Lisa EDS

[Ehlers-Danlos Support UK @ehlersdanlosuk]

Today is PoTS Awareness Day!

Find resources, videos, and information on how this is diagnosed here: https://t.co/IRV01n6cdk

Signpost your GP to the EDS Toolkit and emerging major associations at https://t.co/y4o2mkir3U #PotsAwarenessDay #PoTS

[PoTS UK @UKPoTS]

Today is ⭐️#PoTSAwarenessDay⭐️

✨PoTS on a Page - GP Guide✨

If you are a healthcare professional please download this guide which summarises information about #PoTS

For those seeking a diagnosis or attending medical appointments, please take this along to increase knowledge & awareness of PoTS.

PDF link for this information sheet: https://t.co/twWVJiVrAM

#TeamGP #MedTwitter #HCP #MECFS #EDS @HMSACharity @RCPhysicians @theRCN @DrNeenaJha @DrSdeG @GSTTnhs @BMA_GP @rcgp_ni @DrNighatArif

[Lisa EDS @lisab1998]

Look who’s now got #EDSZebraRocks helping us raise awareness of Ehlers-Danlos Syndrome and the EDS UK petition https://t.co/oHTDrxWZyl

[Ehlers-Danlos Support UK @ehlersdanlosuk]

We were also able to share all of the information and support EDS UK provides to its patients and to health professionals across the four nations.
A well-received session and an amazing opportunity to raise awareness with Welsh rheumatologists!

[Ehlers-Danlos Support UK @ehlersdanlosuk]

We were very fortunate today to be able to take part in the Welsh rheumatologists academic meeting where Dr. Kazkaz represented EDS UK in delivering some training to 27 Welsh rheumatologists on recognising the signs of #EhlersDanlossyndrome and #hypermobilityspectrumdisorders.

[Frances Heley @FrancesHeley]

https://t.co/J0DEK5URQe Thank you to Bannatyne for helping support us with the EDS UK petition. @EDSawareness1 @Ehlersdanlos @Bannatyne

[Frances Heley @FrancesHeley]

200 mile walk planned starting mid August called 'P2P on the Bannatyne Trail'. 🚶‍♀️ I'm linking Bannatyne Health Clubs to get signatures for the EDS UK petition -100,000 signatures needed for a debate. Please share. 😀🦓 @Bannatyne @bbchealth @Ehlersdanlos

[Frances Heley @FrancesHeley]

The misconception that hEDS and HSD are rare means that the government overlooks this condition. It's wrong and unjust. This petition plays a crucial role in enabling a debate which will challenge current attitudes toward EDS and HSD. @bbchealth @TheEDSociety @Bannatyne

[Lister Park parkrun, Bradford @Listerparkrun]

On Saturday it's the NHS 75th birthday celebration. Please wear something blue in support but also how about an additional dash of yellow? The Bradford Ukrainian Club will also be with us as it's the 500th day of the Putin's invasion of Ukraine so come along and give generously

[Frances Heley @FrancesHeley]

Thankyou to Bradford Parkrun for giving us a couple of minutes at the start to talk about EDS and the petition. We appreciate all your support. ❤️ @parkrun @TheEDSociety

[Frances Heley @FrancesHeley]

Today there are 13,400 signatures on the petition created by EDS UK. Getting to 100,000 signatures by November seems impossible unless something changes. Please sign and share. It HAS to get better. @TheEDSociety @Ehlersdanlos @LaraBloom

[Lisa EDS @lisab1998]

https://t.co/CcxvjCLBIF

[David Bainbridge @D_Bainbridge]

Just 18 days left until my #BHF #L2B ride for @ehlersdanlosUK! With miles under my belt and determination in my heart, there's no hill too high or path too tough. Grateful for the journey, and even more so for the cause. Here's to tenacity, and #EDS awareness! 🚴‍♂️💪 #RideLondon

[David Bainbridge @D_Bainbridge]

Stand with Fran, stride with purpose, and echo her journey of #COURAGE , #determination , and #resilience .

This is more than a walk, it's a #Movement for change!

We are powerful together. We are visible together. Let's unify our stripes 🦓💪 #EDS #ehlersdanlos @HMSACharity

[David Bainbridge @D_Bainbridge]

Fran Heley, a tenacious advocate for those affected by #ehlersdanlossyndrome (#EDS), has raised an astounding £4,000 towards her £5,000 goal. She is making an impressive 210 mile walk from Leeds to London to raise awareness for EDS and to aid @ehlersdanlosuk
@TheEDSociety

[Lisa EDS @lisab1998]

@jvsimmonds01 Congratulations Jane very well deserved you’re no small cog in my eyes for all you’ve done and still do.

[Ehlers-Danlos Support UK @ehlersdanlosuk]

Pathway to Parliament!

Fran Heley has raised an amazing £860 so far towards her goal of £2000 in aid of EDS UK. Fran is walking from Leeds to London to raise awareness and support others in limbo for diagnosis and care. https://t.co/ksdYL0Zas6

[Lisa EDS @lisab1998]

.@campaignforleo @SimonHarrisTD People living with #EhlersDanlosSyndrome need a consultant now! https://t.co/6twa8dFlWS via @UpliftIRL

[Physiocure Physiotherapy Clinic Leeds | Est. 2000 @Physiocure1]

The amazing Anna Higo💫
This award from EDS U.K. is so well deserved
Thank you EDS U.K. 🙏⁦@higo_anna⁩ ⁦@GemmaSPearce⁩ ⁦@ProfSheaPalmer⁩ ⁦@ehlersdanlosuk⁩ ⁦@TheEDSociety⁩ ⁦@hEDStogether⁩ https://t.co/okrDjcQrQM

[Lisa EDS @lisab1998]

.@campaignforleo @SimonHarrisTD People living with #EhlersDanlosSyndrome need a consultant now! https://t.co/6twa8dFlWS via @UpliftIRL