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Jacqz-MEwarrior_au

@mewarriorau.bsky.social

ME advocate longing for a cure, or some form of treatment. Mum of 3, grandmum of 3. Lived with the horrendous & disabling disease #ME (not CFS) for 28 years. #MyalgicEncephalomyelitis #pwME #MyalgicE (#MECFS #CFS) #LongCovid #ChronicIllness

95 Followers  |  81 Following  |  6 Posts  |  Joined: 02.10.2023  |  1.6779

Latest posts by mewarriorau.bsky.social on Bluesky

What do the Germans call fluffy toys then?

19.10.2023 14:05 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

Sorry to hear that. I seem to be worsening each year.
This is only my 2nd time on here. I’ve not been a regular, so can’t really compare. I’m still using the blue bird most of the time. I think here will get better as X gets worse, or we’re forced to pay. Take care Ravi.

19.10.2023 14:04 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0

@ravihvj.bsky.social
Hi Ravi. I haven’t seen you for ages. How are you doing? Any improvements?
πŸ’™πŸ¦‹

19.10.2023 13:46 β€” πŸ‘ 2    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0

I am so sorry. πŸ˜ͺπŸ’™

05.10.2023 13:18 β€” πŸ‘ 1    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0
Photo of test kit

Photo of test kit

From UK ME/CFS biobank:

πŸ”¬ Exciting News! Our new study is underway.

🧬 Our focus? Exploring the link between HHV-6 DNA levels and ME/CFS severity.

πŸ“† Over the next 6 months, our participants will be collecting saliva samples for us to analyse.

Want to know more? bit.ly/3Q3vKVm

#MEcfs #CFS #PwME

05.10.2023 11:48 β€” πŸ‘ 20    πŸ” 4    πŸ’¬ 0    πŸ“Œ 0

Same.

05.10.2023 13:04 β€” πŸ‘ 2    πŸ” 0    πŸ’¬ 1    πŸ“Œ 0

A huge loss. May he & Robert RIP. πŸ˜ͺπŸ’”πŸ•―οΈπŸ•ŠοΈ

05.10.2023 11:21 β€” πŸ‘ 3    πŸ” 0    πŸ’¬ 0    πŸ“Œ 0

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