Jade Thomson (@jadethomson17) 's Twitter Profile
Jade Thomson

@jadethomson17

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

ID: 3240628011

linkhttps://www.gofundme.com/stem-cells-for-jade-thomson calendar_today07-05-2015 16:24:09

27,27K Tweet

1,1K Followers

3,3K Following

Janet Dafoe (@janetdafoe) 's Twitter Profile Photo

Article by Whitney Dafoe now published in Healthcare journal dedicated to severe and very severe ME/CFS mdpi.com/2227-9032/9/5/…

MGresko (@mgresko2431) 's Twitter Profile Photo

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. Whitney Dafoe speaks for millions of us.

Janet Dafoe (@janetdafoe) 's Twitter Profile Photo

Perhaps Solve ME should change their name to Solve Long Covid. They didn’t even mention ME in their advocacy day! I feel like we’ve been overlooked again.

Sten Helmfrid πŸ‡ΊπŸ‡¦ (@stenhelmfrid) 's Twitter Profile Photo

#MECFS is a severe, chronic multisystem illness. Some say that you should give hope by trivialising the illness and saying that there is a good chance of recovery, but hope is best given by saying that you take it seriously and won’t rest until there is a cure. #MEAwarenessHour

#MECFS is a severe, chronic multisystem illness. Some say that you should give hope by trivialising the illness and saying that there is a good chance of recovery, but hope is best given by saying that you take it seriously and won’t rest until there is a cure. #MEAwarenessHour
Janet Dafoe (@janetdafoe) 's Twitter Profile Photo

I just listened to the congressional hearings on long COVID. I don’t know whether to scream or cry. All this intense sympathy for people and statements that they can’t wait for 1 to 2 years for solutions. MECFS patients have been suffering for over 40 years with no solutions.

#MEAction Network (@meactnet) 's Twitter Profile Photo

Dr. Collins testified before Congress today that the NIH is going to get out treatments for #longCovid ASAP. So why aren’t they PRIORITIZING ME/CFS research when we know that ME/CFS research is crucial for understanding #LongCovid?

Alisontomyradioooo (@arisonsned) 's Twitter Profile Photo

Please vote and then share for @invest_in_me (Invest in ME Research) πŸ‡ͺπŸ‡Ί to win funding money πŸ’™πŸ’— for the UK/European Centre of Excellence for ME @ FMT research! Each year we give Β£300,000 in grants based on your votes mygivingcircle.org/invest-in-me-r…

#BeMoreSkater Debut single out now (@joncampling) 's Twitter Profile Photo

Please support @invest_in_me (Invest in ME Research) πŸ‡ͺπŸ‡Ί 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 πŸ™πŸ‘Š #WalkTall mygivingcircle.org/invest-in-me-r…

Please support <a href="/Invest_in_ME/">@invest_in_me (Invest in ME Research) πŸ‡ͺπŸ‡Ί</a>
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 πŸ™πŸ‘Š

#WalkTall 

mygivingcircle.org/invest-in-me-r…
Margaret Laverick (@margaretlav) 's Twitter Profile Photo

Each year we give Β£300,000 in grants based on your votes mygivingcircle.org/invest-in-me-r… A few seconds to support Invest in ME Research please πŸ˜€

Jade Thomson (@jadethomson17) 's Twitter Profile Photo

mygivingcircle.org/invest-in-me-r… πŸ’™πŸ’™πŸ’™πŸ’™ please vote for invest in ME πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™

MedlinePlus.gov (@medlineplus) 's Twitter Profile Photo

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: ow.ly/Ceai50GUKwm

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: ow.ly/Ceai50GUKwm
Preetie (@preetilli) 's Twitter Profile Photo

Adam Brooks AKA EssexPR πŸ‡¬πŸ‡§ 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.

@NHS100K (@nhs100k) 's Twitter Profile Photo

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 Sajid Javid Boris Johnson

Jade Thomson (@jadethomson17) 's Twitter Profile Photo

Please vote for @invest_in_me (Invest in ME Research) πŸ‡ͺπŸ‡Ί πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™ #7th place now but lets get to #1st with your help..please vote πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™πŸ’™mygivingcircle.org/invest-in-me-r…

Jade Thomson (@jadethomson17) 's Twitter Profile Photo

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

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