Fractured Humerus Physical Therapy - Pieces Of Bone Moving Feeling
Jan 29, 2014
I sustained a spiral fracture of the distal third of my humerus approximately 3 and a half weeks ago. Im currently in a hard functional brace and able to let my arm hang freely at my side. I began PT earlier this week and have a few questions regarding the process. While most of the exercises are focused on maintaining range of motion and are relatively pain free, some do put small amounts of stress on the fracture site and cause discomfort. Every once in awhile I can feel the pieces of bone moving during the exercises. My arm has also swollen up a bit more (specifically my lower arm) since beginning PT. I assume this is normal. I'm more concerned with the movement of the bone. Is this cause for concern? and will excess movement hinder the bone healing process?
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I suffered radial nerve palsy following surgery for broken humerus 9 weeks ago. The break area has recovered well but im still completely numb around parts of my elbow,thumb and top of my hand. I have only a slight grip and my elbow bends only at a 90 degree angle-Ive heard some numbing never recovers so could this be part of the reason i cant grip or bend?I know it takes 6-12 months for full recovery but im finding the physio very hard and should i be pushing these areas so much?Both areas are as swollen as they were 9 weeks ago which is another concern. Has anyone been through anything similar?
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I had a fall on june 17th 2014. Fell about 20 feet onto a concrete floor. I fractured the humerus, fairly simple fracture straight across the midshaft, no surgery. fracture to the elbow, and got radial nerve damage.
It is now week 14 and although the nerves are back and my wrist is fully functional, both fractures are yet to heal, the humerus fracture is fairly straight, and some callous is appearing, but there is still movement in the fracture site. And the elbow still shows a fracture.
I now have an electromagnetic device to help with the healing, 30 mins a day i can use it for.
Just wanted to know if anyones had success with one?
Also seeing as i broke the elbow the arm has been held in a sling this whole time, without straightening of the arm, so the inside of my elbow is getting very inflamed, but not painful yet, anything i can do to help it?
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After my 2nd THR {4 weeks post op to be exact} I was doing an NHS exercise when there was a crack and my leg gave way. The long and the short of it........Emergency consultant I saw said it would heal but would take a long time.......About a couple of months later I saw the consultant that has done both THR's and he said it would never heal. I would be on 2 crutches or possibly one for the rest of my life.
OK 20 months later I'm still on crutches but the main problem is that the pain has got so much worse. I'm in agony with it especially the first 3 hours or so in the morning. I've got other conditions but can cope with the pain from those....this!!! cant find anything to ease it.
I'm normally a person who is glass half full......but recently I've been very "down" I'm seeing the consultant again on Friday 2nd October....can't come quick enough. Anyone any ideas/ suggestions/or questions for the consultant. I get on well with him but this time I'm going to have to really lay it on thick if that makes sense.
