Well it is a month since my last visit to the hospital to see the vampire darts team and therefore my last monthly dosage of the blue stuff is due. On Monday, the day before my appointment, the ward at the Royal Hallamshire hospital rang me to tell me that they were trying to book the ambulance but were told by them that one was booked already to take me to the Northern General hospital! Needless to say, I knew nothing of this appointment. The next thing was a call from the Northern General asking me if I was keeping the next day's appointment to which I said that no letter had been received and the Hallamshire appointment was more essential. The young lady said she would investigate and call me back which she did and apologised profusely because it was a mix up on their part.
All was well [so I thought] and so the next morning the alarm was set for 5 a.m., so I would be ready for 8 a.m., at 10.30 I was still here and I am supposed to be on the ward before that time so I rang the ward who rang the patient transport department, the ward rang me back 10 minutes later and confirmed my suspicions, the fiasco the day before had resulted in all transport being cancelled. The ward staff were not pleased but there again they didn't know the level of chaos that occurs whenever I try to do anything!
So another appointment was made for me on the Thursday [tomorrow] meaning another early morning start. So we will see what amount of chaos will reign tomorrow!
Regarding my housing situation, everything is a 'wait and see'. The department that awards 'mobility priority' have told me that I am on the system and the assessment will be done when it comes to my turn with no indication as to how long it will be.
The bidding system seems a shambles, we have to bid for properties after only seeing a photograph on the website, then we are allowed to view the properties. Someone has told me that often they have a 'viewing day' when all the interested parties view together, but the housing department know who they are going to offer it to. So why let others view?
I wonder how many people cheat like I do? Using google earth and google maps to look around? I may not know the exact address but a postcode puts me on the correct street and then I can look at the garden size and distance to the bus stops etc. but all this gets me any further towards moving
Well I'm home from the hospital and guess what? They've not done anything apart from make holes in my arms – 2 at each inner elbow with matching purple bruises. Apparently I have got another urine infection AGAIN – The Staff Nurse is going to ring on Monday to tell me if I can take these antibiotics the GP has left for me, or whether I need different ones, in which case she will ring my GP. Another appointment will be made for me in about 2 weeks, it seems as though because of the infections causing delays the original 12 month treatment is more likely to be 18 months. [why did I think it could be possible for me to keep to the schedule]
Friday, 16 July 2010
Friday, 25 June 2010
THE RAMIFICATIONS OF BEING STUCK!
Hello everybody, I'm still here even though it has been a while. I've had the second low dosage chemotherapy treatment but little progress on the housing situation.
Let me tell you about the treatment day. The good points of the day were that I wasn't as bruised as before, they had no trouble finding a vein that would play and so inserted the cannula and took the blood test sample from that; they had football on the television instead of the usual 'magazine' programme, which is usually about Celebrity and fashion, even the recipes, and as I am not interested in either, I find those programmes boring, also a friend who lives near the hospital came to keep me company, and we can and do keep talking for hours! My urine was olive green time not the bright green of last time. Probably because more is staying in my system, it is a cumulative treatment after all.
That evening I let my leg bag fill too much and had what I thought was strong bladder spasms, by the time I realised that it wasn't a spasm it was too late to get to the toilet and so I made a puddle on the floor. [That'll teach me to make sure the bag is emptied regular]
My blood test results are gradually improving so something positive is happening. Maybe next time the effects will last longer. Another indication of my body retaining more of the treatment is the steroid high I have been on for about a week. The feeling of being able to handle anything life throws at me and the overwhelming tiredness afterwards. Plus the steroid flush that I have been warned about but has never happened to me before, and, of course the insomnia, but I've attributed that to my mind overworking due to the imminent move.
The news that I will have to move has counteracted any positive effects of the treatment. I now drag my right foot continually even scraping it on the riser part of the stairs which is not safe. It takes me so much effort to climb the stairs I have no energy to do anything apart from sit on my dressing chair, and the thought that I have to descend the stairs doesn't help either. I have to cling to both handrails so cannot bring even the dirty washing downstairs. Oh the joy of having a bungalow.
My GP has referred me for a wheelchair and, after a discussion she is ordering an electric helper chair. I can't have a self-propelled model unless I want to spend my days travelling in circles and a power-chair would only be provided if I had either a ramped or level access. As Alan has been told by the cardiologist that he cannot push a wheelchair the electric version that is easier for him is the only solution
So I have no independence until I move and that is making me impatient, I have spoken to the Occupational Therapist since and from what she said I am working on an October moving date. Not ideal but I am left with no option really, the workings of Local Government departments are powered by pedals it seems. My MS physiotherapist is prodding them to move quicker if that helps. I bet it doesn't!
