LGD Alliance Europe (@lgda_eu) 's Twitter Profile
LGD Alliance Europe

@lgda_eu

The LGD Alliance Europe is dedicated to patient support, advocacy and research to find treatments and cures for lymphangiomatosis and Gorham's disease.

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linkhttp://www.lgda.eu calendar_today01-03-2016 10:09:53

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LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Come, ask questions, and share your experiences! Join us for our DISH monthly support group on Saturday, May 14 at 10:00 am ET. Open to our global CLA community of both patients and parents. facebook.com/events/s/dish-… LGD Alliance Europe #rarediseases #supportgroups

Come, ask questions, and share your experiences! Join us for our DISH monthly support group on Saturday, May 14 at 10:00 am ET. Open to our global CLA community of both patients and parents.
 
facebook.com/events/s/dish-…
 
<a href="/LGDA_EU/">LGD Alliance Europe</a>

#rarediseases
#supportgroups
VASCERN (@vascern) 's Twitter Profile Photo

We're proud of the work our patient advocates are doing for the patient community, and we're looking forward to hearing about the #ISSVA conference. HEVAS CMTC-OVM LGD Alliance Europe

LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Worldwide LGD Awareness Day in on May 26. Join us in sharing our CLA story. Share your stories using #lgdawareness. lgdalliance.org/legacies-2/jan… #LGDAwareness LGD Alliance Europe #rarediseases

Worldwide LGD Awareness Day in on May 26.

Join us in sharing our CLA story. Share your stories using #lgdawareness.

lgdalliance.org/legacies-2/jan…

#LGDAwareness
<a href="/LGDA_EU/">LGD Alliance Europe</a>
#rarediseases
LGD Alliance Europe (@lgda_eu) 's Twitter Profile Photo

Thank you ISSVA for the great conference in Vancouver. VASCERN was well represented at the conference. See you soon again and keep up the good work for our CLA patients. #networking for #lymphatic and #vascularanomalies #issva22 CMTC-OVM HEVAS

Thank you <a href="/ISSVA_org/">ISSVA</a> for the great conference in Vancouver. <a href="/vascern/">VASCERN</a> was well represented at the conference. See you soon again and keep up the good work for our CLA patients. 
#networking for #lymphatic and #vascularanomalies #issva22 <a href="/CMTCOVM/">CMTC-OVM</a> <a href="/hevas_nl/">HEVAS</a>
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Share your experiences finding medical care for vascular anomalies in a study being conducted by Bryan Sisk and Anna Kerr Must be over 18 years of age or older. Open to US and non-US participants. kerrcommlab.wixsite.com/vacomsurvey LGD Alliance Europe #rarediseases #WUSTL

Share your experiences finding medical care for vascular anomalies in a study being conducted by <a href="/Sisk_MD/">Bryan Sisk</a> and <a href="/DrAnnaKerr/">Anna Kerr</a>

Must be over 18 years of age or older. Open to US and non-US participants. 
 kerrcommlab.wixsite.com/vacomsurvey

<a href="/LGDA_EU/">LGD Alliance Europe</a>
#rarediseases
#WUSTL
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Special Topic Support Group May 28 at 11:00 am Eastern Time Sponsored by the Young Adults and Millennial Support Groups. This special support session is dedicated to family planning and reproductive health. Register Today! us06web.zoom.us/meeting/regist… LGD Alliance Europe #rarediseases

Special Topic Support Group
May 28 at 11:00 am Eastern Time

Sponsored by the Young Adults and Millennial Support Groups. This special support
session is dedicated to family planning and reproductive health. 

Register Today! us06web.zoom.us/meeting/regist…

<a href="/LGDA_EU/">LGD Alliance Europe</a>
#rarediseases
LGD Alliance Europe (@lgda_eu) 's Twitter Profile Photo

We are gearing up to better treatments and cures: The LGDA Europe is joining forces with LGDA USA and LMI to support Team CLA Warriors in the 2022 Million Dollar Bike Ride event. Get involved and be part of the MDBR here: secure.givelively.org/donate/lymphan…

We are gearing up to better treatments and cures:  The LGDA Europe is joining forces with LGDA USA and LMI to support Team CLA Warriors in the 2022 Million Dollar Bike Ride event. Get involved and be part of the MDBR here:  secure.givelively.org/donate/lymphan…
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Share your experiences finding medical care for vascular anomalies in a study being conducted by Bryan Sisk, MD and Anna Kerr, PhD. Must be over 18 years of age or older. Open to US and non-US participants. Questions – Contact (link kerrcommlab.wixsite.com/vacomsurvey) LGD Alliance Europe

Share your experiences finding medical care for vascular anomalies in a study being conducted by
Bryan Sisk, MD and Anna Kerr, PhD.
Must be over 18 years of age or older. Open to US and non-US participants. Questions – Contact

