Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 In a message dated 11/28/2005 4:49:16 P.M. Eastern Standard Time, anne@... writes: I'm wondering if this is a symptom of lyme or not? I find that I am able to fall into these deep, extremely deep sleeps that more resemble unconsciousness than sleep. When I wake up I feel like I've just gotten back from a trip to China. And during these sleep times, I have extremely strange and vivid dreams - more so than in " normal " sleep. It's kind of scary, this unconsciousness thing - and sometimes I can hear things going on outside, phone ringing, dogs barking, but it's like I'm paralyzed and can't get out of the stupor. Does any of this sound familiar to anyone? Or maybe it's just me Anne Hi Anne ;-) If you'd like to email or throw it out here on the board (up to you) I am thinking maybe you are having a reaction to a med ...?? I take many different meds and this sounds familiar to me. I never ever wake feeling rested ...I do at times have vivid dreams etc..but I tend to think it may be from an antidepressant or something else that I may take. If you have fibromyalgia you will never reach the healing part of sleep...I talked about that the other day .....and that is why you wake up feeling as if you dug a ditch all night instead of sleeping. Please feel free to email me or whatever ...but until I know what you take and if its a side effect I can't really say ...except to empathize with you and to tell you that although I CRAVE sleep , I never , ever feel 'rested' ....Kat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 In a message dated 11/28/2005 6:35:55 P.M. Eastern Standard Time, mac_mcd@... writes: 3) Paralyzed I have episodes where I feel like I am paralyzed and just cannot move. I have used terms like, " I know what is going on around me but I am trapped inside my body and can't communicate. " 4) Dreams And then when I completely pass out it is the DREAMS! Vivid, extremely real and upon waking it is obvious did not get any rest. 5) Numbness In conjunction with these episodes I have extreme numbness of the hands and feet. It moves around and varies in intensity sometimes going all the way up the arms or legs. At times it is so bad on waking that I cannot even move my hands or grip anything and I have to look at my feet to make sure they are pointing down before trying to get up. 6) Frequency and Duration It happens a few times a day and lasts from 30 minutes to an hour or two. The brain dullness will last longer but I am able to move and partially interact with people but I'm a little slow talking and have a problem keeping track of ideas. Hi Mac ! I also have ,5 and 6 ..especially the numbness in my hands and feet ....though for me its also VERY painful !!! Usually its my legs and feet ..now moving to my fingers. The joint in my thumb feels swollen and painful ..but its NUMB also if that makes any sense ? I USED to have the dreams ...very real and very strange and repetitive (which has never happened to me before) for about a month I would dream the same things (different situations but same people) in my dreams for about a month ..but I am trying to figure out if I started a new med then ....I have 6 a great deal of the time. I almost feel dyslexic ....I can't get my words out properly , I forget what I am saying mid sentence ....totally FORGET ....I get very confused in places where there are a lot of people ..ie:grocery store etc ....then I can't get it done ..because I am so confused , I forget 1/2 of the things that I need if I don't have a list ....and I usually FORGET the list ! I have a hard time with organization , sitting down to pay bills , etc ...I do a load of wash , put in dryer , dry and forget about it until I am looking for that one shirt ! I surely can relate ....now ...number 3 . I have not had that ..but it definatly sounds neurological. Almost sounds to me as if you are having petit mal seizures ? Have you been to a neurologist (who is LLMD) not some jerk who hands out ritalin to kids ...but one who knows lyme and what it does to your brain ? I am wondering what a few weeks of an anti seizure medication would do ? Are you still seeing your LLMD ? Maybe a small dose of something and that symptom would go away ? I am not a doctor and I don't even want to tell you WHAT I think it may be ...but ....when a person can't move, knows what is going on ,and sort of freezes for a few minutes ..etc ...sounds like a small (petit) mal seizure ..no skaking or anything like that ..just the inability to communicate ..on ending ..I would like to say that it has been my experiencing both professionally and personally that when a doctor is too stupid to know what is wrong with you or unwilling to investigate ...he will usually SAY YOU ARE CRAZY OR FAKING ! Don't let it go Mac ....can I ask you if you stopped your abx because you wanted to ? Just plain sick of it all ? or ..did your LLMD want you to take a break ? If that is too