Guest guest Posted September 20, 2000 Report Share Posted September 20, 2000 I changed from BodyFlex to LifeLift at the recommendation of my good friend Hedra. We had heard of it from the BodyFlex list for several years and finally she broke down and bought it. I was hesitant because I didn't want to add yet another workout video to my collection if it was just more of the same. After she got it she assured me that it was the same, yet much different and I should get it for myself. Darlene had also been recommending the tape to the list for quite some time, so, that is how I first got it. My first two weeks on BodyFlex I lost 8 inches. I kept those inches off. Two years later after breathing for those two years, not consistently but pretty good, I tried LifeLift. After just three days I measured and had lost 6 inches! AND some weight!!! I never lost a single pound using BodyFlex. So, that is what keeps me doing it. I know it works for me, if....I just do it. :-) ~Karma karma@...http://loaves-n-fishes.com more questions hi again1. I notice that several of you started off with the BF program thenswitched to the LL program. WHAT made you investigate further when the BFprogram *turned you off* and find the LL program? I would have thought youmight just stop even doing anything like this.2. oil swishing> If you cannot find the brands listed in the FAQ will anybrand do? waht about the castor oil? the sound of it just makes me cringe,,just what do these oils taste like? I dont feel like gagging when I do this.3. does it matter when you do the LL breaths? is there any gain or advantageto do as many as possible in a row? or can they be spread out all the day ,like a couple an hour?Marie,, > knows I will come up with more questions as I go alonghttp://themail.com/ref.htm?ref=1227417 *** This free e-mail service pays money for messages that are read! This list sponsored by:http://www.lifelift.comhttp://www.angelmagic.comhttp://loaves-n-fishes.comhttp://themail.com/ref.htm?ref=1227417 http://www.amazon.com/exec/obidos/redirect-home/karmasrecommerea/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 20, 2000 Report Share Posted September 20, 2000 Hi Marie, I'm one of those people who made the switch from BF. I had actually heard of LL when I first started with BF, but I was always under the impression that the breathing had to be done with force and intensity to see results. I did see results with BF, but I was starting to dread doing the breathing. I would litterally have to sit there for a couple of minutes and convince myself to " just do it " and it will be over with in 15 minutes. After 3 months of this, I just wasn't enjoying BF, and so I went to le's LL website and absorbed as much info as I could. It wasn't until I read what she said about the breathing that I started do understand that deep breathing could in fact be relaxing and enjoyable. I ordered the original tape plus the 2 twenty min videos. I honestly couldn't believe the difference it made being gentle with the breath. I love doing LL breathing and I often do breaths throughout the day on top of the 20 min workout. Although I did see results with BF, the results I've gotten with LL have been more dramatic and faster ...like I'm sure you will hear from others who have switched. As for oil swishing, I believe as long as the oil is " cold-pressed " then it doesn't matter what brand it is. I have yet to try the castor oil myself, so I can't comment on the taste ...but for some reason I picture a dark, thick oil (I really have no idea what it looks like either). I've been using the peanut oil, and I don't find it offensive at all, but when my husband tried it, he got very dramatic with the gagging and all ...I'm not sure he will try it (peanut oil) again, although he admits it helped with his sore throat! I believe it is recommended that you 40 consecutive breaths in a row for weight reduction, but it's always beneficial to add extra breaths throughout the day. If you can't do 40 breaths all at one time, then do as many as you can and you will still be doing your body some good. I usually do at least a 20 minute routine first thing in the morning, and then add extra breaths (without positions) while watching TV, folding laundry, or sitting here at my computer. The extra breaths I do throughout the day is when I really focus on the tummy tuck and really feeling it in the ab muscles ...this is producing better results for me than all the floor ab positions I was doing with BF. You really can experiment with the program to find what works best for you. Hope this helps, ë Tara > hi again > > 1. I notice that several of you started off with the BF program then > switched to the LL program. WHAT made you investigate further when the BF > program *turned you off* and find the LL program? I would have thought you > might just stop even doing anything like this. > > 2. oil swishing> If you cannot find the brands listed in the FAQ will any > brand do? waht about the castor oil? the sound