English
English Español Português Pусский Deutsch Français Itaaano Nederlands Polski Indonesia العربية ไทย Tiếng Việt Türkçe 繁體中文 简体中文 日本語 한국어
@chronic_hopeful Profile picture

Char | ChronicallyHopeful.com

@chronic_hopeful

M.E. Advocate, Blogger, Artist & Gamer Housebound with #MyalgicE since 2015 #MillionsMissing #pwME #MEcfs #MEawareness Also at @MEawarePics

5KPosts 1KFollowers 836Following
Similar User
A Journey Through the Fog photo

@JourneyFog

Henry Anderson photo

@macanders

Joy In The Seasons photo

@JoyInTheSeasons

PurpleSpeedwell purplespeedwell.bsky.social photo

@PurpleSpeedwell

Deborah Causer photo

@causer_deborah

ME perspective photo

@me_perspective

Moira Dillon photo

@MoiraDillon_ME

Mishka G 🌊 photo

@Mishka0808

ClairME photo

@ClairME_

James Foulger photo

@jifoulger

Patient Dreams photo

@PatientDreams

🌱🛌🦓Margo 🍃🕊🙌🏼🥄 photo

@JessicaMargo99

EndMECFS photo

@EndMECFS

postersandme photo

@postersandme

Andrea photo

@andrea__sweden

Char | ChronicallyHopeful.com Reposted
chronic_hopeful Profile Picture
Char | ChronicallyHopeful.com
 @chronic_hopeful
26 May 2023

WORSHOPS - places still available 1--7th June 2023 ONLINE Starter Workshop - BOOK HERE - salesatdrmyhill.co.uk/7th-june-2023-… 2--14th, 15th and 16th July 2023 -IN PERSON Weekend Workshop - JUST ONE PLACE LEFT - book here - salesatdrmyhill.co.uk/july-14th-15th… #cfs #me #longcovid #naturopathic

Tweet Image 1
0
3
6
0
645
Char | ChronicallyHopeful.com Reposted
chronic_hopeful Profile Picture
Char | ChronicallyHopeful.com
 @chronic_hopeful
25 May 2023

I’m going with Ron to London Invest in ME conference! I hope to see lots of you there! investinme.org/IIMEC15.shtml

33
40
466
5
12K
chronic_hopeful Profile Picture
Char | ChronicallyHopeful.com
 @chronic_hopeful
28 May 2021

I just unlocked the Invisibility Cloak in the Chronic Illness Survey Adventure! Join me in helping reveal the realities of chronic complex disease by clicking here: ctt.ec/Od1dF+ #SC4D #NEISvoid #MEcfs #POTS #MCAS #hEDS

0
0
1
0
0
Char | ChronicallyHopeful.com Reposted
chronic_hopeful Profile Picture
Char | ChronicallyHopeful.com
 @chronic_hopeful
21 May 2021

Symptom Cluster Characterization in Complex Chronic Disease (the Chronic Illness Survey Adventure) is ready for you! Are you ready? Can you help to gather the richest dataset on complex chronic disease symptoms ever? (1/4) #SC4D meaction.net/epi

1
6
21
2
0
chronic_hopeful Profile Picture
Char | ChronicallyHopeful.com
 @chronic_hopeful
16 May 2021

Hey friends! I've just donated £5 to ME research, who can match that and help #EndMEcfs? #MayMomentum is building awareness and accelerating research to end ME/CFS. I donated to OMF to lead research and deliver hope. Join me! omf.ngo/?form=maymomen…

Tweet Image
OMF Home - Open Medicine Foundation
Source: https://t.co/037CVZvsIj
0
2
6
0
0
Mindfully capturing & sharing little seasonal joys in nature. Currently #JoyInSpring 🌸🌼 Mindfulness & Meditation Practitioner #pwME #Spoonie

Joy In The Seasons

@JoyInTheSeasons
Curious & exhausted peace seeker, co-host of @pempodcast23, photographer and blogger. PwME, sidelined social worker, grief dealer, joy peddler, SAFC fan, He/Him

Daniel Moore

@Talmandaniel
30y/o creative, with complex health issues🤞🏼ME/CFS biomedical research. Passion for the wild, for kindness, and helping all people have a voice. Co-author✨

Lizzy H

@hopefullizzy
Life was once Leith, homelessness & a forklift truck. Life is now being chronically ill with ME & writing about it. Autistic. Smorky’s human. She/her.

