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Dreams about falling down/ being unable to use my legs?
I continually have been having dreams about being unable to use my legs or falling down while walking and not being able to get back up. I was diagnosed with Lupus in January and have been taking Cymbalta (20mg) and Tramadol as needed. Would my medications cause weird/nightmarish dreams like this?
I continually have been having dreams about being unable to use my legs or falling down while walking and not being able to get back up. I was diagnosed with Lupus in January and have been taking Cymbalta (20mg) and Tramadol as needed. Would my medications cause weird/nightmarish dreams like this?
foxtrotted
in
LUpus Patients Understanding and Support
10 years ago
For Your Immediate Attention: Heartbleed - what you should do to stay safe from this major online security flaw
Must Read: 1) Log out and log back in to any site where you stay logged in 2) Change your Internet passwords as each site informs you that they've fixed this security problem - Update your HealthUnlocked password NOW - they've patched their servers 3) For at least the next week, keep an eye on any
Must Read: 1) Log out and log back in to any site where you stay logged in 2) