Birdshot is a rare disease. Because of this, it can sometimes be difficult to get the right diagnosis and treatment.
The Government will be implementing a Rare Disease Plan by 2013. This plan SHOULD help all of us, with rare diseases get better services. But will it? The plan is now being consulted on, and the closing date for comments is 25th May.
This is our opportunity to give our opinions, and make sure the rare disease plan meets our needs.
You will remember that BUS has worked with Rare Disease UK (the national alliance for people with rare diseases and all who support them) to help advise the government on what people with rare diseases need. Some of our recommendations have been incorporated, but we are worried that this plan will not fully meet the needs of those of us with Birdshot and other rare diseases.
Individual patients can respond to the consultation, as can patient organisations and healthcare professionals. If you are an individual patient, or a healthcare professional, please take the time to have a look at the rare disease plan, and see if you think it will work for you. The plan can be found at:
If you want to understand why the proposed rare disease plan might not meet needs, Rare Disease UK have produced a very good presentation that you can listen to at:
http://www.anymeeting.com/RDWebinarEngland/EA56D880804C
If you have any concerns at all, following listening to the above presentation, please do submit your comments to the Department of Health. If you need help in designing your comments, Rare Disease UK has provided help – just click on the link below.
Alternatively, you can submit your comments to Rea at info@birdshot.org.uk and she will collate and present them
Many thanks everybody – if we work together, we might be able to get an NHS system that meets our needs!
Is this plan only for patients in the UK or would it include those of us in the USA?
Sorry, I should have said it is the UK plan. Applies only in the UK. Rea