Guest guest Posted February 24, 2007 Report Share Posted February 24, 2007 Hi Marcia: Do you have their email address, I would love to give them a piece of my mind, what little is left that is. Jeanette Response to today's News-Herald editorial The CO-CURE list alerted it's members to an editorial today that disparaged the CDC's use of taxpayers' money for the CFS Awareness campaign. It said (and I quote), " Chronic fatigue syndrome is just not that important. " I submitted the following comment (and believe me, I was really holding back on some of the things I *wanted* to say!). Marcia on Salem, MA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Hi Jeanette! *** Here's the link to that editorial: http://tinyurl.com/29h58v *** You may need to scroll down slightly to see the " Brickbat " section that mentions CFS. Hi Marcia: Do you have their email address, I would love to give them a piece of my mind, what little is left that is. Jeanette Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Awesome response, Marcia!!! You said it all, perfectly. K2 I submitted the following comment (and believe me, I > was really holding back on some of the things I *wanted* to say!). > > Marcia on > Salem, MA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Thanks Marcia Jeanette Re: Response to today's News-Herald editorial Hi Jeanette! *** Here's the link to that editorial: http://tinyurl.com/29h58v *** You may need to scroll down slightly to see the " Brickbat " section that mentions CFS. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Marcia: My comments I submitted to this editorial: How dare this person say that Chronic Fatigue is just not that important. I hope he gets it, and he can feel how it feels. You have no idea what you are talking about, and you should not make a comment like that not knowing anything about this illness. If you did, you would not have said what you said. Maybe you should start doing some real research and find out the real answers. This funding money came from people who wanted to donate to this cause, and they should not be berated for donating to the cause of their choice. Obviously they think it a good cause or they wouldn't have donated their hard earned money.I feel you should make a retraction of your statement and apologize to those who have this debilitating illness. (Marcia-I know that this money came from the CFS group( and was money that was donated to them) Thanks Jeanette Re: Response to today's News-Herald editorial Hi Jeanette! *** Here's the link to that editorial: http://tinyurl.com/29h58v Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 That article was also from the AP News Wire to our Newspaper as well. Would like a copy of my response to the paper? Made me so mad. Oh and Hi in case I didn't introduce myself, my name is b4cjcll or Doe Serena Cochran. Just when we have made great strides to remove the stigma, someone comes along with that. Its politics already in place when the President leaves, " lets see what money can we take to reduce the national debt? " Blessings~~Doe Serena there before the grace of God go I.......... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 25, 2007 Report Share Posted February 25, 2007 Marcia, I'm saying thank you too, I did go read the editorial (more stupid ignorant poison), and your reply, and the others there, were very moving to me. It actually gives me hope that we are getting so fed up we're not going to take it anymore - I don't know what that looks like, but it feels great! Perhaps with all that's going on now, the tide is really beginning to turn. Aylwin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 26, 2007 Report Share Posted February 26, 2007 Marcia, Hooray for you for writing such an informative reply to this " idiot! " I was truly brought to tears by this. I am so tired of not being able to find medical treatment, so tired of being sick and tired, so tired of not being able to do for myself around my home. I moved here 4 years ago and am still not unpacked. I am beginning to seriously doubt if I ever will be. I am sick of having friends not understand the seriousness and hopelessness of this disease. I find myself becoming more and more isolated from the outside world. It is no wonder we become depressed on top of everything else. ----- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 27, 2007 Report Share Posted February 27, 2007 Hi, I came to live with my Mom cause I couldn't work, and she constantly wants me to do things for her. It drives me crazy, and I feel like she has made me her social outlet. I have tried to talk to her about not feeling like talking, and she says, I understand, but them she wants me to look at what's on TV, which is blaring loud, and wants me to send out emails for her, print off music, pay her bills on line, etc...it seems like everyday there is a new request. I try not to even go out of my room most days. I am so going crazy living here. I wish I could afford to move. She is 80 and she doesn't remember or care about how I feel. She knows I have had a migraine for 9 days yet the TV still is so loud you can hear it outside. I think this is a perfect example of not believing I am sick. I want there to be someone who would help me once in awhile, not me having to do stuff here all the time. I never ask for anything, no help with anything, if I can't do it, like my laundry, it sits and waits for me.She makes dinner every night, and I have to clean up the kitchen. I get so sick of all of it. God is really punishing me. I get up and she talks to me about something and my mind is blown, I can't focus on anything after that. I can't get anything done for myself. My mind shuts down, and I am lost.Just a bad situation and she has no clue. She acts like I am there to serve her purpose, and not because I am sick. Really gets to me sometimes. I have to keep reminding myself she has given me a place to live, but now I wish I had never moved in here. The public housing says you have to have some kind of income to qualify, so that is out for now. OK, sorry, she is out of the house right now, and it is nice and quiet. Wish it was like this all the time. I am so sick of that TV going 24/7 all news. How many times can you watch the same story over and over again, and she thinks the world is going to end tomorrow, lol Sorry, just had to vent, no one even has to reply to this, just venting. Thanks for listening. Jeanette Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 28, 2007 Report Share Posted February 28, 2007 Oh Jeanette, I am SO SORRY you are having to go thru this. I wish I had a solution, or at least some wise words, but know that we are out here, feeling your pain and always with a compassionate, understanding ear. Try to take care of yourself and God Bless you always, STL Jane Jeanette French wrote: Hi, I came to live with my Mom cause I couldn't work, and she constantly wants me to do things for her. It drives me crazy, and I feel like she has made me her social outlet. I have tried to talk to her about not feeling like talking, and she says, I understand, but them she wants me to look at what's on TV, which is blaring loud, and wants me to send out emails for her, print off music, pay her bills on line, etc...it seems like everyday there is a new request. I try not to even go out of my room most days. I am so going crazy living here. I wish I could afford to move. She is 80 and she doesn't remember or care about how I feel. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2007 Report Share Posted March 3, 2007 OH.....This REALLY ticked me off, I sent my comments - I'm sure they don't give a rip, but at least I got to give them my 2 cents worth! STL Jane Jeanette French wrote: Marcia: My comments I submitted to this editorial: How dare this person say that Chronic Fatigue is just not that important. I hope he gets it, and he can feel how it feels. You have no idea what you are talking about, and you should not make a comment like that not knowing anything about this illness. If you did, you would not have said what you said. Maybe you should start doing some real research and find out the real answers. Quote Link to comment Share on other sites More sharing options...
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