Guest guest Posted January 28, 2006 Report Share Posted January 28, 2006 In a message dated 1/9/2006 6:11:55 P.M. Central Standard Time, theskweez2001@... writes: Hello from ArizonaMy name is and I am 43 and on Feb 2 I will be having my rightknee replaced and then in about 4-5 months I will have the other onereplaced. I also have had 2 back surgeries, one being a fusion in2001. I live on methadone and various other drugs for pain, bloodpressure, depression and anxiety meds as well as drugs to keep myulcers from bleeding. I am a single mom of an amazing wonderfullyfunny and bright 8 year old girl. I am pretty nervous about thissurgery only because my back is so bad, I know the therapy will betricky but after 30 years in pain with my knees I am looking forwardto a healthier me! What I am hoping to find out is what do I need todo to be ready and prepare myself as well as my home and family to beready? Can someone help and give me some insite? I appreciate anyfeedback and God Bless! in AZ Hi , are you getting ready for your surgery? I went to Wal Mart and bought some easy to eat foods and stocked up on dog/cat food, and feed for my goats, and chickens. Just wondered how you were holding up. I'm very nervous, but the worst part to me is fasting. Really, the pain isn't fun. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 31, 2006 Report Share Posted January 31, 2006 Hi , I am new to this board as well, I was wondering how was it decided for you to have your second tkr in four to five months? Is that the regular routine when both need to be done? Val > > > In a message dated 1/9/2006 6:11:55 P.M. Central Standard Time, > theskweez2001@y... writes: > > Hello from Arizona > My name is and I am 43 and on Feb 2 I will be having my right > knee replaced and then in about 4-5 months I will have the other one > replaced. I also have had 2 back surgeries, one being a fusion in > 2001. I live on methadone and various other drugs for pain, blood > pressure, depression and anxiety meds as well as drugs to keep my > ulcers from bleeding. I am a single mom of an amazing wonderfully > funny and bright 8 year old girl. I am pretty nervous about this > surgery only because my back is so bad, I know the therapy will be > tricky but after 30 years in pain with my knees I am looking forward > to a healthier me! What I am hoping to find out is what do I need to > do to be ready and prepare myself as well as my home and family to be > ready? Can someone help and give me some insite? I appreciate any > feedback and God Bless! > > in AZ > > > > Hi , are you getting ready for your surgery? I went to Wal Mart and > bought some easy to eat foods and stocked up on dog/cat food, and feed for my > goats, and chickens. Just wondered how you were holding up. I'm very > nervous, but the worst part to me is fasting. Really, the pain isn't fun. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 7, 2006 Report Share Posted February 7, 2006 Hi Lynn, You may remember me from another list we are on together. Welcome! <smile> Your speech discrimination scores sound like you are *so* close to being a candidate. Have you thought about attending a different CI center for an evaluation? I know some CI centers are more lenient than others in terms of their guidelines. While 50-60% is the standard (for the best ear), I'm sure there have been CI candidates who have fallen a couple percentage points above the FDA criteria and were still implanted. I'm not an audiologist, but based on your scores, it definitely looks like you are a CI candidate. Medicare and Medicaid may have lower percentages, but if I remember correctly, that percentage was raised sometime last year from 30% to 40%. If you don't mind my asking, do you have an HMO, private insurance or Medicare/Medicaid? That of course may also influence your candidacy since some insurance carriers accept higher speech discrimination score percentages than others. Sorry I can't answer your questions about the Freedom just yet. However, I was able to see the Freedom and noticed that it is a little bigger in size than the 3G, but has a more streamlined fit to the ear. Hope this helps! I wish you all the best during your testing in July! Left ear - Nucleus 24 Contour Advance with 3G Implanted: 12/22/04 Activated: 1/18/05 Right ear - Nucleus Freedom Implanted: 2/1/06 Activation date: 3/1/06 Deafblind/Postlingual Severe-profound hearing loss since 1995 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2006 Report Share Posted February 8, 2006 Lynn, Hi and welcome to the group. My first thought was " well, she could just not understand some of the words and her speech discrimination score would be low enough. " But I don't know your situation or if anyone else has done that or what. It is interesting to read that knew that some CI centers and insurance companies have different standards. I had assumed they would all be the same. I'm now completely deaf after being severely HI since birth. I lost the residual hearing I had right after Christmas. I go Friday to be evaluated at Charlotte, NC center and then to Columbia, SC center on Tuesday. I am comparing them on three criteria: how I like/respect the audies since