Knee :: Back To Work - When And Risks?
Jun 1, 2016
Yesterday I had my 6 week PO review with my surgeon, he was very happy with every aspect of my recovery. However, when I mentioned returning to work, he was adamant that not for another 6 weeks. He said that too many people feel pressure to go back to work too soon, do damage by overdoing it and kick themselves 12 - 18 months later due to some form of correction or achieving less than optimum results.
My work would require about 50/50 office/factory floor walking and an hours commute.
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Can someone please tell me what to expect when having dental work done?
I'm 3 months post TKR and have just found decay, which may need filling or extraction (its quite bad) ... What happens if it gets infected and how would that affect my prosthesis?
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I'm 17 years old I've played volleyball basketball and track my whole high school career and I've always had problems with my knees and ankles but I've been going to the doctor for my knees for like 2 years now and I've had like 3 MRIs they never tell me anything I've tried braces but they don't work. My left knee is way worse than my right but they both hurt. It started out feeling like I just had to crack my knee like if you straighten your elbow and it cracks but then it progressed and know it hurts extremely bad when I start running and I can't stand up after sitting like straightening them hurts horribly bad. Sometimes while I'm sitting they ache and I feel like it's on the inner side of my knee and on my left knee it's on the left side inside and if I go on my tip toe it hurts really bad like a shooting pain kind of it's like a line kinda. And it's also worse when they're cold like I have to drive with the heat on them even when it's 80 degrees outside.
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On August, I over-stretched a ligament on my knee while playing soccer and was on crutches for a month and half. Afterwards, everything was fine and my knee felt normal. It's now April and it is starting to hurt again. Specifically the back of my knee. I didn't have to have any surgery before. Would I need to now? I don't know what to do.
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I am 26. I work in some IT company, and i have sitting job. now I am suffering from sever lower back pain. Doctor said that it is due to long time sitting work. What to do?
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I'm 9 days post op, can anyone tell me, do I have to sleep on my back?
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With my knee pain it hurts the most when I lay down with leg straight out, then it starts to stiffen and pain runs down to the top of my foot up my hip, butt bone from my knee cap. What is my diagnostic and whats the worst condition this can cause if not treated or taken care of.? Please I need advise. I live with a severe ,chronic pain. Even ibuprofen and tramadol pain meds.does not ease the pain..
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About a year ago I got some (maybe 20) red bumps/spots on my back. Some are raised and some are flat against the skin. They don't itch. The doc gave me some steroid cream which faded them but didn't remove them entirely ( a few went away).
The problem is now I have more spots, behind my knee (3 or so), ankle (2) and on my penis (10 or so). Same thing, red spots that don't itch or cause any discomfort. They seem to appear suddenly, it's not a gradual thing. I would think they were insect bites but they don't itch, but that's what they kinda look like. They also don't heal naturally.
I've attached a pic from last year of my back. These ones have faded now but you get the idea of what they look like. I still have that cream, should i use it again or do you think i need to see a GP? I've seen two about my back and neither of them really seemed concerned to be honest, but they weren't dermatologists.
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I'm freaking out so I'll try to make sense. I woke up this morning with a stinging pain in the back of my left knee and I read that this might be a symptom of Deep Vein Thrombosis and it has scared me. I had blood tests done a month ago and they all came back clear. I don't sit too long, don't travel on planes and have no prior family history of clots if that helps.
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I'm 23 weeks and 3 days and my lower back,hips and knees hurt me so bad I can't sleep that well. So is it okay to take a nice warm Epsom salt bath or any other suggestions? I have scoliosis in the lower back and just started showing in my belly area (well it just appeared one morning lol) but I've noticed my back and everything has been really sore.
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Pain in buttock muscles, knee (with additional feeling of bubbling on back of thigh) and groin, is this sciatica?
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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.
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. ....
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I am 25 year old IT engineer facing knee pain along with other spine problems. I have been diagnosed as cervical spondylosis around 8 month back so i was taking physio therapy session since then. During those session i was getting some pain in my right leg knee which i ignored as i have bigger problem to be taken care of. Over the time it increased and since 2 month i am feeling pain while exercising for cervical and when i walk (sometime unbearable ) so I started physio therapy for that too but not getting satisfactory results. In addition to that I was swimming for subsiding my neck , left hand and knee pain but unluckly i got pain in my lower back pain due to swimming which was getting increasing day by day so i started physio therapy for that. I am doing physio therapy for neck , left hand, back and knee. I am very dishearten as suffering from neck , left hand pain with lower back pain and that extra pain has added. Could someone please let me know whether i will be get recovered from that painful life ever?
