Bone / Joint :: Pain After Bone Spur/arthritis Surgery On Shoulder
Feb 11, 2012
I had surgery on June 14, 2011 to remove a bone spur on my left clavicle and to remove arthritis near (but not in) my shoulder joint. It was the worse experience of my life. I was in constant agonizing pain for 2.5 months. Just for the record, I've had two ulnar nerve surgeries on my left AND right elbows and never even needed pain medication. This shoulder surgery apparently did not relieve any of my pain. I still have a dull aching pain through out the day starting in my neck (left side) to my shoulder, and down my bicep to my elbow. I still can not sleep at night, and through out the day while working my shoulder/arm/ neck is killing me. I continue to take an Naproxin and continue to rotate heat and ice. I did physical therapy for the first two months after surgery. My concern is that had arthroscopic surgery, and there was NO rotator damage so why is my shoulder still in pain? My shoulder pops when I do try to rotate it.. and often when I simply reach outward for something..I'm in excruciating pain. I'm a baker, so I am constantly lifting a 34-50lb metal mixing bowl and have to reach many times through out the day. There really is no way to not do my job duties and still retain my job. Any ideas why I'm still having this problem?
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December 2013 had a tkr on my right knee, and the day I cam home from the hospital, I complained on I couldn't lay on my right side. After 2 year of cortisone shots, physical therapy and x rays, doctor took an MRI and told me that I have a bone spur and a torn hip lining. Had surgery for that, and I am still in pain now from both the groin area and the hip. Now I am being told that I need a new hip. Not sure that I want to go through that.
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I had bunion surgery on my feet last year, since then i have been in more pain than before i had surgery. To be honest they weren't actually painful before the surgery, just a pain to wear shoes and they were very bent. now my left foot feels weird and my right foot is extremely painful.
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what to do? i regret having the surgery i want to go back to being my normal super active self. They hurt so much!
I had bunion surgery about 5 months ago. I'm 16 years old and have severe bunions on both feet. I play sports and am constantly running around and going through a lot of shifting and moving. before the surgery the pain was unbearable and felt like I had two broken toes. I went to the doctor after a few years to when the pain was just too much and he told me I needed surgery. I chose to do one foot at a time because I wouldn't be able to walk on it for about 6 weeks so I chose the one that hurt more. I had nerves being pulled on the side by the bunion and my toe was shifted to the side. Now 5 months after I am in the same about of pain as before and then some. My big toe is not only still numb( which the doctor told me was apart of the normal healing process) but the big toe also does not touch the ground. The pain is so bad when I am playing basketball that I need to stop. It's the bottom of my foot under the big toe and around where the bunion was removed that hurts it feels like pins and needles and like I'm walking on rocks. It's very tender on the area, should I be worried/get this checked out? Or should I just deal with it?
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Two years ago I broke my ankle and had pins and plates put in. On Monday I am having them taken out because they are irritating my tendon. I am also having a 'bone spur' basically shaved off and they are going to 'explore' the damage done to the tendon.
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When I had them put in I had a general anaesthetic, but I wasn't asked what I'd prefer. This time, at a different hospital I have been.
I don't know what to do for the best. Obviously I can talk about this when I arrive on Monday I'd just like people opinions on which they prefer and why. Or even which they think would be suitable for my surgery.
I was fine after my anaesthetic last time, no side effects etc I just think I feel more comfortable not being 'put to sleep'... just in case. I'm a bit of a worrier!
I am leaning towards opting for the spinal anaesthetic combined with a bit of sedation as I do think I may get anxious. The only thing that is putting me off is what I will hear. Obviously they will be using screwdrivers etc and the thought of hearing them and knowing what they are doing makes me feel a little queasy!
I am experiencing pain on the bottom of my right heel. I have been told by several people that could be several things....a stone bruise, bone spur, heel spur, plantar fasciitis or tendonitis. Any ideas?
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I am 6 days post-op and had no idea this surgery would be this bad. I decided since I had to have the plantar fasciitis and heal bone spur surgery that I would just get my bunion and hammertoe corrected at the same time. BIG MISTAKE! I was unaware of the pain I would have to go through and the worst part is that because the plantar fasciitis surgery requires a cast for two weeks, I have not been able to ice my foot at all. The first day out of surgery wasn't too bad. My foot was numb but there was a little pain. Day 2 post-op was a little more painful. I did have to take hydrocodone but soon realized that they did not work to relieve my pain at all. I ended up calling my doctor for stronger pain meds. They ended up working great but make me very sleepy. Day 3 was far more worse than the first 2 days because all of the numbing medicine had worn off. I stayed on my couch with my foot propped up and only got up to use the restroom. Day 4 was about the same as day 3. I did go back to work but could only stay 1/2 day due to the pain. After surgery, I had a splint made out of cast material that went up to just below my knee. It was heavily bandaged. I had my first post-op appointment yesterday and the regular cast was put on. I have to say, I was very shocked at how horrible my foot looked. I have 5 incisions and a ton of bruising and swelling. The cast again is only because of the plantar fasciitis surgery which I have had ABSOLUTELY NO PAIN with. When they put the cast on, it felt too tight because of the swelling and it hurts 10 times worse now than it did before the cast. This is currently day 6 post-op and I am back at work with a pillow on my desk to prop my foot up on. Heaven forbid I stand up because when I do, the blood and fluid in my leg and foot race down to the bottom of my foot causing excruciating pain. I can only stand up for about 5 minutes before my breath is completely gone from trying to "take" the pain. I can only hope it gets better from here. Once the cast comes off 13 days post-op, I will then be placed in a walking boot for 2 weeks. I can only dream of that day now because I know I will be able to ice my foot any time I need to. I have not been able to ice my foot 1 time due to the splint and now the cast. I know if I could ice it, the swelling would have a much better chance of going down quicker.
