Big Toe Joint Replacement Operation? Experience?
Oct 23, 2015
If so, I would like to hear how you are getting on. I had the op 10 weeks ago, I am still in pain and have tendonitis. I go to physio and can bend my toe which is great but the pain is still as bad as before the op, hoping its because its still early days after a joint op.
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So I have been advised by 2 different oral surgeons I need total joint replacement of both joints.
For those of who have gone through joint replacement, I would really appreciate knowing:
1) what questions I should be asking the surgeons about the surgery, about the outcomes; about post-op care; risks;
2) what your personal exerpience was - just want to know what to expect.
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I had a replacement hip operation 6 months ago,and I still get pain in the leg,I have a large dent in my leg where the hip has been replaced and a large lump below it as if my muscle has slipped.I have just started with a chiropractor for help in trying to walk correctly,I have been on a stick since the op I don't feel confident without it yet,has anyone else in the group had this problem or something similar,the dent and the lump below it?
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I'm due a hip replacement very soon I know it's bad but I smoke should I give up before op are there more dangers
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Anyone have experience with SI joint injections?
I have been dealing with pain (from nagging to disabling) for almost a year. A year ago, the pain slowly progressed to the point that any position was uncomfortable...sitting, standing, walking, sleeping was impossible (for some reason the pain seems worst at night). At that point, I called my spine surgeon (had a lumbar burst fracture 5 years ago so already had a doctor ), but the first available appointment was a month out...I scheduled the appointment and went to the ER after not sleeping any more than an hour or two for several weeks in a row due to pain. They gave me a Toradol injection, muscle relaxers, and Vicodin. I went home thinking that I would finally sleep...WRONG! All those drugs did nothing to stop the pain! I struggled through the next few weeks until my appointment. My doctor's first guess was a disc problem due to my history; however, MRI showed healthy discs and fracture site looking as good as a burst fracture can After a few more tests, he diagnosed me with an SI joint problem and put me on Relafen for 6 weeks to control inflammation. After 3 weeks, I did see improvement...The pain returned to the "annoying" level. Since that time, the pain has been up and down...Always there, not always awful, but sometimes miserable for weeks at a time. I had a foot/ankle reconstruction in November and had a HUGE flair up after that...I realized that I really had an issue when my back pain was keeping me awake at night, not the heel bone that had been sawed into three chunks! I was hoping this problem would just disappear as mysteriously as it began; but, unfortunately, it looks like it's here to stay. My doctor has recommended an SI joint injection as the next step.
Has anyone had success with SI joint injections? My typical symptoms are left side lower back, hip, and thigh pain from just annoying to feeling like my bones are disintegrating...that's the best description I can come up with I also have a lot of muscle soreness in those areas.
How was the "injection experience?" I've had cortisone injections in my foot before, and they were not pleasant...So, I'm definitely not excited about this. I have a high pain tolerance and have dealt with a lot of medical procedures, but something about someone sticking a big needle in my back doesn't give me a warm, fuzzy feeling.
Did you have increased pain for a few days following the injection? After the ones in my foot, I had fairly severe pain for several days...I think they called it a cortisone flair.
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Since 3 yo I have had pain in my back and up until I was 12 they said that it was growing pains! they then said I had wear and tear at l3/4 and suffered everyday since but been a pain I know that's there but didn't stop me I just grit my teeth and get on! Every few years I have a flare up of it and knocks me for a few weeks then back to usual bearable pains!
April 2013 woken to numbness /tingling legs and feet 3 days later horrendous back pain and it hasn't left since! Been 15 month of living hell! I've tried pt many many times over the years and always made my pains worse! I've eventually seen PM who said they will do facet joint injections in July however I am due to fly on holiday 5wks later! I can't imagine coping on holiday being the way I am atm however if I get worse then I won't be able to go!
Anybody had facet joint injections? Any good for you ? All experience welcome please
I was taken 300mg X2 daily pregabalin (lyrica). 250mg x 3 naproxen daily and 30mg oxycodone 2x daily they have cramped my meds to now 50mg x2 lyrica, 60mg x1 duloxetine and 30 mg X2 oxycodone! All the meds do is take the edge of the pain but if having a flare up then nothing helps!
I have to use crutches constantly just can't walk without at least one because it causes to much pain in my lumber,hips, groin and my legs sometimes give way!
The things I have been diagnosed with are, ddd, spondylosis, osteoarthritis, fibromyalgia. (They said I have loss if disc height and osteophytes too)
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I have had a toe joint replaced - all is not good. Has anyone had this done that I could speak with?
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Just had my procedure and in recovery now, waiting to be discharged!
I have severe prolapse of L4/L5 with bilateral impingement of nerve roots. This results in severe back pain and constant sciatica. Worse on my right side.
Whole process took less than half an hour and I feel just fine after. Was offered sedative, but refused as I'm personally cool with stuff like this and very relaxed/able to keep still.
Very little pain during the actual procedure. In fact the worst bit was the initial injection of local anaesthetic!
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I had total jaw joint replacement a year ago. This was a last resort that resulted from trauma that happened 40 years ago. I am not doing as well as I hoped and suffer from chronic pain. Is there anyone who has had this surgery who could share their post surgery results?
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Anyone know about Big Toe Joint Replacement recovery time? Any successful ops?