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my daughter is thirteen weeks pregnant and has been in touch with chicken pox at the contagious stage. what are the risks to her and her baby. she has seen a doctor and is very upset.
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I am deciding whether or not to get a stapedectomy done, and my doctor told me that it is only a 0.1% chance (1 out of 1000) that i will go completely deaf. i think i am going to go through with it...since i have been partially deaf my whole life, and am excited to hear the difference.
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I recently had an encounter where I accidentally may have used the towel which the sex worker just used to clean herself. What are the risks of stds for this action? Do I need any testing?
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i have been on atorvastatin 20 mg for about 4 years now. i was on simvastatin but i had muscular problems . just lately it's all you have been hearing on the news is there seems to some doubts about statins do the benefits outweigh the risks and what exactly are the risks , does anyone actually know.
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I have had a macular pucker in my right eye for three years. It's not terrible, just very frustrating. It has been changing only a little from year to year.
I have not wanted to try vitreous surgery for epimacular membranes (macular pucker 'repair') because of the risk of some of the receptor cells being damaged as the scar tissue (epimacular membrane) is pulled off the macula. I don't want blind spots.
Yesterday an optometrist told me that I risk getting those same blind spots by not having the surgery - because the scar tissue is pulling the receptor cells away from their blood supply.
Is/are there any data or studies that compare the risks of having the surgery with the risks of not having the surgery - as regards damage to the macular cells?
I know that development of cataracts is a well known complication of having the surgery. And having to risk cataract surgery is another reason I have for resisting the pucker repair.
I am seriously considering getting glasses that adjust for my main problem (things look 15% bigger in my right eye). This condition, caused by the membrane, is called aniseikonia and can be compensated for by getting glasses that minimize the image in my right eye.
If the risks of surgery, and there are many, are greater than no surgery, special glasses will be my choice.
I've read that, on average, the surgery, if successful, gives you back half of the vision originally lost to the pucker. I think that means I would still need special glasses.
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Can taking 8 to 10 dihydrocodeine 30 mg pills a day cause serious health problems? I am aware of addiction issues but what are health risks? Is there risk to kidney function or liver function etc?
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I'm a 25 year old female who has recently moved to Singapore with her partner.
I began attending a specialist in Glasgow in 2010 after minor palpitations that would always disappear on their own or with a forced cough. The longest lasted 10 minutes. They never caused me too much concern and after lots of tests and ECG monitors, which returned nothing, I put it at the back of my mind. My Dr. suggested it was a minor AV Node SVT and that we would just monitor it over time.
Last Sunday morning I woke out of my sleep at 0630 with a severe attack. Nothing would stop it at home. After 15 minutes I made my way to the nearest A&E where I was injected with Adenosine (not pleasent) and was kept under observation for the rest of the day before being sent home being doing that I had SVT. I had no caffeine or alcohol that night and made sure that I rested well.
The following morning I was woke out of my sleep at 0530 (an hour apart - strange) with another severe attack and followed the same process at A&E. Again, I was kept in for observation for the rest of the day before being sent home with Verapamil, to be taken as and when required.
The following day I was tired, extremely anxious and now afraid to be on my own or fall asleep but I had no palpitations. I followed my no caffeine and no alcohol diet hoping for the best but by Wednesday evening, after leaning over, another attack presented itself.
I have an appointment with a specialist here in Singapore on the Thursday the 22nd and it can't come quick enough, this whole thing has flipped my world and has put everything on hold. Even with a supportive partner, not having my family here has been an upsetting experience. My Dr. in the UK has suggested that I have RFA done to cure the condition once and for all. I'm terrified of the risks but don't want to have to take medication for the rest of my life either. My other problem is, do I get RFA done here or back in the UK when i'm home on leave in July? Should I wait or could I be making my condition worse?
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Over a year ago I noticed a change in my vision. It was diagnosed as a macular pucker. I repeated a visit to a retina specialist and she recommends surgery to repair it at an early stage rather than waiting until it gets worse. I live in a large metro area with great doctors and the one I see has good marks.
I can see 20/40 in the bad eye and just fine in the other one. I do wear glasses though. I can tell that my vision is weird as it tries to blend the 2 eyes together but it doesn't stop me from living a normal life.
So, is it worth it to have the surgery like they say or can I just wait it out? If it never changes from what I have I will be fine. I fear the bad results possible with surgery. Why risk a bad outcome and a worse problem than I have now?
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