addy don @Addy4fun
hi here to meet new friends sufferi,ng with me , cfs I live romsey, Hampshire , uk romsey south coast,uk r Joined March 2013-
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@nopostergirl GET A GOOD MICRO BIOLOGIST,IVE GOT CFS,,BECAUSE WEST NILE VIRUS,YELLOW FEVER
DONT JUST SAY I HAVE M E, CFS,,GIVE A REASON OF WHAT CAUSED THIS ILLNESS WITH ANWERS,PROPER DIAGNOSED NAMES
REALLY FIND OUT WHAT HAS CAUSED YOUR M E ,CFS,,THERE IS ALWAYS A ANSWER
to get anythink done to get better is to find microbiologist,lots of blood tests , do it,you might be surprised,
fiends you should get a good microbiologist and find out what is causing your m e , cfs. I did,yellow fever,west nile virus,get blood tests
@MEAssociation I BELIEVE that doctors should give m e cfs patients more indepth blood test,, came back yellow fever and west nile virus.
I SUGGEST THAT EVERYONE SHOULD GET A GOOD MICROBIOLOGIST WHO WANTS TO FIND OUT WHAT IS CAUSING YOU THE M E,,CFS.
I ave antibodies to yellow fever,flavviviruses,,west nile virus,,low grade encephacitis,AFTER A TRIP TO ISRAEL 5 YEARS AGO,ILL FOR 5 YEARS
seeing a microbiologist in Winchester hospital having a lot of blood test, I got results,antibodies towest nile virue yellow fever,
having a lovely day ,every day body aches and head aches,what a life,i hate so very much,
@hayleyszucs my neighbour said to me the other week not working today as I nicely told him to mind his f ing buiesness,i do get pi,,ed off
Are You In Pain? @AreYouInPain
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Janet Winter, PhD @BreathingRemed
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ME Association @MEAssociation
19K Followers 2K Following We raise funds for medical research into ME/CFS and provide support, information & campaign for people in the UK. RPs do not necessarily mean endorsement.
Kat @SpoonieBeauty
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FibroRecovery @FibroRecovery
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Janet Winter, PhD @BreathingRemed
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Sharon Anderson @sharoncurlyy
32K Followers 40K Following 🍃Helping people change their life is my passion🌿 HEALTHY LIVING - WEIGHT LOSS - GUT HEALTH - ANTI AGEING 🍃 it’s our choices that make the difference!
mira 🇳🇱 @Gooische_Vrouw
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Jocelyn @nopostergirl
778 Followers 582 Following Life With Severe Myalgic Encephalomyelitis: A bed-lyin', pill-poppin', muscle-wastin' good time. #pwME #ADHD #neurospicy #POTS #MCS #MCAS
Let's Do It for ME! @LetsDoIt4ME
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19K Followers 2K Following We raise funds for medical research into ME/CFS and provide support, information & campaign for people in the UK. RPs do not necessarily mean endorsement.
@invest_in_me (Invest... @Invest_in_ME
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ME for M.E. @ME_forME
2K Followers 1K Following Just a girl raising awareness for the neuro-immune disease Myalgic Encephalomyelitis. ME is not fatigue, it's Post Exertional Malaise!
Kristin Harris @kristindunreath
1K Followers 328 Following Artist, illustrator & pilates instructor. Ulcerative colitis survivor. Jpouch. Patient Advocate for IBD. Insta: kristindunreathart
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FibroRecovery @FibroRecovery
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Kate Keeling PT @kate_keeling
320 Followers 861 Following I am a PT, TBI and CFS survivor. Im an expert in providing all aspects of Internet Marketing for businesses. Garden, Dogs, Mental Health, Horses, Affiliate M.
hayley_eszti @hayley_eszti
2K Followers 658 Following
Kat @SpoonieBeauty
1K Followers 2K Following Professional Patient, Beauty Nerd, Scifi Nerd. I have a chronic illness and want to live a full life. #spoonie #UMCTD #Fibro #Sjogrens
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Hannah 🥀😷💚�... @PipsMiniTwee
4K Followers 4K Following M.E(Over26Years so far🐦🔥🪫🙄)🥄Depression,Millennial,Vegan🌱Sloth🦥Magpie✨Love:Animals🐾Piercings,Tattoos,Soaps,Crystals💎LipBalm💄J2🖤1R🎵TT🎵+More🫶She/HerYou might like