of it just makes me cringe,, > just what do these oils taste like? I dont feel like gagging when I do this. > > 3. does it matter when you do the LL breaths? is there any gain or advantage > to do as many as possible in a row? or can they be spread out all the day , > like a couple an hour? > > Marie,, > knows I will come up with more questions as I go along Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2000 Report Share Posted September 21, 2000 Hi Marie, Answer to Question #1-BF did not turn me off. I did it for 3 1/2 months. Also was interested in Oxycise (for a change) did it, then quit BF'ing. Started back doing BF (because it works, but you have to keep up with it), but in the meantime, I got LifeLift and started using it. Like how I felt with it AND my results were much faster than BF...hense, I do LL now. Answer to Question#2--Don't know yet haven't tried it, but bought the " Oils That Heal " book. Talks about " castor oil " and such. Maybe I'll have an answer for you when my book arrives. Answer to Question #3--As long as you do 40 breaths you are going to reap rewards. BUT I think 40 during one sitting helps, the breathing throughout the day won't hurt either. I call those " extras " ... Does that help? Hope so. Tig > hi again > > 1. I notice that several of you started off with the BF program then > switched to the LL program. WHAT made you investigate further when the BF > program *turned you off* and find the LL program? I would have thought you > might just stop even doing anything like this. > > 2. oil swishing> If you cannot find the brands listed in the FAQ will any > brand do? waht about the castor oil? the sound of it just makes me cringe,, > just what do these oils taste like? I dont feel like gagging when I do this. > > 3. does it matter when you do the LL breaths? is there any gain or advantage > to do as many as possible in a row? or can they be spread out all the day , > like a couple an hour? > > Marie,, > knows I will come up with more questions as I go along Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2000 Report Share Posted September 21, 2000 My sentiments exactly Karma, I didn't lose a pound with BF, but I lost 5lbs with LL and then some. I lost in 1 week with LL what it took 4 weeks (a month!)with BF. So, it was easy to decide which breathing program I enjoyed most. Also, I want to add, today I feel lighter than ever and my jeans are getting looser! Cool! Happy camper as usual, Tig > I changed from BodyFlex to LifeLift at the recommendation of my good friend Hedra. We had heard of it from the BodyFlex list for several years and finally she broke down and bought it. I was hesitant because I didn't want to add yet another workout video to my collection if it was just more of the same. After she got it she assured me that it was the same, yet much different and I should get it for myself. Darlene had also been recommending the tape to the list for quite some time, so, that is how I first got it. > > My first two weeks on BodyFlex I lost 8 inches. I kept those inches off. Two years later after breathing for those two years, not consistently but pretty good, I tried LifeLift. After just three days I measured and had lost 6 inches! AND some weight!!! I never lost a single pound using BodyFlex. So, that is what keeps me doing it. I know it works for me, if....I just do it. :-) > ~Karma > karma@l... > http://loaves-n-fishes.com > more questions > > > > > My Groups | LifeLift Main Page | Start a new group! > > > hi again > > 1. I notice that several of you started off with the BF program then > switched to the LL program. WHAT made you investigate further when the BF > program *turned you off* and find the LL program? I would have thought you > might just stop even doing anything like this. > > 2. oil swishing> If you cannot find the brands listed in the FAQ will any > brand do? waht about the castor oil? the sound of it just makes me cringe,, > just what do these oils taste like? I dont feel like gagging when I do this. > > 3. does it matter when you do the LL breaths? is there any gain or advantage > to do as many as possible in a row? or can they be spread out all the day , > like a couple an hour? > > Marie,, > knows I will come up with more questions as I go along > > > http://themail.com/ref.htm?ref=1227417 *** This free e-mail service pays money for messages that are read! > > This list sponsored by: > http://www.lifelift.com > http://www.angelmagic.com > http://loaves-n-fishes.com > http://themail.com/ref.htm?ref=1227417 > http://www.amazon.com/exec/obidos/redirect-home/karmasrecommerea/ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2001 Report Share Posted June 20, 2001 In a message dated 6/20/01 9:15:53 PM Pacific Daylight Time, coffey@... writes: The interferon and riboferon (I don't know the names exactly) treatments, are they bad? I have been on interferon and ribivirin as has a lot of people here. This forum also has spouses of people with Hep-C How hard is it on a person? It