Sam Williams
@googleplex1001
Stem cell transplant recipient, Support and Outreach Manager at @AplasticAnaemia and supporter of @AnthonyNolan. All views are my own.
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Really looking forward to finally reading Shirley Nolan’s autobiography this weekend! Such a wonderful And timely re-release to celebrate fifty years of @AnthonyNolan saving lives. Soon to be on the shelves at @StaffsLibraries @HednesfordLib once I’ve finished reading it 📗
Looking forward to a busy day, recruiting new potential stem cell donor to the @AnthonyNolan register at @PrideInLondon today! Come along to see us at a Trafalgar Square, next to Canada House and say hi! 🏳️🌈
"I wish they would understand that every day is different that we are not lazy and that we are all trying our best. Just because what I have is not cancer does not mean it is not serious!" - Claire #RareDiseaseDay #RareDiseaseDay2024 #aplasticanaemia
What do you wish people understood about your Super Rare condition? "I'm still me." - Paula, living with Dyskeratosis Congenita, a rare genetic disorder #RareDiseaseDay #RareDiseaseDay2024 @DC_Action
What do you wish people understood about your Super Rare condition? @fanconihope @PNHSupport @CharitySdsuk @CAnaemiaNetwork @AplasticAnaemia @DC_Action
Hi @PostOffice, would it be possible for you to confirm what the in-branch rate would be if I wanted to purchase around £100 worth of Bahrain Dinar, please?
📢 NEWS: Belumosudil has been approved by NICE for chronic GvHD We’ve been calling for better access to GvHD treatments for a long time, so we’re delighted that a new treatment option will now be available to patients across the UK who have not responded to other therapies.
Hi @easyJet, I’m currently waiting for the delayed EZY 338 BHX-EDI flight. Could you shed any light on the reason for the delay please? Thank you :)
Honoured to be at the Olly Wilkes Memorial Tournament at St George’s Park with @simonwilkes13 @FinnTheFabulou1 and @rianc_harvey to raise awareness of the @AnthonyNolan stem cell register. Here’s to signing up lots of new potential donors! 💚🖤💚
The Better Together for Healthy Bone Marrow Alliance is committed to using the findings of the newly launched #RareVoices report to inform their focus for change and lobbying moving forwards. Read the commitments and recommendations of the report here➡️ bit.ly/3eRNus
We are dedicated to using the findings of the newly launched #RareVoices report to make a difference moving forwards. See our commitments below, and to read in full, click here➡️ bit.ly/3eRNus
The new #RareVoices report by the Better Together for Healthy Bone Marrow Alliance found that 83% of those surveyed wanted access to current research about their condition, new treatments, and treatment methods. Read more here ➡️ bit.ly/RareV
The #RareVoices report found that many people affected by rare bone marrow conditions face significant challenges when trying to navigate the healthcare system. Discover more below ⬇️ bit.ly/RareV
The new #RareVoices report by the Better Together for Healthy Bone Marrow Alliance found that 53% of respondents reported always or often feeling anxious. Read more here ➡️ bit.ly/RareV
Today we’re launching #RareVoices - a new report based on the first ever national community survey of people affected by rare bone marrow conditions. Stay tuned as we uncover important insights. Read the report here ➡️ bit.ly/RareV
Really excited to be a part of the Olly Wilkes Memorial Football Tournament this year, helping to promote @AnthonyNolan and sign people up to the stem cell register. Massive thanks to @simonwilkes13 and family for inviting me 💚🖤💚
⚽️🏴⚽️🏴⚽️🏴⚽️🏴⚽️🏴⚽️🏴⚽️🏴⚽️🏴⚽️🏴 JUST 20 DAYS TO GO. All 24 teams entered into "Our Olly's" Memorial Football Tournament 2023 have now submitted their Players List & Supporter Lists, some wonderful surprises on the Players lists i might add…. tbc
United States Trends
- 1. Rockets N/A
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- 11. Fulton County N/A
- 12. Model S N/A
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- 15. Chris O'Leary N/A
- 16. Optimus N/A
- 17. #PorVida N/A
- 18. #ChicagoPD N/A
- 19. S and X N/A
- 20. Cavs N/A
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