❤️🥰Today is #WorldKindnessDay 🙏🏼😍 May we suggest a donation to LKN as a #RandonActsofKindness and help us to deliver #DeliberateActsofKindness and #LeaveNoOneBehind in our mission to #EndTheNeglect #lymphaticfilariasis #podoconiosis https://t.co/UGjaTZJmZQ

Thanks for all the #Pacific contributors to our #filariasis #MMDP breakout session on digital technologies for bringing support to community health workers and those with #lymphoedema #COR_NTDPacificIslands session yesterday 26 Sept in Brisbane. @NTDnet @COR_NTD @jcu

LKN Foundation is making progress in bringing #lymphoedema #filariasis self care information to those who need it in #Bangladesh. Check out the latest video here https://t.co/GX58zlBWRc. Your support makes all the difference. Donate Here: https://t.co/1QElgPZqbd Thanks

Images and a video from our first workshops in Ethiopia! Please share, subscribe and follow our work https://t.co/3J9hLP5aUw #LF #podoconiosis #LymphedemaAwarenessMonth #lymphaticfilariasis #lymphoedema

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Article on the great work done by Patricia Graves and colleagues @JCU on establishing the #PacELF Library. #LF #Filariasis #Podoconiosis #Lymphedema

With a fantastic donation of 100K we have our skates on! 🎈🎉🥳👏 The Spring newsletter outlines our plans. Please support our fundraising and share 🙏 https://t.co/gB4OwYPmcd #LF #Podoconiosis #lymphoedema #lymphedema #stigma #selfcare #lymphaticmassage #EndTheNeglect #MMDP

Our paper using Bayesian Networks to analyse Lymphatic Filariasis serology from Myanmar has just been published in @TropicalmedMDPI. It suggests benefit in adding antibody testing to post-MDA surveillance.

" Being able to participate in social and economic life activities is to be activities is to be born again " - Fikre Hailkiros, National Podoconiosis Action Network #NaPAN

Delivering results on our QOL surveys in Bangladesh and Ethiopia #14thALAconference #LymphaticFilariasis and #podoconiosis cause debilitating infections, pain, stigma & social exclusion. #lymphoedema #selfcare can reduce pain, increase mobility, restore social inclusion #ALA

A strong and poignant message as we approach the end of #LymphoedemaAwarenessMonth https://t.co/OZ3lVL6IkS

LKN Foundation launching on #WorldLymphoedemaDay March 6th! Read the blog and check it out here https://t.co/ruOx1wHHVu @Jan_FRL @lkn_foundation

Launching the LKN Foundation https://t.co/wGOuSkqyPJ on #WorldLymphedemaDay, March 6 2022. Subscribe to the newsletter here

LKN Foundation is organization focused on #lymphaticfilariasis and #podo -related #Lymphedema. Check out their story at: https://t.co/84CaW7u23Q @lkn_foundation

Congratulations @louisekellyhop1 @CNTD_LSTM @syeed25 @FHailekiros and all co-authors on publication of an important new objective measure for lymphoedema in #lymphaticfilariasis and #podoconiosis endemic areas. https://t.co/QMUPNAZxns

Results on the Bangladesh arm of our enhanced-care study are published.

Our paper on staging systems in #lymphedema is available #openaccess via Lymphatic Education & Research Network @LymphaticResearch @CNTD @LSTM https://t.co/c5MkDMjoQc

On the first #WorldNTDDay, let us be clear: no one in the world should have to suffer from a neglected tropical disease in 2020. It’s time to finally #beatNTDs so that everyone has the chance to live a healthy, productive, dignified life. https://t.co/AjS8CcfRzB

Day 4 Long distances & poor roads hinder many with #NTDs from #accessinghealthcare, especially those with #poormobility #WorldNTDDay #beatNTDS #disabiltyrights #disabilityinclusion #12daysofNTDs #MMDP @COR_NTD @Laura_Deano @shahreen_c @lumenmartins @Sightsavers_Pol