M.E Diary 3 - Signs & Symptoms of M.E/CFS

Go to - www.youtube.com/wizardscar to see my new 'project' about M.E - From M.E To You
It'd be really great to have your support :)

This is my third entry into my diary about having M.E
The first, second and fourth are in my videos section - go have a watch :)

Please watch, comment, subscribe and stuff if you suffer from M.E/CFS or any other type of illness that most people don't understand or even think exsists.

Music;
Mary - The Scissor Sisters
I obv don't own any rights or anything to this song

Category:

News & Politics

Tags:

• M.E
• CFS
• myalgic
• encephalomyelitis
• chronic
• fatigue
• syndrome
• fibromyalgia
• scissor
• sisters
• mary

[redchant]

I'm at almost exactly the same stage of treatment as yourself, very early stages of perring technique treatment, although fortunately I have not had the paranoia/nightmares etc. Lets get better together. Keep converting the illness into a creative output, its fantastic to watch. :)

[plzsupportme]

Thanks!

Where do you go for your treatment?

(If you don't mind me asking)

I'm glad you like my videos.

:)

[fogggygyrl]

This is excellent. Very clever and creative. Thank you!

[plzsupportme]

Thanks.

:)

[jimbobg65]

What treatment are you having? I wouldn't trust ANY treatment that made me feel awful. No use putting your body through something it doesn't want. If it's good for you, you will feel good from it. If it's bad for you, you will feel bad. Your body knows what's what, and if someone sells you something that makes you feel awful under the guise of 'helping' you, I wouldn't touch it with a barge pole.

[computers734]

I pay for it later on! the thing thats i hate the most is the brain fog. Some of the time its so bad thats its like im out of it on drugs. Even tho i was told by my doc i had M.E i stil come across people who think its a load of sgit and should just get over it.

[computers734]

Hi. I really liked the video! I have had M.E for over 2 years now and its good to know im not alone and others know what its like. I didnt know what was wrong with me for a long time and was out of my head with worry. I was tested for all sorts of things. The amount of times i was at the docs was unreally. Finally the doc said i had M.E. Got singed of work too. But now i can tell people whats wrong rather than saying i dont know. At times im not too bad and can go for walks or a cycle but......

[Tiffysmyhorse]

hi

i just read your comment and thought i'd add that i have perrin technique treatment in oxford...helix house....if that is more convienient. also i am going through GCSE's and really struggling with concentration..any tips apprietiated! great movie it really does put everything into perspective.

[Timebandit720]

Do you have the web address for the Lightning Course in Wales? (Do you kmnow if the treatment is available anywhere else?) I've tried allsorts of herbal "treatments" but their effect was minimal. I started my own part time business using the computer, (flexi-time!)which helps to give me a focus, but apart from the occasional night seeing friends, I can't do much else really.

[antares4141]

google homopathic medicine on quackwatch the dr's there are not part of conspiracy they generously give their time (time they could be making $300 an hour) to try to fight quackery. Good dr's will always be successful regardless of the quacks that rob desperate people of their limited resources, on the other hand quacks can't make it without deceiving their mark's. Lightning process cost's money so does homopathic medicine which is one of the biggest health frauds of all time! Please look itup

[Tiffysmyhorse]

i'm having it at the moment, i can feel the difference even though i still have a long way to go, after al i have a back up if it doesn't work...a lightening course in wales!

[Tiffysmyhorse]

in wales there is someone who can help, its a lightening course for like 3 days, someone who has suffered for 15years with ME/CFS is now perfect again. i am currently having help from a homopathic doctor which has helped a bit but i still have a long way to go, at the end of the day its worth a try you have nothing to loose! were all in the same boat really but i'm still at school (boarding) , my parents don't understand what its like, i have GCSE's this year and i can't concentrate :( we'll see

[TangledUpInDylan]

Thank you so much for this video - I nearly started crying with the relief of not feeling so alone! I hope things are going well for you x