES makes me feel extremely lucky to be alive. My life may be agony but with the right balance of pain meds I live life all I can and don't let my disabilities define who I am. Ok I want this subject dropped before this gets out of hand. I came to this group for support and to give advice not to have flame wars with members. I have made my point and will ignore any further emails on this thread. M. Hussli wrote: > Excuse me A. Habok - I was merely asking a question! We're all in the > same boat here (messed up spines & necks) and I was merely trying to > learn something. > > I don't know what would be left to do after they cut out part of the > boney structure. Where would they screw in the hardware if they cut > out the back part of the vertebrae? These are the questions I have. > > I guess your problem is lumbar - while I have herniations, bone spurs, & > stenosis in all three levels... my c-spine is the most severe right now. > > I'm sorry you misunderstood. And I don't know how you think I was > "going on". Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2004 Report Share Posted September 7, 2004 kristina is following Dr Fox's aftercare program. Fox is retired from doing open bypass surgery, so when you go to him you end up having bypass or band surgery with a different Dr at his clinic, but he also has a working relationship with Rumbaut and for a large fee, he sends his patients willing to be banded in mexico, to rumbaut. (personally, i said to heck with that fee and called rumbaut and made my own appt for banding 2 yrs ago) i never went back to fox.....i had no interest in following his bypass aftercare program, and instead chose to follow rumbauts aftercare for the banded. Fox likes all his clients to lose very quickly and thats why he makes everyone who goes thru his office follow his bypass instructions i.e. no milk, etc. too strict....not neccessary... Sandy Landry Landco@... Lynnwood, Wa. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2004 Report Share Posted September 7, 2004 Yes, I've heard this before. Jessie Ahroni was one of the very first rumbaut/Fox clients. Hopefully, as she becomes more confident in her own knowledge, she will be able to make good choices for herself. Weight loss is fine, but clears for a month does not provide adequate nutrition. Band loss (as you know) is supposed to be slow and heqalthy, bot an unhealthy crash like bypass. Sandy R > kristina is following Dr Fox's aftercare program. Fox is retired from > doing open bypass surgery, so when you go to him you end up having > bypass or band surgery with a different Dr at his clinic, but he also > has a working relationship with Rumbaut and for a large fee, he sends > his patients willing to be banded in mexico, to rumbaut. (personally, i > said to heck with that fee and called rumbaut and made my own appt for > banding 2 yrs ago) i never went back to fox.....i had no interest in > following his bypass aftercare program, and instead chose to follow > rumbauts aftercare for the banded. > Fox likes all his clients to lose very quickly and thats why he makes > everyone who goes thru his office follow his bypass instructions i.e. no > milk, etc. > too strict....not neccessary... > > Sandy Landry > Landco@W... > Lynnwood, Wa. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 25, 2005 Report Share Posted October 25, 2005 I don't know about the rest of you, but I don't get flyer attachments, so if the course information can be posted directly, that would be very helpful. That aside, I would like to add to the testimonials. I was present when Svetlana and Pietr worked with Lily for the second time this summer here in Austin. Svetlana and Pietr were in town to do a couple of workshops I was sponsoring and Lily's parents drove her down from Arkansas. I drove S & P to meet Lily, her parents, and a gentleman who had arranged their lodging at the golf club here in the Austin area. I heard Lily's parents give their still enthusiastic testimonial in their own words from their own mouths, and they said that no one can believe or understand why their daughter is so far ahead of the curve than all the other kids with similar situations in their support group. I personally watched as Lily practiced a staircase over and over again. Before working with P & S, she slithered down partially on her rear end, partially twisting, always to the same side, clearly not moving normally. By mid morning, Lily was moving up and down the stairs bilaterally in a very typical infant way. At the end of a long day, Lily started laughing. She explored every conceivable type and pitch of laugh. I only wish I had a video of the 6 adults present and Lily, because we couldn't help eventually laughing with her, and we hooted for probably close to a half hour. Additionally, since I also use Svetlana's work, I would like to share some of those experiences: 1) an autistic spectrum girl who tested 20 points higher in spring of 2004 than she had in the spring of 2001, after experiencing Brain Gym and Neurokinesiology. She learned to tie her shoes, and many other practical activities, including getting started on a bike, but not being able to steer it. Since her appointments with Svetlana this summer , she is now actually riding her bike. 2) a mildly CP boy who also takes 2 medications for ADD His mother has send three communications regarding his marked improvement in speech , behavior (school evaluations)and reading. I could go on and on..... EduK and NeuroK are so rich !! Sharon Heller Quote Link to comment Share on other sites More sharing options...
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