Today I remember my Mum. The best Mum in the world, obviously!
My Mum died far too early in her life, aged 53. It always serves as a reminder to me to live life as if tomorrow was your last day, make the most of what you have and be grateful, don't sweat the small stuff, be true to yourself and try to make a difference in someone elses life.
Monday, September 29, 2008
Meningioma Facts
Meningioma Tumours are fairly rare and account for 30% of diagnosed tumours in the UK each year.
90% of meningiomas are benign, 6% are atypical, and 2% are malignant.
The word benign is misleading in this case as, when benign tumours grow and constrict the brain, they can cause disability and even be life threatening.
90% of meningiomas are benign, 6% are atypical, and 2% are malignant.
The word benign is misleading in this case as, when benign tumours grow and constrict the brain, they can cause disability and even be life threatening.
Sunday, September 28, 2008
Brain Tumours and Driving Regulations
Found some very interesting stuff recently which could be very important to some of you. I'm sharing this info because nobody mentioned it to me at all.
I have found that there are strict rules laid down by the DVLA (Drivers and Vehicle Licensing Assoc.) regarding epilectic fits and Brain Tumours. Now, bear in mind that the hospital will not contact the DVLA, but it is your responsibility to do so and your doctor will advise you how to go about this.
If you have had an epileptic fit, the Drivers and Vehicle Licensing Association will not allow you to drive for a year after your last fit and this period of time may be increased depending on your own circumstances and medical assessments.
If you have a benign meningioma (which is what this particular blog concentrates on) and have not had any seizures, the DVLA requires that you do not drive for at least six months after surgery. No-one made me aware of this and I'm not sure if I was supposed to know this sort of thing and whether it would have affected my insurance - but I didn't and I did drive. So this is why I am telling you, just in case :D)
If your occupation involves driving vehicles, such as a LGV (large goods vehicle) or a PCV (passenger carrying vehicle) you will not be able to drive for at least five years after surgery. If you have had any seizures you will not be able to drive this type of vehicle until 10 years after your last fit.
I'm not sure in the circumstances that you would feel it appropriate to take the risk anyway but in some instances you may require a medical assessment before your driving licence is renewed.
I have found that there are strict rules laid down by the DVLA (Drivers and Vehicle Licensing Assoc.) regarding epilectic fits and Brain Tumours. Now, bear in mind that the hospital will not contact the DVLA, but it is your responsibility to do so and your doctor will advise you how to go about this.
If you have had an epileptic fit, the Drivers and Vehicle Licensing Association will not allow you to drive for a year after your last fit and this period of time may be increased depending on your own circumstances and medical assessments.
If you have a benign meningioma (which is what this particular blog concentrates on) and have not had any seizures, the DVLA requires that you do not drive for at least six months after surgery. No-one made me aware of this and I'm not sure if I was supposed to know this sort of thing and whether it would have affected my insurance - but I didn't and I did drive. So this is why I am telling you, just in case :D)
If your occupation involves driving vehicles, such as a LGV (large goods vehicle) or a PCV (passenger carrying vehicle) you will not be able to drive for at least five years after surgery. If you have had any seizures you will not be able to drive this type of vehicle until 10 years after your last fit.
I'm not sure in the circumstances that you would feel it appropriate to take the risk anyway but in some instances you may require a medical assessment before your driving licence is renewed.
Labels:
benign meningioma,
brain tumours,
epilectic fits,
seizures
Tuesday, August 26, 2008
MRI Results
The exam was complete and I nervously asked the technologist if all looked good and clear. As is the usual procedure, she advised that the Radiologist had been down to have a quick look and had been out to speak to my husband.
The pulse quickened and my mouth went dry until I saw her smile. She obviously sensed my concern and fear and smiled the smile of relief and success, not the smile of sympathy or concern. This girl had been on the same path with me 2 years earlier and knew what they had found then so she must have felt a small amount of exhilaration that the images were clear. I cannot imagine what turns up in their day to day examinations. Nobody likes to be the bearer of bad tidings. They operate the equipment that is advanced enough to help diagnose a problem. Discovery is one thing, fixing it is another!