personal I am so sorry ...I don't want to pry ...I am just trying to help , I hope you know that ! If you want to talk more about it ...email ....I can definatly relate to lots of your symptoms , but of course not all ...I think we all get bits and pieces of each others things ..depending on what we have going on in our bodies ....hang in there and God Bless ...Kat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 In a message dated 11/28/2005 6:57:37 P.M. Eastern Standard Time, dona@... writes: natural pain patch " on my temples overnight Hi Dona I have never heard of a natural pain patch ? Do you know what is in them ? I have neuralgia in other places , do they help ? I understand about the side effect but I was just wondering did it help you ? I was just thinking ...Anne also , that if I fall into a deep sleep after a pain med or anti anxiety I will ALSO have a very difficult time waking up fully . It takes coffee ....(I am quitting it ) to wake me up to be functional. ALSO ....the numbness in my body especially my fingers lasts a good while AFTER I do wake. I seem to do this more during a herxheimer reaction which I am having now. I just can't get LIMBER ....I can't stretch out properly ..feels like my hamstrings are tightening up on me ....and I can't touch my toes like I could ..things like that ....Kat ...ps ..dona ..have you seen outback jack ? I've been looking high and low for that guy ? ;-) I also need a new pair of uggs size 8 ...just trying to put a smile on your face .....nice to see someone from so far away ! WOW ! Take care ! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 In a message dated 11/28/2005 9:33:57 P.M. Eastern Standard Time, dona@... writes: Oh Outback Jack.. he got married to the girl he picked on the show.. they made a really great match. Hi Dona ! He would have made a much better match with me although the one he picked was the one I would have picked for him ..she was adorable ! I also have many pairs of uggs ....but since Oprah started giving them to people they are so difficult to get and so expensive here in the states ~! Just ridiculous but I get them anyway ..sometimes from ebay . Anyway ...that patch sounds almost like our 'lidocaine' patch ..does nothing for me either ! I would be afraid to put something like that on my face ? Does your face hurt ? At times I have had 'skin' pain on my cheeks. Very strange and I always thought it was allergy or sinus infection or something. Never thought about it being lyme. It feels as though it is numb , but when you touch it really hurts ! I'm tellin you , there is not many spots on me that don't hurt ! Now ..from sitting here ..my bottom hurts ! but that's just the chair ;-) ! Take care ..nice to talk to you also ! Is there a great deal of lyme in Australia ? Kat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 This is exactly what I have been experiencing for the past year. 1) Lyme duration I was bitten 13 years ago with a reinfection 8 years ago 2) Stopped abx I have been untreated by abx for a year and a half and it started about 3 months after I stopped the abx. 3) Paralyzed I have episodes where I feel like I am paralyzed and just cannot move. I have used terms like, " I know what is going on around me but I am trapped inside my body and can't communicate. " 4) Dreams And then when I completely pass out it is the DREAMS! Vivid, extremely real and upon waking it is obvious did not get any rest. 5) Numbness In conjunction with these episodes I have extreme numbness of the hands and feet. It moves around and varies in intensity sometimes going all the way up the arms or legs. At times it is so bad on waking that I cannot even move my hands or grip anything and I have to look at my feet to make sure they are pointing down before trying to get up. 6) Frequency and Duration It happens a few times a day and lasts from 30 minutes to an hour or two. The brain dullness will last longer but I am able to move and partially interact with people but I'm a little slow talking and have a problem keeping track of ideas. 7) Medical Opinions Columbia University references something like this in their neurological symptoms. As with a lot of things to do with Lyme my LLMD just nodded her head and said nothing about it and one regular medical professional working for my insurance company said that I was faking it. he said in his report that there was nothing that that could cause these kind of episodes. So it looks like its is you and I that have these symptoms. Anne Shroeder <anne@...