Guest guest Posted April 22, 2012 Report Share Posted April 22, 2012 Hi all-- I am awfully close to 60. Parents did live a very long time as well as one grandparent (in late 90's all). With exception of my mom, all were damn sharp in terms of their minds later into their time when it did come. What zi mean by this is .. dad could still do the daily NY Times crosswords; he read, could carry one easily a conversation except for when he got very tired (this because he ate very little; they had to build him up quite a bit when he finally had to go into a nursing home via a damn broken hip). For me, I was diagnosed with Fibro/ ME/ CFS in 2002. I know I had all of 'this' because of symptoms which I'd lived with for a long damn time (they'd worsened over perhaps a bit longer than a decade; just undiagnosed). I am near 14 years in recovery for alcoholism and addiction. Question; seems as if I've lost a great deal of being able to figure out things which used to be simple for me. Maps when traveling would be a good example. Currently it is my damn electronics (my Mac notebook I am trying to switch to; had used one exclusively when they first came out). I also have had a ton of problems with a damn digital camera; I was previously conversant with SLR cameras and processing in colour (did darkroom work with E-6 slide system and B & W dark room which I just LOVED). My brain is just .. not working. Feel so damned hopeless, overwhelmed by problems -particularly financhial, some of my own making, some .. just the times. I DO have a diagnosis of major depression. Do many others also find problems in understanding things which once came easy or .. easier? Is the way you think, the way in which your brain 'works' rather foreign as compared to the before-I-got-sick-era? I was told by the shrink I have (pill doctor I call 'the shrink'; can no longer afford a therapist or 'talk therapy' doc) that I have a 'thought disorder' because I tend to jump from topic to topic. I will be writing or speaking and sort of .. it's like my mind will leap ahead and go to something else sort of although there is a relation to the original thing I was saying or writing. I write, I always have to go back, re-read so as to correct myself so what I've written makes sense. I tried damn hard when I saw her to get her to name the diagnosis she'd given me but she refused; said 'I don't like to label people.' The hell she doesn't; I think there is likely a 'name' for the so-called thought disorder for which I was placed on some MOST disagreeable meds and these same meds were given as well to other patients by other docs who are in treatment with my ME/CFS/Fibro doc. (At that time it was ADD stuff; it did terrible things to me and I stopped taking them; the nurses at his office seemed to also be against them -the ADD stuff- as the side effects were nasty; who wants chronic headaches as a side effect?!) Forgive me if I've posted this previously OR if this has been a subject before. It is bothering me now a great deal and I simply need some feedback from others. Thanks in advance! Oh; for me, exercise is kind of out in terms of keeping my brain sharp as it sends me to bed when I overdo things and now I am at a point when the exercise is down to less than ever. (This I believe is because of stress as I have a multitude of stress caused symptoms at the moment). Thanks to all for even 'listening; a load from my mind. Jane, the one with the hound, NYC Quote Link to comment Share on other sites More sharing options...
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