Guest guest Posted August 26, 2007 Report Share Posted August 26, 2007 Hey Bob, my last collapse has given me much more severe problems this way. I think that CoQ10 can help, also B12 shots, fish oils…there are a number of things but these are big for me. Not that I’m “all better”, but these things have improved some, over time. Of course as soon as I actually go out my brains melt! (Stimulation) Whether or not it’s the supplements or just time I’ll never really know, but they feel like they’re doing some good. I’m sure others will have other ideas too. Good Luck, Aylwin xox Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 26, 2007 Report Share Posted August 26, 2007 Hey Bob, my last collapse has given me much more severe problems this way. I think that CoQ10 can help, also B12 shots, fish oils…there are a number of things but these are big for me. Not that I’m “all better”, but these things have improved some, over time. Of course as soon as I actually go out my brains melt! (Stimulation) Whether or not it’s the supplements or just time I’ll never really know, but they feel like they’re doing some good. I’m sure others will have other ideas too. Good Luck, Aylwin xox Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2007 Report Share Posted August 27, 2007 HI Bob, Have you had your blood oxygen ratio tested? I know we all have this same problem with memory loss as I am terribly afflicted too. My understanding (if I can say this right) is that after a nite of sleep, we wake up as if we had not slept at all. Upon testing, my oxygen level ratio drops below 82% at night and I stop breathing 5.7 times in 1 1/2 hour. My doctor believes if I use oxygen at night, it will not only improve my recovering sleep but feed the cells that can actually reverse the problems with memory and other aspects of this DD. It may be worth your while to check it out? I do not know where you live (USA or otherwise) but there are nurses that will bring the finger thingie (great term eh?) with a box attached to monitor your oxygen levels at nite so that Medicare will cover the Oxygen tank and fills free. I am still in the process of getting mine or would let you know if it really helped or not, but my lil doggy was upset by the machine and would not let me sleep to get a good study. I have to redo the testing again before I get my oxygen tank. (has to be below 98% for collective 5 min throughout the night to qualify and I slept 1 1/2 hour!..after throwing him outside) , " Bob " wrote: > > Hi Everyone, > i'm having alot of cognitive problems at the moment... > i've got problems with the following: > no mental clarity > foggy head > bad memory (long term and short term memory recall problems) > > i was wondering if anyone has found anything that helps at all? > any tips or advice would be very much appreciated, > Bob > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 27, 2007 Report Share Posted August 27, 2007 Hi Bob! I have severe cognitive issues due to FMS/CFS/severe anxiety and due to the almost 20 different medications I take. I have found the following to be helpful: -I read in a magazine for improving memory that BRIGHT YELLOW helps increase memory. They suggested using Yellow Post It's around the house to help remember things. -Word Searches, Reading, and puzzles of any kind help to stimulate memory and to keep the brain active and has recently shown according to an article I read to help prevent dementia. -I make a ton of lists-to do lists, sometimes, I will even write down on a slip of paper, what I am going into a room to do so that I don't forget. -I try to get enough rest and take naps as needed as that sometimes helps me as well. Even though it is a very frustrating situation, I have learned to use laughter and humor! I find if I get aggravated over the issue, that I only get myself anxious and that makes my memory worse. I hope this helps. I can empathize with how you are feeling. I am not able to drive anymore due to my cognitive issues, and have even been tested for early alzheimers 2 years ago when I was only 33. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2007 Report Share Posted September 4, 2007 That sounds like a really hard situation. There are things to take for sleep and it is horrid that she won't give you something. But not to allow counseling when dealing with chronic illness and all the repercussions is really cruel. I can't understand that. Sandrea Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2007 Report Share Posted September 4, 2007 So sorry Bob that the doc is not all that helpful! THAT is so frustrating and sadly, we've all been there. And I'm with you on the subtle differences of what they say and what they MEAN! Documentation is HUGE in this ratrace............I wish I had some great words of advice????? Just hang in there and hopefully, someone here can suggest another physician that may be somewhat local for you - Good Luck! STL Jane Bob wrote: Hi everyone, i'd like to thank you all so much for your suggestions about improving congitive dysfunction... i'm already taking fish oils, evening primrose oil and CoQ10, so i'm going to look into getting Vit B12 shots.. even tho i know that this will be no mean feat in the UK! Be a better Heartthrob. Get better relationship answers from someone who knows. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2007 Report Share Posted September 4, 2007 Hi Bob, sounds like you need a new doc…someone who won’t even try to help you manage any part of this through simple massage, or sleep aids sounds pretty useless, not to mention uncompassionate. Any way you could get the B12 on prescription and give your own injections? Diabetics do it all the time, I did my own Gamma Globulin injections years ago (It helped me until I became allergic to the preservative). The do or a nurse could teach you. Good Luck with it, Aylwin xox ps I find if I get it too often I get a bad brain & body inflammatory response, so take it easy and find your right dose/frequency if you can get it at all <sigh>. It does help. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 7, 2007 Report Share Posted September 7, 2007 Hi a, Lupus sounds a lot like my CFS. I would have thought it would be considered more " respectable " to have Lupus than it is CFS as it seems more folks know about Lupus or at least have heard about it. I guess not. I find it harder to read the all caps print actually, but maybe others don't. Sorry, not up to writing much now. Sandrea Quote Link to comment Share on other sites More sharing options...
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