> wrote: I'm wondering if this is a symptom of lyme or not? I find that I am able to fall into these deep, extremely deep sleeps that more resemble unconsciousness than sleep. When I wake up I feel like I've just gotten back from a trip to China. And during these sleep times, I have extremely strange and vivid dreams - more so than in " normal " sleep. It's kind of scary, this unconsciousness thing - and sometimes I can hear things going on outside, phone ringing, dogs barking, but it's like I'm paralyzed and can't get out of the stupor. Does any of this sound familiar to anyone? Or maybe it's just me Anne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 HI Anne I just had to respond to this one.. . Yes I have experienced what you describe.Its called sleep paralysis and I find it very scary. I have been told that its just because your Muscles don't wake up with your mind. It only happens to me a couple of times a year but I have found that if I take anything that has a sedative effect or pain killing effect it will happen. The last time it happened to me I had worn a " natural pain patch " on my temples overnight to try and help with my facial neuropathy and it turned out to be the worst " sleep paralysis " experience I have ever had.. I didn't feel " real " for hours after I woke up . Dona (Australia) _____ From: [mailto: ] On Behalf Of Anne Shroeder Sent: Tuesday, 29 November 2005 1:32 AM Subject: [ ] Bizarre sleep, bizarre dreams? * I'm wondering if this is a symptom of lyme or not? I find that I am able to fall into these deep, extremely deep sleeps that more resemble unconsciousness than sleep. When I wake up I feel like I've just gotten back from a trip to China. And during these sleep times, I have extremely strange and vivid dreams - more so than in " normal " sleep. It's kind of scary, this unconsciousness thing - and sometimes I can hear things going on outside, phone ringing, dogs barking, but it's like I'm paralyzed and can't get out of the stupor. Does any of this sound familiar to anyone? Or maybe it's just me Anne -unsubscribe <mailto: -unsubscribe ?subject=Unsubscribe> * Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 In a message dated 11/28/2005 10:50:30 P.M. Eastern Standard Time, dona@... writes: There is a lot of lyme in Australia but not many people know about it.its quite tragic .. the situation with doctors is disastrous.. There just aren't any.. The only infectious diseases specialist who knows a little bit about it is too scared to expose himself for fear of being attacked and the only doctor that I know of that treats it .. doesn't understand the longevity of lyme disease and will take you off meds when you get a negative blood test result .if y ou have symptoms after that they are put down to a million other excuses.. .. . I would give anything to be able to put together a list of doctors in Australia that could treat and understand lyme but I don't think it will ever happen. Its so totally depressing. OH ..that is just awful ! When you explained the pain in your face my OWN started to hurt for you ! You poor thing ....I am so sorry you are in such pain. I do hope that your doctor provides relief for this. So many are so afraid to prescribe pain medication here, but mine does and thank God for her because some days I just hurt so bad. Do you have a good LLMD ? Of course you may test negative after you've been on ABX ..but that is not a 'true result' .....it just happens ! Its late and I am tired ..but please keep in touch ...Take care of yourself ...and find Jack for me please ? heehee ! I'm very pleased to have met you ! kat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 In a message dated 11/28/2005 11:47:34 P.M. Eastern Standard Time, donnap@... writes: It sounds crazy, but my doc told me there is an institute in Philadelphia (I think that's the city - big city in PA) for kids with seizures, usually really severe ones that even meds can't control, and they are having really good success with getting these kids' seizure meds reduced, and some even off meds. I kind of laughed when he suggested it, but the masks are cheap, and I stay brain fogged enough on my own without meds that can make me even more out of it, so I gave it a go. So far, so good. He is most likely speaking about the University of Penn hospital in Philly ...its very good ....I am so sorry you are so sick ....wow ..tonight has been quite an eye opener for me ..lots of sick lymies tonight ...keep coming back and posting ..was nice to hear from you ! I hope that you feel better ...Kat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 Mac Mc wrote: > one regular medical professional working for my insurance company said that I > was faking it. he said in his report that there was nothing that that could > cause these kind of episodes. > > So it looks like its is you and I that have these symptoms. Well, you can just add me to the list of someone with fake symptoms. lol Mine are not so extreme with the numbness and paralysis, but the dreams are as though I'm in someone else's brain, because I don't dream that way. And when I wake up, fully awake and walking around, it's as though there's a movie still playing in my head. A med-psych I talked to called them " pseudo-hallucinations. " Ain't we got fun! deanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 HI Kat The pain patch I used is called a Body Eze Patch