varies from person to person. I personally hated it, but would NEVER suggest to anyone, not to try it if the Dr. feels that you are a candidate for the treatment. I have a friend that the treatment did not bother her at all. I think a lot of it is your over-all health at the time of treatment. Will I still be able to go to work? Yes Also is it true that you could have this for years and your liver count not be high? Yes this is unfortunately true. I had it for almost 20 yrs before I found out. I was told just Friday evening by the doctor's receptionist that I have Hepatitis C. So far I had a blood test for a check up and my liver count was high. They ordered a hepatitis screening and I came back positive for C. Yesterday I had another blood test done that has to be sent off that counts some sort of numbers. The 2nd test is a called a PCR which measures the amount of active virus. Tomorrow I go for a liver ultrasound. Next week I see a gastrointerologist. Does this sound like the normal steps? Yes What's next? You could have a biopsy done and a Genotype test done. Do you have any advise for me? Yes, learn as much as you can about this disease. As you educate yourself, you might find that you become frustrated with the Dr's knowledge or sometimes "lack of" . This is not always the case either but it can be. The main thing is to take good care of yourself. If you are a drinker, quit. Learn about what is liver friendly and what is not. There are a lot of very good sites with tons of info on this subject. Stay positive, even if you have to run in circles to do so. I am learning that after all of this time with treatment and now off for 1 1/2 yrs that there most definately is life after Hep-C. If you have not been vaccinated, there is a vaccine for Hep-A and I think Hep-B also. Since I was a "carrier" of Hep-B and never sick from it (that I knew of) I didn't have to get that vaccine. As you can guess I'm pretty scared. It'll be ok and it is perfectly normal to be scared. So was I and everyone else. You are not alone BC. We are all here for you. BTW, my name is Janet I don't post a lot but I'm always around. Take good care of yourself and try not to worry. Janet Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2001 Report Share Posted June 21, 2001 Do you have any advise for me? As you can guess I'm pretty scared. Of course you're scared, bc. But it's not a death sentence. There are others on this list who know a lot more than I, but I'll tell you what I know. My husband (well, we're separated) has probably had the virus since the 1970s, and he's 50 now. He's also an alcoholic, so when his liver functions were high, we attributed it to alcohol. But even when he abstained they were out of the normal range, so he was tested specifically for Hep C--and it was positive. Other than hearing the results from the receptionist (my husband's doctor called him personally in the evening), it sounds like the appropriate path (gastro). He/she will probably want you to have a liver biopsy to see if there is any cirrhosis (scarring/damage) yet. This involves, usually as an out-patient, inserting a long needle into the liver and extracting a very tiny sliver of the organ. Then you lay perfectly still for several hours with weight on the entrance point to prevent bleeding. There are some on this list who have had bad experiences with this procedure; others didn't. For my husband, it was a breeze. He has some cirrhosis, but elected not to try the interferon/ribovarin. The statistics just weren't convincing that it was worth the side effects that some experience (sick as a dog and depression, big time). You need to be very cautious about the medications you take, because many are not liver friendly. As the pharmacist. And don't drink. Alcohol exacerbates the problem. Every time my husband would fall off the wagon, he would be sick for weeks ) If you're interested in alternative treatments, a good book is The Green Pharmacy, by Duke (can't remember his first name). He recommends taking Milk Thistle and also eating artichokes (same family) to cleanse the liver. A good place to learn more is the National Institutes of Health web page, where you can find layperson and technical fact sheets. It's www.nih.gov, and then select the Institute for Digestive Diseases (NIDDK or something like that). By the way, I was tested myself last spring and do not have it. We never used any kind of barrier protection, so I believe it's not easily contracted. Of course we didn't share toothbrushes or razors, where blood could be transferred. Write any time you want. Tree Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 22, 2001 Report Share Posted June 22, 2001 thank you for the info on alternative treatment. Here in Hawaii, I suppose elsewhere too, the Alt. methods to address this disease is very much accepted and appreciated so A Big MAHALOS to you! ( that means thank you)----Ted Re: more questions Do you have any advise for me? As you can guess I'm pretty scared. Of