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In early January of this year (2008) I was working out at the gym one day with weights. I heard a "pop" in my upper right arm. Did not think much of it. Continued working out with weights for another 3 days. One night a terrible throbbing pain started in my upper right arm. It was bad. I knew it was not a "normal" pain. I went to my family doctor and had xrays. Everything came back normal. The pain continued. It was terrible. I went back to my family doctor the next week. By this time, I had terrible pain in my arm, and lost some range of motion in my shoulder. My doctor sent me for an ultrasound. It showed that I had a Shoulder Impingement/Frozen Shoulder. I thought, at the time, that this was the most terrible thing in the world. Boy, was I wrong. I began physio on my arm, took anti-inflammatories and painkillers. My ROOM came back, shoulder got better. I was still having terrible pain in my arm. That same "throbbing, pulsating" pain. I was not sleeping at this point. I went to see a few sports and rehabilitation doctors. I got a cortizone shot in my shoulder for the pain. Did not work. I requested another ultrasound from my doctor. It showed that I had a partial bicep tear. I thought that that was the cause of all my problems in the first place. So I began treating that. I had another cortisone shot in my bicep. It made things worse. I was a terrible mess. On painkillers, NSAIDS, anti-depressants, etc. I was at my "witts-end". On another last ditch attempt visit with my family doctor, he prescribed me antibiotics because he believed that I had an infection. My arm was swollen, sore to the touch, very painful, I had a fever, etc. The antibiotics worked. My swelling went down, the pain started to go away, I started to feel like myself again. I thought I was cured. In the meanwhile I had a bone scan. It came back "not normal". My pain doctor who made me have the bone scan told me to go to the hospital right away because he thought that I had cancer in my bone. At this point I was feeling better after being on antibiotics for only a few days. I was devastated. I could barely even believe it - in fact - I did not believe it. I was admitted to the hospital where I had numerous testing done. MRI, CT Scans, Xrays, bloodwork, etc. I was being treated for a bone infection and was on intravenous meds for 4 days. On my fifth day in the hospital, my doctor changed her diagnosis and told me out of the blue that she believed that I had cancer in my arm bone. Either Lymphoma or Sarcoma. Needless to say - I was in a state of shock. I was sent for a biopsy of my arm bone. I had to wait approximately 3 weeks from the date I was told that I had cancer until the day I received the results from the biopsy. I was told that I did not have cancer and had chronic Osteomyelitis. I was so happy to hear this news. I just went to go see an infectious disease doctor today. She told me that the damage to my humerus was bad and that it would not be "the same"anymore. I can't do any weightlifting anymore. I am on oral antibiotics for at least three months. I have a Staph bacteria that somehow nested in my arm bone. I am just thankful that it is not cancer. I do hope though that my infection goes away and NEVER comes back and that the damage to my humerus does not affect my every day to day life.
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I broke my humerus (upper arm) bone in half about two weeks ago. It is a oblique break in the middle of the bone. They had me take x-rays yesterday so they expected me to straighten my arm. Well buddy my bones started grinding and popping and OW! needless to say say they didn't didn't get me to straighten it... Ah whatever they got pictures of it straight the day I broke it thanks to painkillers. It is in a sling and perfectly aligned according to what they did get yesterday and two weeks ago. I am 20 I don't smoke and i don't drink. That is my story now my questions are. 1: how long until I can straighten my arm without the bone moving and snapping? They expect more x-rays in 2 weeks but if this thing moves its not happening! (because I'm a wuss I know) 2: how terrible does therapy really hurt? Should I take pain pills beforehand? I've heard some scary stories about therapy after a break. 3: do I I have have to worry about breaking it again in therapy or when I do decide to straighten it out? May be a stupid question but last time my arm was broken i was 2 so... 4: I have a numb spot on my arm, that from the bone or did I give myself frostbite from non stop ice packs? It's above my elbow, below the break. And lastly how long until it's completely healed? I'm a CNA I kinda need the thing :/ thanks for taking taking time to read this please help me out a little. I have borderline PPD and a hint of wimp so I appreciate any HONEST information!
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It all started three years first got a raw feeling around my anus them it started to itch bad day and night it felt like worms I took 3or 4boxes of worm tablet enough to kill a cow. I had a Sigmoidoscopy and colonoscopy with no results it continued on the itching isn't as bad now but it still there mostly at night . It starts now at night when I'm in bed or when I'm relaxed . When Tgt starts it feels like ive to poo not a heavy feeling but like little bit of pressure in there but it feels like it's moving around I try to poop but nothing comes out .
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My mom is 88. In August of 2012 she fell and broke her left humerus. Our first Dr. did an external fixation and we administered a bone stimulator conscientiously for 3 1/2 months, a half hour every night. After about six months the external fixation became progressively loose.
We obtained a new orthopedic surgeon who deemed that another surgery would be necessary. He did an internal fixation with synthetic bone graft. After about a year that has failed. Now we have total failure of the arm …. (looks like two elbows), x rays reveal floating screws, wire wrap coming undone from the plate, and most recently painful surges from the shoulder all the way to the tips of her fingers.