and you can check out the ingredients at www.greenridge.com.au <http://www.greenridge.com.au/> Its drug free. I cant remember it being incredibly effective but its pretty cheap and worth a try I guess , but I highly recommend not to use it on the head or face because of what happened to me. I wake up feeling like Im a hundred years old myself but once I get the blood moving I start to limber a little. I don't really feel able enough to get out and about until around 3 in the afternoon , then I hit the mall for a couple of hours but it's a slow walk around even then. I love coffee but unfortunately it does really bad things to me.. I let myself have one decaff a day though just for the heck of it. BTW I love my ugg boots!!!.Ive got 3 pairs. lol...its only cold enough here to wear them for a few months which is a shame. Oh Outback Jack.. he got married to the girl he picked on the show.. they made a really great match. Nice to talk to you Dona _____ From: [mailto: ] On Behalf Of KATL1957@... Sent: Tuesday, 29 November 2005 12:25 PM Subject: Re: [ ] Bizarre sleep, bizarre dreams? In a message dated 11/28/2005 6:57:37 P.M. Eastern Standard Time, dona@... writes: natural pain patch " on my temples overnight Hi Dona I have never heard of a natural pain patch ? Do you know what is in them ? I have neuralgia in other places , do they help ? I understand about the side effect but I was just wondering did it help you ? I was just thinking ...Anne also , that if I fall into a deep sleep after a pain med or anti anxiety I will ALSO have a very difficult time waking up fully . It takes coffee ....(I am quitting it ) to wake me up to be functional. ALSO ....the numbness in my body especially my fingers lasts a good while AFTER I do wake. I seem to do this more during a herxheimer reaction which I am having now. I just can't get LIMBER ....I can't stretch out properly ...feels like my hamstrings are tightening up on me ....and I can't touch my toes like I could ..things like that ....Kat ...ps ..dona ..have you seen outback jack ? I've been looking high and low for that guy ? ;-) I also need a new pair of uggs size 8 ...just trying to put a smile on your face .....nice to see someone from so far away ! WOW ! Take care ! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 HI Kat Last winter we had an absolute glut of ugg boots on the market.. .you could get real cheapies for $12 and of course the real sheepskin ones.. Maybe it was Oprah that triggered the market over here too.. I love them. They are just about the most comfortable things out. I broke a toe a couple of years ago and all I could wear were ugg boots.. they saved the day then for me.haven't looked back since. Unfortunately I have neuropathy in my trigeminal nerve.. have been like this for 6 years now.. every second of my life.. Its like having razor blades and fish hooks racing around my face all the time.. for the first 3 years it was I wanna die stuff but it's a lot better than it was and I can function around it . only because of bicillin. I would be dead without it... I give myself a shot of bicillin every second day.I expect it to be like that for the rest of my life but that's fine by me.. There is a lot of lyme in Australia but not many people know about it.its quite tragic .. the situation with doctors is disastrous.. There just aren't any.. The only infectious diseases specialist who knows a little bit about it is too scared to expose himself for fear of being attacked and the only doctor that I know of that treats it .. doesn't understand the longevity of lyme disease and will take you off meds when you get a negative blood test result .if y ou have symptoms after that they are put down to a million other excuses.. .. . I would give anything to be able to put together a list of doctors in Australia that could treat and understand lyme but I don't think it will ever happen. Its so totally depressing. Dona _____ From: [mailto: ] On Behalf Of KATL1957@... Sent: Tuesday, 29 November 2005 1:40 PM Subject: Re: [ ] Bizarre sleep, bizarre dreams? In a message dated 11/28/2005 9:33:57 P.M. Eastern Standard Time, dona@... writes: Oh Outback Jack.. he got married to the girl he picked on the show.. they made a really great match. Hi Dona ! He would have made a much better match with me although the one he picked was the one I would have picked for him ..she was adorable ! I also have many pairs of uggs ....but since Oprah started giving them to people they are so difficult to get and so expensive here in the states ~! Just ridiculous but I get them anyway ..sometimes from ebay . Anyway ...that patch sounds almost like our 'lidocaine' patch ..does nothing for me either ! I would be afraid to put something like that on my face ? Does your face hurt ? At times I have had 'skin' pain on my cheeks. Very strange and I always thought it was allergy or sinus infection or something. Never thought about it being lyme. It feels as though it is numb , but when you touch it really hurts ! I'm tellin you , there is not many spots on me that don't hurt ! Now ..from sitting here ..my bottom hurts ! but that's just the chair ;-) ! Take care ..nice to talk to you also ! Is there a great deal of lyme in Australia ? Kat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 I had sleep paralysis too since I was very little. My brother had it too. Have not an episode in over 5 yrs. I sleep 9-12 hrs a night. I don't think it has anything to do with Lyme. You are stuck between the awake stage and the sleeping stage, hence hallucinations. It does occur with sleep deprivation, and side effects of meds. I am sure there are other reasons that it may occur. In , " Dona Stobie " <dona@i...