If anyone would like to chat...

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Pink_lilly_2101
New Member


Date Joined Dec 2006
Total Posts : 6
   Posted 12/8/2006 8:45 AM (GMT -7)   
Hi my names Mandy, im an 18 year old female. Aswell as suffering from depression i have also suffered from CFS since a bad bout of viral meningitus combined with glandular fever 3 years ago. I was unaware of how many people suffer from the same thing and thought i was alone, its good to know there are other people who can relate to my situation, if anyone would like to chat id be happy to.

:-) Mandy :-)

Post Edited (Pink_lilly_2101) : 12/8/2006 9:07:54 AM (GMT-7)


karateguy
New Member


Date Joined Nov 2006
Total Posts : 10
   Posted Yesterday 9:50 AM (GMT -7)   
Hi Mandy,

It's great to see your here but unfortunate also as I know how you feel. My name is Lew and I have had CFS for 10 years now. If their is anything I can help you with feel free to contact me.

Lew

sparker
Regular Member


Date Joined Oct 2006
Total Posts : 114
   Posted Yesterday 8:08 PM (GMT -7)   
I'm Patrick and I'd chat with with you if you'd like.. in fact I'd chat with anyone if they'd like.

I suffer from depression along with some other still unknown fatigue problem.. going on 5+ years of trying to find out what the heck it is.
12/04/2006: Adrenal fatigue - awaiting endo blood test results.

5000mg/Vitamin C     800mg/Vitamin E     500mg/Carnitine
1000mg/Vitamin B5    100mg/vitamin B6    200mg/SAMe
 400mg/Magnesium     500mg/L-Tyrosine    100mg/CoQ10
 450mg/Licorice Root 500mg/DL-Phenyl.    ADRENergize
 250mg/Korean Ginsng 500mg/Niacin        Resveratrol


Pink_lilly_2101
New Member


Date Joined Dec 2006
Total Posts : 6
   Posted Yesterday 10:02 PM (GMT -7)   
Hiya guys

Thanks for replying, like i said before i had no idea that there were so many other people suffering from the same condition as me. Its unfortunate for others but in a way im glad im not alone, id love to chat to anyone one who wants to, it doesnt have to even relate to CFS but i know how it is to feel alone and like nobody understands or that you cant talk to others because they look differently upon you, so chat away those who feel like it . :-) I can also be contacted at blondie_0014@hotmail.com & on msn messenger at the same address, take care all.

:-) Mandy :-)

Pink_lilly_2101
New Member


Date Joined Dec 2006
Total Posts : 6
   Posted 12/11/2006 5:31 AM (GMT -7)   
Hi Meg

I agree, i was due to start university at the start of this year but due to CFS i had to leave school in year 11 and my dream of being a lawyer was shot down. As a result i work part-time when i can while all my friends are off gettin g their degrees and making something of themselves....i feel very left out confused but yeah you have to make it what you can hey

:-) Mandy :-)

Pink_lilly_2101
New Member


Date Joined Dec 2006
Total Posts : 6
   Posted 12/13/2006 1:53 AM (GMT -7)   
Yeah thats is a coincedence, i keep hoping ill get there some day but im starting to retire to the fact that by the time im well enough ill be to old or not want to anymore. Im in Australia what about you?

:-) Mandy :-)

Pink_lilly_2101
New Member


Date Joined Dec 2006
Total Posts : 6
   Posted 12/15/2006 6:48 AM (GMT -7)   
My main syptoms are dizziness & muscle aches. Nausea hasnt been that bad for me although when i push myself i get it.


:-) Mandy :-)

karateguy
New Member


Date Joined Nov 2006
Total Posts : 10
   Posted 12/18/2006 6:54 PM (GMT -7)   
I too have the symptoms you talk about Mandy and I wish I could tell you that there is some cure but unfortunately they haven't found one yet. I feel for you as I have been working with CFS for over 10 years now. i will say that when you get good days take full advantage of them.

Lew

Pink_lilly_2101
New Member


Date Joined Dec 2006
Total Posts : 6
   Posted 12/19/2006 3:50 AM (GMT -7)   
I have tried antibiotic, herbal & alternate therapy but none have worked for me, however i really hope they do for you . :-)

Thanks for the advice, when i do have good days i take full advantage of them but i find that i pay for good days by being extremly tired for the next few days.

:-) Mandy :-)

karateguy
New Member


Date Joined Nov 2006
Total Posts : 10
   Posted 1/11/2007 12:57 PM (GMT -7)   
Pink Lilly,

I sounds like you are doing everything you can be doing. It's a hard road to travel but we haven't been given any choice.

fudgey
New Member


Date Joined May 2007
Total Posts : 2
   Posted 5/26/2007 12:43 PM (GMT -7)   
HI
I AVE M.E./CHRONIC FATIGUE AND HAVE HAD THIS FOR 5 YRS NOW! I WOULD LOVE TO CHAT ANYTIME WITH YOU AS ITS GOOD TO CHAT WITH PEOPLE WHO UNDERSTAND WHAT THIS BLOODY THING IS AND JUST HOW DISSABILING IT CAN BE.
I NO LONGER WORK AND AM REGISTERED DISSABLED DUE TO THIS CONDITION BUT HAVE TO COPE BEST AS I CAN AS I HAVE 2 KIDS WHO NEED ME
TAKE CARE

agnesgo
New Member


Date Joined Sep 2008
Total Posts : 17
   Posted 9/25/2008 3:31 PM (GMT -7)   
Hi pink,would love to hear from u,ao we can support each other,all my love agnes 41xx
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