Sisters@Heart

A non-profit org that improves the lives of those affected by heart disease and stroke. Three moms/survivors on a mission.

[ISurvivor Lisa Deck @lbdeck]

Come follow our new non profit organization! @SistersAtHeart3 We're excited to be on Twitter! @markkane37 @BrianDeck1 https://t.co/2gef8uEjVn

[Downtown North Attleboro @north_downtown]

Great turnout for last nights DNAC meeting at @angletreebrew and for our donation of $2000 to @SistersAtHeart3. Sisters At Heart is a local charitable organization that gives back to individuals and families affected by heart disease. They do wonderful and important work.

[Ken Taylor @KenRayTaylor]

I’m happy to be part of @HealtheVoices' next #HealtheVoicesHCP session! We'll discuss how caregivers and HCPs can use social media to improve relationships that support positive patient outcomes. Register: https://t.co/mrjCOLcxcy #GenerationCare

[RareNewEngland @RareNewEngland]

Calling all students interested in Genetics! Join us for a 1-hour webinar featuring professionals in the fields of industrial, clinical, and laboratory genetics March 15th at 6:30 PM ET. Register here: https://t.co/ce36OFdtD8
#raredisease

[RareNewEngland @RareNewEngland]

#rarediseaseday
https://t.co/HoBldOLJNm

[North Attleborough Middle School @NorthMiddle1]

Spirit Day Success! Thank you to all who joined us in raising awareness for Heart Health on Friday!

[RareNewEngland @RareNewEngland]

For our 7 for Rare campaign, we want you to share with us 7 words of encouragement for rare disease families. Comment below! #7anything4rare #raredisease

[North Attleboro High @NorthHigh1]

Congratulations to North football captains, Tyler DeMattio- Running Back, Jared Vacher- OLine, and Tyler Bannon- Linebacker. All three made the 2021 MHSFCA Division III All-State team! #GOBIGRED!!

[RareNewEngland @RareNewEngland]

Our newest World of Rare Disease episode features Dr. Stanley Crooke who shares his career and involvement with the rare disease community, including his foundation, @n_lorem. Check it out: https://t.co/pVZqXT3BzT
#raredisease

[RareNewEngland @RareNewEngland]

Our support groups are happening this Tuesday (12/14) and we would love to see you there. Sign up at the link below #raredisease
https://t.co/CptonmaOEo

[Barbara Conner @BConnerFXC]

Over the next weeks & months, tens of thousands of college admission decisions will be released. Your value & worth are not tied to whether you are admitted, deferred, wait-listed, or denied. Trust the research you did to find #FiveFirstChoiceColleges for your Apply List!

[RareNewEngland @RareNewEngland]

Raise A Glass For Rare🍷 Start your Holiday shopping now!
Chateau STE Michelle $12.99
Klinker Brink “ Brick Mason” Red Blend $14.99
Wine available at City Spirits locations in Attleboro/North Attleboro, MA.
#raredisease

[RareNewEngland @RareNewEngland]

RNE's Annual Conference will be held virtually on Saturday, October 23rd. We will host a day of education and information to the rare disease community. Caregiver and Patient tickets are FREE this year. Don't forget to register! #raredisease #virtualRNE
https://t.co/xlZCZnyPXX

[RareNewEngland @RareNewEngland]

Enter our 2021 Conference Raffle for a yeti cooler (image below) or a $100 Amazon gift card! $10 for 1 entry or $50 for 10 entries. Use this link to enter: https://t.co/u4A5q76U9l

Register for the conference at: https://t.co/OuP7Ao0bR5
#raredisease #rne #virtualRNE

[North Attleboro High @NorthHigh1]

Let’s make sure North leads the way! North Attleboro Food Access Collaborative Spirit Day! Details below…donate today!

[RareNewEngland @RareNewEngland]

Save the date and register for Rare New England’s Virtual Conference on October 23rd! Tickets are free for rare disease patients and caregivers. Register here: https://t.co/C7GBLFQvFW
#raredisease #rarenewengland #virtualRNE

[Sisters@Heart @SistersAtHeart3]

@sshingledecker And on the beach is always a bonus!

[ISurvivor Lisa Deck @lbdeck]

Pls answer & RT. Need some input from my #patient friends. I’m crowdsourcing for a presentation. What do you wish #pharma knew about you as a patient? How should #industry interact w/ #patients? #patientadvocate #RareDisease #chronicillness @wegohealth @savvy_coop @healthevoices

[Sharon Rose Nissley @Rose_of_Sharon8]

Friday is Klippel-Feil Syndrome Awareness day. KFS constantly affects my body in ways I never could have imagined. My choice is to do what I can, even though it hurts tremendously & I struggle. I use my body as hard as I can & find peace wherever I can. #raredisease @KFS_Freedom

[Moyamoya Foundation @moyamoyafdn]

House Calls: Moyamoya Disease - Weill Cornell Medicine Events https://t.co/ZbiM0TOnHN

This free virtual event (webinar) is Aug 3rd, at 5:30pm click the link to register.