1. Home
  2. Detail

@nuno.galvao: Em cada etapa que a vida me traça, Carrego fardos que tenho de enfrentar, Uns dias mais forte, noutras uma desgraça, Em ciclos onde a força tende a vacilar. Nas agruras que cada jornada me revela, Às vezes brilho, noutros naufrago, Lido com a dor,... a luta é tão singela... Que em dias bons, maus ou assim assim sou transformado. Sigo, oscilando nesse vaivém, Entre as alturas de triunfo e a sombra da dor, Sou um ser em busca de um porto além, Onde em dias frágeis, ainda sou de valor. Por Nuno Galvão #poesia #poetry #poetsofinstagram #poetrytiktok #poetrycommunity #trending #trend

Nuno Galvão
Nuno Galvão
Open In TikTok:
Region: PT
Thursday 18 January 2024 00:36:09 GMT
3
2
0
1

Music

Download

No Watermark .mp4 (0.2MB) No Watermark(HD) .mp4 (0.2MB) Watermark .mp4 (0MB) Music .mp3

Comments

There are no more comments for this video.
To see more videos from user @nuno.galvao, please go to the Tikwm homepage.

Other Videos

𝗜𝗧𝗔𝗖𝗛𝗜 𝗨𝗖𝗛𝗜𝗛𝗔 𝗘𝗗𝗜𝗧 🫀🥀𝗥𝗮𝘁𝗲 𝗘𝗱𝗶𝘁 𝗽𝗹𝗲𝗮𝘀𝗲 𝘀𝘂𝗽𝗽𝗼𝗿𝘁 🤨🔥 #lorditachi #hero #fypシ゚viral #foryoupage #anime
𝗜𝗧𝗔𝗖𝗛𝗜 𝗨𝗖𝗛𝗜𝗛𝗔 𝗘𝗗𝗜𝗧 🫀🥀𝗥𝗮𝘁𝗲 𝗘𝗱𝗶𝘁 𝗽𝗹𝗲𝗮𝘀𝗲 𝘀𝘂𝗽𝗽𝗼𝗿𝘁 🤨🔥 #lorditachi #hero #fypシ゚viral #foryoupage #anime
hihihi. 🤍✨ . . . . . . . .🤍✨
hihihi. 🤍✨ . . . . . . . .🤍✨
Did you know Sarcoidosis is a disease that causes inflammation in different parts of the body? It takes over major organs. Eyes, lungs, brain etc. In my case it took my vision. I had no warning. No slow decline I could prepare for. I lost my vision within 3–4 weeks. One day I was living life normally doing photography, capturing moments, building memories for other people and the next, everything started disappearing faster than I could understand it. I had a 7 month old, 4 and 5 year old as well. My world went from clear to gone in a matter of weeks. There was no adjustment period. Just shock, fear, and having to rebuild a life I didn’t recognize anymore. The first year and a half, I lived in the gray. I couldn’t tell if the boys had left a light on or if it was day or night. I was even on medication just to help me wake up and function through the day. I have had two stem cell treatments. After the first one, I started to see light again. I could finally tell if a light was on or off in the house. I could tell it was daytime or nighttime. After the second treatment, I began to see colors. Everything is just extremely, extremely blurry. . And I want more. Because even the smallest return of vision gave me something I hadn’t felt in a long time: hope. A few years later I began doing blind photography and learned how to work, feel, and capture moments in a completely different way than before. It wasn’t about what I could see anymore, but about emotion, connection, and trusting something deeper than sight. Sarcoidosis took so much from me without warning but it didn’t take my fight, my creativity, or my desire to keep going. I’m still learning, still healing, still hoping. And I’m sharing my story so others know they’re not alone in the fight they never asked for. #SarcoidosisAwareness #VisionLoss #BlindButNotBroken #VisionLossAwareness #AutoimmuneDisease
Did you know Sarcoidosis is a disease that causes inflammation in different parts of the body? It takes over major organs. Eyes, lungs, brain etc. In my case it took my vision. I had no warning. No slow decline I could prepare for. I lost my vision within 3–4 weeks. One day I was living life normally doing photography, capturing moments, building memories for other people and the next, everything started disappearing faster than I could understand it. I had a 7 month old, 4 and 5 year old as well. My world went from clear to gone in a matter of weeks. There was no adjustment period. Just shock, fear, and having to rebuild a life I didn’t recognize anymore. The first year and a half, I lived in the gray. I couldn’t tell if the boys had left a light on or if it was day or night. I was even on medication just to help me wake up and function through the day. I have had two stem cell treatments. After the first one, I started to see light again. I could finally tell if a light was on or off in the house. I could tell it was daytime or nighttime. After the second treatment, I began to see colors. Everything is just extremely, extremely blurry. . And I want more. Because even the smallest return of vision gave me something I hadn’t felt in a long time: hope. A few years later I began doing blind photography and learned how to work, feel, and capture moments in a completely different way than before. It wasn’t about what I could see anymore, but about emotion, connection, and trusting something deeper than sight. Sarcoidosis took so much from me without warning but it didn’t take my fight, my creativity, or my desire to keep going. I’m still learning, still healing, still hoping. And I’m sharing my story so others know they’re not alone in the fight they never asked for. #SarcoidosisAwareness #VisionLoss #BlindButNotBroken #VisionLossAwareness #AutoimmuneDisease

"Me limaron la cara con un martillo" #MalaPraxis #NegligenciaMedica #Testimonio #Cirugia #Polemica #Influencer @...jay...jay
💫 مسائكم عالمي 💫 #صقرالعالمي_2026 #اكسبلور_explorer #صخب_جمهور_النصر #بطل_دوري_روشن #النصر_بطلاً_لدوري_روشن2026
💫 مسائكم عالمي 💫 #صقرالعالمي_2026 #اكسبلور_explorer #صخب_جمهور_النصر #بطل_دوري_روشن #النصر_بطلاً_لدوري_روشن2026
cykarmaryn seni yadymdan 🥹🍂
cykarmaryn seni yadymdan 🥹🍂

About

Legal