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Effective protection and cleaning, easy to clean: made of high-quality non-woven materials, can prevent accidental spills, pet fur, stains, normal wear and tear. It can be cleaned regularly to avoid cleaning large recliners, which is very convenient
Elastic strap fixing: This sofa cover is equipped with elastic straps to ensure that it will not wrinkle, shift or slide. Can be adjusted according to personal needs
A variety of colors, One Size: This series has 8 colors, you can choose according to your needs, there is only one size: The length of this product is 200cm, width is 171cm. Please estimate the required size before purchasing and whether it is suitable After your needs, you can place an order
Ideal gift: This product is very suitable for family, home, dormitory, living room, etc. It is also very suitable for people who keep pets. It is a little happiness at home and a thoughtful gift for good friends.
【100% Service 】It is the core of providing our customers with high-quality products and services. If you have any questions, please contact us to ensure that you are completely satisfied.
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Stay up-to-date with all things lupus and LUPUS UK with our quarterly email newsletter!
LUPUS UK is the only national registered charity supporting people with systemic lupus and discoid lupus and assisting those approaching diagnosis. We presently have over 5500 Members and a number of Regional Groups around the UK who arrange medical talks, publish local newsletters, set up local occasions and organise fundraising events.
LUPUS UK also produces an informative national magazine with lupus articles, letters, reports, and photographs, and operates a strong Grant Programme for research purposes and welfare.
I learned almost everything I know about lupus from LUPUS UK and that knowledge gave me the confidence to get control back in my life and do almost everything I used to be able to do including running. It also helped my husband, family and employer to know what lupus is and how we can make life work together.
My mom was diagnosed with lupus nearly 15 years ago! Every day is a challenge! We have our ups and downs. Thanks LUPUS UK for the work that you do!
Contact LUPUS UK first to find out about the condition from those that know the facts; Books and random internet sites can just confuse the issue.
LUPUS UK has been a good source of information for me and my family over the last two years.
I'm so happy I ran...I'm so pleased that I've raised over £2,500...but most of all I'm so proud of my husband & how he deals with lupus & all the other complications that come with it!!!
Most people are unaware of this mysterious condition. People should know how hard it is to live with it. I was diagnosed with SLE some time back, and my life hasn't been the same since.
The LUPUS UK site is for informational purposes only and should not be a substitute for professional medical advice, examination, diagnosis or treatment. However, do not delay seeking or disregard medical advice based on information on this site. Always seek the advice of your local family physician or other qualified health professional before starting any new treatment or making any changes to existing treatment. Medical information changes rapidly and while LUPUS UK make efforts to continually update the content on the site, some information may be out of date.
LUPUS UK is a certified member of the Information Standard scheme. Any pages on this site that display this logo have undergone all the measures required by this standard, so you know it is information you can trust.
LUPUS UK shall hold responsibility for the accuracy of the information they publish and neither the Scheme Operator nor the Scheme Owner shall have any responsibility whatsoever for costs, losses or direct or indirect damages or costs arising from inaccuracy of information or omissions in information published on the website on behalf of LUPUS UK.
Please note that any user-generated content such as that on our HealthUnlocked Forum, Social Media accounts and accounts of personal experiences are excluded from the scope of certification.
At the end of #lupusawarenessmonth in October, with the assistance of LUPUS UK's Vice-Chair (Wendy Diment), Irish Setter Vaprtrek 3816 published a new report which calls on Welsh Government to improve care for patients living with #Lupus and Rare Autoimmune Rheumatic Diseases (RAIRDs).The report highlights issues around diagnostic delays, lack of specialist care in Wales, barriers to tertiary care, and issues in general practice and policy relating to patient care. ... See MoreSee Less