Phoebe Boag

@PhoebsBo
Myalgic Encephalomyelitis ME + POTS 38 years Donor to the @mecfsbiobank for 10 years & @DecodeMEstudy Please watch https://t.co/rPfzhZQ6po #pwME

Katy B

@KatyBruce108
CFS(!) & POTS diagnosis, ME symptoms - trying to accept. Still me. Sense of humour intact. Proud “Anti-Recovery Activist” justjo@bskysocial

Jo

@cfs_jo
Advocate & sharer of bio research for INFECTION ASSOCIATED CHRONIC DISEASES inc MECFS, Long COVID, MCAS, Dysautonomia, Vaccine injuries, FMS, Sjogrens & Lyme 🔬

Wading through treacle

@kimisgubbed
Writer with ME/CFS & Lyme & son w/#MECFS & #Lyme; love to travel, read & spend time outdoors w/family & friends; write 2 blogs & author of chronic illness book.

Suzan Jackson

@livewithmecfs
A global network fighting for equality for Myalgic Encephalomyelitis. #MEAction #MillionsMissing https://t.co/JhhNZoFYJi

#MEAction Network

@MEActNet
M.E. inactivist, person-centred counsellor (see link), former flaneur, recovering poet (Rack & Waterloo Press)

Dan Wyke 🦠➡️🧠🔥

@Dan_Wyke
Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos.

Adam

@ABrokenBattery
We raise funds for medical research into ME/CFS and provide support, information & campaign for people in the UK. RTs do not necessarily mean endorsement.

ME Association

@MEAssociation
ME/CFS | Long COVID

Billy Hanlon

@bhanlon15
I'm Beth, embroidery & craft are my buzz. #socialist #pwme #disabled insta: thecraftymissb https://t.co/H4UqOa9igd

Crafty Miss

@CraftyMissB
ME/CFS patient advocate, @OpenMedF science correspondent. Bedbound. Former: biochemist in training, Powerlifter, PT, Gym Manager. Jazz grad/Musician. F1/Boxing.

Ben H

@benh_mecfs
Working to improve the quality of life of M.E. patients using every available means and opportunity #SocialEnterprise #pwME Linktree - https://t.co/TNEwofcNnm

ME Foggy Dog

@MEFoggyDog
I share #ChronicIllness & #ChronicPain info fr VARIOUS #perspectives. #Lupus #Sjogrens #AntiphospholipidSyndrome #epilepsy #MentalHealth #anxiety #depression

A Chronic Voice

@AChVoice
Family, faith, footy, friends, books, classical music, rescue cats, #fibromyalgia #pwME #hEDS #spoonie #SCS #chronicpain. Also now on blue sky @rainbowsteph

Stephania

@RainbowStephan
Community Builder / Passionate Collaborator / Chair - #MedicalEducation Group / #ResearchPartner / #MECFS #LongCovid Advocate / #PwME / #MCAS / #POTS / #Fibro

Sabrina Poirier (On Hiatus)

@Sabrina_Poirier
UK branch of global grassroots movement @MEActNet. Empowering patients to fight for the #MillionsMissing with ME. Health equality & biomedical research now!

#MEAction Network UK

@MEActNetUK
#ME #MECFS #LongCovid #BildungAberSicher #Petition #MECFS. ➡️https://t.co/EuFUEYyf9j ⬅️

KK

@KSannara

Tthotat

@TthotatiPaq

Porytee

@PoryteeYlA4kN
Love your own self

Leesa

@Rewckore9tam

Grueslson

@GrueslsonrWV9_

Florance

@holm_florance33
Danced around the ME/CFS spectrum for 6 years, currently landed in Moderate/Housebound. I write a bit about the ME story. #ME #CFS #ChronicFatigue #pwMe

KJ Cassells

@myyearcrash

Toughckeigh

@Toughckeigh0Qp

Nupyshee

@Nupyshee9XQV
ME/CFS..........

Martin

@fmartin467

SigridChrist

@10y7cVrA3Ix36
📢This is a twitter cryptonews aggregator, just like https://t.co/hEGyjSoQiX, but this is for you who is on Twitter! 😚✨💎** Read pinned post for more info👇🏾

CryptoDoctor Godswill 📈🩺

@TheDoctorGods
Teacher & social worker: environmental & health humanities, community development, linguistics, queer & disability pride. Workplace violence survivor.

Debbie Filippaki, BSW (Hons)

@filippakid

Seelea

@Seelea156498

CleanTheAir

@CleanTheAir2024

Sarah Reedman

@sassyreeds

Terresa Chatmon

@TerresChatm
30 | Disabled from #mecfs for a decade | Disability rights advocate | Formerly homeless | Artist | See highlights tab for my free graphic art | she/her | 333

Kendra

@SurvivingCFS
When something doesn't feel right, it's because it's not. #ChronicPain #ChronicIllness #Fibromyalgia #CFS #Housebound #DisabledPeopleDemand #Invisible #Advocacy

N.K.C

@888NatNatNatNat
ME/CFS for 7 years now. Diagnosed 3 years ago. Musician - Gardener - Plant lover 🪴 Artistic

CreativeGuy🌈

@CreativeGuyDK
Full Body Rejuvenation! Vital Reaction® is a #health and #wellness company specializing in molecular #hydrogen. #LongCovid #MECFS #CKD #Fatigue #millionsmissing

Vital Reaction®

@h2vitalreaction

Wateen Federici

@FedericWate
Riksförbundet för ME-patienter. Vi har organiserat personer med diagnosen ME/CFS och deras anhöriga sedan 1993. Twittrar sedan 2016.

RME

@RMEsverige

Richard

@Richard52884321

James Tooms

@JamesTooms
In recovery since 09/09/23 | #ActuallyAutistic | M.E | Fibro | GAD | Gamer | Music is life | Dancing to the beat of my own drum | Writer for LadiesGamers.

Annii

@SylveonUmbreonx
Poet | Abolitionist | Environmentalist | Bedbound with Long COVID and M.E. 🍉 🌲 🐦 🛌 😷 #disabilityjustice

brokenwingpoet

@brokenwingpoet
Pasient-sentrert fellesskapsplattform for langtidssyke Covid-pasienter i Norge. #longcovid #healthequity #healthjustice #dataprivacy. Del av @CareConnectlc

Lange Covid-pasienter i Norge

@pwlcNorway
Mum of 2, I have M.E, so am plodding along nicely in the slow lane, professional resting is hard you know!

kelly

@KellyHartfield1
#Disabled & 10x #ChronicIllness inc #pwME for 20 yrs + prob #AuDHD please #WearAMask whovian, history grad, Christian, grey/demi, #ClimateActionNow

Nic

@LilNic000
22 | #pwME for 8 years

Hannah Avery

@Hannaheavery
The voice for Long Covid in Ireland. An advocacy group comprised of Long Covid patients fighting for awareness of LC & adequate services in Ire for all patients

Long Covid Advocacy Ireland

@LCAIreland
Justice is like air; without it we cannot survive; We’re suffocating from lack of Justice! #DisabilityJustice #pots #ptsd #depression #migraines #mecfs etc

Justice is like air

@JusticeIsAir
30yo avid reader living with chronic illness 📚✨️ #MEcfs #fibromyalgia #anxiety #depression #trauma #PCOS #booktwitter #booktwt

Amy Osborne

@busywithmyb0oks
♿️ chronisch krank - ME/CFS, POTS, FIBRO, SFN, MCAS & mehr l Bell 10-20 l hauptsächlich auf Instagram l für mehr Aufklärung, gegen Ableismus und Vorurteile 💬

mein.mecfs.tagebuch

@mecfs_diary

Elçin Seçkin

@elcinseckin
♿️ ME/CFS, POTS, SFN, FIBRO & MORE - raising awarness for the chronically ill 🤍 25 years old // Germany // happily married // also on Instagram and Facebook //

regis.chronic.diary

@regichronically
A patient led initiative bringing autoimmune patients together to share experiences, support and raise disease awareness. Join our #autoimmunechat community

Autoimmune Chat

@AutoimmuneChat
Hannah Elliott, Marketing & Comms Consultant in heritage sector. Tweets about culture, nature and life's small delights and ironies. Any views my own.

Hannah Elliott

@HannoMingrace

LB

@Lindaroo32
Your ❤️ is a weapon the size of your fist - keep loving, keep fighting. #longcovid 🐝

Laura Collison

@lauracollison
Female Muscle, Models and Other Stuff 18+. I do not own any of the Photos or Videos posted. DM for Removal, Credits, Promo or Collaboration 🌈✨

Jay Muscle

@JayMuscle1
👩‍🦽‍➡️2 living kids,1 angel baby,Girlguiding leader,DBT, participation worker, poverty campaigner, disability advocate.

