Top Tweets for #itpwarrior
Rare Disease Day 2026 – 28 February
Immune thrombocytopenia (ITP) is a rare autoimmune condition, but its impact on daily life can be significant and long-lasting.
This Rare Disease Day, we’re raising awareness of ITP and recognising the vital role of the ITP Support Association in providing trusted information, support, and advocacy for people living with ITP and their families.
Together, we’re working to ensure no one affected by ITP feels alone.
💜 #RareDiseaseDay #ITP #RareButNotAlone #itpawareness

Meet #ITPwarrior Samantha who doesn't let her ITP diagnosis define who she is as a teacher, researcher and reader. Read her story at https://t.co/NZ8ONcs9bM.
#ITP #chronicillness #ITPdiagnosis #chronicillnesswarrior

Meet #ITPwarrior Kristin who is raising $2,100 for 21km as she and her husband Dave take on the Queenstown Half-Marathon this Saturday in New Zealand! Join us in supporting Kristin and Dave at https://t.co/8xmQz3cqrF.

Meet #ITPWarrior Prisma. She was diagnosed with ITP during her pregnancy and worked with her hematologist over the years to find a treatment that has helped her to start feeling better than ever. Visit https://t.co/NZ8ONcs9bM to read Prisma's story. #ITP #ITPinPregenancy

Meet #ITPWarrior Sei: "I've learned that I like to play for fun and love to compete, but I always prioritize my health before sports." Diagnosed at with ITP at age 6, Sei has been able to keep a watchful eye his platelet count. Read more at https://t.co/NZ8ONcs9bM

Tiny Warriors, Mighty Hearts 💜 This September we recognize the strength of all families navigating their ITP journey, especially little warriors. We stand together to raise awareness about ITP and the all the challenges children face in this rare condition. #itp #ITPwarrior

Meet #ITPWarrior David: “[Having ITP] has thrust me into a small, elite group of people with similar experiences and struggles.”
Read more about David’s journey to manage his platelet count and navigate life with ITP at https://t.co/sibkB2KaXL.
![PDSA_ITP's tweet photo. Meet #ITPWarrior David: “[Having ITP] has thrust me into a small, elite group of people with similar experiences and struggles.”
Read more about David’s journey to manage his platelet count and navigate life with ITP at https://t.co/sibkB2KaXL. https://t.co/hjqZdEOyIv](https://pbs.twimg.com/media/GJH08fkXIAAyVLI.jpg)
Meet #ITPWarrior Joshua: “It’s amazing to think how scared I was of needles, and now I give [shots] to myself!”
Diagnosed six years ago at age 10, Joshua joined the ITP POKE-R Club and found support in PDSA. Read more about his journey with chronic ITP: https://t.co/CcpKz83C69.
![PDSA_ITP's tweet photo. Meet #ITPWarrior Joshua: “It’s amazing to think how scared I was of needles, and now I give [shots] to myself!”
Diagnosed six years ago at age 10, Joshua joined the ITP POKE-R Club and found support in PDSA. Read more about his journey with chronic ITP: https://t.co/CcpKz83C69. https://t.co/JIs31hIKZv](https://pbs.twimg.com/media/F8ND-hRWgAA7VVL.jpg)
Meet #ITPWarrior Julie: “I was told my ITP might stop me...”
Read about Julie’s courage and determination to not give up at https://t.co/r2xFjclqJO.

Meet #ITPWarrior Chloe: “I hope one day I can work in a pediatric hematology/oncology unit and comfort and care for children just like me.”
Read more about Chloe’s journey to take control of her ITP at https://t.co/0NGT9ZxJCc.

Meet #ITPWarrior Jennifer: “I just don’t think too much about it as I try to enjoy how lucky I have been.”
Read more about how Jennifer navigated her treatments and now maintains a manageable platelet count: https://t.co/MoQ1W3PLi6.

Meet #ITPWarrior Rhona: “Being diagnosed with ITP at such a young age was especially difficult.”
Read more about how Rhona has come to better understand her ITP and gained a new perspective on life in the process: https://t.co/ObOXMwA1UP.

Meet #ITPWarrior Joe: “Unfortunately, within a week my platelets plummeted back to below 10,000 and I was readmitted.”
Read more about his journey to advocate for himself: https://t.co/ND4h0636bH.

Meet #ITPWarrior Alisia: “My [Color Guard] dream was over, but I knew my health came first.”
Read Alisia’s ITP story at https://t.co/oyYfEZSVYT.
![PDSA_ITP's tweet photo. Meet #ITPWarrior Alisia: “My [Color Guard] dream was over, but I knew my health came first.”
Read Alisia’s ITP story at https://t.co/oyYfEZSVYT. https://t.co/qI4rC0Acyo](https://pbs.twimg.com/media/FjaDxx1XkAI-vYC.jpg)
Meet #ITPWarrior Marcia: “I’m an ITP Warrior and proud of it!”
Read how Marcia builds community with fellow ITP patients: https://t.co/jsxf8KotVC.

@Glimberri @Cykotiq @Shinzakura and various viewers (no @ unfortunately 😢), friends, and family for your contributions, I love you all and sincerely thank you from the bottom of my heart! 💜💜💜
#ITPKnowledgeIsPower
#ITPAware
#ITPWarrior
Meet #ITPWarrior Barbara: “That was the start of a [18]-year journey which has included about 12 hospitalizations due to a platelet count under 7,000.”
Read more about what Barbara has learned during her roller coaster journey with ITP: https://t.co/hCyy3jno1u.
![PDSA_ITP's tweet photo. Meet #ITPWarrior Barbara: “That was the start of a [18]-year journey which has included about 12 hospitalizations due to a platelet count under 7,000.”
Read more about what Barbara has learned during her roller coaster journey with ITP: https://t.co/hCyy3jno1u. https://t.co/wyVQeuOfWF](https://pbs.twimg.com/media/FeVnkMCWIAQESeJ.jpg)
Sporting purple for the last day of September and ITP Awareness Month. It's been a privilege to bring awareness to this condition, and I look forward to doing this again next year.
#ITPKnowledgeIsPower
#ITPAware #ITPWarrior

Meet #ITPWarrior Tia: “Before my diagnosis, I was a gymnast and a figure skater, but I had to give up both sports because of the risk of bleeding.”
Read more about how Tia prioritizes her mental health and refuses to let ITP define her at https://t.co/N9Mm9AgBwu.

Meet #ITPWarrior Kristy: “I want to remind others that nobody should ever have to go through this alone, and there is always hope.”
Read about how Kristy learned to embrace life again after her diagnosis at https://t.co/e9pvHQiW5k.

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