Rosanna
rosannawregor.bsky.social
Rosanna
@rosannawregor.bsky.social
Cosmopolitan, DVM, caregiver for soulmate with very severe ME, the barbell keeps me sane.
Reposted by Rosanna
Available to buy now: One Red Leaf at a Time Greetings Cards.

All proceeds go to our #MEcfs research @uoe-igc.bsky.social.

Thank you @drjogreer.bsky.social & Dr Clare Raynor!

theredtreeandme.substack.com/p/one-red-le...
#oneredleafatatime
One Red Leaf at a Time Greetings Cards - Raising funds for research into Myalgic Encephalomyelitis
Since so many of you have asked, greetings cards featuring images from the Red Leaf Creative Collaborative are now available to purchase.
theredtreeandme.substack.com
November 16, 2025 at 12:36 PM
Reposted by Rosanna
Who do you think is behind door number 5?
#ThereForMEAdventCalendar
December 4, 2024 at 5:00 PM
Reposted by Rosanna
Thank you @rory-stewart.bsky.social l for your advocacy for people with #LongCovid & #MyalgicEncephalomyelitis My 17 yo daughter had Covid Pneumonia in Sept 21. V. sick since & now bedbound & tubefed #SevereME. She needs an NHS #ThereForME Please invite @binitakane.bsky.social on your podcast.
Fantastic to have @rory-stewart.bsky.social on board for the #ThereForME Christmas campaign! 🎄

@restispolitics.bsky.social covered Long Covid this year and we’d love to see them come back to it in 2025 (+ links to ME!) 🙏
It’s Rory Stewart! @rory-stewart.bsky.social is one half of @restispolitics.bsky.social podcast, which covered Long Covid earlier this year.

His message: “My Christmas wish for people with Long Covid is that you are able to feel welcome, accepted and cherished over the holiday season.”
#ThereForME
December 4, 2024 at 10:30 AM
Reposted by Rosanna
Who do you think is behind door number 4?
#ThereForMEAdventCalendar
December 3, 2024 at 5:00 PM
Reposted by Rosanna
Big thanks to @natashadevon.bsky.social for her advocacy and for her Christmas message 👏👏👏👏
@lbc.co.uk presenter @natashadevon.bsky.social is #ThereForME!

Her message: “For people affected by ME and Long Covid, please know that you are in my thoughts this Christmas and I will continue to advocate for you whenever I can. Sending you so much love, Natasha Devon”

#pwME #pwLC
December 3, 2024 at 9:26 AM
Reposted by Rosanna
@lbc.co.uk presenter @natashadevon.bsky.social is #ThereForME!

Her message: “For people affected by ME and Long Covid, please know that you are in my thoughts this Christmas and I will continue to advocate for you whenever I can. Sending you so much love, Natasha Devon”

#pwME #pwLC
December 3, 2024 at 9:00 AM
Reposted by Rosanna
Up and running again for #ME people!
I have sent an amended version of the template letter to my MP, it would be great if we had as many MPs as possible attending.

💥APPG Inaugural Meeting - 17 December 2024 - All-Party Parliamentary Group on ME
📢 APPG on ME

We're delighted to announce Jo Platt MP has agreed to be put forward to Chair the APPG on ME! 🤝

📆 Inaugural meeting: Tue 17 Dec, 5pm - 6.30pm

Invite your local MP 👇

appgme.co.uk/meetings/app...

@thereforme.bsky.social will assist Action for ME in sharing APPG updates!

#pwME #MECFS
December 2, 2024 at 10:58 AM
Reposted by Rosanna
Here's the clue for tomorrow's #ThereForMEAdventCalendar. Can you guess who it is? Find out tomorrow at noon.
December 1, 2024 at 5:01 PM
Reposted by Rosanna
Can you guess, can you guess?
As promised, here's a clue for tomorrow's #ThereForMEAdventCalendar. Can you guess who it is?
November 30, 2024 at 7:01 PM
Reposted by Rosanna
And the fun begins… 😍

Can you guess who’s #ThereForME for 1 December?
As promised, here's a clue for tomorrow's #ThereForMEAdventCalendar. Can you guess who it is?
November 30, 2024 at 5:08 PM
Reposted by Rosanna
Atlas of the plasma proteome in health and disease in 53,026 adults 👩‍🔬🥼👨‍🔬🧪. #proteomics #proteome #plasma #MedSky 👇👇

www.cell.com/cell/fulltex...
Atlas of the plasma proteome in health and disease in 53,026 adults
A large-scale proteomics study involving 53,026 individuals maps 2,920 plasma proteins to 406 prevalent diseases, 660 incident diseases, and 986 health-related traits, identifying promising biomarkers...
www.cell.com
November 23, 2024 at 7:49 AM
Reposted by Rosanna
We are sad to announce that #ThereForME has suspended our collaboration with the ME Association.

We feel that concerns from the community must be heard. The door remains open to continue our collaboration once action is taken and concerns addressed.

More here 👇
November 18, 2024 at 8:43 PM
Reposted by Rosanna
Canadian H5 patient: sequencing confirms Influenza A (H5N1), clade 2.3.4.4b, genotype D.1.1.

Not the same genotype that is infecting dairy cattle and dairy workers in the US. Responsible for poultry outbreaks in Canada.

How the patient was infected remains unknown

www.canada.ca/en/public-he...
Statement from the Public Health Agency of Canada: Update on Avian Influenza and Risk to Canadians
The Public Health Agency of Canada (PHAC) today confirmed a human case of avian influenza (also known as bird flu) caused by influenza A(H5N1) virus in Canada.
www.canada.ca
November 13, 2024 at 8:36 PM
Reposted by Rosanna
Please sign and share this petition to help Karen a severe ME patient who is not getting the help she so desperately needs from the hospital! It is so close to the 10,000 signatures!
www.change.org/p/save-karen...
October 16, 2023 at 4:36 PM
Reposted by Rosanna
OMF's Annual Directors Gathering brings together all our CRC directors and the esteemed SAB member, Dr. Maureen Hanson. 🤝 During these three days, this group discusses the state of research within OMF and in the broader research community. 👉 Stay tuned for more details.
October 13, 2023 at 4:24 PM
Reposted by Rosanna
New from Scotland:

"People With #LongCOVID and #MyalgicEncephalomyelitis/#ChronicFatigueSyndrome (ME/CFS) Exhibit Similarly Impaired Vascular Function"

Free fulltext:
www.amjmed.com/article/S000...

#MEcfs #CFS #PwME #MyalgicE #PwLC #postcovid  #postcovid19 #LC
October 12, 2023 at 12:17 PM
Reposted by Rosanna
We have a dedicated page for #MECFS scientists who are looking for ways to fund their biomedical research. We hope this will be a useful collection of resources to those who are studying ME and also #LongCOVID

europeanmecoalition.com/resources-fo...
October 5, 2023 at 2:55 PM
Reposted by Rosanna
Well it’s spooky szn! And nothing is spookier than having a LDN incurable and disabling complex chronic illness like #MECFS. That’s why all month long I’m fundraising for Open Medicine Foundation. Donate/share/etc so we can raise as much money as possible! openmedicinefoundation.crowdchange.co/35021
Open Medicine Foundation | Fundraisers
Open Medicine Foundation (OMF) envisions improved health care for people with chronic complex diseases.
openmedicinefoundation.crowdchange.co
October 1, 2023 at 3:10 PM