Linda Arundale @FloBarker_1
West Yorkshire based healthcare worker. Love all things science. Dedicated follower of good coffee and cats!. Leeds, West Yorkshire, UK Joined September 2013-
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What are the symptoms of achalasia? 💚 Achalasia is a condition that affects the nerves and muscles of the oesophagus (food pipe), mainly where it meets the stomach. This makes it harder for food and fluids to pass down, leading to difficulties with swallowing.
September is Achalasia Awareness Month.💚 Approximately 2 to 3 in 200,000 people are diagnosed with achalasia each year. Although it is rare, we must raise awareness because for the people affected by it, it is very real. And it needs to be better known.
On Rare Disease Day 2025, we unite to advocate for those living with achalasia, emphasizing the importance of their needs within the health system. If you can, share your achalasia stories. Together, we can make a difference and increase awareness and recognition of achalasia.
In a historic first, the word Achalasia has been spoken in the House of Commons, thanks to @VikkiSlade72 asking an important question on the provision for rare diseases, such as FND and Achalasia. Today, Achalasia has finally been recognised in Parliament - a massive step-change!
We are so pleased to see this latest publication on the development and testing of a non-surgical achalasia intervention. We encourage any future research that can help us better understand how people with achalasia can manage their symptoms.
We are so pleased to see this latest publication on the development and testing of a non-surgical achalasia intervention. We encourage any future research that can help us better understand how people with achalasia can manage their symptoms.
September is Achalasia Awareness Month.💚 Achalasia affects 1 in 100,000 people, meaning it is rare. Although it is rare, it is crucial we raise awareness because for the people affected by it, it is very real. And it needs to be more known. (🧵1/4)
Here at Achalasia Action we aim to bring people together and to help everyone improve their understanding of achalasia. We provide a friendly and well-informed community to support those with oesophageal motility and peristalsis problems. #AchalasiaAwarenessMonth #Achalasia
Our guest speakers at our meeting on July 1st 2024 at 5:30 BST. Should be a fascinating evening. We hope to see you there. There are only 100 places available for this meeting. https:/www.meetup.com/achalasia-104/events/301688027/ #Achalasia #AchalasiaAction #CharitySupport
There is no "one size fits all" for Achalasia! Remember, everyone's experience with Achalasia is different, so find what works best for you! 🩵 There is LOTS of useful information and tips on our website! These include: Nutrition Spasms Medication Problem Foods #CharitySupport
We're here to help support those affected by Achalasia. Need help or information? Check out our website or drop us a DM "Uniting for a Rare Swallowing Condition" #Achalasia #AchalasiaAction #AchalasiaDisorder #AchalasiaSupport #AchalasiaCommunity #RareDisease #CharitySupport
We are a volunteer-led charity founded in 2020, we aim to improve the lives of individuals affected by Achalasia and their loved ones. This is our Charitable Purpose, which we strive to meet "Uniting for a Rare Swallowing Condition" #Achalasia #AchalasiaAction #CharitySupport
Amazing news, this #DonationDay Yorkshire Cat Rescue has been paid £398.76! Thank you to everyone who supports us through @easyuk! Why not get involved? Watch your online shopping turn into free donations for us! Sign up now: easyfundraising.org.uk/causes/yorkshi…
It was amazing to see @ronnieo147 speak about #achalasia and #achalasiaaction on #rarediseaseday yesterday!! If you know of anyone else who might be willing to use their platform to raise awareness of this rare condition pls DM us!
It was amazing to see @ronnieo147 speak about #achalasia and #achalasiaaction on #rarediseaseday yesterday!! If you know of anyone else who might be willing to use their platform to raise awareness of this rare condition pls DM us!
On #RareDiseaseDay, we'd like to say thanks to our co-founder and Trustee Amanda Ladell for everything she has done for the #achalasia community. Without her, Achalasia Action might never have been created! You can read her #achalasiastory here: achalasia-action.org/blog/amanda-la…
On this rare day of the year I’m recognising Rare Diseases Day 2024. I have Achalasia Type 1. It's a truly life affecting condition in so many ways. Read more here: achalasia-action.org #AchalasiaSupport #AchalasiaAction #RareDiseaseDay
Can you believe it’s been FOUR weeks since #TheakstonsCrime? WIN a big bag of goodies from this year’s Festival to see you through the end of summer! And as we celebrated 2 decades of crime, we made sure that there are 20 books! 👍 Simply Like & Retweet to enter. T&Cs in comments
Just been sent this 😂
33 funniest snapshots of British life this year as shared on ‘Casual UK’ on Reddit thepoke.co.uk/2021/12/31/33-…
Conservative Govt seems to have sneaked this out quietly - their consultation on taking free prescriptions away from over 60s by aligning the exemption with State Pension (66 - later 68). Women in this age group already hit hard by losing State Pension. gov.uk/government/new…
This #WorldHealthDay we want to thank #sonographers for everything they do! We & your patients appreciate your important contribution, especially during the past year. Thank you! ❤️🤗 @SCoRMembers

michaeljwhelan @mikejwhelan
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