Jade Thomson

M.E severe sufferer, fibro & lyme disease patient. Love all my family and my pooch. Love music, films and chocolate. My son is my world #nevergiveuphope

[Jade Thomson @JadeThomson17]

💙💙 how far can we get teddy!💙💙 Raising much needed awareness for M.E/cfs a neurological disorder that has no treatment or cure 💙💙
#ME #CFS #MyalgicEncephalomyelitis
#raisingawareness #share #nocure #Awareness

[Jade Thomson @JadeThomson17]

💙💙 how far can we get teddy!💙💙 Raising much needed awareness for M.E/cfs a neurological disorder that has no treatment or cure 💙💙
#ME #CFS #MyalgicEncephalomyelitis
#raisingawareness #share #nocure #Awareness

[Jade Thomson @JadeThomson17]

Please vote for @Invest_in_ME
💙💙💙💙💙 #7th place now but lets get to #1st with your help..please vote 💙💙💙💙💙💙💙💙💙💙https://t.co/XYyNsMD94Y

[Jade Thomson @JadeThomson17]

Please vote for @Invest_in_ME
💙💙💙💙 8th place now lets get to first!!!!
https://t.co/XYyNsMD94Y

[@NHS100K @NHS100K]

The NHS is already under immense pressure and crumbling , if these mandates go ahead then it will have a devastating impact as a whole. Not only NHS staff but the general public will be affected hugely @sajidjavid @BorisJohnson

[Preetie @Preetilli]

@EssexPR Yes.. I now have 18 triple vaccinated NHS colleagues off sick with covid on my ward. 10 patients (majority vaxxed) I'm tested every 3 days and I had a PCR due to outbreak. I test negative..and yet I'm the only unvaccinated staff member on my ward and I'm set to lose my job soon.

[Jade Thomson @JadeThomson17]

@JennyRohn Lfts are for no symptoms. Pcr is when you're symptomatic 🤦‍♀️😒 i can't deal with this level of stupidity

[Jade Thomson @JadeThomson17]

@JennyRohn Ffs the instructions tell you to do nose and throat 😒😒

[MedlinePlus.gov @medlineplus]

Did you enjoy a post-turkey nap yesterday?

While turkey does contain tryptophan, an essential amino acid that your body uses to help make melatonin and serotonin, it was probably the excess of carbs that made you tired.

Learn more about tryptophan: https://t.co/46OKFBWOFm

[Jade Thomson @JadeThomson17]

@AvrilFoundation @InfusioFFM have taken all my money for my treatments that was all fundraised for and not one person from this company has been in touch with me, They have left me still housebound/wherlelchair bound & now without any money to get help from anywhere else.

[Jade Thomson @JadeThomson17]

@AvrilFoundation i was having #stemcelltreatment @InfusioFFM 'EVO' i fundraised for my treatments there,i was due back to have my ACT after my stemcells that was all paid for, covid hit & now ive heard the company has apparently gone into liquidation without telling me

[Alisontomyradioooo @arisonsned]

Please vote and then share for @Invest_in_ME to win funding money 💙💗 for the @CofEforME @ FMT research!

Each year we give £300,000 in grants based on your votes https://t.co/XCYJt25Kv1

[AKA #BeMoreSkater Debut single out now. #STF @joncampling]

Please support @Invest_in_ME
A charity doing amazing work for people with #ME or to give it it's I'll name #myalgicencephalomyelitis

Simply VOTE for #InvestinME at #Myfundingcircle to help them share in a big charity funding giveaway 🙏👊

#WalkTall

https://t.co/HAGMhzUWxL

[Jade Thomson @JadeThomson17]

Please vote for invest in ME 💙💙💙💙💙💙 @Invest_in_ME 💙💙💙💙https://t.co/XYyNsMD94Y

[Margaret Laverick @margaretlav]

Each year we give £300,000 in grants based on your votes https://t.co/ZvyYZf80sq
A few seconds to support Invest in ME Research please 😀

[Jade Thomson @JadeThomson17]

Please vote for invest in ME 💙💙💙💙💙💙 @Invest_in_ME 💙💙💙💙https://t.co/XYyNsMD94Y

[Jade Thomson @JadeThomson17]

https://t.co/XYyNsMD94Y 💙💙💙💙 please vote for invest in ME 💙💙💙💙💙💙💙💙💙💙

[Jade Thomson @JadeThomson17]

https://t.co/XYyNsMD94Y 💙💙💙💙 please vote for invest in ME 💙💙💙💙💙💙💙💙💙💙

[Janet Dafoe @JanetDafoe]

Article by Whitney Dafoe now published in Healthcare journal dedicated to severe and very severe ME/CFS

https://t.co/dN98DY34fG

[MGresko @MGresko2431]

Millions of us are living with post viral myalgic encephalomyelitis. I am a 21 year 'long-hauler'. Patient testimony/history is the very best research, particularly with a disease that the medical mafia dismisses. @DafoeWhitney speaks for millions of us.