Sam Williams Profile
Sam Williams

@googleplex1001

Followers
643
Following
2K
Media
237
Statuses
2K

Stem cell transplant recipient, Support and Outreach Manager at @AplasticAnaemia and supporter of @AnthonyNolan. All views are my own.

Cannock, England
Joined July 2011
Don't wanna be here? Send us removal request.
@googleplex1001
Sam Williams
2 years
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 📗
1
0
11
@googleplex1001
Sam Williams
2 years
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! 🏳️‍🌈
3
1
22
@googleplex1001
Sam Williams
2 years
…it hasn’t been available as an option for redelivery. It would be so much more convenient if they were able to offer this, rather than me travelling further to another branch. It’s odd as they offer Pick Up and Drop Off for other carriers there.
0
0
0
@googleplex1001
Sam Williams
2 years
Hi @RoyalMailHelp , is there a particular reason why I can’t select Hednesford @PostOffice as an option to have a parcel redelivered to, when other local branches are able to offer the service? Ever since the branch opened a few years ago…
1
0
0
@AplasticAnaemia
The AAT
2 years
@fanconihope @PNHSupport @CharitySdsuk @CAnaemiaNetwork @DC_Action "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
2
3
3
@AplasticAnaemia
The AAT
2 years
@fanconihope @PNHSupport @CharitySdsuk @CAnaemiaNetwork @DC_Action 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
1
2
3
@AplasticAnaemia
The AAT
2 years
What do you wish people understood about your Super Rare condition? @fanconihope @PNHSupport @CharitySdsuk @CAnaemiaNetwork @AplasticAnaemia @DC_Action
2
3
6
@googleplex1001
Sam Williams
2 years
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?
1
0
1
@AnthonyNolan
Anthony Nolan
2 years
📢 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.
2
16
63
@googleplex1001
Sam Williams
2 years
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 :)
2
0
0
@googleplex1001
Sam Williams
2 years
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! 💚🖤💚
1
2
16
@AplasticAnaemia
The AAT
2 years
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➡️ https://t.co/DBiyPlM6WM
0
4
7
@AplasticAnaemia
The AAT
2 years
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➡️ https://t.co/DBiyPlMEMk
0
4
7
@AplasticAnaemia
The AAT
2 years
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 ➡️ https://t.co/CiWmeCNHgy
0
5
7
@AplasticAnaemia
The AAT
2 years
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 ⬇️ https://t.co/CiWmeCNHgy
0
3
4
@AplasticAnaemia
The AAT
2 years
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 ➡️ https://t.co/CiWmeCNHgy
0
4
5
@AplasticAnaemia
The AAT
2 years
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 ➡️ https://t.co/CiWmeCN9r0
0
4
10
@googleplex1001
Sam Williams
2 years
…card. We were told that we need to send a copy of her death certificate in by post, but weren’t given an address for this. Could you please advise us where to send the paperwork, please?
0
0
0
@googleplex1001
Sam Williams
2 years
Hi @NatWest_Help, my mother in law died recently and my husband, acting as executor of her estate needs to close down her credit card held with NatWest. We’ve managed to close her current account via the online form, but we were told that we couldn’t use this for her credit…
2
0
1
@googleplex1001
Sam Williams
2 years
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 💚🖤💚
@simonwilkes13
simon wilkes
2 years
⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿⚽️🏴󠁧󠁢󠁥󠁮󠁧󠁿 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
1
0
6