Rocio Saracho πŸ‡²πŸ‡½ πŸ‡ΊπŸ‡² πŸ‡¦πŸ‡Ί

62 Followers
162 Following
157 Posts

Here as part of the #TwitterMigration of 2022. Living in Wurundjeri land.

Mum to 2 humans and a Golden Retriever. Avid runner taking a break due to #LongCovid #Dysautonomia.

#StillMasking because #CovidIsNotOver

Interested in #ClimateChange #science, #Covid, #LongCovid, #POTS, #CleanAir, #auspol.

Americans will really do anything to avoid using the metric system.
Having migrated from Twitter I have far fewer followers that are bots, crypto bros or Russian trolls, but there are also good things about Mastodon.
@irenetosetti yep that's me. I only had a sore throat and some mild gastro issues. Perfectly healthy and super active prior to #COVID19 , no pre-existing conditions. Three weeks after positive Covid diagnosis, chest pain, palpitations, shortness of breath. First diagnosis was pericarditis, and weeks afterwards #Dysautonomia. That's #LongCovid, the gift that keeps on giving. #CovidIsNotMild #WearAMask

RT @[email protected]

”We found that a staggering 90% of people living with long COVID initially experienced only mild illness with COVID-19.” https://www.cbsnews.com/news/most-people-who-ended-up-with-long-covid-started-with-a-mild-case-new-study-shows/

πŸ¦πŸ”—: https://twitter.com/AkuKarvinen/status/1611995432543985664

Most people who ended up with long COVID started with a mild case, new study shows

The researchers found "a staggering" 90% of people living with long COVID only had a mild illness to start β€” but people who were hospitalized were more likely to develop the lasting symptoms.

CBS News
I have to get on a plane next week. Need some tips to minimize Covid infection risk. N95, personal mini HEPA filter (hope its allowed on the plane) what else?. It's a long flight (10+ hours), so I would have to drink/eat at some point.
@irenetosetti unfortunately a lot of people don't realize how debilitating it can be.

RT @[email protected]

THREAD: latest Long Covid Data

ONS has released its latest Long Covid stats. I'm just going to show results for those with Long Covid for *at least 12 weeks*.

Numbers are steady but high, at just under 2 million people (about 3% of population). 1/6

πŸ¦πŸ”—: https://twitter.com/chrischirp/status/1611090167011368979

Prof. Christina Pagel πŸ‡ΊπŸ‡¦ on Twitter

β€œTHREAD: latest Long Covid Data ONS has released its latest Long Covid stats. I'm just going to show results for those with Long Covid for *at least 12 weeks*. Numbers are steady but high, at just under 2 million people (about 3% of population). 1/6”

Twitter
@Tatiana_Trifan how is this not acknowledged amongst most medical professionals. It took me months of debilitating symptoms to get help. One cardiologists suggested my fluctuations in heart rate were caused by anxiety, but couldn't explain why my heart rate was consistently low sitting or laying down and would sky rocket the minute I stood up. I asked him to measure the difference sitting and standing and explain how it was possible for me to bring my heart rate back to normal within seconds by laying down. I told him that if I was able to control my heart rate and make it go up and down within seconds I wouldn't be consulting him. He wasn't impressed. πŸ€·β€β™€οΈ
Another cardiologist said #POTS was not possible at my age. It was because of my own research that I pursued consultation with a specialist in #Dysautonomia. Sure enough that has been one of the many gifts from #LongCovid. I just wish it wasn't that hard to get help.
@valwen so sad there are so many similar stories. I was super fit and three weeks after my "mild" Covid infection, I found my self in the Emergency Department. It took months of debilitating symptoms and hospital admissions to find help. Most doctors bluffed me off. One cardiologist suggested my symptoms were due to anxiety and another one was certain #POTS was not possible at my age. It was because of my own research that I pursued to consult a disautonomic disorders specialist. Sure enough I became part of the statistics of #LongCovid as I developed #dysautonomia post Covid. If it wasn't because I never gave up looking for answers I would probably still be bedridden bouncing from doctor to doctor, being reassured I was in perfect health. There's still a long way to "recovery" (whatever that means) but treatment has been very helpful. I just wish it wasn't that hard to get help. Who knows if I would have deteriorated as much if I had gotten help sooner.
Long COVID made me an advocate for myself as symptoms were ignored with treatments hard to access

Long COVID made me retreat from the world, entering into the realm of invisible illnesses where sufferers are ignored, dismissed and struggle to find the help they need.

ABC News