Sunshine Glitter👼🏻🦸🏼‍♀️👩🏼‍🦽🧜🏼‍♀️

@Racheewheels
🌧 Health & Wellness for the Body & Spirit 🌧 #IIH #ChronicIllness #Advocate #Outreach #Ministry #Health #Writer

Weather in April

@AprilMNormand
🗝#FreePalestine🗝#GoVegan🐮#StopGenocide🌿#CeasefireNOW🕊#WaterForGaza🫒#HelpGazaChildren💕#PrayForGaza🌳#PrayForPeace🌻#StopEcocide🌍#RIPAaronBushnell

🕊️🗝️🇵🇸KRISTA🔱Cruz🦊

@KRISTAC52846823
Podcast amplifying voices of people with Multiple Chemical Sensitivity (MCS) and research about the illness. Subscribe where you get your podcasts! 🎙️🎧✨

The Chemical Sensitivity Podcast

@podcastingmcs
Live Authentically. Cmplicted by chrnic dis-ease. 23 yrs w #MyalgicEncephalomyelitis, Covid Competent

BaziaZeb

@BaziaZeb
Writing my memoir about 18 years of life as the #patient - Tuberculosis & AI 🩺 Rep’d by @ASaunders7 @thesohoagencyuk

Tilly Rose

@tillyroseauthor
A documentary that seeks to shine a light on and tell the stories of those suffering with myalgic encephalomyelitis and Long COVID.

Movie About M.E.

@Movie_About_ME
gender is weird. all pronuns accepted. tired. antifascist. chronic illness.

tmsizemore

@bookwormlite
Caregiver for very severe ME/CFS son, advocate and fundraiser for End ME/CFS PROJECT at OMF and CFSRC at Stanford. The rest of my life is on hold...

Janet Dafoe

@JanetDafoe
Ph.D. in physics, also interested in mathematics and science theory. Loves to apply general knowledge of science to other fields, for example ME/CFS.

Sten Helmfrid 🇺🇦

@StenHelmfrid
Former professional ballet dancer | Bed/sofa-bound M.E. patient | Using Twitter to raise awareness for #MyalgicE | #art2cureME #pwme #millionsmissing

Anil van der Zee ©

@AnilvanderZee
Mindfully capturing & sharing little seasonal joys in nature. Currently #JoyInSpring 🌸🌼 Mindfulness & Meditation Practitioner #pwME #Spoonie

Joy In The Seasons

@JoyInTheSeasons
Curious & exhausted peace seeker, co-host of @pempodcast23, photographer and blogger. PwME, sidelined social worker, grief dealer, joy peddler, SAFC fan, He/Him

Daniel Moore

@Talmandaniel
💙Art, Nature, Books, Some Music. Severe ME 32 years, would love to be released from this one room. Daughter severe 38 years. Furious about treatment of ME.

Carole Bruce

@CaroleBruce17
Life was once Leith, homelessness & a forklift truck. Life is now being chronically ill with ME & writing about it. Autistic. Smorky’s human. She/her.

Phoebe Boag

@PhoebsBo
With ME 35 years (30 yrs severe). 95% of posts on #MEcfs/#LongCovid/#chronicillness. 26 publications in peer-reviewed journals. @IrishMECFSAssoc trustee 27 yrs

Tom Kindlon

@TomKindlon
Severe ME/CFS patient and advocate. Photographer, filmmaker, artist, creative. Sick since 2004, bedridden since 2013. Never. Giving. Up. ✊

Whitney Dafoe

@DafoeWhitney
Writer with ME/CFS & Lyme & son w/#MECFS & #Lyme; love to travel, read & spend time outdoors w/family & friends; write 2 blogs & author of chronic illness book.

Suzan Jackson

@livewithmecfs
News, interesting information and commentary on ME/CFS. Mostly inactive these days.

ME/CFS News

@MECFSNews
A global network fighting for equality for Myalgic Encephalomyelitis. #MEAction #MillionsMissing https://t.co/JhhNZoFYJi

#MEAction Network

@MEActNet
M.E. inactivist, person-centred counsellor (see link), former flaneur, recovering poet (Rack & Waterloo Press)

Dan Wyke 🦠➡️🧠🔥

@Dan_Wyke
Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos.

Adam

@ABrokenBattery
Senior Fellow in Public Health and Journalism, Center for Global Public Health, UC Berkeley. My academic position is largely funded by donations from patients.

davidtuller

@davidtuller1
We raise funds for medical research into ME/CFS and provide support, information & campaign for people in the UK. RTs do not necessarily mean endorsement.