course you're scared, bc. But it's not a death sentence. There are others on this list who know a lot more than I, but I'll tell you what I know. My husband (well, we're separated) has probably had the virus since the 1970s, and he's 50 now. He's also an alcoholic, so when his liver functions were high, we attributed it to alcohol. But even when he abstained they were out of the normal range, so he was tested specifically for Hep C--and it was positive. Other than hearing the results from the receptionist (my husband's doctor called him personally in the evening), it sounds like the appropriate path (gastro). He/she will probably want you to have a liver biopsy to see if there is any cirrhosis (scarring/damage) yet. This involves, usually as an out-patient, inserting a long needle into the liver and extracting a very tiny sliver of the organ. Then you lay perfectly still for several hours with weight on the entrance point to prevent bleeding. There are some on this list who have had bad experiences with this procedure; others didn't. For my husband, it was a breeze. He has some cirrhosis, but elected not to try the interferon/ribovarin. The statistics just weren't convincing that it was worth the side effects that some experience (sick as a dog and depression, big time). You need to be very cautious about the medications you take, because many are not liver friendly. As the pharmacist. And don't drink. Alcohol exacerbates the problem. Every time my husband would fall off the wagon, he would be sick for weeks ) If you're interested in alternative treatments, a good book is The Green Pharmacy, by Duke (can't remember his first name). He recommends taking Milk Thistle and also eating artichokes (same family) to cleanse the liver. A good place to learn more is the National Institutes of Health web page, where you can find layperson and technical fact sheets. It's www.nih.gov, and then select the Institute for Digestive Diseases (NIDDK or something like that). By the way, I was tested myself last spring and do not have it. We never used any kind of barrier protection, so I believe it's not easily contracted. Of course we didn't share toothbrushes or razors, where blood could be transferred. Write any time you want. Tree Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2001 Report Share Posted August 18, 2001 hello welcome !!! carragene is not good för us. bye irene more questions Right I now have two books, 'The Eat Right Diet' which is a UK version of the 'Eat Right 4 Your Type' by D'Adamo (turns out one of my roommates bought it a few years back) and 'Cook Right 4 Your Type'. I've read both and have a few more questions. 1) I bought some Rice Milk today and after checking CR4YT I realised its no good (at least that brand) because it has safflower oil in it. my question is if I were to use this brand, is the amount of safflower oil in it really that significant and would it really be that much of an issue? 2) I know I'm allowed Cranberries, but does that also include Ocean Spray type Cranberry sauce/jelly? 3) Gravy! Are there any UK er4yt-ers that can recommemend a pre- prepared (just add water) gravy that would be okay? 4) Whilst shopping today I also bought what I though was soya milk (bought some the other day and thought it was disgusting, but figured different brands might vary) anyway, turns out it was Soya dream, an alternative to single cream. Its quite nice (got a creamy texture/taste to it) and I would like to use it as part of my diet, but I'm not sure whether the ingredients are okay. Checking the packing its made of water, hulled soya beans, veg oil, fructose syrup, emulsifer, stabilisers, xanthan gum, carrogeenan, sea salt and natural tocopherol. Thanks Clive Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2001 Report Share Posted August 20, 2001 Clive - The fructose syrup is probably corn syrup and I don't think we're allowed gums such as xanthan gum. Kate ----Original Message Follows---- From: clivegriffiths@... Reply- Subject: more questions Date: Sat, 18 Aug 2001 16:15:35 -0000 Right I now have two books, 'The Eat Right Diet' which is a UK version of the 'Eat Right 4 Your Type' by D'Adamo (turns out one of my roommates bought it a few years back) and 'Cook Right 4 Your Type'. I've read both and have a few more questions. 1) I bought some Rice Milk today and after checking CR4YT I realised its no good (at least that brand) because it has safflower oil in it. my question is if I were to use this brand, is the amount of safflower oil in it really that significant and would it really be that much of an issue? 2) I know I'm allowed Cranberries, but does that also include Ocean Spray type Cranberry sauce/jelly? 