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If keeping up with trends means I get to keep spreading awareness for her rare genetic disorder then put me in, coach. May is Neurofibromatosis Awareness Month. NF is a rare genetic disorder affecti
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This trend has me 🥹😭 I’ll do whatever it takes until the whole world has heard of Neurofibromatosis. Until there is a cure. Until no parent has to wonder if they’ll outlive their child from a progr
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Medical devices make the best toys anyway💛 *Feel like I need to make it clear this is a joke, and we would be lost without the incredible team of hemonc nurses. They are angels on earth🫶🏻 . . . .
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This is our 2nd year of celebrating Rare Disease Day🦄 I’ll admit that I never thought this is what my motherhood journey would like, but I can confidently say I would not ever change it. GK’s rare
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First, I know this person didn’t mean it to offend or upset me. I truly believe they thought it was a kind thing to say. However, whether the intent was innocent or not, it was still really hurtful.
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Rare disease awareness month feels like the perfect time to share this showing the faces of some of the most incredible NF fighters 💙 NF1 is a rare genetic disorder that causes tumors to form along
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February is Rare Disease Awareness Month🦓 Even though Neurofibromatosis (NF1) is the *most common* rare disease affecting 1 in every 2000 births, it’s still widely unknown and misunderstood. It is
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February is Rare Disease Awareness Month! 🦓💜 Our daughter has a rare genetic disorder called Neurofibromatosis type 1. It’s affects nearly 1 in every 2000 births, making it the most common rare dis
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Her diagnosis absolutely rocked me. The dark cloud that seemed to follow for so long felt never ending. But one day I woke up and realized I couldn’t keep going this way. We have zero control over
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Sometimes I’ll get a reel that goes to the dark side of the internet, so I recently received a comment saying if “we knew she wasn’t going to be healthy, we should have unalived her.” So I want to m
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Can you do me a huge favor and SHARE + SAVE this reel to help us reach a bigger audience 🫶🏻 K, cool. ILY. NF (Neurofibromatosis) is a rare genetic disorder that affects 1 in every 2500 births. It
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Peace out, 2024. Hope to see ya never! . . . . #pediatricbraincancer #pediatriccancerawareness #childhoodcancer #childhoodcancerawareness #kidsgetcancertoo #braincancer #braincancerawareness #brainca
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About @joyforgeorgia

Amanda | Neurofibromatosis + Pediatric Brain Cancer Awareness is a Instagram micro influencer. With 17.7K followers and 144 posts, joyforgeorgia's account shows a follower-to-following ratio of 13.9:1. This profile demonstrates strong community engagement within its niche. View all content anonymously on Pictame - no login required.

joyforgeorgia's engagement rate sits at 2.40%. This is right in line with the 2.5% average for accounts with 10K-100K followers — a healthy, steady performance.

Out of the last 12 posts, 92% are videos and 8% are photos. Notably, videos tend to get 2.0x more engagement than photos. Content shows up about every 11 days. Captions lean detailed, averaging 902 characters.

2.40% engagement rate — right on track for 10K-100K follower accounts.
92% videos, 8% photos. Videos get 2.0x more engagement here.
Posts about every 11 days.
13.9:1 follower-to-following ratio.

FAQs About @joyforgeorgia

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joyforgeorgia
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@joyforgeorgia

Amanda | Neurofibromatosis + Pediatric Brain Cancer Awareness

Public
Posts
144
Followers
17.7K
Top Hashtags
#nf1#endnf#neurofibromatosis#makenfvisible#braintumor#rarediseaseawareness#rarediseases#raredisease

Explore the most impactful hashtags used in recent posts. These tags highlight the core interests and trending topics that define this profile's digital influence and content strategy.

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Popular Hashtags

#ootd#streetstyle#blogger#influencer#photographer#naturephotography#landscape#travelphotography#architecture#portrait#wanderlust
Following
1.3K
Avg. Likes
381
Avg. Comments
44
Engagement
2.40%

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