I'll be spending a lot of time with them, experience of the surgeon with CI surgery and which one can get me a CI first. in SC Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2006 Report Share Posted February 8, 2006 Hi , I thought you were on this list, also. We are on several mail lists together. I haven't thought of going to another CI center. My " CI Center " is a doctor's office in Birmingham. I am seeing a doctor who was recommended to me, and he is the one who really started talking to me about getting a CI. I like him, and really want to stay with him. The doctor wants very much to implant me, but I don't want to get stuck with the bill. I have private Blue Cross insurance (small group plan), so have to abide by their guidelines. The doctor says they won't give a pre-approval letter, other than to say that a CI is a covered service. He says they won't specifically approve a patient without lots of caveats that allow them to still deny coverage, so he has found it to be a waste of time to even bother with it. He says Blue Cross has basically agreed to cover the implant if you are at the 50% or less threshold, and even then, they have given some patients a hard time. He said he recently implanted one man with zero speech discrimination, and after surgery, the patient got a huge bill from the hospital. The doctor says Blue Cross will end up paying this, but he is having to help this patient force them to pay. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2006 Report Share Posted February 8, 2006 Hi Lynn, Welcome. I have the Freedom sitting on my left ear and the 3G on my right ear. I removed both of them and rested them one on top of the other to compare them physically. The Freedom is bigger, I am guessing about a 1/4 inch in length and width. The advantage of the Freedom over the 3G is that it is digital and offers more than the 3g. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2006 Report Share Posted February 8, 2006 said: Hi and welcome to the group. My first thought was " well, she could just not understand some of the words and her speech discrimination score would be low enough. " But I don't know your situation or if anyone else has done that or what. It is interesting to read that knew that some CI centers and insurance companies have different standards. I had assumed they would all be the same. , My doctor told me that I was too astute as a hearing impaired person. He felt that I had gotten too good at guessing and filling in the blanks, and for this reason scored just a little too high on the test. I admit, I did my best on the test. I probably should not have concentrated so hard. Only a few less words answered correctly on the sentence tests, and I would have qualified. Maybe I wasn't as ready for the CI then as I thought. It may be for the best to wait until July anyway. The timing may be a little better then, and I will have had a chance to go to the HLAA/SHHH convention. I have never met anyone " in person " who had a CI, and I would really like to. The mail lists are wonderful, but there is nothing like meeting and interacting with someone in person. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2006 Report Share Posted February 8, 2006 " " <wdywms@...> said: Hi Lynn, Welcome. I have the Freedom sitting on my left ear and the 3G on my right ear. I removed both of them and rested them one on top of the other to compare them physically. The Freedom is bigger, I am guessing about a 1/4 inch in length and width. The advantage of the Freedom over the 3G is that it is digital and offers more than the 3g. Hi , The size of the Freedom doesn't sound so bad to me. I had someone tell me that it was MUCH larger than the 3G, so I feel much better about the size now. Some others have written me off list and told me that it was very light and they didn't even know they were wearing it. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2006 Report Share Posted February 11, 2006 Welcome to the boards Wanda.... I'm in Kentucky myself. Hope how soon you can get things scheduled after making the best decision for your case needs. Long recoverying are hard... I've had a few myself~ but remember to think positive~ all things happen for a reason & have purpose... I'm sure you'll pull through the struggles and hopefully have a better quality of life when all is said & done. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 11, 2006 Report Share Posted February 11, 2006 Hi Wanda, I just wanted to welcome you to this group and wish you luck and a speedy recovery. Well you have a nice day . Susie -------------- Original message -------------- From: "Wanda" <granny_6@...