Help Support Geeky KOOL's Morgan Straughan Comnick - Geeky KOOL At Geeky KOOL, we are more than just a team—we are a family. Today, we are reaching out to our community to ask for support for one of our own:

Help Support Geeky KOOL’s Morgan Straughan Comnick

www.geekykool.com/help-support...

#SupportMorgan
#CommunitySupport
#StrongerTogether
#GoFundMe
#Fundraising
#MutualAid
#PayItForward
#LupusWarrior
#LupusAwareness
#SpoonieSupport
#ChronicIllness
#InvisibleIllness
#LupusSupport

#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

#LupusAwareness

#LivingWithLupus

#ChronicIllness

#AutoimmuneWarrior

#LupusSupport

#HealthJourney

#InvisibleIllness

Did you know we have a guide for #teachers that provide them with information on #lupus?

You can download the guide for free on our website: https://lupusuk.org.uk/youth-resources/ 🧑‍🏫

#LupusCommunity #LupusSupport

This month is #NationalHeartMonth. #Lupus can impact heart health and it is important to know more about its effects.

You can find out more about how lupus affects the heart through our publication here: https://bit.ly/4bkGMk6

#LupusAwareness #LupusSupport #LupusCommunity #SLE

When you give, you’re not just donating. You’re standing alongside everyone living with lupus. 💜

Thank you!

#Lupus #LupusUK #LupusAwareness #LupusSupport #Charity #InternationalDayOfCharity #CharityDay

The poster highlights the prevalence of people in the UK living with #lupus and signposts our support services to those who may not have heard of us. 

#LupusUK #1in1000 #KnowLupus #LupusSupport #MakeLupusVisible #LupusAwareness #InvisibleIllness

Go purple for World Lupus Day

We’d love to see what you get up to! Share your photos via DM or by tagging us or emailing Nakita@lupusuk.org.uk

#Lupus #LupusUK #1in1000 #KnowLupus #LupusSupport #LupusCommunity #MakeLupusVisible #LupusAwareness #InvisibleIllness

Parents, carers, or friends of someone with lupus are welcome to complete the survey and attend a focus group. 

Your voice matters, and we are listening. Thank you for sharing your views! 💜

#Lupus #SLE #LupusCommunity #LupusSupport #Survey #PatientSurvey #FocusGroup

Clinical Trials Talks Whether you're thinking about joining a trial or just curious about the process, this podcast offers patient-friendly insights into clinical trials.

Thinking about lupus clinical trials? Join Dr. Philip Mease as he explains what clinical trials involve and how they might benefit you! Perfect for anyone considering this next step on their health journey.

🎙️ Listen Now! creakyjoints.org/clinical-tri...
#LupusSupport #ClinicalTrials #LupusChat

If you are unable to attend a focus group but would still like to share your views, you can complete our "Living with lupus" survey here: https://www.surveymonkey.com/r/lupusuk-survey-social

Thank you 💜

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#Lupus #SLE #LupusCommunity #LupusSupport #Survey #PatientSurvey #FocusGroup

Your life with lupus: what you need, what you want | Lupus UK Your life with lupus: what you need, what you want by Nakita | Mar 4, 2025 | Blog, Latest News Lupus UK is 35 years old in 2025, and we are taking this opportunity to develop our aims and priorities for the coming years. Your voice matters, and we are listening. We want to understand the needs and w...

All questions are optional and the survey is anonymous. Please email any questions to HeadOffice@LupusUK.org.uk.

For more information, visit https://lupusuk.org.uk/2025/03/04/survey/

#Lupus #SLE #LupusCommunity #LupusSupport #PatientSurvey

#FightLupus #LupieProblems #Lupus #SLE #Lupie #LupusProblems #LifeWithLupus #LupusAwareness #LupusSucks #LupusSupport #LupusTruth #laziness