|Member Since||01/05/2009 06:11 PM|
|Last Online||04/24/2012 03:37 AM|
|Occupation:||employed full time!|
|A little about me:||Like many of you, I am not new to FMS. I was diagnosed with FMS in the early 2000s. Prior to the onset of FMS, I had good health and rarely took more than tylenol. In fact, I was against taking medicine. My how things have changed! My FMS showed up after passing kidney stones, although now, I can see that I had symptoms as a child. More about me: I am a single mom from Arkansas with a 14 yr old daughter and 10 yr old son. I work full time - more like all of the time. I look forward to meeting everyone!
|Hello Chronic Pain Members, Please do not be shy in joining in on the support group- do not just sit on the sidelines/be passive - if you can post then do so okay :-)! Know that at least 5 % of you could realistically join in at least once a month- which would be around 93 of you guys as there are 1,871 members here (maths was never my strongest point yet it is roughly that number) yet not even close to that are joining in at the present! Yes, you all have chronic pain yet so does this Group Leader(me) who has moderate severe to severe chronic pains as well as am a GL in 3 different support groups yet still post as often as possibly can plus take time to find some good posts/links for you! Some of you here have less pains than myself yet for whatever reason do not join in, too. Not saying you have to post every single day or every week yet, this support group will be more dynamic if you are proactive in making this group your own! Variety is the spice of life, too!! If you see a post you like then say so- you do not have to write an essay just a few words. If you need support- ask for it- you would find many people would respond including myself! As long as you keep it respectful, no spamming/promoting any product or treatment, plus do not talk about controversial treatments that spammers like to attach themselves to, and, you post links when appropriate then post freely!
You see something inspirational- share it!
You have some good news- let us know.
You are struggling in some way- lean on us!
Know there are some of you who really cannot post- to weak to type anything- am not talking to you- you carry on just getting inspiration from the posts okay then hopefully when you feel brighter you can join in plus know that we are all here for You! Lean on me via pm anytime, too, as care deeply!
This group hug is mostly for that(at leas) 5% of you who could join in regularly!
Let us keep this board active as well as have lots of faces- not just this batgirl's(bat avatar), okay!
Just needed to give some of you guys a gentle kick of motivation.
Truly hope it will make a difference- will be watching the Chronic Pain SG closely!
Keeping all my fingers as well as toes crossed that will see plenty of new faces as well as some familiar ones post in the next few days/weeks! Thanks in advance to you each- super gentle super grateful hugs winging their way to you all!!
Sending you each ultra gentle hugs, healing light as well as warmest wishes, Namaste Clarita :-)
namaste = the light in me honours the light in You :-)
Many thanks :-)
(i) Angels tremendously as well as tenderly bless every single one of you/much good karma to you each(i) may this serendipitously as well as sublimely so be so!
|The wealth is turning wonderful,remember to enjoy the sunshine it is healing:-)
|Hello :-), Group Hug time from your Group Leader Clarita,
Please check out all the new posts over on Chronic Pain Support Group plus if you are able to join in then please freely do so plus thanks in advance for this- this would be fabulous(only if you can post as your pains are not too high or you are not too busy or both of these) if able to join in then do so - refuse to sit on the sidelines- be active/proactive as the more that join in the better it is for the dynamics of the group :-) so the better it is for us all!
Very warm welcome to all new members here- make your fine selves at home with us :-)!
Respect is vital- hence my rant of a post earlier- always treat your fellow chronic pain community member with the upmost respect as well as show them gratitude whenever they take their time to help You. Manners cost little yet make a big difference. Always be civil, adult like as well as treat each other as equals, too.
Bullies will be given zero tolerance by us GL's, too.
Though, on the whole this is a supportive fabulous community even though it has been a little quiet in its voices recently(soon to change hopefully)!
It is a real honour to serve as a GL here alongside Mike and Fibroforever.
Huge heartfelt thanks for all the supportive kind messages receive regularly via private messages from you lovely people here as well as the wonderful hugs- touches me deeply to know that you care plus appreciate what do for You. So huge heartfelt thanks.
All those here holding on tightly keep holding on tightly plus know that it will pass/ease up! Lean on us here for support , too.
If you are in a good phase or just want to show you care then please reach out to your fellow chronic pain member with some words of encouragement or support.
Take excellent care of You- each one of You here, plus take brilliant care of one another. Be kind as we are all each fighting hard battles- as the saying goes!
Choose to be the best you can be plus learn to be your own best friend- make it so!
Look forward to seeing new posts as well as new faces on the support group- all who can make it happen.
Sending you my warmest wishes plus super soothing hugs, namaste Clarita :-)
namaste= the light in me honours the light in you
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