> Hello My name is Wanda I live in Ohio I am in the process of scheduling surgeries and thought I would join this list I am having an osteotomy of the femur to correct gross misalignment due to an old fracture Then 2-3 weeks after the ostetomy they will be doing my 2nd total knee revision I will be non weight bearing for 9-12 months I also have a total hip on the same leg that is showing signs of loosening on radiographs so it will have to be replaced after the osteotomy and knee revision are healed It is going to be a long recovery but I am hopeful some of my pain and the instability will be much more tolerable have a great night all Wanda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 12, 2006 Report Share Posted February 12, 2006 Hi Wanda I live in Ohio too - Marietta. Where do you live? I am about to have a hip resurfacing with Dr. De SMet in Belgium on March 15. I don't have any insurance and can't afford getting my hip resurfaced in the US. I am 61 and don't want to have a THR and am lucky enough to have enough good bone density to go the hip resurfacing route. I am sorry that you will have such a long recovery. I think it is good to join a group like this to have people to talk to. Many here have had THR and knee replacements and understand what you are facing. There is a lot of good support here. Keep in touch. Pat in Ohio Introduction Hello My name is Wanda I live in Ohio I am in the process of scheduling surgeries and thought I would join this list I am having an osteotomy of the femur to correct gross misalignment due to an old fracture Then 2-3 weeks after the ostetomy they will be doing my 2nd total knee revision I will be non weight bearing for 9-12 months I also have a total hip on the same leg that is showing signs of loosening on radiographs so it will have to be replaced after the osteotomy and knee revision are healed It is going to be a long recovery but I am hopeful some of my pain and the instability will be much more tolerable have a great night all Wanda No virus found in this incoming message.Checked by AVG Free Edition.Version: 7.1.375 / Virus Database: 267.15.6/257 - Release Date: 2/10/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 Welcome Warren. Glad you are on the list. I look forward to your input. On Mar 1, 2006, at 9:57 AM, warren brodey wrote: > My level of electrosensitivity is mild. Mostly I just get tense and > tired around machines and dislike the feeling intensely. Have been > working with reducing these kind of effects with some success. Now I > can work with my computer most of the day. Before I just had to leave > it without finishing what I was doing. > > I am a medical doctor but now I don't see patients, actually I > haven't for a long time. When I began working at MIT and NASA in the > 60's I moved into the field of man-machine interfacing . I have been > working with engineers and cybernetic solutions to problems. I prefer > working independently, softly and gently like a cat, since I am not an > institutional person. > > I still help people. That is inbuilt. > > For the last 4 years I have been trying to be clear about the > problems generated by exposure to electrical fields outside the body > and their effect on the electrical signal fields inside the body. > > I have found out that inside the body the electrical fields work > gently like putting a key in a lock and opening a garden door. Outside > fields like those that cause electro sensitivity are more like more > battering ram, sledge hammer stuff comparitively. > > Trying to be clear about the process and to be helpful is not so > easy but I know a lot more than I did when I got interested. > > So thats an intro. I will read some of the old materials on this > forum. Maybe I'll be clearer when I have done that. > > > > > --------------------------------- > > Bring photos to life! New PhotoMail makes sharing a breeze. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 1, 2006 Report Share Posted March 1, 2006 Welcome, Warren, Nice to meet you! When you were a doctor treating people, what was your specialty, if I might ask? My best to you, Diane warren brodey <to.bclear@...> wrote: My level of electrosensitivity is mild. Mostly I just get tense and tired around machines and dislike the feeling intensely. Have been working with reducing these kind of effects with some success. Now I can work with my computer most of the day. Before I just had to leave it without finishing what I was doing. I am a medical doctor but now I don't see patients, actually I haven't for a long time. When I began working at MIT and NASA in the 60's I moved into the field of man-machine interfacing . I have been working with engineers and cybernetic solutions to problems. I prefer working independently, softly and gently like a cat, since I am not an institutional person. I still help people. That is inbuilt. For the last 4 years I have been trying to be clear about the problems generated by exposure to electrical fields outside the body and their effect on the electrical signal fields inside the body. I have found out that inside the body the electrical fields work gently like putting a key in a lock and opening a garden door. Outside fields like those that cause electro sensitivity are more like more battering ram, sledge hammer stuff comparitively. Trying to be clear about the process and to be helpful is not so easy but I know a lot more than I did when I got interested. So thats an intro. I will read some of the old materials on this forum. Maybe I'll be clearer when I have done that. --------------------------------- Bring photos to life! New PhotoMail makes sharing a breeze. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2006 Report Share Posted March 23, 2006 > > Thanks for the SmartShelter link I have begun to read the ES testimonial, very interesting. I know only too well how ES can dessimate a career. I also will not let an employer kick sand in my face, when they begin to think about the implications of employing an ESSER it is only a matter of time before they do ! I think that most managers have been bodysnatced by Vodafone perhaps they think ES is contagious. We talk about DC as not being offensive to ES, but I guess it depends on how simple the circuitry is, and how its put to use - I am writing this on a Laptop on battery, and I am rapidly feeling uncomfortable and fogged/hystamiened out ! It has a wifi card which can be disabled, on checking available networks I see that my Neigbour has 3 router devices on the go, all day/night no wonder my tinitus has got worse and I feel like I ve gone ten rounds with Mike tyson in the morning - Have you got any spare plots at your place ? best wishes Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2006 Report Share Posted March 23, 2006 > We talk about DC as not being offensive to ES, but I guess it depends > on how simple the circuitry is, and how its put to use - I am writing > this on a Laptop on battery, and I am rapidly feeling uncomfortable > and fogged/hystamiened out ! As far as I know, all laptops use a florescent backlights, and that all of these backlights require high voltage AC to run, so there is a low voltage DC to high voltage/high frequency AC inverter in your laptop which could be causing you problems. It will be interesting to see what symptoms will be like when all backlights are replaced by LEDs sometime in the next several years, as LEDs won't need AC power. Marc Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 23, 2006 Report Share Posted March 23, 2006 Lol Espaules at the body snatching. Sorry of your problem there Freika. Sounds like lots of us, too much chemical/radiation exposure. Want to look at the smartshelter site too. I think the MC/EMF problem is probably so entwined, because chemistry and electricity are themselves, frequencies and all. You can hardly separate the two really when it comes down to it. I do think a lot more people have this problem than realize it, as in post about the high blood pressure. They aren't use to feeling energy fields, and are still looking for solid defined physical problems as the cause, when many times that may only be part of it. Good luck on your adventures. ~ Snoshoe > > > > Thanks for the SmartShelter link I have begun to read the ES > testimonial, very interesting. I think that most > managers have been bodysnatced by Vodafone perhaps they think ES is > contagious. > > We talk about DC as not being offensive to ES, but I guess it depends > on how simple the circuitry is, and how its put to use - I am writing Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 24, 2006 Report Share Posted March 24, 2006 Hi Frieka, I love the name! I also feel like a Freak of Nature sometimes! I noticed on another list that someone recommended BioPro chips to you. I didn't find those helpful at all for me even though I bought the most expensive package and stuck them all around. I sent them back. If you buy them I hope you have a better experience. nn -------------- Original message ---------------------- From: freika natur <freikanatur@...> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 24, 2006 Report Share Posted March 24, 2006 > sometime in the next several years, as LEDs won't need AC power. > > Marc > Thanks Marc - Cant wait hey ! Out of intrest today I travelled around Brighton as part of my work as a Building Surveyor, Boy that place is cooking ! needless to say as I felt really fried on one route I happened to note that alongside there was one of British Telecoms main offices, crowned with a myriad of anttenea - nice to know that they dont mind sharing the radiation with their beloved employees !! Driving really tires me out. I drive a year 2000 Fiat punto 1.2 which does not give me many problems,(cant drive 2.0ltr Renault Scenic - Thats a killer to me I become like a mad dog after a while) only I have a dodgy right ankle (to list one suspicious symptom)like varicouse veins inflamed Dr says ankle is aged for some reason !! this is the same side closest to wheel arch high EMFS there ! I also have folliculitis on thighs perhaps this could be attributed to lying belly down on a metal sprung mattress for years ( Iam 1000m away froma 3g mast accross open feilds 32db power ?) ? I am about to change to a foam mattress, have tried a foam topper recently and have awoken feeling more refreshed could be placebo I know but I am going to go with it despite my lurking mistrust of foam with so many chemicals there ? Back to the driving and cars, I am bored with the fiat I want speed and perfomance and style I need a change, so I test drove a Ford KA Sport very quick nippy, guess what - did my head in !!! Transponder in key, microwaves here there and everywhere, I think that my creator is having a laugh cos 2 days later a Ford KA Sport, different model turns up on forecourt with number plate .....EMF, - Thats weird ! Next GRIPE - As you know from my last post I talked about WIFI devices used in my neighbours house, GEE who is regulating this stuff ! whats to stop me from going out and buying fifty Wifi routers, transmitters and turning them on for the heck of it ? This requires positive action serious and present ! If my neighbour does not relent ie turn off his wifi at night to offer some compromise I will take this to all the powers that be, he knows I am ES so I am about to write him a letter to put him on notice that I feel he is damaging my health and my family for that matter, I hope to get backing of ES-UK here. We must try to fight this I am so angry right now !!! and I will not die in a corner ! cheers Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 24, 2006 Report Share Posted March 24, 2006 > > > We talk about DC as not being offensive to ES, but I guess it depends > > on how simple the circuitry is, and how its put to use - I am writing > > this on a Laptop on battery, and I am rapidly feeling uncomfortable > > and fogged/hystamiened out ! > > As far as I know, all laptops use a florescent backlights, > and that all of these backlights require high voltage AC to run, so there > is a low voltage DC to high voltage/high frequency AC inverter > in your laptop which could be causing you problems. It will be interesting > to see what symptoms will be like when all backlights are replaced by LEDs > sometime in the next several years, as LEDs won't need AC power. > > Marc > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 Hello Carol,I have not had surgery,but do have neck discs that are messed up. Sorry that I can't help you with that. I just wanted to welcome you to the group and let you know that there are a lot of good folks in this group. Someone will be able to answer you question about the surgery. MAY YOU HAVE A BETTER DAY TOMORROW THAN YOU HAD TODAY. TAKE AS BEST CARE THAT YOU CAN AND BE SAFE. LARRY carol herbin <cherbin1@...> wrote: brand new to the group -- so glad to find it! i'm looking for information about cervical fusion surgery -- its successes, its challenges and the process. i went to a neurologist about other issues (mostly carpal tunnel) and through the MRI's and x-rays, was referred to a neurosurgeon who is telling me i should have both anterior and posterior surgeries to remove disc(s) and fuse vertebrae because i have cervical instability, stenosis and spondylosis. my spinal cord seems to be compressed from about C-5 to T-1. i had multiple whiplash injuries over the years (lucky me -- i seem to have a target on the back of my car!) so i've dealt with neck pain for a very long time, but was more than surprised at this call for immediate surgery. i've never known anyone who was completely satisfied and/or pleased with the result of it. and i'm hoping i'm wrong and there are successes out there to encourage me -- OR someone with some other alternatives to the situation. so -- here i am. hoping to learn. thanks for reading a post that turned longer than i expected. carol REMEMBER ALL OF OUR MEN AND WOMEN IN THE ARMED SERVICE OF OUR NATION PRAY THAT THEY MAY BE SAFE AND SOUND IN BODY AND MIND Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 Thank you, Larry! I'm looking forward to lots of input so I can make some kind of reasonable decision(s). I appreciate the friendly welcome. c Re: introduction Hello Carol,I have not had surgery,but do have neck discs that are messed up. Sorry that I can't help you with that. I just wanted to welcome you to the group and let you know that there are a lot of good folks in this group. Someone will be able to answer you question about the surgery. MAY YOU HAVE A BETTER DAY TOMORROW THAN YOU HAD TODAY. TAKE AS BEST CARE THAT YOU CAN AND BE SAFE. LARRY carol herbin <cherbin1@...> wrote: brand new to the group -- so glad to find it! i'm looking for information about cervical fusion surgery -- its successes, its challenges and the process. i went to a neurologist about other issues (mostly carpal tunnel) and through the MRI's and x-rays, was referred to a neurosurgeon who is telling me i should have both anterior and posterior surgeries to remove disc(s) and fuse vertebrae because i have cervical instability, stenosis and spondylosis. my spinal cord seems to be compressed from about C-5 to T-1. i had multiple whiplash injuries over the years (lucky me -- i seem to have a target on the back of my car!) so i've dealt with neck pain for a very long time, but was more than surprised at this call for immediate surgery. i've never known anyone who was completely satisfied and/or pleased with the result of it. and i'm hoping i'm wrong and there are successes out there to encourage me -- OR someone with some other alternatives to the situation. so -- here i am. hoping to learn. thanks for reading a post that turned longer than i expected. carol REMEMBER ALL OF OUR MEN AND WOMEN IN THE ARMED SERVICE OF OUR NATION PRAY THAT THEY MAY BE SAFE AND SOUND IN BODY AND MIND Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 Hi Carol I had a single level cervical fusion several years ago. My neuro fused from C5-C6 but he didn't use any rods or cages in my neck. He did the surgery thru