Hey everyone, I have some good news :)
I went to the hospital on the 20th of June and had my x-rays and met up with the consultant to discuss my progress. It was agreed that the bones had meshed together quite well and now was the next part of the process- to slacken the frame off.
(This might be a bit awkward to explain, but I'll try my best.)
Above picture is my leg with my Illizarov Frame. The green arrows point to my rods which are attached to the rings. Basically these are all screwed together to hold the bone steady so it heals straight and everything fuses together as it should.
This is a better look at the rod, you can see the nuts holding the rings straight (meaning the pins hold the bone).
At the hospital, I had these nuts slackened off so the rings are free standing and the bone can freely move.
If you look closely, you can see the nuts aren't screwed down. I remained like this for one week and then had the rods and nuts taken out completely.
I'm now being held together with cable ties. The ties are there mainly for peace of mind as it's a bit unnerving to only have pins in your leg.
We now have to watch my leg and make sure it doesn't bend or move and all being well, the pins will come out on the 9th of July!!!
Showing posts with label pain. Show all posts
Showing posts with label pain. Show all posts
Monday, 1 July 2013
Sunday, 13 January 2013
Walking again.
The idea of the external fixation is that you can weight-bare through it straight away. In theory, after my operation, I would've got up and walked away. But life isn't that easy.
Physiotherapy started the day after my operation. I was given a walking frame and had to make my way from the bed to the chair, an easy enough task, so you'd think.
I was in agony lowering my leg from the bed to the floor, the blood rushing to my leg also brought feeling. I was with two physios, each helping me from the bed to the frame. I managed to stand and hobble over to the chair by the side of my bed. Something that would've taken a normal person seconds, took me fifteen minutes. Evey time I bent my leg, a hot pain would rush to my knee and when I tried to walk, my leg wouldn't respond in the way I wanted it to. There were moments where I thought my leg was out in front of my body but in actual fact it was parallel.
I got through my physio with thanks to only my mother. Without her, I would still be stuck in hospital struggling to get up from my bed. My mother devised a system where I would get up and down from my chair five times to earn a gold star. We spent hours in one night on getting just one star, to ease my leg into be bent and straightened over and over. By the time the physiotherapist came the next morning, I could get up with ease.
The next step of my recovery was walking with the walking frame. Like I mentioned above, it was difficult to get my leg to respond and when I wanted to move my foot forward, it would hang limply, not responding. Again all night, we practised walking with the frame, ever so slightly. I'll admit, I cried a lot through my physiotherapy. It hurt every time I moved and to put pressure on the bones was excruciating. When the physio returned the next day, I could walk a short distance with my frame. I was happy and was told I could go home if I progressed to the crutches.
Little did I know that crutches would be my downfall. I hated my crutches right from the start. They didn't support me in the way the walking frame did and the tile floors, to me, seemed slippery. I practised slightly with the crutches but less support from them meant more stress on my leg. Soon, I had blisters on my hands, my arms ached and I cried in pain every time I stood up. My medication was doubled to deal with the pain but done little to help me walk.
At this point, it was two days until Christmas and I desperately wanted to go home. I had to prove to the physiotherapist that I could walk. I grabbed my crutches and screamed inside every step I took but I walked the required length. This was good news, I could manage the length of an average room. The bad news however, there was another task I had to complete before I was allowed home; stairs.
I still don't know how I managed those steps but my determination to go home for Christmas was greater than my pain. I was dismissed from hospital on Christmas eve.
Physiotherapy started the day after my operation. I was given a walking frame and had to make my way from the bed to the chair, an easy enough task, so you'd think.
I was in agony lowering my leg from the bed to the floor, the blood rushing to my leg also brought feeling. I was with two physios, each helping me from the bed to the frame. I managed to stand and hobble over to the chair by the side of my bed. Something that would've taken a normal person seconds, took me fifteen minutes. Evey time I bent my leg, a hot pain would rush to my knee and when I tried to walk, my leg wouldn't respond in the way I wanted it to. There were moments where I thought my leg was out in front of my body but in actual fact it was parallel.
I got through my physio with thanks to only my mother. Without her, I would still be stuck in hospital struggling to get up from my bed. My mother devised a system where I would get up and down from my chair five times to earn a gold star. We spent hours in one night on getting just one star, to ease my leg into be bent and straightened over and over. By the time the physiotherapist came the next morning, I could get up with ease.
The next step of my recovery was walking with the walking frame. Like I mentioned above, it was difficult to get my leg to respond and when I wanted to move my foot forward, it would hang limply, not responding. Again all night, we practised walking with the frame, ever so slightly. I'll admit, I cried a lot through my physiotherapy. It hurt every time I moved and to put pressure on the bones was excruciating. When the physio returned the next day, I could walk a short distance with my frame. I was happy and was told I could go home if I progressed to the crutches.
Little did I know that crutches would be my downfall. I hated my crutches right from the start. They didn't support me in the way the walking frame did and the tile floors, to me, seemed slippery. I practised slightly with the crutches but less support from them meant more stress on my leg. Soon, I had blisters on my hands, my arms ached and I cried in pain every time I stood up. My medication was doubled to deal with the pain but done little to help me walk.
At this point, it was two days until Christmas and I desperately wanted to go home. I had to prove to the physiotherapist that I could walk. I grabbed my crutches and screamed inside every step I took but I walked the required length. This was good news, I could manage the length of an average room. The bad news however, there was another task I had to complete before I was allowed home; stairs.
I still don't know how I managed those steps but my determination to go home for Christmas was greater than my pain. I was dismissed from hospital on Christmas eve.
Labels:
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external fixation,
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fainting,
fibula,
gas and air,
hospital stay,
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inury,
needles,
nhs,
pain,
phobia,
physio,
physiotherapy,
skating injury,
surgery,
tibia
The operation
On the 18th of December at 3pm, I was wheeled down to operation. Luckily for me, they took my needle phobia into consideration and the anesthetic was administered through a mask. All I remember is going to sleep and waking up in immense pain.
The worst part about waking up was the compression pillows on my feet. The pillows basically inflate up and down to keep the blood flowing. It was painful because the pillows would squeeze my foot tightly (think like having your blood pressure taken but on your foot) before deflating. Later, when I was recovering, the pillows were put on my feet only at night and they became more of an annoyance rather than painful.
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| Sexy picture of me taken by my mother. |
The worst part about waking up was the compression pillows on my feet. The pillows basically inflate up and down to keep the blood flowing. It was painful because the pillows would squeeze my foot tightly (think like having your blood pressure taken but on your foot) before deflating. Later, when I was recovering, the pillows were put on my feet only at night and they became more of an annoyance rather than painful.
Resetting the mistakes
After my x-rays, I was wheeled into the fracture clinic into a private bay. I was given shots of morphine and gas and air was placed around my mouth. My partner was told to wait outside and it was explained that in order to put a cast on, the bones would have to be reset. I didn't know what that meant and was a bit hazy on what was happening. The next thing that happened was one of the worst experiences of my life.
To have bones reset means that they will literally manipulate the ends of the broken bone so that they are in a better position. This means they take the bones and crunch them together, hold them and then plaster it. It makes me sick to even think about what happened. I was in agony, I screamed, I lashed out so much that a nurse restrained me and then I passed out. Or I think I passed out because all I rememeber mostly is pain and darkness and screaming.
I wish I could say this process happened only once. I had my bones reset four times in total.
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