3) Gravy! Are there any UK er4yt-ers that can recommemend a pre- prepared (just add water) gravy that would be okay? 4) Whilst shopping today I also bought what I though was soya milk (bought some the other day and thought it was disgusting, but figured different brands might vary) anyway, turns out it was Soya dream, an alternative to single cream. Its quite nice (got a creamy texture/taste to it) and I would like to use it as part of my diet, but I'm not sure whether the ingredients are okay. Checking the packing its made of water, hulled soya beans, veg oil, fructose syrup, emulsifer, stabilisers, xanthan gum, carrogeenan, sea salt and natural tocopherol. Thanks Clive _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com/intl.asp Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2003 Report Share Posted January 5, 2003 In a message dated 1/5/03 12:47:56 AM Eastern Standard Time, dsherm112@... writes: > What type of changes show up on X-rays for AS? 1.) Anteroposterior Pelvis XRay: Usually sufficient as only XRay confirmation Reveals Bilateral and symmetric sacroiliitis 2.) Spine XRay other findings: Bony sclerosis appears as squaring of vertebrae Syndesmophytes between vertebrae Classic " Bamboo " spine (<10%) appearance 3.) Special XRay views: Ferguson's View (specialized sacroiliac view) 4.) Other studies with limited indications: Bone Scan CT or MRI spine Besides these XRay findings, I remember something like *joint space narrowing*, *bony erosions* and the word *fluffy* on my own shoulder chart. Usually, AS starts in the spine, SI region. It can start in other joints, but this is more rare. What you describe about your shoulder sounds like it is age related...quote: " I have degenerative disks and osteoporosis type changes .. " I believe many older people have degenerative and osteoporosis disease (my own husband has these findings on his shoulder XRays). The person who read your XRay would have mentioned any AS type findings and your doctor would have given you that DX. Hope this helps. Best regards, Connie (granny) AS/IBD/chronic iritis/glaucoma Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 14, 2003 Report Share Posted November 14, 2003 Evel, I have to agree with Dora about not using the number of implants done at a center as an important consideration when choosing. I was only # 4 or 5 at Walter Army Med. in D.C. They have had marvelous results so far. The surgeon is great and the audis are doing a wonderful job also. Even tho it is a fairly new CI program, there is alot of drive and motivation to get the best results possible. LouAnne War Implanted 11-06-02 Hook-up 12-10-02 Message: 2 > Date: Thu, 13 Nov 2003 08:38:22 -0600 > From: " Dora Weber " <dora_weber@...> > Subject: More questions > > Hi Evel > > I don't think the number of implants done at a center is the most important consideration..afterall ,even the largest centers,started with that first patient.I think the reputation of the center and the skill of the surgeon and the knowledge of the Audiologists are most important. > > > Dora Weber > Nucleus Volunteer Advocate > dora_weber@... > > Bilateral > N22-96 > N24C-01 > Cochlear Otosclerosis > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2004 Report Share Posted January 3, 2004 More Questions > > What should I do now? See a rheumatologist or orthopedist? Either one, but you may have more luck looking for a doctor and not a speciality if you know what I mean. You might even try a pain specialist, especially if they work a lot with knees. > > Do any of you get better during the summertime when the weather is warmer? I don't, but it does seem to hurt a lot more when a weather front is moving in. Mike Bernhardt Park City MT Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 3, 2004 Report Share Posted January 3, 2004 Have you had an MRI? That would be better for showing CP or anything else wrong with your knee. Do you sleep with your knees bent? If you have CP, that could irritate it at night. However, the fact that you can walk around & do whatever else you do during the day & not have pain is mystifying. I'd recommend an orthopedic surgeon & ask for an MRI. Ann More Questions Is Chondromalacia only related to the knees? Can someone help me, who has perhaps gone down the same road? Three mos. ago I developed bad pain in my right leg. It would wake me up in the early morning hours, but during the day, it was perfect. I have had x-rays which should slight arthritis, and was diag. with CP of the right knee. Dr. put me on two Aleve before bedtime. No help. Back to Dr. in two weeks as recommended and given 200 mg Celebrex (take one pill before bedtime). No help. Called Dr. and said to take one 200 mg Celebrex when I get up and one when I go to bed. No help. Then I added to this cocktail, one Ultracet at bedtime, which seems to help alot, but my doc only gave me 6 pills and is out of town for another week. I still hurt, and am only on Celebrex now. What should I do now? See a rheumatologist or orthopedist? Do any of you get better during the summertime when the weather is warmer? Thanks in advance. Kate ------------------------------------------------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2004 Report Share Posted June 29, 2004 CK wrote: >Also kelp. It seems to be most useful cut up and sprinkled on salads. Is this how you use it? I sprinkle it on salads or use in soups. >And flax oil. Is it used as a supplement, or something to cook in? A " supplement " in that it has essential fatty acids not found in most foods. I never heat it on the stove, I put it on stuff cold from the refrigerator, like say I made a sweet potatoe and instead of butter when the potato cools down I will sprinkle kelp and flax oil on it. By the way, the only brand of flax oil I have found that I can get down is Barrican's -- I get it at Wild Oats in refrigerated section. I cannot tell you how many I have bought over the years and threw them out after one spoonful. This stuff isn't half bad :+) ^. .