the front of my neck to the back. I also had several bone spurs in there he removed and spinal stenosis where my spinal cord was being squished so bad it was causing me horrible pain. The surgery I consider a success I still have to be careful of my neck and I no longer lift anything heavy (I have several horses so lifting 50lb bags of grain and 75 lb bales of hay were part of my weekly work) I had to be really careful for several months after my surgery until the bone grafts healed as my neck was just like building blocks stacked one on top of each other without the cages and rods for support my recovery was a little slower I think, But I am happy with the outcome. As far as things that are different, it took me awhile to be able to turn my head a decent amount to the left ( like when I was driving and backing up I needed too do this) and I still can not turn as far that way as to my right. Also swallowing was tough after surgery I guess because of the way they go in there and squish and move everything around. I still once in awhile find it hard to swallow things but from what I have heard from other people here that seems to be prety common. Do you know what kind of surgery your dr is thinking of doing?? How many levels and what kind of hardware is he planning on using? Be sure and ask him what kind of recovery time you can expect, he should be able to give you an idea although everyone is different. Also I'd ask him what you think your chances are for a good recovery from the surgery as far as it being a success?There are several other people here who have had cervical fusions some good, some bad so I am sure you will get more input from them. If you have any questions feel free to ask, and welcome to the group. Best wishes Sharon Group Owner > > brand new to the group -- so glad to find it! > > i'm looking for information about cervical fusion surgery -- its successes, > its challenges and the process. > > i went to a neurologist about other issues (mostly carpal tunnel) and > through the MRI's and x-rays, was referred to a neurosurgeon who is telling > me i should have both anterior and posterior surgeries to remove disc(s) and > fuse vertebrae because i have cervical instability, stenosis and > spondylosis. my spinal cord seems to be compressed from about C-5 to T-1. > > i had multiple whiplash injuries over the years (lucky me -- i seem to have > a target on the back of my car!) so i've dealt with neck pain for a very > long time, but was more than surprised at this call for immediate surgery. > > i've never known anyone who was completely satisfied and/or pleased with the > result of it. and i'm hoping i'm wrong and there are successes out there to > encourage me -- OR someone with some other alternatives to the situation. > > so -- here i am. hoping to learn. > > thanks for reading a post that turned longer than i expected. > > carol > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 Hi Carol I had a single level cervical fusion several years ago. My neuro fused from C5-C6 but he didn't use any rods or cages in my neck. He did the surgery thru the front of my neck to the back. I also had several bone spurs in there he removed and spinal stenosis where my spinal cord was being squished so bad it was causing me horrible pain. The surgery I consider a success I still have to be careful of my neck and I no longer lift anything heavy (I have several horses so lifting 50lb bags of grain and 75 lb bales of hay were part of my weekly work) I had to be really careful for several months after my surgery until the bone grafts healed as my neck was just like building blocks stacked one on top of each other without the cages and rods for support my recovery was a little slower I think, But I am happy with the outcome. As far as things that are different, it took me awhile to be able to turn my head a decent amount to the left ( like when I was driving and backing up I needed too do this) and I still can not turn as far that way as to my right. Also swallowing was tough after surgery I guess because of the way they go in there and squish and move everything around. I still once in awhile find it hard to swallow things but from what I have heard from other people here that seems to be prety common. Do you know what kind of surgery your dr is thinking of doing?? How many levels and what kind of hardware is he planning on using? Be sure and ask him what kind of recovery time you can expect, he should be able to give you an idea although everyone is different. Also I'd ask him what you think your chances are for a good recovery from the surgery as far as it being a success?There are several other people here who have had cervical fusions some good, some bad so I am sure you will get more input from them. If you have any questions feel free to ask, and welcome to the group. Best wishes Sharon Group Owner > > brand new to the group -- so glad to find it! > > i'm looking for information about cervical fusion surgery -- its successes, > its challenges and the process. > > i went to a neurologist about other issues (mostly carpal tunnel) and > through the MRI's and x-rays, was referred to a neurosurgeon who is telling > me i should have both anterior and posterior surgeries to remove disc(s) and > fuse vertebrae because i have cervical instability, stenosis and > spondylosis. my spinal cord seems to be compressed from about C-5 to T-1. > > i had multiple whiplash injuries over the years (lucky me -- i seem to have > a target on the back of my car!) so i've dealt with neck pain for a very > long time, but was more than surprised at this call for immediate surgery. > > i've never known anyone who was completely satisfied and/or pleased with the > result of it. and i'm hoping i'm wrong and there are successes out there to > encourage me -- OR someone with some other alternatives to the situation. > > so -- here i am. hoping to learn. > > thanks for reading a post that turned longer than i expected. > > carol > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 oh, thank you! what wonderful information! the surgeon actually changed his mind from the first time we talked to the second, so that was one of the things that threw me a little. he plans to do C3 to C4 from the front -- remove the disc and fuse. then he would flip my half-dead self over and do the remainder from the back -- C5 to T1. he has warned me about the swallowing (altho he did say it would more than likely completely go away in a few days AND since he added on the posterior part of the surgery, he told me i probably wouldn't be too worried about it because the back incision would hurt much more). i have not asked about hardware. i appreciate that heads up. i'll ask. i'm actually trying to track down a second opinion on the process now, but finding it difficult to find anyone who will even review my films, reports and diagnosis. i'm thrilled to find someone who is pleased with the outcome. i don't know anyone personally who's had the procedures, and i only know similar surgeries from years ago -- with mediocre results. so far, he's told me a 12-week recovery/recuperation period, but hasn't been too specific about that and what it would entail. i work from home -- doing legal transcription and training by phone for home-based call center workers -- so i'm hoping i'll be able to return to those some time within that 12-week period. thanks again. very encouraging information! c Re: introduction Hi Carol I had a single level cervical fusion several years ago. My neuro fused from C5-C6 but he didn't use any rods or cages in my neck. He did the surgery thru the front of my neck to the back. I also had several bone spurs in there he removed and spinal stenosis where my spinal cord was being squished so bad it was causing me horrible pain. The surgery I consider a success I still have to be careful of my neck and I no longer lift anything heavy (I have several horses so lifting 50lb bags of grain and 75 lb bales of hay were part of my weekly work) I had to be really careful for several months after my surgery until the bone grafts healed as my neck was just like building blocks stacked one on top of each other without the cages and rods for support my recovery was a little slower I think, But I am happy with the outcome. As far as things that are different, it took me awhile to be able to turn my head a decent amount to the left ( like when I was driving and backing up I needed too do this) and I still can not turn as far that way as to my right. Also swallowing was tough after surgery I guess because of the way they go in there and squish and move everything around. I still once in awhile find it hard to swallow things but from what I have heard from other people here that seems to be prety common. Do you know what kind of surgery your dr is thinking of doing?? How many levels and what kind of hardware is he planning on using? Be sure and ask him what kind of recovery time you can expect, he should be able to give you an idea although everyone is different. Also I'd ask him what you think your chances are for a good recovery from the surgery as far as it being a success?There are several other people here who have had cervical fusions some good, some bad so I am sure you will get more input from them. If you have any questions feel free to ask, and welcome to the group. Best wishes Sharon Group Owner > > brand new to the group -- so glad to find it! > > i'm looking for information about cervical fusion surgery -- its successes, > its challenges and the process. > > i went to a neurologist about other issues (mostly carpal tunnel) and > through the MRI's and x-rays, was referred to a neurosurgeon who is telling > me i should have both anterior and posterior surgeries to remove disc(s) and > fuse vertebrae because i have cervical instability, stenosis and > spondylosis. my spinal cord seems to be compressed from about C-5 to T-1. > > i had multiple whiplash injuries over the years (lucky me -- i seem to have > a target on the back of my car!) so i've dealt with neck pain for a very > long time, but was more than surprised at this call for immediate surgery. > > i've never known anyone who was completely satisfied and/or pleased with the > result of it. and i'm hoping i'm wrong and there are successes out there to > encourage me -- OR someone with some other alternatives