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If there is anyone out there looking for advice on bunion/hammertoe surgery....please do not think that this will be a walk in the park. This surgery was my 21st surgery. I am 33 years old and have had 14 knee surgeries alone. I have had 3 total ACL reconstructions and the rest scopes to clean out torn cartilage. I have had bunion surgery in middle school on each foot, hammertoe surgeries on each foot, a c-section, and a few other minor surgeries. THIS SURGERY BY FAR IS THE WORST I HAVE EVER HAD. Do not take that lightly. I was on crutches for 9 months with my first ACL reconstruction so it was not easy but I never would have imagined anything ever being worse than that. I now have 4 screws in my foot along with 1 dissolvable pin in my second toe. I can bear very little weight on my foot but hope each day I can put more and more weight on it.
If you are considering having plantar fasciitis surgery and need bunion/hammertoe surgery or it was suggested to just get it all done at once.....DO NOT DO IT! From the experience I have in the past 6 days, I have learned that there is VERY LITTLE pain associated with plantar fasciitis surgery. The only discomfort I have had with that part is the incision rubbing against the splint/cast. Because the plantar fasciitis surgery requires a cast for 2 weeks and a walking boot for 2 weeks and if you are considering bunion/hammertoe surgery at the same time, you will have WORSE pain with the bunion/hammertoe part of it than the fasciitis because of the splint/cast.
I am due to get my other foot done (bunion/hammertoe only) in December and I am seriously considering not doing it. Please consult with your doctor before considering all of these corrections at one time. My doctor made it sound like it would be a very simple and easy surgery to recover from. HE WAS WRONG! If you do decide to have the surgery, make sure you plan to take at least a full week off of work.
I have a problem and need advice! My family is known to have history of arthritis. I am 34, male and I am afraid I have this disease too. I feel tingling in my temples. Is this a symptom of arthritis?
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I have been having back pains in my upper back between the shoulder blades as if I need to pop my back but I can't. i feel like there is tension all the way up my neck and i always have headaches. When I twist my upper body, there is a loud pop coming from my chest that does not normally hurt, but sometimes the pain is a 10. I have no idea what is the cause.
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I am a 47 year old female. I had Microfracture Knee surgery on January 12, 2016 and it was not a success. My doctor said that I am still bone on bone and will need a partial knee replacement. He uses the Oxford Partial Knee and says it is the best one to go with. I was able to get a Synvisc injection on May 12, 2016. My doctor and I are both hopeful that this will give me some time to make this big decision. I have had a really hard time recovering from the microfracture surgery. I was on crutches for five weeks and my knee got stuck in a bent position. I was in therapy for three months and I still cannot walk with a straight knee. The thought of undergoing another surgery is so scary. I just want to be normal again and do all the things that I used to do before.
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For the past 18 months I have experienced joint & bone pain, predominantly in my fingers, hands, wrists and elbows but also affecting my forearms, feet, ankles, knees, hips and shoulders. I have spent months trying to ignore it and at other times have kept detailed diaries, but can find no pattern relating to the area and level of pain and what I may have been doing, eating, drinking or how well I've slept.
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I am nearly always fatigued ... I do work hard but even when I have time off, I'm exhausted to the point of needing to nap or walking around like a zombie. I used to run a lot and completed marathons, but now can't face a short jog.
Whenever I go to give blood, 4 out of 5 times my blood is too low in iron. It's not considered a dangerously low level for me but it is too low for the blood service to accept. The last time I went I succeeded in giving blood but was borderline and they only just accepted me.
Diarrhea; like many women I usually have this around the first couple of days of my cycle. However in recent months this is happening more frequently. Again there is no pattern relating to what I eat, where I eat or who prepared it. When it happens I get cramps and an urgency to go, but no nausea, sickness or loss of appetite.
Finally, I've recently begun getting pins and needles in one hand / fingers in a pattern that suggests carpal tunnel syndrome. It lasts for a few days then fades.
All of these things could be related or entirely unrelated, I just don't know. Also, one or two on their own might be easier to deal with but combined they can really get be down. My doctor has recently given me blood tests for arthritis and they came back normal. Any other ideas please?
I have been diagnosed with hallux rigidus (accompanied by a bone spur, joint space narrowing and mild sesamoiditis). The pain came on suddenly (sharply) in September 3013 and progressed rapidly to constant aching and tenderness by November). Although the podiatrist says the arthritis is "mild", I am definitely concerned that I already have lost joint space. As I am only 45, with a number of additional biomechanical conditions in other areas of my body, its very important for me to avoid any surgery that could potentially throw anything else out of alignment.
