Doctor Ali stroked the soles of my feet. My toes curled. I squeezed his hand with my left hand, then my right. So far so good. Then the bad news hit me. I still felt as if my legs and arms were tied down. I couldnât move them. My hands wiggled. My feet wiggled. My legs and arms were immobile. I looked at Doctor Ali with tears in my eyes.
âMy arms and legs donât move,â I sobbed.
âI was afraid they wouldnât,â he said. âIt is early yet. Now you are with us, we can try to find out what is wrong.â
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Three months later I was discharged from hospital in a wheelchair. My arms and legs still donât work. There is a faint possibility that something could be done, but not on the National Health Service. The cost would be enormous.
Then Greg did something that I wouldnât have agreed to if I had known about it. He went to his bosses who owned a TV station and a national scandal-rag newspaper. They planned a campaign to raise money for treatment. He even got my parents to co-operate. Between all of them they set up a massive media launch.
The first I knew about it was on the national news on TV. There I was as the local beauty queen five years ago, the home movies of me winning a skiing competition, and even rock climbing. Then there were pictures of me being evacuated on a stretcher surrounded by TV crews. The story ended with an appeal âCan you help Jan to walk again?â
I was angry. My private grief had been splashed across the TV news. It got worse. The scandal-rag printed pictures of me on their Page Three, topless. I thought those photos had been destroyed but I was the Page Three girl for a week. On Saturday they printed the one with just my hand covering my cunt. I had been wearing a G-string but they edited that out. I was nude for their million or so readers to drool over.
What hurt even more than the exposure of my body was the thought that thousands of men might be jacking off over my picture and enjoying themselves. All I could do was stay still while Greg humped me. He could put his cock into my fingers and I could squeeze. He could put it in my mouth and I could suck. He had to move my legs to penetrate me. I couldnât hold him or cuddle him. That made me cry.
I argued with Greg about it. I hurt him. I know I did but I was hurt as well. I didnât like being a charity appeal. I felt that he had sold my body or at least images of it.
I came round after a couple of weeks. I had thousands of âget-wellâ messages from strangers. A group recorded a pop record for the appeal, then played a âBirthday Concert for Janâ. I had to be wheeled on to the stage. Greg held my arm up while I wiggled my fingers at the crowd. Their response was amazing. Ten thousand people sang âHappy Birthdayâ to me. I cried. My tears were shown live on TV to five million.
The money rolled in. After the concert the total had reached two million pounds. For what? For a faint chance that someone might be able to help me.
More important than the money was an offer from a medical research unit near Cambridge University. They worked mainly on robotic arms and legs for people who were missing a limb or two. They thought that they might be able to do something for me because it was the nerve signals that were wrong.
Greg drove me to Cambridge. At the door of the unit I met Doctor Ali again. He had come, bringing my medical notes, to discuss my case with the researchers. Three TV crews recorded my arrival. Microphones were thrust into my face. I answered the questions as blandly as I could. How could I answer âWhen do you think you will walk again?â when I hadnât been given any hope yet?
All I could say was to thank those who were supporting me, and even praying for me. The prayers helped. Even though I was not religious, the idea that Christians, Muslims, Hindus and other groups were praying for my recovery was comforting. I felt as if all those people were giving me a cuddle. Whenever I was beginning to feel depressed or upset the thought of those prayers brought me hope again.
The first hour in the laboratory raised my hopes sky high. Electrodes attached to my arms and legs made them twitch and move. I could even flick the switches with my fingers and move my limbs myself. The movements were crude and uncontrolled but⌠My limbs were wasted with disuse.
The researchers, Doctor Ali, and Greg were all pleased. I had several hugs. After some practice I managed a swing an arm to tap Greg on his rump when he wasnât looking. That made him jump, then both of us burst out laughing.
Greg and I moved to the research unit, with our own TV crew. We had several mobile homes placed on a field, plumbed and wired in with adaptations for my wheelchair in my one. Greg had one as well. I enjoyed the limited independence that a few gadgets gave me. I could use the telephone, the TV, the computer and even make a cup of tea with commands from a keypad under my fingers. I still needed help to drink the tea.
Doctor Ali and a team of nurses were there as well. They were paid with money from the charity. They were happy. I wasnât a demanding patient and I was making progress. The TV crew recorded everything. There was a weekly programme for a quarter of an hour every Friday night showing what was being done. The programme had a high viewing rating and brought in more money each week.
The researchers were happy as well. They were being paid and their facility was getting national coverage once a week. They were attracting funds and more research into different fields. The funds meant that they could treat more limbless people most of whom wanted to meet me. Why not? Their courage and persistence in face of difficulties were amazing. They seemed to think that it was a big deal to meet me and sometimes get a cameo role on the TV programme.
Eventually the researchers had a trial system for my right arm. They had inserted pick-ups into my upper arm that could be stimulated by electrodes on the skin. They connected the electrodes to a keypad under my left hand. They told me what to do. I tried. My right arm lifted from my lap. I swung it sideways. It felt like controlling a fairground coin in the slot crane. Left. Up a bit. Right. Down a bit.
I played for hours. At the end I was tired but I could reach to a table in front of me, pick up a cup off a saucer and bring it to my lips to drink. It was half full of water. I had a plastic sheet draped across me or I would have been soaked through. The first dozen cupfuls I poured down my front, recorded faithfully by the TV crew. They also caught my delight when I drank my first sip without spilling.
After that progress seemed to be at a crawl again. I was fitted with more pick-ups in my left arm and in both legs. The legs were difficult. Raising and lowering them was easy. Walking was impossible. I had to be slung in a harness and suspended from a gantry so that I wouldnât fall. Each time I lifted one leg I would overbalance to be caught by the harness. I couldnât move the second leg to compensate for the change of weight.
The keypad system was a dead end. I practised hard to regain the strength in my limbs. Yet after weeks of practice I still couldnât control my major muscles. Press 1034 then (enter) to lift right arm and turn my hand over wasnât natural. The researchers and doctors went back to the design basics. The doctors prodded and probed to find the exact point where the link between my damaged brain and the nerves controlling my muscles ended.
Some research found on the Internet provided the breakthrough. An American university had been doing some defence contracts on thought control of aircraft. The spin-offs from that had led to them linking a sensor on the scalp to a mechanical arm. They could pick up a coin from a table by thinking at the arm. Some of the researchers flew to the US university and stayed for three months while I went slowly crazy trying to remember thousands of keypad numbers. By the time they got back I had managed to walk three steps before collapsing. Those steps were a great hit on the TV programme, as was my slow âRoyalâ arm wave to my fans.