Eliana
Region: US
Tuesday 20 October 2026 00:18:16 GMT
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jubliagooblia :
She risked a lot for this interview. I’m forever grateful for her sacrifice and for bringing attention to this disease. She’s helping so many people.
2026-10-20 01:03:20
464
Anja 🎨 :
From the article: "A lot of people that have this illness that I've spoken to have said to me 'I don't get believed, people think I'm lazy'. I've never experienced one person that doesn't believe me and that's because, why would an athlete just suddenly stop after 20 years? "
2026-10-20 00:33:13
598
brenna :
fantastic i have covid right now and now im scared
2026-10-20 02:23:59
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Kalah Lalley :
Majority of doctors treat me like my ME is a choice/laziness. Yet another neurologist told me yesterday that I just need to build my stamina. I feel so alone and so hopeless.
2026-10-21 01:39:32
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Taylor :
The indiscriminate nature of disautonomic diseases is so upsetting. I've seen your content and understand the amount of research you do. Have you found out if there is anything in common with those who have come down with these conditions that could have been prevented? I know that professionals say that conditions like MECFS are idiopathic but I was just curious to hear your take ❤️
2026-10-20 00:30:39
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danyel diaries :
Oh I’ve never heard of ebv called glandular fever
2026-10-20 17:57:57
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Heather D. Norris :
And people act like wearing a mask in public is somehow ridiculous
2026-10-21 21:17:21
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beautiful moments🫶 :
i have ME and long covid 😳now in a pem its🤮
2026-10-20 08:28:36
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nokechic07 :
Same girl as you. I was running 5Ks and in CrossFit, as well as kickboxing and yoga. Sept 2020 COVID infection almost ☠️me. I have POTs and MCAS.
2026-10-20 18:27:00
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chill.im.chronically.ill :
I was a gym ambassador, lifting 5x / week, cardio 6x a week and working full time. already had several chronic illnesses. developed dysautonomia after a ebv reactivation (mono). pots took a lot from me. the gym is just one of them.
2026-10-20 11:29:33
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.𖥔 ݁ ˖ ˚⊹₊⋆ :
i caught EBV at the peak of my fitness and i was almost in remission from my autoimmune disease 💔 i'm extremely mild compared to others with similar experiences, but i feel the worst i have ever felt in my entire life. it is so much worse than anything i've experienced before. it is worse than when my immune system attacked my brain
2026-10-20 02:12:19
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Soph :
Thank you for your videos! Our society is so ableist, so many people believe they have immunity from disability bc they are fit… no one is immune from disease or a disabling injury/ accident
2026-10-20 02:59:45
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𝔞𝔪𝔞𝔯𝔞𝔫𝔱𝔥𝔦𝔰 :
before POTS I was a near Olympic swimmer. Now I can barely stand.
2026-10-21 00:03:34
10
Chelise :
Same for me after one covid infection. It’s been a wild 5 years.
2026-10-21 01:34:30
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Cynthia :
My heart goes out to her . I believe i got ME: / CFS after getting covid in 2022 .
2026-10-20 09:39:56
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ᴠᴀᴍᴘɪʀᴇ ɪꜱ ᴇᴍ :
As someone who's entire life was flipped upside down by Covid, thank you for sharing this story 🥰
2026-10-20 02:31:19
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preston :
can completely change your life. been an athlete my whole life, got diagnosed with pots, me/cfs, and eds in 2017. cannot even imagine trying to be an athlete again
2026-10-21 21:49:20
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Gina Grows 🌈♾🪴😷🍉 :
I was the healthiest and most active I’d ever been as a dancer around age 13 (did 5 1/4 hours of dance a week after school/gym class/etc) and that’s when I developed POTS. I remember everyone talking about how “allergies are worse this year”. It was when swine flu was going around. I wish I knew about masks back then.
2026-10-20 13:53:51
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sjdjournal :
this is a magnificent video. thank you for sharing this!!!
2026-10-20 00:26:00
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Neff :
Are you aware if there’s any research regarding what makes an individual more susceptible to long covid/POTS? I had thought that I was more susceptible because of diabetes (even though it’s well controlled). But if an Olympic athlete, the paradigm of health and fitness, can get POTS, no one is safe.
2026-10-20 00:41:15
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Vanessa Flintt :
Sounds like mold to me
2026-10-21 14:56:47
0
Change.org :
Hey Eliana! We DM'd you about teaming up on this ❤️It's in Inbox > crossed-out bubble > Filtered requests, from Change.org ✔️
2026-10-22 17:44:24
2
AmyD 🏴 :
I’m really glad more people are starting to talk about ME/CFS, POTS, adrenal insufficiency and the many ways chronic illness can affect someone—whether it follows COVID or comes from another cause. Maybe it’s my algorithm, but it feels like awareness is growing, and that matters. Keep talking about it. 💛 💜
2026-10-24 08:41:39
2
Michelle :
I think one of the most frustrating things is that temporary disability is literally only 52 weeks and permanent disability doesn’t pay enough for you to survive on if you live in certain places like the place where I live so it’s like I have to work but working could also cause me to crash so what do I do?
2026-10-24 19:20:46
2
Dee :
I used to train for Olympia as a swimmer and now I can barely make dinner and docs don’t care
2026-10-21 11:09:52
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