to the situation. > > so -- here i am. hoping to learn. > > thanks for reading a post that turned longer than i expected. > > carol > ------------------------------------------------------------------------------ No virus found in this incoming message. Checked by AVG Free Edition. Version: 7.1.405 / Virus Database: 268.12.2/441 - Release Date: 9/7/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2006 Report Share Posted September 7, 2006 oh, thank you! what wonderful information! the surgeon actually changed his mind from the first time we talked to the second, so that was one of the things that threw me a little. he plans to do C3 to C4 from the front -- remove the disc and fuse. then he would flip my half-dead self over and do the remainder from the back -- C5 to T1. he has warned me about the swallowing (altho he did say it would more than likely completely go away in a few days AND since he added on the posterior part of the surgery, he told me i probably wouldn't be too worried about it because the back incision would hurt much more). i have not asked about hardware. i appreciate that heads up. i'll ask. i'm actually trying to track down a second opinion on the process now, but finding it difficult to find anyone who will even review my films, reports and diagnosis. i'm thrilled to find someone who is pleased with the outcome. i don't know anyone personally who's had the procedures, and i only know similar surgeries from years ago -- with mediocre results. so far, he's told me a 12-week recovery/recuperation period, but hasn't been too specific about that and what it would entail. i work from home -- doing legal transcription and training by phone for home-based call center workers -- so i'm hoping i'll be able to return to those some time within that 12-week period. thanks again. very encouraging information! c Re: introduction Hi Carol I had a single level cervical fusion several years ago. My neuro fused from C5-C6 but he didn't use any rods or cages in my neck. He did the surgery thru the front of my neck to the back. I also had several bone spurs in there he removed and spinal stenosis where my spinal cord was being squished so bad it was causing me horrible pain. The surgery I consider a success I still have to be careful of my neck and I no longer lift anything heavy (I have several horses so lifting 50lb bags of grain and 75 lb bales of hay were part of my weekly work) I had to be really careful for several months after my surgery until the bone grafts healed as my neck was just like building blocks stacked one on top of each other without the cages and rods for support my recovery was a little slower I think, But I am happy with the outcome. As far as things that are different, it took me awhile to be able to turn my head a decent amount to the left ( like when I was driving and backing up I needed too do this) and I still can not turn as far that way as to my right. Also swallowing was tough after surgery I guess because of the way they go in there and squish and move everything around. I still once in awhile find it hard to swallow things but from what I have heard from other people here that seems to be prety common. Do you know what kind of surgery your dr is thinking of doing?? How many levels and what kind of hardware is he planning on using? Be sure and ask him what kind of recovery time you can expect, he should be able to give you an idea although everyone is different. Also I'd ask him what you think your chances are for a good recovery from the surgery as far as it being a success?There are several other people here who have had cervical fusions some good, some bad so I am sure you will get more input from them. If you have any questions feel free to ask, and welcome to the group. Best wishes Sharon Group Owner > > brand new to the group -- so glad to find it! > > i'm looking for information about cervical fusion surgery -- its successes, > its challenges and the process. > > i went to a neurologist about other issues (mostly carpal tunnel) and > through the MRI's and x-rays, was referred to a neurosurgeon who is telling > me i should have both anterior and posterior surgeries to remove disc(s) and > fuse vertebrae because i have cervical instability, stenosis and > spondylosis. my spinal cord seems to be compressed from about C-5 to T-1. > > i had multiple whiplash injuries over the years (lucky me -- i seem to have > a target on the back of my car!) so i've dealt with neck pain for a very > long time, but was more than surprised at this call for immediate surgery. > > i've never known anyone who was completely satisfied and/or pleased with the > result of it. and i'm hoping i'm wrong and there are successes out there to > encourage me -- OR someone with some other alternatives to the situation. > > so -- here i am. hoping to learn. > > thanks for reading a post that turned longer than i expected. > > carol > ------------------------------------------------------------------------------ No virus found in this incoming message. Checked by AVG Free Edition. Version: 7.1.405 / Virus Database: 268.12.2/441 - Release Date: 9/7/2006 Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.