I haven't told my mother yet about having to move, some days she just isn't on this planet. Her planet must be light years away from mine because I never see her in transit. She is trying the care home again next week, which will give all the family a break from her ringing each of us for nothing.
Let me tell you about the treatment day. The good points of the day were that I wasn't as bruised as before, they had no trouble finding a vein that would play and so inserted the cannula and took the blood test sample from that; they had football on the television instead of the usual 'magazine' programme, which is usually about Celebrity and fashion, even the recipes, and as I am not interested in either, I find those programmes boring, also a friend who lives near the hospital came to keep me company, and we can and do keep talking for hours! My urine was olive green time not the bright green of last time. Probably because more is staying in my system, it is a cumulative treatment after all.
That evening I let my leg bag fill too much and had what I thought was strong bladder spasms, by the time I realised that it wasn't a spasm it was too late to get to the toilet and so I made a puddle on the floor. [That'll teach me to make sure the bag is emptied regular]
My blood test results are gradually improving so something positive is happening. Maybe next time the effects will last longer. Another indication of my body retaining more of the treatment is the steroid high I have been on for about a week. The feeling of being able to handle anything life throws at me and the overwhelming tiredness afterwards. Plus the steroid flush that I have been warned about but has never happened to me before, and, of course the insomnia, but I've attributed that to my mind overworking due to the imminent move.
The news that I will have to move has counteracted any positive effects of the treatment. I now drag my right foot continually even scraping it on the riser part of the stairs which is not safe. It takes me so much effort to climb the stairs I have no energy to do anything apart from sit on my dressing chair, and the thought that I have to descend the stairs doesn't help either. I have to cling to both handrails so cannot bring even the dirty washing downstairs. Oh the joy of having a bungalow.
My GP has referred me for a wheelchair and, after a discussion she is ordering an electric helper chair. I can't have a self-propelled model unless I want to spend my days travelling in circles and a power-chair would only be provided if I had either a ramped or level access. As Alan has been told by the cardiologist that he cannot push a wheelchair the electric version that is easier for him is the only solution
So I have no independence until I move and that is making me impatient, I have spoken to the Occupational Therapist since and from what she said I am working on an October moving date. Not ideal but I am left with no option really, the workings of Local Government departments are powered by pedals it seems. My MS physiotherapist is prodding them to move quicker if that helps. I bet it doesn't!
I haven't told my mother yet about having to move, some days she just isn't on this planet. Her planet must be light years away from mine because I never see her in transit. She is trying the care home again next week, which will give all the family a break from her ringing each of us for nothing.
Sunday, 13 June 2010
BLOOD TESTS AND ASSESSMENT
Well the woman from the Council is coming this Tuesday to see if access can be done for me or whether I will have move. I do need however to see the doctor, I feel as if I am imposing on the telephone.
Now it is Thursday and the woman came and went [useless] and her recommendation to her Manager is going to be that adaptations could not be done to this house and therefore the only option is to move to either a ground floor flat or a bungalow. Of course big mouth here mentioned Alan's ground floor flat, but we can't go there because of the dog, [bless her] that being one reason among many, so we have only one option, that is a bungalow.
This brings along two more problems - there are very few empty ones and those that are empty are in areas we don't want to live in and become members of the ethnic minority. Also when I asked her if there was any help with moving she said no, the thought of the logistics of moving has brought on another relapse, I am now finding stairs a 90% challenge whereas before they had rated a 50% challenge. So unless someone in the MS department knows of help I can apply for we are left facing a large bill for the packing and moving, when we get somewhere that is, we could be waiting about two years!
Don't you agree with me that the local authority are saving thousands by not doing any work and so giving me a moving grant to cover my costs is not too much to ask?
So now we are waiting for the outcome in writing. Once we get that we can say we want a bungalow and start the search hopefully with Medical Priority
My GP told me aswell, after consulting with her colleagues and MS specialists, that the bladder spasms are part of MS and can't be controlled with medication [thanks I really wanted to know that it would be with me for life]
The next treatment is on Tuesday when I see the vampire darts team again.
Now it is Thursday and the woman came and went [useless] and her recommendation to her Manager is going to be that adaptations could not be done to this house and therefore the only option is to move to either a ground floor flat or a bungalow. Of course big mouth here mentioned Alan's ground floor flat, but we can't go there because of the dog, [bless her] that being one reason among many, so we have only one option, that is a bungalow.