> wrote: > > HI Anne > > I just had to respond to this one.. . Yes I have experienced what you > describe.Its called sleep paralysis and I find it very scary. I have been > told that its just because your > > Muscles don't wake up with your mind. It only happens to me a couple of > times a year but I have found that if I take anything that has a sedative > effect or pain killing effect it will happen. The last time it happened to > me I had worn a " natural pain patch " on my temples overnight to try and > help with my facial neuropathy and it turned out to be the worst " sleep > paralysis " experience I have ever had.. I didn't feel " real " for hours > after I woke up . > > Dona > > (Australia) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 Hi all, I've been lurking on this list for a few years now - way too ill to post and/or answer, but have to respond to this one. Don't know if it will really help you much, but you may be able to put a name to what you are experiencing. I too experience this " trapped inside my body and can't communicate " episodes. Frequently, unfortunately. For me they seem to be triggered by almost anything, but especially extra stress when I am more fatigued than usual (I am couchbound 95% of my day), and from sensory overstimulation of any kind. I have described these episodes to my three specialist doctors - my LLMD, my CFIDS doc and my Environmental doc - without mentioning to any of them that I had asked any of the others about these episodes. All three docs gave me the same answer - Paroxysmal Limbic Discharges - seizures that originate in the limbic portion of the brain. My LLMD prescribed a bunch of seizure meds which I refused to take. One of my other docs suggested wearing a mask - like a surgeon's paper mask - several times a day for maybe twenty minutes at a time, (if I remember correctly). If you are claustrophobic, (I am) cut a hole in the mask to let in room air. I cut my hole, about the size of a quarter, into the folds of the mask, so that on better days I don't need the full quarter size hole, and on bad days, I open the mask fully. This has cut way back on the frequency of the seizures. Also, my husband has learned that when I'm too out of it too long, he taps me gently and I snap out of it - a lot quicker than when my body decides to end it! It sounds crazy, but my doc told me there is an institute in Philadelphia (I think that's the city - big city in PA) for kids with seizures, usually really severe ones that even meds can't control, and they are having really good success with getting these kids' seizure meds reduced, and some even off meds. I kind of laughed when he suggested it, but the masks are cheap, and I stay brain fogged enough on my own without meds that can make me even more out of it, so I gave it a go. So far, so good. Donna in NC Re: [ ] Bizarre sleep, bizarre dreams? > 3) Paralyzed > I have episodes where I feel like I am paralyzed and just cannot move. I > have used terms like, " I know what is going on around me but I am trapped > inside my body and can't communicate. " .. > > Anne Shroeder <anne@...> wrote: > > I'm wondering if this is a symptom of lyme or ..<snip>.... It's kind of > scary, this unconsciousness thing - and sometimes I can hear things going > on outside, phone ringing, dogs barking, but it's like I'm paralyzed and > can't get out of the stupor. Does any of this sound familiar to anyone? > Or maybe it's just me > > Anne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 HI Kat Its nice to have met you too. I don't take any pain medication. nothing would touch the sides of the pain I am in . The only thing that would knock this pain would be something like morphine and I Don't want to be half dead or feeling sick because of pain meds.. . I just live around it.. its amazing how we get used to things. It was a lot worse years ago when all I did was cry all day . so I have to be grateful for somthign. if I stay on my bicillin and get enough of it I can function to a reasonable degree.. AT least I can get to the shops and cook and do some stuff around the house.. that's all I ask for.. If I bump into Jack at the mall Ill send him over for you..and Ill get him to bring you a pair of ugg boots