ME Association

@MEAssociation
Activist/Organizer: ChronicIllness, disability, ME/CFS, Lyme, LongCovid, women | Writer: WashPost, MarieClaire, NPR, Ms, Newsweek | Playwright: Many productions

Rivka

@Rivkatweets
@arisonsned.bsky.social Cat and Dog botherer. YP counsellor retired. Want my bike and my health back 🩵

Alisontomyradioooo

@arisonsned
ME/CFS patient advocate, @OpenMedF science correspondent. Bedbound. Former: biochemist in training, Powerlifter, PT, Gym Manager. Jazz grad/Musician. F1/Boxing.

Ben H

@benh_mecfs
Working to improve the quality of life of M.E. patients using every available means and opportunity #SocialEnterprise #pwME Linktree - https://t.co/TNEwofcNnm

ME Foggy Dog

@MEFoggyDog
#ThisIsME is a multi-platform campaign raising awareness for Myalgic Encephalomyelitis and Chronic Fatigue Syndrome (ME/CFS). DM us to be featured.

#ThisIsM.E.

@ukthisisme
Person Centred Counsellor. ME Sufferer. Social Justice & Equality. LFC. #MyalgicEncephalomyelitis #autismawareness #YNWA #MentalHealthMatters

Phil Stewart 💙

@PhilStewart23
I want a happy, peaceful life! 23 years of neurological problems #chronicillness #disabled♿️ #fibro #dyslexic #dyspraxic #ME Mother of 5❤,nana.🇧🇧

Lina

@greenecharmer9
Ill w/ severe Myalgic Encephalomyelitis. Neuroimmune disease. Bedridden/housebound. Interested in raising awareness of what M.E. is (& isn't). London, UK

Alice Woolf

@me_awareness
To improve the lives of all people affected by ME/CFS and Fibromyalgia through advancing awareness, care, treatment and research.

Massachusetts ME/CFS & FM Association

@MassMECFS
Official Twitter account for Simmaron Research, a non-profit scientifically redefining ME/CFS. Visit our site to learn more.

Simmaron Research

@RedefiningMECFS

Bettie Hough

@bettiehough
Philosopher - ethics, politics, music | Slowly writing a book on Isaiah Berlin | Grew up in USSR, Isr, UK. Home is London | Living with ME since 2003. | 🔗 🎥

Vlad Vexler

@VladVexler
A group of physiotherapists with a special interest in Myalgic Encephalomyelitis (ME) with the aim to improve physiotherapy management for people with ME

Physios For ME

@PhysiosForME
The world's largest study ever into #MEcfs. #pwME info@decodeME.org.uk - 0800 196 8664 #DecodeMEStudy #pwME #MillionsMissing

DecodeME the ME/CFS Study

@DecodeMEstudy

Windsänger

@windsaenger_1
Founded over 70 years ago, Marshalls' heritage & expertise is in supplying seeds, bulbs, plants & garden care products. Ran by gardeners for gardeners.

Marshalls Garden

@MarshallsSeeds
Founded in 1888. 135 years later and we still offer the finest quality seeds at real value for money backed up by good old fashioned service!

Kings Seeds

@KingsSeeds_UK
Est. 1894, we are UK suppliers of quality flower and vegetable seeds, bedding, bulbs, fruit bushes, trees and horticultural tools, plus gardening advice!

Dobies

@DobiesOfDevon
Our 2023 Catalogue & VegBook offers fresh seeds of over 2500 items, with something for everyone, including old, new and interesting, rare species and varieties

Chiltern Seeds

@ChilternSeeds
Mr Fothergill's in the UK. Supplier of flower & vegetable seeds and plants, with one of the UK's most extensive seed ranges. #vegetablegarden #flowergarden

Mr Fothergills Seeds

@mrfothergill
Gardening advice you can trust. Get the latest tips from the horticulture industry in the UK’s best-selling kitchen garden magazine. Subscribe now. #GrowWithGYO

Grow Your Own

@GYOmag
🌱 Experts in the garden since 1855, everything you need for your garden in one place. We’re with you all the way! #yourtmgarden

Thompson & Morgan

@ThompsonMorgan
Historic #gardening company still going strong after 200 years. Royal Warrant holder and best known for the quality of our Veg and Flower seeds and plants

Suttons

@suttons_seeds
Welcome to the official Twitter page of Iceland foods! Follow us for all things food, exclusive new products, & ice cold deals! ❄🍽

Iceland Foods ❄️

@IcelandFoods
The official Aldi UK Twitter page. This week our Social Media Team are available Monday to Saturday 8am-8pm and Sunday 10am-4pm.

