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@ellie_teale: Your new fav dinner bowl 🍱 full recipe in bio!! @Mike’s Hot Honey @nutiva @Caraway Home @lundbergfarms @Primal Kitchen Foods @Yellowbird Foods @gimmeseaweed #healthymeals #mealprep #Foodie #nutrition #quickrecipes

Ellie Teale
Ellie Teale
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Region: US
Thursday 24 July 2025 21:41:57 GMT
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gimmeseaweed
gimmeseaweed :
So delicious!💚💚💚
2025-07-25 21:15:35
0
jess__burgess
jess :
You should try the poke salmon from Costco! Sooo good and tastes fresh even though it’s frozen
2025-07-24 22:06:08
0
meghanp_06
Meghan 🇨🇦 :
I make this very often and it’s so so yummy! I will have to try your version, it looks delicious!
2025-07-24 23:41:09
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Chiếu mây điều hoà lót lụa cao cấp, chiếu mềm mịn mát, thoáng khí, được bo viền kỷ càng tỷ mỹ, có chun cài 4 góc, có đầy đủ kích thước cho từng cỡ giường#xuhuong #xuhuongtiktok #viral #trending #tongkhogiadungphanthanh #phunuvietnam #danongdichthuc #phunu #sinhvien #noitrothongminh #chieumaydieuhoa #chieumaydieuhoalotlua #chieumaydieuhoacaocap #chieumaylotlua #chieumayvienlua
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The sound of glowing, hydrated skin and lips 💖🎀💅🍓
The sound of glowing, hydrated skin and lips 💖🎀💅🍓
The FDA acknowledged the data behind this gene therapy is strong. But instead of working with the company to resolve manageable manufacturing concerns, they rejected the application. Now, families are being told to wait another 6 to 12 months while a new application is prepared and reviewed. In Sanfilippo, that’s a lifetime. It means speech lost. Mobility gone. Memories erased. We know FDA Commissioner Marty Makary and CBER Director Vinay Prasad have voiced their commitment to rare disease families. We’re asking them to take action on their words and sit down with us, now, before we lose more time and more children. This isn’t just about Sanfilippo. Other rare disease patients are facing similar delays, and we need reform. Our kids are losing their voices, so we need yours. Please tag and share with FDA, Congress, the media, and anyone else who can help. #ApproveHopeNow #NoMoreDelays #WalkTheTalkMakary #SanfilippoSyndrome
The FDA acknowledged the data behind this gene therapy is strong. But instead of working with the company to resolve manageable manufacturing concerns, they rejected the application. Now, families are being told to wait another 6 to 12 months while a new application is prepared and reviewed. In Sanfilippo, that’s a lifetime. It means speech lost. Mobility gone. Memories erased. We know FDA Commissioner Marty Makary and CBER Director Vinay Prasad have voiced their commitment to rare disease families. We’re asking them to take action on their words and sit down with us, now, before we lose more time and more children. This isn’t just about Sanfilippo. Other rare disease patients are facing similar delays, and we need reform. Our kids are losing their voices, so we need yours. Please tag and share with FDA, Congress, the media, and anyone else who can help. #ApproveHopeNow #NoMoreDelays #WalkTheTalkMakary #SanfilippoSyndrome
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#vibing #dancedance #accountability #yup #truth #talkaboutit #keepitreal #hitthemwiththetruth #fyp #fafo_og #facts #liars #amen #facts #iykyk #viral #fans

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