FFNSNG

Neuromuscular support NG is a foundation whose passionate aims are to improve patients' lives & also connect families and professionals to wrestle the disease.

[FFNSNG @nmsupportng]

It’s few days to #RareDiseaseDay #RareDisease is whispered and explained in hush tones in Nigeria. Join us to break this silence!!! Let’s #Roar for #Rare

[FFNSNG @nmsupportng]

@OneLuckyGirl_28 A cure for muscular dystrophy 🙏🙏🙏

[FFNSNG @nmsupportng]

@colgate_ng As////

[FFNSNG @nmsupportng]

This is good news!!! 🤸🏻‍♂️🤸🏻‍♂️🤸🏻‍♂️🤸🏻‍♂️

[Parent Project Muscular Dystrophy (PPMD) @ParentProjectMD]

The United Nations has officially designated September 7th as World Duchenne Awareness Day, marking the UN’s first formal acknowledgment of a day dedicated to a rare disease!

[FFNSNG @nmsupportng]

It’s that time of the year

[World Duchenne Awareness Day 🎈 @DuchenneDay]

👊 Join us in raising awareness on World Duchenne Awareness Day! 🎈

Download high-resolution logos and other essential materials directly from the official WDAD website. Don’t forget to use the hashtag #WDAD2023. Together, we can make a difference!

👉 https://t.co/tB6lIldral

[FFNSNG @nmsupportng]

Always 💯

[World Duchenne Awareness Day 🎈 @DuchenneDay]

🎈 Join us in raising awareness for Duchenne and Becker Muscular Dystrophy!

For #WDAD2023, September 7, show your solidarity by sharing this support pledge. Spread the word and show your support using the hashtag #WDAD2023.

🤝 Together, we can move mountains!

[FFNSNG @nmsupportng]

Breaking barriers! Let’s include Africa.

[World Duchenne Organization @worldduchenne]

This year's World Duchenne Awareness Day theme is "Duchenne: Breaking Barriers."

Together, let's raise awareness and empower the Duchenne community worldwide. 🌟

Want to learn more? Check out the press release with detailed information. #WDAD2023
https://t.co/FMO8gCorst

[FFNSNG @nmsupportng]

@EU_BIND This is very great. Is it focused on Africa?

[FFNSNG @nmsupportng]

@Quickteller Hello Quickteller, I must say that I am very disappointed with your services. You deducted my money from my bank, failed to give me code and also did not refund my money. I’ve sent countless emails and yet no response from you. Why? Why? Why? This is so wrong!

[FFNSNG @nmsupportng]

Done.

[Africa Agility @AfricaAgility]

Application ends soon!

Don't miss this golden opportunity to start your tech career.

Click on this link - https://t.co/Mpmf7KR96F to apply (the link is available in our bio)

[FFNSNG @nmsupportng]

Do you remember when you joined Twitter? I do! #MyTwitterAnniversary

[FFNSNG @nmsupportng]

Just posted a photo https://t.co/DP0XWWBZge

[FFNSNG @nmsupportng]

Raising Rare Disease Awareness Nonstop!

Go raise awareness till you get to the corners of the earth.
#awareness
#support
#rarediseaseday2022 https://t.co/vABy8ncKPh

[FFNSNG @nmsupportng]

Prayers for Peace in Ukraine and other parts of the world 🤲🏼

[EURORDIS-Rare Diseases Europe @eurordis]

We stand in solidarity with people in Ukraine and wish to extend support to 🇺🇦 rare disease community.

We are calling on the international community to protect those caught in the conflict, with no access to humanitarian aid.

https://t.co/r141NWb1vX
📸 "Happy together", Ukraine

[FFNSNG @nmsupportng]

@BukarDanyaya None that we know of.

[FFNSNG @nmsupportng]

It’s few days to #RareDiseaseDay #RareDisease is whispered and explained in hush tones in Nigeria. Join us to break this silence!!! Let’s #Roar for #Rare

[Lade™ @CFCLade]

Please we need your support to ensure a successful rare disease day event 🥺🙏🏼
If you want to make your donations, please send us a dm or contact us on 08174634976 or 08077821007.
If you know anyone or brand that can support this.
Continuation 👇🏽

[FFNSNG @nmsupportng]

Just posted a photo https://t.co/jahXnoaEi2

[FFNSNG @nmsupportng]

Just posted a photo https://t.co/7xybdLvHCf

[FFNSNG @nmsupportng]

Your story helps others to share and grow through what you go through.

#shareyourrare

Repost @rarediseasedayofficial https://t.co/qrxllvEqLK