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I have been closely following success stories of PRP and stem cell therapies and am definitely encouraged by anecdotal evidence (from forums and testimonials, as well as patients I've encountered personally). It appears that with a skilled and experienced practitioner, PRP can kickstart healing, and stem cells can actually help grow back cartilage. There is one physician in Chicago (Hauser at Caring medical) who even treats mild bone spurring with injections of HCl (which helps dissolve it).
I'm wondering if anyone has tried any regenerative therapy for their big toe (or anywhere on the foot - all data can be helpful) and how they fared. Also please write if you are interested and considering it, as it will undoubtedly be helpful to exchange ideas and information.
My vagina opening is wide enough to fit a tampon, which i've done on many occasions however, anything larger than this and it doesn't seem to stretch anymore. The actual skin can stretch fine and does but at the opening is a small ridge of bone. Once you reach past this bit of bone, inside the vagina it can stretch fine, it's just that one ridge, i can put my finger round it and hook it but I can't actually move the bone (obviously)So my problem is just that when I come to having sex, nothing will fit. I think this bone is the pubic bone which is just sunk down too far. I can also feel it right behind my clitoris and urethra opening like everything has been squashed down into one small area. It doesnt come very far up on my front 'mound' but comes too far down underneath in my vaginal area.Is this normal? Has anyone experienced this? What should I do?
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for the past week I had severe joint pain and weakness, muscle weakness, bone pain in extremities ( had a blood test for lupus and RA[ no family history of either] Starting to get a bit better as long as I rest. recently sexually active with one person, now I just noticed feeling swollen like I was getting a UTI ( hurt when I urinate), but noticed it hurt in my vagina not urethra, checked and there are 4 small red bumps in my right labia minora and 1 in my left labia minora-odorless, feels inflamed and hurts now. Is this related to possible lupus or separate problem? I feel exhausted and run down.
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I found a paper recently that contained some insights that might be worth thinking about." Studies of Osteoporosis (OP) and drug treatments have challenged the concept that denser bone means stronger bone. Bone strength, or resistance to fracture, is not easily measured by routine DXA as it is a function of both density and quality".
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(Cleveland Clinic, Angelo Licata 2009).
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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I had my operation on Tuesday for capsular release, mua and bone shaved.... the op wasn't too bad to be honest and i started wednesday with physio straight away, movement is still limited and i feel a bit down today as i suppose i was hoping for some miracle, i know it's going to be hard work and im prepared for that and im doing exercises every two hours, have got a lot of pins and needles today and feel like i have no strength at all in my arm, did anyone else feel like this after the op. x
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So I dislocated my knee in January of this year. I was given a device that isolates my knee cap and hold it in place. I wore the device off and on over the year whenever my knee would feel sort of irregular. I worked out routinely to help strengthen my knee, it helped the pain somewhat, but mostly just made me feel better about the way I looked, and kept me healthy. I haven't worked out since some time before Thanksgiving. Starting this week i've started to feel this new akward feeling behind my kneecap, sort of like the ligament behind my knee cap is tightening, sort of similar to how it felt when I dislocated my knee, but not exactly the same. I get the pain after fully bending my knee, for example when I am on my knees doing my job stocking shelves at work, when I stand to my feet I can usually feel the pain. I try doing a couple of different stretches when to make the feeling go away a bit, but it comes back, and then it eventually goes away again.
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My knee "pops" (makes a loud popping noise and pressure) pretty regularly now but when I get off of work and off of my knees I experience the discomfort much less. I want to start exercising again on Monday, but I am scared I might dislocate again. I will try using the knee cap device again tomorrow, but I feel as though whenever I use the device, it makes my knee feel like jello the next day, and make me want to use the device again, even though I was advised by my doctor that I should not need to use it regularly. ....
I'm a 29 year old male. I have been diagnosed with rheumatoid arthritis in October and my doctor put me on Enbrel. He told it's a miracle drug promising me it would change my life. I took my 5th injection today and I still don't see any major difference in my body. I still have morning stiffness and pain, and I still have a couple of swollen joints. I'm waiting for the Enbrel to take effect, but I'm starting to get worried that it's not working with me. My doctor said that after few weeks I could expect significant pain relief, but I'm still in pain. I've also heard that Enbrel can take effect anywhere from a few days to couple of months and that it doesn't work for all people equally. Anyone here with the same symptoms or Enbrel experience I'd love to hear your feedback. What was your experience with Enbrel?
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I have been having TERRIBLE pain in foot when I step down found out by x-ray I have a 8.4 mm Bone spur on top of my foot it also said on the report that there was a question of a 3 to 3 mm focus of hyperostosis associated with the Plantar aspect of the Calcaneus what does this part mean and also I am allergic to the Shots to relieve the inflammation and have a appt. with a Podiatrist I have used ice and heat also taking Ibuprofen and rested it as much as possible I also put things in my shoe to help still can't walk real good what can a Podiatrist do for me now ?
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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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