Cast? Chevron Osteotomy Hallux With Distal Soft Tissue Realignment
Jul 21, 2015
I had Chevron osteotomy hallux with distal soft tissue realignment and pip joint fusion on my second toe yesterday. I have padding and bandages and an orthopedic boot. I go back on Thursday to the dressing clinic for a Mitchels bootie. I have been told that this is a plaster of paris cast. Has anyone on here had one and if so how long did you wear it for? Also I have a pin sticking out from my 2nd toe, when is this likely to be removed? Apart from the dressing clinic appointment this Thursday my next appointment is to be in 6 weeks to see my surgeon. Surely the pin should be removed before this?
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I had a fusion of my big toe on October 28, 2009. As I approach my first anniversary, I am happy with the results. My joint was severely damaged. The surgeon said I had two choices, cheilectomy and fusion. He did not think the cheilectomy would work for me and if it did, it would only likely last a year. I did some research and realized that I was headed for a fusion. I decided on that and I am glad I did.
My recovery has been good. I did have a couple of scares when the radiologist suggested there might be a bone infection. Fortunately, that turned out not to be the case. I suspect he was confusing healing with signs of infection. At any rate, now that it is a year later, I have pretty much no pain. I am walking every day, usually at least a mile or two each morning. Sometimes I walk up to five or seven miles in one walk. My foot is up for the task. I have started curling for the season now, and my foot is great. The last time I curled, my foot was very sore (pre-surgery). It was so nice to curl without pain! Also, with all my walking, I am in better shape than before, so I curled amazingly well. Scary.
There is some misinformation about fusions I'd like to address: Your gait will be altered with a fusion - my gait was altered by the sore foot and limited range of motion from the arthritis. Now my gait is normal, I toe off the big toe again. That means that now my hip feels better. You won't be able to run or be active - fusion is actually recommended for people who wish to remain active. At least if the foot is damaged beyond a certain point. I am more able to run now than I was pre-surgery because I have a stable foot that does not hurt. Surgery is painful - yes, I had about four days of pain that required medication. After that, as long as I had my foot elevated, I was fine. I think bunion surgery is much more painful
Fusion is certainly a drastic procedure that probably should not be considered lightly. At the same time, if it is the right procedure it is fabulous.
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I am a 40year old woman. I have suffered from hallux rigidus for the last 6 years because of trauma.
Before surgery (which happened in april 013) I had tried all sorts of medications, injections, magneto therapy, you name it I have done it.
In April 2013 I had an osteotomy (NO cheilectomy) to correct it. After 10 months I can finally say the pain has gotten so much worse.
I can't do many things, my foot hurts even if it is not bearing my weight (not walking). Being so young I don't know what do do.
It is ruining my life, personal life (I can't go anywhere cause whenever I walk I am in so much pain) and professional life.
The doctor that operated suggested to do a cheilectomy or a fusion, but considering the result of this operation I am really scared any new intervention will make things worse.
Can anyone suggest a real expert in Europe? Or any other suggestion, I am really desperate.
Many thanks to all of you for reading my post, and thanks to anyone who would be so nice as to try and suggest someone or something.
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On Dec 3 I had a decompression osteotomy on my right toe for hallux rigidus. My doctor told me I would be running at 2 months and completely back to normal at 3. It is over 2 months and I still have a lot of pain and swelling. Running is out of the question and I am still limping.
I am interested in others' experiences with this surgery. I am supposed to have it done on the other foot as well, but I am simply worried that my right foot may end up worse off than when I started.
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I am due to have a bunion removed next month but because of arthritis in my big toe I am also having a 'fusion'.
I would love to hear from anyone who has had this operation to know their experiences.
Was it very painful - how long off work . what (if any) height heels can be worn after. I have been told maximum of 1 inch - is this correct?
Although my toe/bunion is painful, it is so difficult to know what to do especially as I can find no-one who has had this op?
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Last February 11, 2014, I fractured my leg (distal tibia and fibula). My doctor calls it Pilon Fracture. Spiral comminuted fracture of the distal tibia and fibula involving the articulations.
February 15, 2014, I went through MIPO (minimally invasive plate osteosynthesis). 4 weeks(March 11) after the operation, my doctor advised me to put some weight on it and so I did. 4 weeks(April 11) later, I had an xray and it appears like nothing's changed from my 1st x ray 4 weeks ago. I tried to put more weight on it but surprisingly, it doesn't hurt nor caused me any discomfort.
How long does a distal tibia and fibula fracture that went through MIPO heal? Exactly when would I walk again without my crutches?!
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I have just set up an appointment for a ulnar shortening osteotomy here soon and was hoping to possibly get some advise as to what I should expect for my recovery. I had torn my cartilage about four years ago and had it fixed six months ago. For the past two months I have been in a lot of pain and we have found out that my ulnar is pressing into the cartilage and making the injury worse.
I have had a few arthroscopic surgeries and know the recovery to expect for those but this will be my first non-arthroscopic surgery. I believe that my pain level and recovery will be worse and longer due to the plate and screws going in and the larger incision. Also I work at a desk job and am thinking that will take longer to get back to due to the maneuvering of the arm and wrist.