too...lol Dona _____ From: [mailto: ] On Behalf Of KATL1957@... Sent: Tuesday, 29 November 2005 4:19 PM Subject: Re: [ ] Bizarre sleep, bizarre dreams? In a message dated 11/28/2005 10:50:30 P.M. Eastern Standard Time, dona@... writes: There is a lot of lyme in Australia but not many people know about it.its quite tragic .. the situation with doctors is disastrous.. There just aren't any.. The only infectious diseases specialist who knows a little bit about it is too scared to expose himself for fear of being attacked and the only doctor that I know of that treats it .. doesn't understand the longevity of lyme disease and will take you off meds when you get a negative blood test result .if y ou have symptoms after that they are put down to a million other excuses.. .. . I would give anything to be able to put together a list of doctors in Australia that could treat and understand lyme but I don't think it will ever happen. Its so totally depressing. OH ..that is just awful ! When you explained the pain in your face my OWN started to hurt for you ! You poor thing ....I am so sorry you are in such pain. I do hope that your doctor provides relief for this. So many are so afraid to prescribe pain medication here, but mine does and thank God for her because some days I just hurt so bad. Do you have a good LLMD ? Of course you may test negative after you've been on ABX ..but that is not a 'true result' .....it just happens ! Its late and I am tired ..but please keep in touch ....Take care of yourself ...and find Jack for me please ? heehee ! I'm very pleased to have met you ! kat [ _____ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 Some people who have had Out of Body experiences tell of hearing noises that aren't there , that sleep paralysis thing. Some of these " dreams " people feel are out of body experiences. I have had what people would have called hallucinations at night before going to sleep. I hear footsteps and other noises that are not there. I've had a couple of times where like a huge spot light flashes in my room and I look out the window from bed and all of a sudden it's daylight out and I see my husband , clear as day outside walking around (but it's really dark). This has happened several times. One time I yelled out because I thought I saw my son on the deck outside my window shining a flashlight in my room. Of course no one was out there. I have had an out of body experience. The more I am treated for lyme, the less these things happen. It's almost like lyme does something to the brain which may connect us to different vibrations or realities. I know that sounds weird but anything is possible Anne Shroeder <anne@...> wrote: I'm wondering if this is a symptom of lyme or not? I find that I am able to fall into these deep, extremely deep sleeps that more resemble unconsciousness than sleep. When I wake up I feel like I've just gotten back from a trip to China. And during these sleep times, I have extremely strange and vivid dreams - more so than in " normal " sleep. It's kind of scary, this unconsciousness thing - and sometimes I can hear things going on outside, phone ringing, dogs barking, but it's like I'm paralyzed and can't get out of the stupor. Does any of this sound familiar to anyone? Or maybe it's just me Anne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 In a message dated 11/29/2005 10:35:37 A.M. Eastern Standard Time, bluesky@... writes: > I am sure there are other reasons that it may occur. The only times this has happened to me was when I was having intense Lyme flare-ups. Deanna My grandmother used to tell me it would happen if you ate before going to bed ? Go figure ...who knows ..but they are disturbing to those who have them, for SURE ....to be honest , when I was having them , I kindof liked them and would try to go back to sleep and finish ! I had some very strange ones with the BAD herx , and I even thought I was talking to my Dad ...he passed away 5 years ago .....but I swear he was pushing me very lightly to go back. Then I would feel like I was floating ..not scared , really nice and soft ...and then I would land somewhere in NYC near Broadway ...and go back UP again .....over and over ...NOW ...analyze THAT ! ha ! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 In a message dated 11/29/2005 2:11:56 P.M. Eastern Standard Time, mac_mcd@... writes: Under Typical Symptoms among patients with neuropsychiatric Lyme Disease: Hi Ducky ! ;-) WHY do they have to call it neuropsychiatric disease ? To me ,that says crazy ....is it ME ? Lyme is not a psychiatric disorder anymore than hallucinations are to a detox patient. ITS a PHYSICAL thing ...and should be called neurophysical or neuropathy ..or something ..but I think when you add the word psychiatric to something...OTHERS automatically think its a 'crazy' thing that we have ...and not a symptom of a disease that we have gotten from a TICK BITE ....do I make any sense ? ly I have enough problems ..even convincing my family that I am so ill....PHYSICALLY ....that to attach psychiatry into it just makes it all the more difficult for people to accept ....K Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 wrote: > I am sure there are other reasons that it may occur. The only times this has happened to me was when I was having intense Lyme flare-ups. Deanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 To me these symptoms seem to be listed at Columbia University: http://www.columbia-lyme.org/flatp/lymeoverview.html#symptoms Under Typical Symptoms among patients with neuropsychiatric Lyme Disease: Sleep disturbance Multifocal numbness or tingling in hands or feet Brain fog: ... " depersonalization or derealization " in which a person's sense of self and place are altered. .... partial complex seizures, multiple-sclerosis like illness, dementia-like illness, Guillain-Barre syndrome, strokes, Tullio phenomenon. Fluctuating Symptoms: worse on some days, remarkably better on others, without clear cause. Since Lyme disease keeps changing the symptoms as it progresses I think that sometimes we are like the blind men and the elephant only seeing the part of it that we have experienced and not realizing that maybe these other symptoms are just different stages of the disease. To me, if it looks like a duck, quacks like a duck and walks like a duck, it is probably a duck. So since the grouping of these symptoms is included in the Columbia findings these are probably all ducks, I mean, Lyme symptoms. bluesky <bluesky@...> wrote: wrote: > I am sure there are other reasons that it may occur. The only times this has happened to me was when I was having intense Lyme flare-ups. Deanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 In a message dated 11/29/2005 5:09:57 P.M. Eastern Standard Time, mac_mcd@... writes: It is a dream-like state during the day that accompanies the freezing up episodes or the extreme sleepiness that results in an hour of unwanted sleep. I have not noticed this before but since you said it I will share something ....and I am not really sure if it was just because I was very tired , but after my doc appt this morning , I ran to the pharmacy to drop off my rx ...to be delivered ...because I was so foggy and so tired all of a sudden. I came home and tried to do a few things ..and bam ...I was exactly like you say in this post Mac ...not so sure about the freezing ...but I was just so foggy and out of it I could do nothing ....I sat in my recliner ....and fell into the deepest sleep. I did not dream that I remember , but I could not wake up. I slept for a good 2 hours and am still very groggy ! I just feel so out of it .....go figure ? Kat ps ..you can come to NJ and hypnotize me when you need a break from them thar hollars down thar ! heehee ! k Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 In a message dated 11/29/2005 5:10:41 P.M. Eastern Standard Time, mac_mcd@... writes: It is all just a matter of semantics (the meaning each of us personally applies to words). This is the reason we look to a dictionary to make sure we all agree on the real meaning of certain words. I agree with you about this ! ITS other people ...those OTHER people who don't have lyme that just wait for a word like psychiatric to think we are not SICK WITH A DISEASE .....kind of like my Mom ...grrrrrrr ! I love her to pieces ...but she just doesn't " GET IT " ....do you understand what I am saying ? SO many people out there in 'that other world' love to judge and pass judgement and I believe you can only understand lyme if you have it. It just upsets me how a word can make people think something that is untrue ? Maybe I am being nit picky ....and I'm sorry ....maybe its my own 'issue' and the way that I have been treated by family and friends ....not sure ...but for some reason it hurts my feelings ! Again ...GO FIGURE ! Something awful can happen and I can deal with it ...but something so tiny and small can really upset me ! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 KATL1957@... wrote: " My grandmother used to tell me it would happen if you ate before going to bed ? " I don't know about anyone else but it is not dreams at night that I am talking about nor is it freezing up upon waking in the morning. It is a dream-like state during the day that accompanies the freezing up episodes or the extreme sleepiness that results in an hour of unwanted sleep. Now about your dream. BL (before Lyme) I was a certified hypnotherapist and I did a lot of study into the nature of the subconscious mind. Jung believed that dreams were communications from our subconscious mind but that the subconscious only speaks a language of symbols, not the same language of words that we speak. I believe that dreams fall into one of three categories: 1) Reliving past events which our subconscious wants to help us resolve some issues. 2) Sorting out present events which our subconscious wants to help us resolve some issues. 