Ricky Chotai (he/him) (@ricky_chotai) 's Twitter Profile
Ricky Chotai (he/him)

@ricky_chotai

📍Manchester
🏢 Membership & Governance @nusconnect
🦋Trustee @LUPUSUK

#northern | #LoveSUs | #politics | [email protected] | Views: own

ID: 56190920

linkhttp://www.rickychotai.co.uk calendar_today12-07-2009 21:05:36

24,24K Tweet

1,1K Followers

4,4K Following

Lupus Europe (@lupuseurope) 's Twitter Profile Photo

🚨 Calling all men living with #lupus! 🦋 Lupus Europe is hosting a dedicated event for 𝘆𝗼𝘂‼️ Join us for informative sessions, peer support discussions, and a chance to connect with others. ✉️ Send your motivation letter now to [email protected]!

🚨 Calling all men living with #lupus!

🦋 Lupus Europe is hosting a dedicated event for 𝘆𝗼𝘂‼️

Join us for informative sessions, peer support discussions, and a chance to connect with others.

✉️ Send your motivation letter now to secretariat@lupus-europe.org!
Lupus Europe (@lupuseurope) 's Twitter Profile Photo

🩺 Calling doctors: #EasyLupus is the easyread version of #LupusGPT. Made to give easy & valid info on #SLE for patients in many languages. Currently in beta & being tested. Go to: easy.lupusgpt.org to try the tool & e-mail [email protected] with any feedback!

🩺 Calling doctors:

#EasyLupus is the easyread version of #LupusGPT. Made to give easy & valid info on #SLE for patients in many languages. Currently in beta & being tested.

Go to: easy.lupusgpt.org to try the tool & e-mail secretariat@lupus-europe.org with any feedback!
Ricky Chotai (he/him) (@ricky_chotai) 's Twitter Profile Photo

So I got banned from Instagram for breaking their terms. Dunno what I did wrong 🤷🏽‍♂️. If you miss dull photos from my life my new account is here. instagram.com/rickychotai?ig…

Lupus Europe (@lupuseurope) 's Twitter Profile Photo

🌟 Yvonne Norton Grant: A unique opportunity that will cover all expenses for a European #lupus patient who has positively impacted the lupus community but lacks the means to attend the #LupusConvention. 💜 In honour of a great lady. For more info: [email protected]

🌟 Yvonne Norton Grant: A unique opportunity that will cover all expenses for a European #lupus patient who has positively impacted the lupus community but lacks the means to attend the #LupusConvention.

💜 In honour of a great lady.

For more info: secretariat@lupus-europe.org
Lupus Europe (@lupuseurope) 's Twitter Profile Photo

‼️ Researchers at UCL are studying how Muslim patients with autoimmune rheumatic diseases, including #lupus, manage medications during #Ramadan. 🙏 Please take this quick 10-minute survey and  share it in your networks 🌍. Your help is key! qualtrics.ucl.ac.uk/jfe/form/SV_23…

‼️ Researchers at <a href="/ucl/">UCL</a> are studying how Muslim patients with autoimmune rheumatic diseases, including #lupus, manage medications during #Ramadan.

🙏 Please take this quick 10-minute survey and  share it in your networks 🌍. Your help is key!

qualtrics.ucl.ac.uk/jfe/form/SV_23…
NUS UK (@nusuk) 's Twitter Profile Photo

Thank you The SU at UWE for hosting and inviting us to the South West students' unions meet up! It was so great to talk to so many people who are passionate about student activism and we can't wait to work more with you over the next year!

Thank you <a href="/TheSUatUWE/">The SU at UWE</a> for hosting and inviting us to the South West students' unions meet up! 

It was so great to talk to so many people who are passionate about student activism and we can't wait to work more with you over the next year!
LUPUSUK 💙 (@lupusuk) 's Twitter Profile Photo

5 DAYS TO GO! Applications for our Autumn 2024 research funding round must be received by LUPUS UK before 5pm on Friday 30th August. Please email [email protected] for more information, including application forms and conditions for grants. #Lupus #LupusResearch #SLE

5 DAYS TO GO! 

Applications for our Autumn 2024 research funding round must be received by LUPUS UK before 5pm on Friday 30th August.

Please email HeadOffice@LupusUk.org.uk for more information, including application forms and conditions for grants.

#Lupus #LupusResearch #SLE
LUPUSUK 💙 (@lupusuk) 's Twitter Profile Photo

Please take one minute to nominate us in the #MovementForGoodAwards. As a small charity, this grant will make a huge difference💜 The next draw will take place on the 23rd September. Nominate us here: lnk.bio/s/MovementForG…🔗 #Lupus #SLE #SmallCharity #Grant #LupusCommunity

Please take one minute to nominate us in the #MovementForGoodAwards. As a small charity, this grant will make a huge difference💜

The next draw will take place on the 23rd September.

Nominate us here: lnk.bio/s/MovementForG…🔗

#Lupus #SLE #SmallCharity #Grant #LupusCommunity
Ricky Chotai (he/him) (@ricky_chotai) 's Twitter Profile Photo

Thanks for offering this and happy to share far and wide. Organisations like The Wren Project and LUPUSUK 💙 are so important to supporting the Lupus Community. 💜💜💜 #lupus #lupusmen #lupusuk #lupuschat

Ricky Chotai (he/him) (@ricky_chotai) 's Twitter Profile Photo

With the 🦋 Lupus Europe team and our amazing patients, we’re turning survey data into 🔥 abstracts! So much valuable info from the Lupus Community across Europe. Can’t wait to share this with EULAR and the wider #lupus community! #kicklupus 💪💜

Where Is Lorraine? (@lorrainekwatch) 's Twitter Profile Photo

Lorraine Kelly hosted her own show this morning. Congratulations #Lorraine, you have hosted 100 out of 174 (57.5%) episodes this year. This is the first episode she has hosted since 18 July. She missed 31 episodes consecutively.

Lorraine Kelly hosted her own show this morning.

Congratulations #Lorraine, you have hosted 100 out of 174 (57.5%) episodes this year.

This is the first episode she has hosted since 18 July.

She missed 31 episodes consecutively.
Lupus Forum (@lupusforum) 's Twitter Profile Photo

The countdown is on, there is just one week to go till our 'Inequities in accessing lupus treatment' webinar! Taking place from 17:00 BST on 16th September, join our expert faculty members for 90 minutes of discussion. There's still time to register: ow.ly/zE3J50SHWg6

The countdown is on, there is just one week to go till our 'Inequities in accessing lupus treatment' webinar!

Taking place from 17:00 BST on 16th September, join our expert faculty members for 90 minutes of discussion.

There's still time to register: ow.ly/zE3J50SHWg6