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I just had my ulna shortening op on Monday and have been discharged from hospital with a normal bandage. Has anyone else had this? I'm a bit concerned as most post I've read people usually have a cast after the surgery. My surgeon was quite adamant on not placing a cast, but I feel quite unsafe. In fact he wanted to take this bandage off on the day after the surgery. Can anyone recommend any kind of splint I can buy that would help me to feel a bit safer, I have a hyper 4 year old and don't want to risk being hurt. Especially as I can't take all kinds of painkillers, most strong ones give me palpitations and shortness of breath.
I just feel like I've been hacked up with very little after care. My surgeon was very rude and upset to find I had to stay overnight after the surgery. I was very sick from the general and morphine.
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About two weeks ago I had a nasty tangle with a rusty old swing set, and to make a long story short, the swing set kicked my butt and gave me a spiral fracture in my tibia (about halfway down my shin) and a hairline fracture through my fibula (right up near my knee.)
I've got the sucker casted and have been staying off of it, but recently had a nasty scare. I fell off my front porch (about three feet from the ground, which is solid concrete where I was sitting,) and only managed to keep from seriously hurting myself because I knocked my poor cousin over as he was walking by.
Again, I'm fine, but it got me to wondering: How likely is it that, had my cousin not been there, I could have broken my leg despite it being in a thigh-to-toe cast?
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After 1 arthroscopy, 1 bone graft, 2 ACLr my surgeon now thinks I may need a pkr or osteotomy. I know it's an impossible question to ask - but someone may have been through the same thing - if I have a pkr will the pain go? I'm reluctant to go through anymore surgery but I'm struggling walking sometimes.
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I am scheduled for an ulnar shortening osteotomy next Friday, and I am having panic attacks about the procedure so I figured I would ask others to share their experiences and maybe someone could answer some questions for me.
First, I am having this procedure due to my winning the genetic lottery and having an abnormally long ulna. This didn't start giving me pain until about a year ago. I woke up one morning and my right wrist hurt like I had slept on it wrong. When the pain didn't go away I went to a local urgent care to see if I possibly sprained it - I had been doing a lot of yoga at the time. They took x-rays, said it must be a strain or pulled muscle, gave me a splint and sent me on my way. For the last year I wore a brace on and off when my wrist gave me pain. The pain has never been constant, it comes and goes. The most disturbing thing about it is that when I rotate my wrist there is something in there that snaps and cracks - probably the TFCC, I learned from my research. I finally decided to see an orthopedist about my wrist as I figured it might be carpel tunnel from my office job. My ortho showed me the long ulna bone in the x-rays, which there is no denying - the ulna is visibly longer than the radius, even to an untrained eye. My MRI shows that there is wear on my TFCC, but no tear. I am developing cysts on my lunate bone, which is from the pressure from my long ulna. My doctor said that the way to fix this was the ulnar shortening osteotomy, which is coming next week.
My concerns about doing the surgery are varied. I am terrified of how much pain I might be in when I come out of the surgery. I know I will have painkillers, but I really don't want to stay on those for any longer than is necessary. I have read other boards about this and it seems like some people had more pain after the procedure than others. I am afraid that this will not be beneficial in the long run. I mentioned earlier that I enjoyed yoga, but my wrist pain has prevented me from doing yoga for the last year. Ultimately, I would like to be able to return to yoga, but since this surgery is essentially breaking my arm for me and then putting a plate in to hold it together, I have doubts about ever being able to return to yoga after this. I am also wondering if this is absolutely necessary. Like I said, the pain is not constant - it wasn't bothering me at all last week. However, since it's degenerative I imagine that this is not unusual, and that if I wait it will progress into being painful more often and that eventually my cartilage will tear. I am 31 years old, and while I don't consider this even close to being "old," it is also easier to bounce back from surgery the younger you are.
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I had a horse fall and have managed to fracture my left tibia in a spiral complex formation.
They decided not to operate and I have now been in a cast for 7 weeks and have another 3 weeks until my next visit to the fracture clinic
Has anyone else been in a cast this long and non weight bearing? How long until I will be able to ride again once the cast has come off?
I am getting really bored at home now because my work won't let me return until I am walking and the doctor keeps signing me off!
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My 6yr old son suffered a bad comminuted fracture to the tibia whilst on a bouncy castle. He was initially placed in a full back slab for a few days but was then meant to be changed to a full lightweight cast. Unfortunately the doctor deemed it far too unstable to mess around with and so has been left in the back slab with a full cast over the top. Its been on 2 weeks and has another 4 to go AT LEAST. i'm really worried about his recovery as he already had low muscle tone and hip instability.
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Hello... I am having an ulnar shortening done on Friday and I am starting to get really nervous about it. I noticed many people on here who have had this procedure talk about having a fiberglass cast for a couple of weeks after the surgery. My surgeon said after I week and a half I would be put in a removable splint and would not have a big cast like I did when I had my TFCC reconstruction. I was wondering if anyone else had heard this??
Also how long does it take to be able to do "normal" activities again? I am a nursing student and have to begin clinicals again in August.
