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Top News In லூபஸ் ஒன்றுபட்டது Today - Breaking & Trending Today

Woman raffling Manchester city centre apartment after loss of mum left her wanting to do something 'big'


Woman raffling Manchester city centre apartment after loss of mum left her wanting to do something big
Because something big happened to me, I wanted to do something big.
07:19, 17 MAY 2021
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Sushma Sharma is often told by her friends that she does things the “unconventional” way. ....

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'Be passionate, be over enthusiastic': Meet Rosie, Perthshire's 'bikepacking' entrepreneur


She explored the landscape by horse, walking or running.
Rosie discovered the joy of cycling off-road in 2016 and started ‘bikepacking’ (exploring by bike) around the UK.
Having found her passion, she decided to become a cycle guide and started a business under her name.
© Supplied by Rosie Baxendine
The Blairgowrie-based adventurer is also trustee of Highland Perthshire Cycling.
 
Q. How and why did you start in business?
I have a passion for the outdoors, especially going into the wilds to immerse myself in the surroundings.
Bikepacking is a fun and unique way to travel and explore more remote places.
I enjoy helping people to experience this, from talks to groups about kit, to guided overnight trips and longer epis adventures. ....

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Lupus: Welsh centres of excellence could 'extend lives'


BBC News
By Chris Wood
image captionCampaigners say centres of excellence could help lupus patients in Wales
Calls have been made for specialist help in Wales to treat an incurable, life-limiting condition which takes an average of six years to diagnose.
An estimated 2,000 people in Wales are affected by lupus.
Campaigner Wendy Diment said centres of excellence would extend the lives of lupus patients in Wales.
A Welsh Government spokeswoman said health boards could refer people for further treatment if it was not available locally.
There is currently no cure for lupus and it occurs when the immune system mistakenly attacks healthy parts of the body. ....

United Kingdom , City Of , Melanie Sloan , Chris Wood , Hywel Dda , Andrew Carruthers , Wales James , Paul Howard , Paul Davies , Cambridge University , British Society For Rheumatology , Wendy Diment , Welsh Government , Lupus United , Mrs Diment , Senedd Member , Lupus United Kingdom , Cymru Versus Arthritis , British Society , ஒன்றுபட்டது கிஂக்டம் , நகரம் ஆஃப் , மெலனி ஸ்லோன் , கிறிஸ் மரம் , ஹிவெல் டட , ஆண்ட்ரூ கற்றுத்தேர்ஸ் , லேஸ் ஜேம்ஸ் ,

Lupus: 'No-one seemed willing to treat me during Covid'


Lupus: No-one seemed willing to treat me during Covid
By Katy Prickett
Some people living with the incurable autoimmune disease lupus have had treatments delayed or cancelled during the coronavirus pandemic. But they also told Cambridge University researchers they now feel more understood by society, as everyone has had to protect themselves and adapt to a slower pace of life. The BBC has spoken to three patients about their experiences.
There is always the fear of organ damage
image copyrightAnisah Patas
image captionAnisah Patas was told her symptoms were all in her head for years before she was diagnosed aged 12 ....

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