how do I do it ... I dont know!
Im not sure how I do it really!!
Im on a huge amount of prescription drugs including numerous painkillers from codiene, NSAIDS right up to ketaprofen and morphine as well as numerous other non-painkiller drugs - I have over 120 tablets a day and thats just prescription ones not the supllements!! I also have weekly injections and drip therapy / Iv treatments when I can afford them. I have severe cfs/m.e, lordosis,scoliosis and kyphosis of the spine, mitochondria failure and now depression too! My horse is my lifeline, he is my reason to get up every day and face the world and my reason to keep on and he is what gets me out of the darkest times. I now have a lot of help from my mum who does the field for me the days she can which helps enormously, and since starting with the RDA Ive learnt thinsgs and equiptemtn to help e.g rainbow reins, extra rolls on the saddle, bareback etc.
I couldnt do it without such an incredible bond between harry my horse and I, some days I feel utterly horrendous, and when Im in hospital on drips I have his photo by my bed and I know he will look after me and help keep me brave so we can be together again when Im a bit better. I cant put into words how much he means to me, and that is really how I do it, because he means the whole world and more to me, and so you find a way to be together somehow. I need a mounting blcok to get on, the rainbow reins, extra saddle rolls and harry has been trained to respond to me and my aids as I need rather than the general aids which I cant always give.
I guess an element of sheer bl**dymindedness comes into it too, mum would say stubborn but I prefer 'determined'!!
I also use just about everything going, heat pads, wheat bags, tens, tiger balm, deep heat, extra warm layers, wrap around exercise sheet, bandages,magnets,aromatherapy,hydrotherapy,physio,bowen,homeopathy,dietry supplements,hypnotherapy cds,fully supported rest with cushions to support, a special giant pillow type ting to lie on as lying in bed is too painful, you name it and I probably use it / have it / have tried it!!
Im not sure how I do it really!!
Im on a huge amount of prescription drugs including numerous painkillers from codiene, NSAIDS right up to ketaprofen and morphine as well as numerous other non-painkiller drugs - I have over 120 tablets a day and thats just prescription ones not the supllements!! I also have weekly injections and drip therapy / Iv treatments when I can afford them. I have severe cfs/m.e, lordosis,scoliosis and kyphosis of the spine, mitochondria failure and now depression too! My horse is my lifeline, he is my reason to get up every day and face the world and my reason to keep on and he is what gets me out of the darkest times. I now have a lot of help from my mum who does the field for me the days she can which helps enormously, and since starting with the RDA Ive learnt thinsgs and equiptemtn to help e.g rainbow reins, extra rolls on the saddle, bareback etc.
I couldnt do it without such an incredible bond between harry my horse and I, some days I feel utterly horrendous, and when Im in hospital on drips I have his photo by my bed and I know he will look after me and help keep me brave so we can be together again when Im a bit better. I cant put into words how much he means to me, and that is really how I do it, because he means the whole world and more to me, and so you find a way to be together somehow. I need a mounting blcok to get on, the rainbow reins, extra saddle rolls and harry has been trained to respond to me and my aids as I need rather than the general aids which I cant always give.
I guess an element of sheer bl**dymindedness comes into it too, mum would say stubborn but I prefer 'determined'!!
I also use just about everything going, heat pads, wheat bags, tens, tiger balm, deep heat, extra warm layers, wrap around exercise sheet, bandages,magnets,aromatherapy,hydrotherapy,physio,bowen,homeopathy,dietry supplements,hypnotherapy cds,fully supported rest with cushions to support, a special giant pillow type ting to lie on as lying in bed is too painful, you name it and I probably use it / have it / have tried it!!