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Broke fibula and tibia Feb 17, 2016. Had surgery March 1, and had 2 screws put a n fibula and a plate on tibia. After 8 weeks in cast and NWB I am now in a boot. I am doing exercises for therapy but after walking on it for about an hour leg hurts and ankle and foot swell. Also get sharp twinges now and then in ankle area. Has anyone else had these problems and how long before you can put full weight on it and be able to work. I'm a waitress and have to be on my feet for 4 hours or longer without sitting.
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I had a Hemorrhoidectomy in October of 2012 and I did have some complications with it. It is now 3 years later and things have gotten a little worse. Over time I have developed some internal scar tissue at the site of the wound (this was confirmed today by a Colorectal Surgeon) which has resulted in me having a hard time defecating and constant constipation. The outside of my anal opening is a little irritated as well and he gave me a topical cream for it. However, he told me not to worry about the scar tissue....that I wouldn't have never known it was there until he told me. However, I knew something was wrong because of the narrow stools. So I'm not trying to determine if their are any OTC creams i can use internally to smooth out or get rid of the scar tissue. I remember reading somewhere awhile back about non surgical treatments for scar tissue due to Hemorrhoidectomy surgery but I can't remember where.
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This is not cure, but it really worked for me for 8 mths to reclaim my life. I have hemorrhoids since 2012, and bleeded furiously at times. I have tried several methods to cure, tried pushing in the piles using KY gel during work or soap when bathing. But no success. Then one day I tried using wet tissues to push in. Worked like a charm! Even when I have diarrhea and had to go toilet 3 times, it still worked!!
This is how I would advise...
Right after your bowel business, take 3 wet wipes (pref the flushable type - otherwise do not throw into toilet bowl).
I use the first for cleaning. I would wipe twice with it (mine is 19x20 cm)
Then I would fold the second into half, wipe once, then fold again.
Position 2 fingers onto the center of the wet wipe (now quarter-sized) and push gently into anus.
First push at the center of piles (I have 2 big and 1 small, the smaller one most painful).
Push gently in, while relaxing your anal muscles.
Withdraw fully till the tips of your fingers are just touching the anus, then push in again.
Repeat one or twice more, then begin targeting the piles, pushing them in.
Total of 6-8 times shd do the trick.
Third wet wipe? Just a spare. I usually used it to confirm that it is clean.
But why wet tissues? Because they provide enough traction to draw the piles in, but wet enough to make it painless, and tough enough not to break.
Tips:
1. Experiment with different hands when pushing. I used to do it with the hand I normally wipe with, but my first finger started to ache after 3 months. Then I tried the other hand, and behold, angle is such that it is much easier to push in. And because it takes less effort, my finger of that hand has not ache even now.
2. Squeeze your anal muscles gently after the piles have been push in. If you feel a slight sensation of piles being drawn in fully, then you'll know it is done. Even if not, as long as your piles is no longer painful nor interfere your life, it shd be considered ok.
The whole thing only takes one more min in the toilet. And by using flushable wet tissues, it is so convenient, you can just throw into the toilet bowl, at home or outside.
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I have been dealing with undifferentiated connective tissue diseases for a few years. I am now being treated for Fibromyalgia and Rheumatoid Arthritis.
These are very painful at times.
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So I took the abortion pill, which resulted as successful. However, weeks later I was walking in my house and felt something moving out of my vagina, similarly to how I would feel the tissue and such while on my period, but significantly more. I ran to my bathroom thinking I was getting my period at an off time due to the abortion, but there was a large glob of tissue and blood that had exited my body. After that, there was nothing for a week or so later when I started getting my actual menstrual cycle again. Was this a result of the abortion? Is it normal?
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I have undifferentiated connective tissue disease and am off all meds. Currently I can barely walk. I am getting so used to it that it almost feels normal but of course it's far from normal. The pain is about an 8 out of 10 and i've never experienced anything over a 4 or 5. It was always fatigue before!
Can anyone tell me what i can do about this foot pain?
More than anything I just want to know what it is? It started when I began a job where i stand all day. Is it a kind of RA? I am desperate for answers. If I knew something would work I would do it. Anything but go back to prednisone....I"m starting to think that would be better too though!
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Four months ago I had microfracture surgery to repair cartilage damage in my big toe joint. Recovery has been very slow due to swelling. I began experiencing overheating in that foot just a few days following surgery. While my foot also gets quite warm if I stand or sit for too long, these more dramatic episodes occur only at night.
By overheating, I mean that the surgery foot turns bright red, and gets exceptionally warm... the big toe joint area gets downright hot to the touch (there is no infection present) and feels as though there is a space heater sitting about an inch in front of my foot.
The episodes originally occurred every night and lasted up to 2 hours before normal temp. returned. Gradually, the duration has shortened to 30-45 minutes, occurring only 3-5 times a week. The only way I have found to prevent this from happening (and it only works sometimes), is to leave my bare foot uncovered when I go to bed - no blankets or sheets over it.
Has anyone else experienced something similar? Nobody can seem to explain why this is happening - it delays my sleep well into the night and is definitely not helping the residual swelling I still have to subside.
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