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Background. I've had symptoms of Condylar Resorption for 6 years. Well technically I have not had ANY condyles for the last 2 years. I'm not in extreme pain. I have maybe 4 or 5 days a month where I can't function well from headaches, jaw, tooth, basically all over pain from the neck up. The rest of the time its livable but constant. I've been in two different jaw splints but since the last one broke two years ago, I have not wanted to invest in more as they are quite spendy. My pain is not extremely bad but if you press anywhere on my face it does hurt. Only my back teeth touch, my chin has receded, I can't breathe through my nose and I can fit my tongue through my front teeth. I'm concerned about my teeth not touching because my dentist said it would cause problems down the road if they continued to not touch. I'm also wondering if my top and bottom jaw just banging together is going to cause problems too. I have small children and having a major surgery that could make me permanently worse is not something I want to do to them. I am also getting this surgery done by Dr. Larry Wolford if that has anything to do with it. The first "TMJ Specialist" I saw thought his splints would miracle cure it. The last two I have seen have both said my only option to fix my bite and joints is surgery but I have not talked to one since the splint broke 2 years ago.
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I am only 41 and have terrible foot pain and limited mobility. I had bunion surgery in 2010 but had terrible scarring issues and have had 2 since surgeries to remove scar tissue, which haven't helped but made it worse. And now I am told there has been tendon damage due to all the scarring and the bones are rubbing together and my options will be fusion or joint replacement in the future. I am very active and don't know the right option for me. It is very upsetting and impacts my life every day. My doctor is the head of podiatric surgery at the hospital so I feel he made the right decisions but I don't know where to turn for a second opinion.
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My 24 year old son was diagnosed with TMJ Arthritis and the surgeon wants to do a bilateral TMJ joint replacement. That seems extreme to me. I would like to know if anyone has had a jaw joint replacement and if you have had jaw problems post surgery.
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Saw an orthopaedic consultant yesterday who confirmed, after an xray, that the osteoarthritis in the big toe joint is getting worse. He suggested two different types of surgery: a fusion of the bone or a replacement of the joint. I am leaning towards the latter although I don't know much about it and the consultant admitted the success rate isn't great! Has anyone had it done or know more about it?
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Can people with OP have joint replacements? Do the joints 'Accept' the new joints? Is a diagnosis of -3.5 serious, or just average?
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I had Big Toe Replacement Op 10 weeks ago, I am still in pain and also have Tendonitis. I go to physio and can bend my toe, but the pain is no better than before the op.
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I've had TMJ/TMD issues for 33 years after a dog bite at 12. In total I've had 5 surgeries on both sides of my jaw with a 6th to repair an ear canal and eardrum that a surgeon cut into while in surgery. The last time I had surgery it was a 10 hour surgery with 2 doctors, one on each side. So needless to say I'm not looking forward to any more.
I seem to grow bone in the left joint space (my disk and ball joint are long gone) and the right side my body absorbs the tissue they put in and I', bone on bone. Therefore I'm living with daily chronic pain for the last 20 years.
I've heard that the joint replacement has gotten better. It doesn't take away all pain, but it's a different pain.
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Had knee replaced 2009. Last year developed cellulitis and septic arthritis one day prior to having other knee joint replaced.
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I've done extensive surgery and am terrified to have this procedure done. I'm only 23, and feel that it might lead to years of complications.
I do need a surgery to fix some jaw problems I'm having. I was told that I am bone on bone, and that the fat graft I had put in is no longer present. Does anyone on here have experience with this?
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I finally scheduled my total bilateral joint replacement for Jan. 15, 2014. As you can imagine I am very nervous. Just yesterday I had screws removed from my latest surgery on September 13th. Back on September 13th, I was to have undergone a bilateral arthrotomy with fat grafting but unfortunately I had some scary complications and that particular procedure was not done. I ended up having an exploration of the left neck, open reduction and internal fixation of the left mandible, extraoral vertical ramus osteotomy and condylectomy and an open left TMJ arthroplasty. Plus I had a left cranial base bleed which I was sent emergently from the OR to interventional radiology to locate and control and bleed and spent several days on a ventilator in the ICU.
Currently, my bite is so off to the left side that it is not even funny. I look like Rocky from the movie "Rocky" when he is screaming...."Adrianne!!" and his mouth is sort of way off to one side.
Can anyone out there who has had TMJ Concepts joints replaced lend me any guidance or advice? I am unable to chew and have been on a non chewing diet since March and am only able to open my mouth two fingers and talking hurts quite a bit.
I know I am making the right decision for me as I have been dealing with this for years.
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I have been in pain off and on for about 5 years now and xrays show that i have greatly reduced and/or missing joint cartilage and bone spurs including bone cysts that seem to come and go. The Ortho surgeon said from the x rays alone, I needed a full replacement. Most days its painful to walk for too long or bend, twist etc which does interfere a lot with my life and i often find it hard to sleep or reach a deep sleep. Id love to travel but but can never tell when my hip will feel okish and when it will be agony! Every day can be different! I have been told pain like this comes and goes and is all part of the slow deterioration of the joint. As my surgery date looms in the next week i am starting to feel maybe i don't need it ( hip is feeling okish today!) or am i just getting cold feet? Im mid 50s and pretty healthy and active but this hip has certainly held me back especially in the last year. I've never had a big Op but some websites say sooner is better than later. Any ideas or thoughts?.
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