3) Visions of future events which our subconscious wants to help us resolve some issues. The best, and in my opinion the only, person to interpret a dream is the dreamer themselves because that dreamer can get in touch with their own subconscious and " have a feeling " or just " suddenly realize " what the meaning of the the symbols in the dream is. Sometimes the dreamer needs a guide to assist and that is where hypnosis can be helpful. So to interpret your dream you need to look within and see what it means to you. Just remember that the subconscious only uses symbols to try to communicate ideas to your conscious mind so don't even try to view the events litterally. One of my biggest problems since the onset of the neuro symptoms is that not only can I not hypnotize others I cannot be hypnotized any more. My mind cannot concentrate in that manner any longer. Go figure? Mac KATL1957@... wrote: In a message dated 11/29/2005 10:35:37 A.M. Eastern Standard Time, bluesky@... writes: > I am sure there are other reasons that it may occur. The only times this has happened to me was when I was having intense Lyme flare-ups. Deanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 KATL1957@... wrote: " WHY do they have to call it neuropsychiatric disease ? To me ,that says crazy " It is all just a matter of semantics (the meaning each of us personally applies to words). This is the reason we look to a dictionary to make sure we all agree on the real meaning of certain words. The term neuropsychiatric means exactly what you are saying when you say " neurophysical or neuropathy " . Neurophysical is not a word and neuropathy refers to the deadening of the nerve paths often seen in Lyme patients as the numbness in the hands and feet. So what is a neuropsychiatric disease? According to The American Heritage® Dictionary of the English Language, Fourth Edition Copyright © 2000 by Houghton Mifflin Company. neu·ro·psy·chi·a·try - " The medical study of disorders with both neurological and psychiatric features. " neu·rol·o·gy - " The medical science that deals with the nervous system and disorders affecting it. " psy·chi·a·try - " The branch of medicine that deals with the diagnosis, treatment, and prevention of mental and emotional disorders. " men·tal - " Of or relating to the mind; intellectual " (Lyme fog, etc.) e·mo·tion·al - " Of or relating to emotion " (Lyme rage, etc.) So the Lyme Disease Neuropsychiatry department at Columbia University (the only one of its kind in the world) deals with: The diagnosis, treatment, and prevention of mental and emotional disorders caused by the effects of Lyme disease on the nervous system. A lot of their work at Columbia has already shown that there is a big difference between clinical psychiatric disorders and those same disorders in Lyme patients and that the treatments for the clinical disorder do not work with the Lyme patient even though psychologists and psychiatrist continue to try to treat Lyme sufferers with popular clinical remedies such as analysis, and prescription sleeping aids, antidepressants, and even anti-psychotics. These same psychologists and psychiatrist convince their patients that they have a clinical disorder rather than exploring the possibility of a symptom being Lyme related. KATL1957@... wrote: In a message dated 11/29/2005 2:11:56 P.M. Eastern Standard Time, mac_mcd@... writes: Under Typical Symptoms among patients with neuropsychiatric Lyme Disease: Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 Mac, Wow! Interesting post. Thanks. Be well, > > In a message dated 11/29/2005 10:35:37 A.M. Eastern Standard Time, > bluesky@g... writes: > > > > I am sure there are other reasons that it may occur. > > The only times this has happened to me was when I was having intense Lyme > flare-ups. > > Deanna > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 29, 2005 Report Share Posted November 29, 2005 ----Original Message----- From: [mailto: ] On Behalf Of KATL1957@... I was just so foggy and out of it I could do nothing ....I sat in my recliner ....and fell into the deepest sleep. I did not dream that I remember , but I could not wake up. I slept for a good 2 hours and am still very groggy ! - That's exactly it! It's that falling asleep during the day for no good reason. It started happening to me last winter. I figured it was that (1) I was cold and wanted to just get snuggly, (2) I was bored with my work (I work from home a few days a week on the computer), (3) I was depressed because I'm so bored with my work. LOL But even over the summer this happened. I'd feel just uncontrollably tired when I was having a perfectly good day. Go to lie in the hammock to rest a bit and 5 hours later wake up and not know where I was or what day it was. But how do we know this is really a symptom of lyme? Anne Quote Link to comment Share on other sites More sharing options...
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