^ ~ " There are many paths to enlightenment. Be sure to take one with a heart. " ~ Lao Tzu ~ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2004 Report Share Posted June 29, 2004 Return the liquid - clearly states that only the capsule version should be used. Yes, cut up and sprinkle. Flax - only as a supplement. Never heat it. ABO Specifics Inc. - http://www.foodforyourblood.com More questions Hi everyone, I bought a few things today and need to know how to use them. I bought a tincture of bladderwrack. It says to add 30-40 drops to a small amount of warm water, daily. Is this what you've all used? Can it be added to tea? Does it have a taste? Also kelp. It seems to be most useful cut up and sprinkled on salads. Is this how you use it? And flax oil. Is it used as a supplement, or something to cook in? Thanks! Carolyn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2004 Report Share Posted June 29, 2004 Okay, thanks. So what is the brand name of the capsule? Is it under some other name than bladderwrack? -- because I didn't see any capsule supplements named bladderwrack, and when I asked, the clerk at the health food store got me only the liquid (and she looked near the kelp too, but there was nothing there). Thanks, Carolyn > Return the liquid - clearly states that only the capsule version > should be used. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2004 Report Share Posted June 29, 2004 You can get it from me if you'd like. Item #1002 ABO Specifics Inc. - http://www.foodforyourblood.com Re: More questions Okay, thanks. So what is the brand name of the capsule? Is it under some other name than bladderwrack? -- because I didn't see any capsule supplements named bladderwrack, and when I asked, the clerk at the health food store got me only the liquid (and she looked near the kelp too, but there was nothing there). Thanks, Carolyn > Return the liquid - clearly states that only the capsule version > should be used. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 30, 2004 Report Share Posted June 30, 2004 Thanks. I'll ask my nutrionist (the one who pointed me to this meal plan) what she thinks. By the way, I did return the liquid. Carolyn > You can get it from me if you'd like. Item #1002 > > ABO Specifics Inc. - http://www.foodforyourblood.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2005 Report Share Posted August 11, 2005 : gave you a very good answer. As for how long implants last, I have had my Nucleus 22 implant for over 17 years and it is working great. Implanted December 1988, Activated January 1989 Legally blind most of my life Totally deaf for part of my life Nan Rosen _www.rosetwig.com_ (http://www.rosetwig.com/) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2005 Report Share Posted August 11, 2005 Hi, (turn off the caps lock - it's considered shouting) The implant hasa more or less infinite lifetime. If it doesn't fail, it will outlast you. Depending on the brand and model, you may use button cells (675 size) for the behind the ear models, or AA or AAA size for the body worn porcessors. The batteries in the BWP may be rechargable. Life of the batteries is largely dependant on the programming that the processor runs. For example my BTE processor uses three hi power 675s every two days. I purchase them in packs of 60 from the centre that did the CI. Cost to me is $60 per box, but I did the first box with the CI. Again depending on where the CI is done, you may get a larger free supply. However, I consider that $1 per day for hearing is cheap at the price Returns for adjustments are quite frequent in the early days and taper off after six months or so. Again, it depends on how well the CI works for you. NZ > MORE QUESTIONS > > > CAN ANYONE TELL ME HOW LONG THESE IMPLANTS LAST. WHAT THEY > RUN ON, LIKE > WHAT KIND OF BATTERIES. HOW DO I PURCHASE THE BATTERIES. WHAT IS THE > COST? HOW OFTEN DO YOU RETURN TO THE DOCTOR TO HAVE ADJUSTMENTS? > MUCH THANKS > LINDA > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2005 Report Share Posted August 12, 2005 > Hi, > (turn off the caps lock - it's considered shouting) > The implant hasa more or less infinite lifetime. If it doesn't fail, it will > outlast you. > Depending on the brand and model, you may use button cells (675 size) for > the behind the ear models, or