If anyone can move mountains, it is Trudy Lapinskis. In spite of having the UK’s worst case of a rare neurological syndrome and suffering considerable pain, her only thought is to raise awareness among the medical professionals so others are spared the same agony.
She enlisted the support of her MP Malcolm Moss.
who raised it as a debate in Westminster this week.
She wants improved understanding of pain to help all pain sufferers, as well as those with her chronic pain disorder, reflex sympathetic dystrophy.
Here is part of Malcolm’s speech which highlights how pain sufferers have been let down in the UK:
“Pain management does not fit easily into the target-driven, rapid-treatment ethos of the modern NHS. The recent NOP survey shows that now 14 per cent. of patients with pain have seen a pain specialist compared with only 7 per cent. in 2002, but what of the other 86 per cent? Facilities for pain management are much more developed in the USA and parts of Europe.
“Specialist services exist in most hospitals in the United Kingdom, but their services are stretched, and some hospital services, such as at Oxford, have been withdrawn. In Southampton, the service closed and has been relocated in primary care, and at other hospitals—for example, East Sussex—there are threats of closure. Relocating a pain service in primary care should be achieved with adequate funding and planning, not by a sudden decision to close existing services or to dispense with the appropriately trained personnel.
“It has been estimated that 10 specialist sessions in pain management are needed for every 100,000 of population, but nowhere in the United Kingdom achieves that, and services are scarcer in the midlands and Wales.
“I end by paying tribute to a constituent of mine who suffers immense pain with stoicism and great bravery. She is planning a huge conference at the Methodist Central Hall in London in December and has attracted prominent speakers in this field from all parts of the world. I hope that her courage will begin to open the doors to knowledge about this condition for other pain sufferers.”
The reply from Health Minister Andy Burnham referrred to a 1999 government report into services for patients with pain management which recommended that a review be held into local provision of pain services, looking particularly at the provision of more specialised treatments on a networked basis. Has this been done?
He ended by saying: “In conclusion, we recognise the need to broaden the access that patients with a variety of conditions have to high-quality care and pain management services. We recognise that there is still some way to go to ensure that all people who need it have access to such care, but we have started to implement a number of initiatives to stress the importance of pain management.”
Trudy has had her day of glory, she should be feeling well chuffed. There is further good news for her too, she will soon be getting her parking permit and next month she will be joining the Queen for tea at Buckingham Palace.
Dear Ellee,
Thankyou so much for all your kind words and i would also like to thank Mr. Moss too. I feel honoured and flattered about all the kind words said about me and that Mr. Moss dedicated the debate to myself. The debate moves us a step closer to my ultimate goal in raising awareness to the highest level. The conference planned for 5th December for medical professionals only will hopefully not only aim to get everyone with rsd diagnosed, treated early with the correct treatment but also prevent anyone from ending up with the degree of disability that i have. Achieving my goals helps me to cope with my rsd. Hopefully i will be able to raise the sponsorship through donations etc.. to enable the conference to go ahead. There is one guarantee and that is i will pursue every avenue and never give up the fight. Thanks again for all you and Mr Moss have done for me in helping with my campaign to raise awareness. Mr Moss’s debate was excellent, lets hope it will make a difference to all those who suffer with chronic pain who live with it everyday including those with rsd.
Very best wishes
Trudy
Trudy, it’s thanks to you all this happened. You are a real star and I admire you greatly. I know your conference will be a great success and I hope it achieves your aims, to make the medical profession more aware of the symptoms so others do not suffer as you have.