I left the MRI suite to be greeted by my smiling husband Roy. All clear he said - NO BRAIN TUMOUR - congratulations! Once again I burst into tears, but of relief this time! All that was left was to pick up the report the following day. I had studied the pictures in disbelief the first time so was really looking forward to looking at the new set.


ABSOLUTELY FABULOUS!
The pulse quickened and my mouth went dry until I saw her smile. She obviously sensed my concern and fear and smiled the smile of relief and success, not the smile of sympathy or concern. This girl had been on the same path with me 2 years earlier and knew what they had found then so she must have felt a small amount of exhilaration that the images were clear. I cannot imagine what turns up in their day to day examinations. Nobody likes to be the bearer of bad tidings. They operate the equipment that is advanced enough to help diagnose a problem. Discovery is one thing, fixing it is another!
I left the MRI suite to be greeted by my smiling husband Roy. All clear he said - NO BRAIN TUMOUR - congratulations! Once again I burst into tears, but of relief this time! All that was left was to pick up the report the following day. I had studied the pictures in disbelief the first time so was really looking forward to looking at the new set.
Labels:
Brain Tumour,
meningioma,
MRI,
MRI examination,
MRI Results
Saturday, August 16, 2008
MRI Examination
Off I toddled for my 5pm appointment. Once again, my husband was at my side, feeling just as anxious as me, I have no doubt.
The procedure seemed very straight forward this time. A canula was inserted into a vein in my hand ready for the contrast dye. A very sweet male nurse showed concern at having to do this to me and was very sympathetic to the fact that I may feel a little discomfort. The old hand that I am, I chuckled and assured him that a small jab in the hand was nothing but I appreciated his bedside manner.
Everyone was pleased to see me looking so well and couldn't believe it had been 2 years since removal of my benign meningioma tumour.
Funnily enough, I arrived feeling far more nervous this time than I did last time when I had no inkling of what the results would be.
All jewellery was left at home, I put on the fabulous hospital gown, was strapped in to the head cage and ready to go.
The familiar clicks and knocks started and half way through the procedure the contrast dye was administered. It took about 40 minutes this time and I started to think about the results as I was laying there as still as possible.
If it's all clear I would be ecstatic and would stop thinking about it all again for a while but I began to feel like I was teetering on a precipice because if it wasn't, it would all start again.....would it be in the same location, what kind of tumour, what treatment would be possible and oh, so many questions not to mention the fears.
You also start asking yourself the "why me" question and the sad thing is research has still not come up with anything conclusive.
The procedure seemed very straight forward this time. A canula was inserted into a vein in my hand ready for the contrast dye. A very sweet male nurse showed concern at having to do this to me and was very sympathetic to the fact that I may feel a little discomfort. The old hand that I am, I chuckled and assured him that a small jab in the hand was nothing but I appreciated his bedside manner.
Everyone was pleased to see me looking so well and couldn't believe it had been 2 years since removal of my benign meningioma tumour.
Funnily enough, I arrived feeling far more nervous this time than I did last time when I had no inkling of what the results would be.
All jewellery was left at home, I put on the fabulous hospital gown, was strapped in to the head cage and ready to go.
The familiar clicks and knocks started and half way through the procedure the contrast dye was administered. It took about 40 minutes this time and I started to think about the results as I was laying there as still as possible.
If it's all clear I would be ecstatic and would stop thinking about it all again for a while but I began to feel like I was teetering on a precipice because if it wasn't, it would all start again.....would it be in the same location, what kind of tumour, what treatment would be possible and oh, so many questions not to mention the fears.
You also start asking yourself the "why me" question and the sad thing is research has still not come up with anything conclusive.
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