Liam Hugo

🏋️‍♂️: JM Warrior 👨‍👩‍👧‍👦: Loving Brother 🕺: Exquisite Dancer 🧠: Imaginative Thinker 🍵: Monstah Potion Creator

[Cure JM Foundation @curejm]

Tomorrow is Giving Tuesday & if we win the Holiday Challenge=$150K for JM research! 3 things you can do:
1. Between 12 AM EST TOMORROW to 12 AM Wednesday, donate at the link below
2. After you make a gift, spread the word & encourage others to give!
We can do this TOGETHER!

[Luke Ryan @LukeARyan]

We’re honored to represent the newly diagnosed families of children with #juvenilemyositis an #autoimmune diesease which affects 1 in 500,000 kids. Tune in for the webinar and we’ll answer questions about our journey and mission to #CureJM

[Cure JM Foundation @curejm]

Join us and walk strong for our little heroes.

[Luke Ryan @LukeARyan]

Our family’s @curejm story is about to air again on @boston25 (5:45p) here’s the link in case you are outside of the area. https://t.co/z5rzcftI7C #autoimmune #curejm #myositis

[Cure JM Foundation @curejm]

Liam's story.

[Cure JM Foundation @curejm]

"Although a lot is known about symptoms, diagnosis and treatment of JM, the underlying reason why a person develops the disease is still unknown. Collecting samples for genetic analysis from families and patients is of paramount importance.” https://t.co/wesHBsaxet

[The Myositis Association @TheMyositisAssc]

This research could help move the needle toward understanding and cure for all myositis diseases...even in adults. Thanks @curejm! #MyositisAwareness #CureMyositis

[Cure JM Foundation @curejm]

Get expert advice on treatments & side effects, nutrition & exercise and how to advocate for your JM child in your school and community.
https://t.co/DQJt45QmcE

[Cure JM Foundation @curejm]

When Liam was diagnosed with JM, his parents had never heard of it.
Once diagnosed, the Ryan family was moved to join the Cure JM mission.
Through hard work, the Ryan family raised $30K for much-needed research. Thank you @LukeARyan & the Ryan family! https://t.co/DovDTZdwaa

[Daniel Miller @Daniel_Miller8]

@curejm @CureJM4Liam @boston25 We are all in this together!

[Cure JM Foundation @curejm]

@Daniel_Miller8 @CureJM4Liam @boston25 Your support is amazing, @Daniel_Miller8 We're so grateful for the great story you created about Liam & your continued support of our collective cause. Thank you!

[Daniel Miller @Daniel_Miller8]

5 year-old @CureJM4Liam is battling a very rare disease - #JuvenileMyositis This past weekend we all gathered to celebrate his Birthday and raised over $25K for @curejm research. @boston25 #KeepFightingLiam

[Daniel Miller @Daniel_Miller8]

Coming up at 8 on @boston25 Morning News - A Lexington family is on a mission to find a cure after their son is diagnosed with a rare autoimmune disease. 📲https://t.co/XKNLT6m1kM

[Luke Ryan @LukeARyan]

Much love to our friend @Daniel_Miller8 and @boston25 for telling our story. Watch #Boston25 today starting at 8am and throughout the day to see our #CureJM Story

[Boston 25 News @boston25]

Lexington 5-year-old in battle with rare childhood disease https://t.co/tKsUJXIywH

[Cure JM Foundation @curejm]

What did you miss? Session videos, photos, & lay summary of research posters from our recent National Family Conference.
https://t.co/Tw0RZfh0XP