Guest guest Posted April 9, 2008 Report Share Posted April 9, 2008 Welcome Bobi Jo, It is hard to explain to family and friends that you are sick all the time because you " don't look like you are sick " . I get that a lot from my family, " well you don't look like you are sick " when I just want to crawl in a hole and disappear. I can't seem to get it through my family's heads that it hurts to stand and do the dishes, they argue with me all the time and tell me that I only say that so then I can get out of doing the dishes but in the end I am the one that does them because they have been sitting there for 3-4 days without anyone touching them. I bought a book so they could read about it so you might want to do that. > > Hello all, > I've been reading some of the posts over the last few weeks, but > haven't taken the time to introduce myself. I'm 28 & stay at home > with my 2 energetic boys ages 2 & 4. I was diagnosed with FMS about a > year ago, but I've been suffering with accumulating symptoms since > somewhere b/t late childhood & early adolescence. My diagnosis was > validating in that I realized that all the different health problems > I experience are connected, & I'm really not crazy (My last doctor > always treated me like I was a hypochondriac)! But it brought with it > a whole new set of problems. Like, how do I explain to everyone that > the Fibro affects every aspect of my life, every single day, w/o > sounding like a broken record? How do I explain this to my friends & > family? So far I'm not doing so hot. I don't understand why it's so > hard for people to believe that I'm ill. I do get around after about > noon and function somewhat normally, but I'm in pain the entire time. > I get sick of complaining, but if I don't say I'm hurting, people > assume I'm " getting better. " There are days I just wish I could > evaporate, & I cry alot. > I am so glad I found you all. It is so sad that there are so many who > suffer like me, but it is also nice to find a group of people who > understand. > Blessings, > Bobi Jo > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2008 Report Share Posted April 9, 2008 Welcome to the group Were're all in the same boat here together, and we learn from each other how to live with Fibromyalgia. Some of our days here on the board are " vent " days and just letting it out is encouraged. Postings contain bits of information that will help to cope with the day to day symptoms and frustrations of living with Fibromyalgia. A few postings contain off the cuff musings, because you have to laugh once in awhile. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2008 Report Share Posted April 9, 2008 Hi BobiJo,welcome to the family. Its sad that we go through what we do and then have to deal with people not understanding. It does get better. I just wanted to say welcome and I am 34 so being young is another factor. We feel we should be living life so differently,especially with children. If you need to talk you can email me personally.Take care. Be Blessed, Shundra Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2008 Report Share Posted April 9, 2008 Hi Bobi Jo, I'm glad you are with us here. I know how you feel. I was actually elated when I was diagnosed with fibro because it explained so very many health issues I was having. Big and little. Every day is a struggle, but you are among friends here. Hugs, /Mi Hi, I'd like to introduce myself Hello all, I've been reading some of the posts over the last few weeks, but haven't taken the time to introduce myself. I'm 28 & stay at home with my 2 energetic boys ages 2 & 4. I was diagnosed with FMS about a year ago, but I've been suffering with accumulating symptoms since somewhere b/t late childhood & early adolescence. My diagnosis was validating in that I realized that all the different health problems I experience are connected, & I'm really not crazy (My last doctor always treated me like I was a hypochondriac)! But it brought with it a whole new set of problems. Like, how do I explain to everyone that the Fibro affects every aspect of my life, every single day, w/o sounding like a broken record? How do I explain this to my friends & family? So far I'm not doing so hot. I don't understand why it's so hard for people to believe that I'm ill. I do get around after about noon and function somewhat normally, but I'm in pain the entire time. I get sick of complaining, but if I don't say I'm hurting, people assume I'm " getting better. " There are days I just wish I could evaporate, & I cry alot. I am so glad I found you all. It is so sad that there are so many who suffer like me, but it is also nice to find a group of people who understand. Blessings, Bobi Jo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 10, 2008 Report Share Posted April 10, 2008 > > Welcome Bobi Jo, > > It is hard to explain to family and friends that you are sick all the > time because you " don't look like you are sick " . I get that a lot > from my family, " well you don't look like you are sick " . When it comes to my family's uttering the famous FM phrase, " Well,...you don't look sick " . My response is always a well thought out, " Bite Me!! " And I even show them a place to start if they can't figure it out on their own. Quote Link to comment Share on other sites More sharing options...
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