This brings along two more problems - there are very few empty ones and those that are empty are in areas we don't want to live in and become members of the ethnic minority. Also when I asked her if there was any help with moving she said no, the thought of the logistics of moving has brought on another relapse, I am now finding stairs a 90% challenge whereas before they had rated a 50% challenge. So unless someone in the MS department knows of help I can apply for we are left facing a large bill for the packing and moving, when we get somewhere that is, we could be waiting about two years!
Don't you agree with me that the local authority are saving thousands by not doing any work and so giving me a moving grant to cover my costs is not too much to ask?
So now we are waiting for the outcome in writing. Once we get that we can say we want a bungalow and start the search hopefully with Medical Priority
My GP told me aswell, after consulting with her colleagues and MS specialists, that the bladder spasms are part of MS and can't be controlled with medication [thanks I really wanted to know that it would be with me for life]
The next treatment is on Tuesday when I see the vampire darts team again.
Friday, 28 May 2010
MY EXPERIENCE OF THE VAMPIRE DARTS TEAM
Well what a week! I had the chemotherapy at the second attempt but it was still fun! Of course my veins don't ever want to co-operate. 4 attempts later and they did get some blood to test and I was left with 4 bruises on my left arm, one of which appears to travel down a vein leaving a nice elongated mark. Of course there was the essential urine test. The first being from the bag was too contaminated so this had to be taken from before the bag, as directly from the catheter as possible. A nurse was told to use a syringe on the valve, but I didn't realise it would leave a small hole in the valve. It wasn't until I stood up later that I noticed the damp patch [damp? It was more wet!], and, as is my want, I changed into my baggy, thin cotton trousers as soon as I returned home and so ended the day very soggily as well as bruised.
Fitting the cannula was awkward, and these were nurses who only did that all day, all week. A very tall surgical registrar wandered into the ward at that point and was instantly persuaded by the nursing staff to do the job, much blood everywhere later the cannula was fitted and taped into place.
The royal blue coloured infusion began. It probably took about two hours to drip into my vein [my watch needs a battery] then it was replaced by a bag of steroid solution so about 5 hours after I had first set out I was home and very tired. There were some people who had brought their partners but the said partners just sat patiently and read their newspaper. I couldn't help wondering just why they were there.
When I was finished infusing an appointment was made for 1 month later. Apparently the course consists of once a month for three months and then every three months until next April.
Luckily because the chemotherapy is only a weak solution the only side-effect, apart from the bruises, is bright green urine that fascinated me! I don't think people who haven't got a collection bag get the full effect of this colour change. They don't know what they are missing!
Unfortunately, my bladder spasm medication stopped working at the same time, I thought it just needed time to settle down but no, it got worse. The doctor has changed my medication and I hope it works because the local pharmacy that I use has changed their policy so do not deliver prescriptions unless requested by the doctor, [which it was] yet it still took 2 days to reach me!
So it is all quiet on the medical front at the moment until I go to see the vampire darts team in mid June. I am still falling to my right and waiting for the equipment and adaptations team to do the assessment with regard to the wheelchair etc, They gave me a date of July so I will have to see and miss all the decent weather,
Fitting the cannula was awkward, and these were nurses who only did that all day, all week. A very tall surgical registrar wandered into the ward at that point and was instantly persuaded by the nursing staff to do the job, much blood everywhere later the cannula was fitted and taped into place.
The royal blue coloured infusion began. It probably took about two hours to drip into my vein [my watch needs a battery] then it was replaced by a bag of steroid solution so about 5 hours after I had first set out I was home and very tired. There were some people who had brought their partners but the said partners just sat patiently and read their newspaper. I couldn't help wondering just why they were there.
When I was finished infusing an appointment was made for 1 month later. Apparently the course consists of once a month for three months and then every three months until next April.
Luckily because the chemotherapy is only a weak solution the only side-effect, apart from the bruises, is bright green urine that fascinated me! I don't think people who haven't got a collection bag get the full effect of this colour change. They don't know what they are missing!
Unfortunately, my bladder spasm medication stopped working at the same time, I thought it just needed time to settle down but no, it got worse. The doctor has changed my medication and I hope it works because the local pharmacy that I use has changed their policy so do not deliver prescriptions unless requested by the doctor, [which it was] yet it still took 2 days to reach me!
So it is all quiet on the medical front at the moment until I go to see the vampire darts team in mid June. I am still falling to my right and waiting for the equipment and adaptations team to do the assessment with regard to the wheelchair etc, They gave me a date of July so I will have to see and miss all the decent weather,
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