Her bones are obviously very osteoporotic. Our Dr. has suggested another surgery with a longer plate. I worry about another surgery (T.I.A. and clotting) and after two failures why would a third be successful?
Is there any new technology regarding 'profound osteoporosis bone fixation'?
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Has anyone had physical therapy for rectal prolapse? and if so did it help at all?
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I've had great success with PT for various muscle groups on the past. But sciatica is neurological. Can PT fix my nerves? Or will it alter where the nerves "run" by shifting muscle strength?
Just hard for me to believe PT can address tingly pain (which I have in right buttocsk and down leg).
Does MRI (which I've had plus x-rays) indicate if PT is a viable option vs. shots or....?
Should 5 PT sessions be enough to tell if PT will do the trick or not?
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Feeling clueless and desperate, so needed to write it off and maybe get some feedback.
I'm 27yo now and for over 2 years I've been having heel pain. It started after running a couple of miles with a lot of uphill parts and sore achilles tendons after a couple of days. Ignorant of achilles injuries, I continued training hard until the pain was to much to bear.
What followed was months of
> manual/friction therapy
> extracorporeal shock wave therapy
> NSAIDS (until it ruined my stomach)
> physical therapy
The pain evolved from being in my achilles to more on the inside of my heel.
Since medical imagery never revealed anything, I had an EEG.
The foot specialist examining me saw a good enough reason to go ahead and open my foot up to perform a tarsal tunnel release surgery.
But after 2 weeks of a half-open cask and some additional weeks of recovery, the pain was still there.
Eventually going into taking natural anti-inflammatories (think turmeric) and just trying to go easy, the pain kind of evolved again to being more on the bottom of my foot now close to and on the heel.
Having had custom orthotics (which didn't help), acupuncture, some more physical therapy, I'm just completely lost..
This influences my life so much.. I'm in an active job, -was- an complete sports lover, loved to go walking, go out in the weekends.. It's all accompanied with a lot of pain, making me miserable and desperate.
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So I know my anxiety increases a lot prior to my period, but is it normal to experience physical symptoms of anxiety without feeling mentally anxious? I guess you can. I posted about digestive problems so that appeared without me actually feeling anxious. It's just unnerving. Yesterday was normal, today I woke up with diarrhea and the shaky feeling inside me. Tonight I feel tingling in my arm and tightness in my shoulders and head. But I don't "feel" anxious. My period is probably just a few days away. This is so hard to deal with!
I feel like this is another women's issue that no one talks about. I had no idea it could go on for so long and cause such a laundry list of symptoms. Why isn't there more discussion about it? It's like when I went through infertility. Another taboo women's topic.
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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.
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.
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I am 42 yrs old and had a Partial Knee Replacement done on Jan 6th...outpatient...went to first PT the next morning. Wasn't too bad...2nd was a little rougher and I was in more pain. 3rd visit had a different therapist and she pushed me beyond what I thought I was ready for. She basically forced bended my knee and forced straighten it..said it's to keep scar tissues from interfering with recovery...this was extremely painful. I am curious to if this is normal protocol on your 3rd visit of PT..which was 7 days post op...I was in soo much pain I could not go to my next PT. Plus I have bruising on my ankle from her force bending with her body weight...I figured I would go back on Monday when my normal Therapist will be there....I have made progress with bending and straightening and don't think I should be rushed like that...I am still in alot of pain but am able to walk around house without crutches. I have been icing and elevating along with doing my homework PT.
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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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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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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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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".
(Cleveland Clinic, Angelo Licata 2009).
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To those who've already lost it, I'm just wondering how much it was cause mine has been lost in pieces. So, I dunno if I lost it all or not...
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I'm 17 female and I know it's gross but I'm worried today and yesterday I had light brown stool with black in it the black piece was long I'm scared I have been taken vitamins the past two days but my stomach hurts and nobody will take me to the Dr should I be worried
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So i have been losing pieces of it. I am 40 weeks. I was worried because i was told there's usually blood in iy and i don't have any and it's coming out a little at a time since yesterday... Anyone else have this?
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