Jennie Jacques

Jennie Jacques Instagram – Hello šŸ‘‹ I’m still M.E.
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I went from high flying in my career #actress @historyvikings @netflix @bbc @itv various fun roles! Completing my @spartanrace trifecta šŸ’ŖšŸ©±šŸƒā€ā™€ļø& more! To buying my own London šŸ” (independently) #firsttimehomebuyer – to being bedridden & dependent on my partner, at times even to wash my hair 🧼 šŸ’•
For a long time I couldn’t get out in a wheelchair ā™æļø #dysautonomia – sitting up (even in bed!) was out of reach.

I caught a virus 🦠 2018 which is still affecting my mobility (physically, cognitively) 2024 šŸ’© #mecfs #chronicpain

This is NOT ā€œnewā€ or ā€œmysterious.ā€
There are #millionsmissing with it. Sadly. And many more with #longcovid – as predicted.

I’m hopeful @decodemestudy puts us on the map šŸ—ŗļø & scientists like @polybiorf continue pioneering šŸ’„

I’m in a fortunate percentage šŸ€ to see improvement – though slow (and sometimes unpredictable!) I hold on to this, dearly ā¤ļø ā˜€ļø

I used to feel like there was an ā€œoldā€ Jennie and a ā€œnewā€ one. I grieved my old self… but (more recently) I’m accepting I’m still just ME… 😊 hence the collection of mixed pics! #tbt

I encourage you to look up #severeme today šŸ™ on #severemeawareness 8th August 🌻

As a person at the milder end (which is still disastrous to navigate) having experienced only small tastes of the more severe… I can vouch for the monsterous gravity of #me

I pray šŸ™ for the science to continue to catch up. And for the unforgivable GAP between ā€œdoctorsā€ and science to bridge šŸŒ‰

I could not clear a nasty virus from my blood 🩸 for some time šŸ•°ļø (years – this part is unusual, but NB* viruses do persist in tissues too!)
EBV Viremia was my diagnosis with ME/CFS… and although I had a good infectious diseases team, no one could help… severe viral hepatitis and other things (pesky kidney stones, chronic UTI’s etc) hindered my recovery… my immune system took a hit šŸ’„
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I post today for any person suffering with the same (or similar) in hope they feel heard. And to encourage healthy folk to donate to @mefoggydog and post a PJ pic to acknowledge #severemeday šŸ’™šŸ¦‹
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Please sign letter āœ‰ļø for a protocol in our #nhs hospital šŸ„ for Severe ME. Link in bio; Foggy’s website! | Posted on 08/Aug/2024 15:53:22

Jennie Jacques Instagram – Listen šŸ‘‚ ā€˜ere @historyvikings has sailed onto @netflix @netflixuk and Queen Judith has a message for you all;
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ā€œIf you can spare a moment of time to sign a letter āœ‰ļø to help me & #millionsmissing with #mecfs I will be over the moon šŸŒ You will see just how important this is if you visit my YouTube channel @jenniejacques1 & listen to the interview with @mefoggydog – please help us.ā€
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#mecfs #neurology #nueroimmunology #severeme #mecfsawareness #me #eds #hypermobility #dysautonomia #pots #orthasticintolerance #lymediseaseawareness #ebv #chronicfatiguesyndrome #longcovidawareness
Jennie Jacques

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