(link kerrcommlab.wixsite.com/vacomsurvey)
<a href="/LGDA_EU/">LGD Alliance Europe</a>
LGD Alliance Europe (@lgda_eu) 's Twitter Profile Photo

You can also support Team CLA Warriors in the 2022 Million Dollar Bike Ride event. Want to know how? Download the Team CLA Warriors toolkit here: ​ drive.google.com/file/d/1_XTNHt…

You can also support Team CLA Warriors in the 2022 Million Dollar Bike Ride event. Want to know how? Download the Team CLA Warriors toolkit here: ​
drive.google.com/file/d/1_XTNHt…
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

The Orphan Disease Center’s MDBR Young Investigator grant is a $25,000 award that supports early career researchers pursuing research ideas related to lymphatic anomalies. orphandiseasecenter.submittable.com/submit/223019/… #MDBR2022 #UPENN #research #rarediseases LGD Alliance Europe

The Orphan Disease Center’s MDBR Young Investigator grant is a $25,000 award that supports early career researchers pursuing research ideas related to lymphatic anomalies.

orphandiseasecenter.submittable.com/submit/223019/…

#MDBR2022

#UPENN

#research

#rarediseases

<a href="/LGDA_EU/">LGD Alliance Europe</a>
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

EXTRA! EXTRA! READ ALL ABOUT IT! May 26 is Awareness Day and LAUNCH DAY for special initiatives that honor our origins and patient community! LGD Alliance Europe

EXTRA! EXTRA! READ ALL ABOUT IT! May 26 is
Awareness Day and
LAUNCH DAY for
special initiatives
that honor our origins and patient community!
<a href="/LGDA_EU/">LGD Alliance Europe</a>
LGD Alliance Europe (@lgda_eu) 's Twitter Profile Photo

Today is #LGDAwarenessDay! Join our celebration! Become a member and make a small monthly contribution that will enable us to keep working to support, educate and give hope to patients with CLA's and their families. Become a member here: lgda.eu/get-involved

Today is #LGDAwarenessDay! Join our celebration! Become a member and make a small monthly contribution that will enable us to keep working to support, educate and give hope to patients with CLA's and their families. Become a member here: lgda.eu/get-involved
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Bikers Wanted! Plan on attending UPenn’s 2022 Million Dollar Bike Ride on June 11th. Don’t forget to register at milliondollarbikeride.org/registration/#… Can’t attend in person, there is a virtual spin class on June 6th at 7:00 pm. LGD Alliance Europe #MBDR2022

Bikers Wanted! Plan on attending UPenn’s 2022 Million Dollar Bike Ride on June 11th. Don’t forget to register at milliondollarbikeride.org/registration/#…
Can’t attend in person, there is a virtual spin class on June 6th at 7:00 pm. 

<a href="/LGDA_EU/">LGD Alliance Europe</a>
#MBDR2022
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Dr. Michael Dellinger to present "New Diagnostic Tools and Treatment for Central Lymphatic Abnormalities". A webinar series on complex lymphatic anomalies. Watch the recorded webinar. (link to youtube.com/watch?v=1ZCx8U…) LGD Alliance Europe #rarediseases #czinitiative #RareAsOne #CZIscience

LGDAlliance (@lgdalliance) 's Twitter Profile Photo

Join Taylor and Liz, moderators for LGDA’s support groups, on their @NotSoRarePodcast as they share their experiences. ·podcasts.apple.com/us/podcast/not… · open.spotify.com/episode/5kgWoF…... LGD Alliance Europe @NotSoRarePodcast

Join Taylor and Liz, moderators for LGDA’s support groups, on their @NotSoRarePodcast as they share their experiences.
·podcasts.apple.com/us/podcast/not… · open.spotify.com/episode/5kgWoF…...

<a href="/LGDA_EU/">LGD Alliance Europe</a>

@NotSoRarePodcast
vascular development lab (@makinenlab) 's Twitter Profile Photo

Looking forward to this conference on Vascular Anomalies in Brussels from 31 Jan to 3 Feb 2023, organized by the V.A. Cure network! Deadline for abstract submission 15 Nov 2022. vacure-conference.net

Looking forward to this conference on Vascular Anomalies in Brussels from 31 Jan to 3 Feb 2023, organized by the <a href="/VACure1/">V.A. Cure</a> network! Deadline for abstract submission 15 Nov 2022.
vacure-conference.net
LGDAlliance (@lgdalliance) 's Twitter Profile Photo

DISH A friendly reminder! Our monthly The DISH (Drop in and Share) support group will meet on Saturday, August 13 at 10:00 am Eastern Time! Join here: us06web.zoom.us/j/94210215213?… LGD Alliance Europe

DISH 
A friendly reminder! Our monthly 

The DISH (Drop in and Share) support group will meet on Saturday, August 13 at 10:00 am Eastern Time!   Join here: us06web.zoom.us/j/94210215213?…  

<a href="/LGDA_EU/">LGD Alliance Europe</a>