AA or AAA size for the body worn porcessors. > The batteries in the BWP may be rechargable. > Life of the batteries is largely dependant on the programming that the > processor runs. For example my BTE processor uses three hi power 675s every > two days. > I purchase them in packs of 60 from the centre that did the CI. Cost to me > is $60 per box, but I did the first box with the CI. Again depending on > where the CI is done, you may get a larger free supply. However, I consider > that $1 per day for hearing is cheap at the price > Returns for adjustments are quite frequent in the early days and taper off > after six months or so. Again, it depends on how well the CI works for you. > > > NZ > > > > MORE QUESTIONS > > > > > > CAN ANYONE TELL ME HOW LONG THESE IMPLANTS LAST. WHAT THEY > > RUN ON, LIKE > > WHAT KIND OF BATTERIES. HOW DO I PURCHASE THE BATTERIES. WHAT IS THE > > COST? HOW OFTEN DO YOU RETURN TO THE DOCTOR TO HAVE ADJUSTMENTS? > > MUCH THANKS > > LINDA > > Sorry did not know that was considered shouting.. Will not do that again.. Much thanks > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2005 Report Share Posted August 12, 2005 > Hi, > (turn off the caps lock - it's considered shouting) > The implant hasa more or less infinite lifetime. If it doesn't fail, it will > outlast you. > Depending on the brand and model, you may use button cells (675 size) for > the behind the ear models, or AA or AAA size for the body worn porcessors. > The batteries in the BWP may be rechargable. > Life of the batteries is largely dependant on the programming that the > processor runs. For example my BTE processor uses three hi power 675s every > two days. > I purchase them in packs of 60 from the centre that did the CI. Cost to me > is $60 per box, but I did the first box with the CI. Again depending on > where the CI is done, you may get a larger free supply. However, I consider > that $1 per day for hearing is cheap at the price > Returns for adjustments are quite frequent in the early days and taper off > after six months or so. Again, it depends on how well the CI works for you. > > > NZ > > > > MORE QUESTIONS > > > > > > CAN ANYONE TELL ME HOW LONG THESE IMPLANTS LAST. WHAT THEY > > RUN ON, LIKE > > WHAT KIND OF BATTERIES. HOW DO I PURCHASE THE BATTERIES. WHAT IS THE > > COST? HOW OFTEN DO YOU RETURN TO THE DOCTOR TO HAVE ADJUSTMENTS? > > MUCH THANKS > > LINDA > > Sorry did not know that was considered shouting.. Will not do that again.. Much thanks > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2005 Report Share Posted August 12, 2005 > : > > gave you a very good answer. As for how long implants last, I have > had my Nucleus 22 implant for over 17 years and it is working great. > > > Implanted December 1988, Activated January 1989 > Legally blind most of my life > Totally deaf for part of my life > > Nan Rosen > _www.rosetwig.com_ (http://www.rosetwig.com/) > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2005 Report Share Posted August 12, 2005 Hi and all, Yes, I agree regarding the implant probably " outlasting you " . August 7th, I just celebrated my 21st birthday as a CI user! I've never had to have the internal implant replaced, although I have had several upgrades to my external components. C. N22 21 years! -- MORE QUESTIONS > > > CAN ANYONE TELL ME HOW LONG THESE IMPLANTS LAST. WHAT THEY > RUN ON, LIKE > WHAT KIND OF BATTERIES. HOW DO I PURCHASE THE BATTERIES. WHAT IS THE > COST? HOW OFTEN DO YOU RETURN TO THE DOCTOR TO HAVE ADJUSTMENTS? > MUCH THANKS > LINDA > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2005 Report Share Posted August 12, 2005 All, Interesting thread here. While I well believe that to be the case, I was told that given the advances (and my relatively " young " age - late 40's) they were making with these CIs that I was probably would have a new implant maybe 20 years from now. Not so much because it doesn't work or become " obsolete " per se but because they will be so much better by then. One operation was enough for me (assuming I never have to replace it because it doesn't work anymore) but I think I would be willing to get an enhanced version that let's me hear more like the normal hearing folks do...umm definitely food for thought... In meanwhile, I will pleasantly enjoy my new CI for some years to come. Dale <cicampbell@...> wrote: Hi and all, Yes, I agree regarding the implant probably " outlasting you " . August 7th, I just celebrated my 21st birthday as a CI user! I've never had to have the internal implant replaced, although I have had several upgrades to my external components. C. N22 21 years! -- MORE QUESTIONS > > > CAN ANYONE TELL ME HOW LONG THESE IMPLANTS LAST. WHAT THEY > RUN ON, LIKE > WHAT KIND OF BATTERIES. HOW DO I PURCHASE THE BATTERIES. WHAT IS THE > COST? HOW OFTEN DO YOU RETURN TO THE DOCTOR TO HAVE ADJUSTMENTS? > MUCH THANKS > LINDA > > Quote Link to comment Share on other sites More sharing options...
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