Aldi Stores UK

@AldiUK
Welcome to Lidl GB’s official Twitter. Have a question? We’re here from Mon-Sat 8am-8pm & Sun 9am-5pm. Customer Privacy Policy: https://t.co/wpdkw7QySq

@LidlGB

@LidlGB
Welcome to the official Asda Twitter page. Our customer service team are always happy to help at @AsdaServiceTeam.

Asda

@asda
More gifs, puns & hashtags, all in 280 characters 💚 #MoreReasons

Morrisons

@Morrisons
Welcome to the official Tesco Twitter! Got a query? We're here to help from 6am-11pm. Visit https://t.co/WoRlLkKfv7 for more information.

Tesco

@Tesco
Welcome to the official Sainsbury’s Twitter page. We’re here daily helping to bring good food to your feed and to answer any of your questions.

Sainsbury's

@sainsburys
Acting, writing, larking, encouraging such fun. Mainly https://t.co/lIdNOpnmJn Me shop is here https://t.co/Spj2cvKBkl

Miranda Hart

@mermhart
I solved my own case of post-viral ME/CFS. Then built a new model of ME/CFS that may also apply to Long COVID. Neuro Research Team, Mt. Sinai. Views are my own.

Jeff Wood

@jeff_says_that
Missing @Tinu with every ounce of my being. #ForTinu. Please read her story & help her family. Views are my own.

Charis Hill | they/them | Free Palestine 🇵🇸

@BeingCharisBlog
Made in Great Britain - Helping you find, shop and buy products made in the UK and support British artisans and makers. Join us, support us. Buy British.

🇬🇧Made in Great Britain 🇬🇧 Buy British 🇬🇧

@British_Made

mary dimmock

@marydimmock
Surviving #MyalgicE #AAG to tell the story, patient&advocate w/ a JD, into: MEdicine, Social justice & the Arts, Human neutrino/MEdical apolide/gnarled Pacer

PwME 4 bioMEdical research

@ValeBodi
Malato di ME/CFS. Ogni giorno soffro. Ogni giorno conservo la speranza e cerco una cura. Mostly in Italian and some in English.

DanieleCFS

@DanieleCfs

Paolo Maccallini

@PaoloMaccallini
La costanza premia

Maria Pia Cavalet

@CavaletMPia
Hosted this week by Sam Cheesman @samcheesman

OurCofELike

@OurCofELike
Advocating for People with Myalgic Encephalomyelitis (M.E.) in Ireland, for Severe ME in particular. info@meadvocatesireland.com

ME Advocates Ireland

@MEAdvocatesIre
#MEICC #ME in -87 🦠 happily Married since-95. Housebound/bedridden since -09 #severeME 🛌♿️💊#MyalgicEncephalomyelitis #POTS #MyalgicEncapalomyelitt

Renate #severeME #MyalgicE #ICC

@Renate17597475
HUGO → very severe M.E. + CCI/AAI + POTS. 24/7 bed-bound in darkened room. No parents or siblings, but with great fighting spirit. #TEAMHUGO

HELP SAVE HUGO

@helpsavehugo
A website on severe ME, created by Naomi Whittingham

A Life Hidden

@ALifeHidden
Caledonian Kitty Luxe Nails & Beauty by @CaledonianKitty 🛍️ • Lifestyle • Accessories & More • Giveaways • 📧 jocaledoniankitty@gmail.com • SHOP/LINKS ⬇️⬇️⬇️

CALEDONIAN KITTY LUXE 🎀💅

@CalKittyLuxe
Positive & inclusive place for all bloggers. Include @BloggersHut OR #BloggersHutRT for a retweet! Ran by @eenasaurus & @wasabaee_ 💖

Bloggers Hut ✨

@BloggersHut
My goal is to encourage & equip you to impact the world by living the Word. | Writer for @HumanDefenseINI | 💙 #CharliesArmy #alfiesarmy

Lois | Where Truth Lives

@WhereTruthLives
#spoonie FT sick since 12/2014 #ChronicFatigue #ChronicPain When brain & body behave: #blogger & #advocate #DogCatTurtleWrangler #wife #feminist #ally she / her

dSavannah = #disabled #MEep (#pwME)

@dSavannahCreate
A place for hints, tips, tools & inspiration for parents with chronic illness or chronic pain. Helping parents do & be their best. Follow our blog for more.

WhoaMumma

@WhoaMumma
My Medical Musings is a Blog, Book, Podcast & FB group for people living with chronic illness. It's a community of friendship, genuine care & understanding.

My Medical Musings

@Med_Musings
United States Trends
Who to follow

Something went wrong.


Something went wrong.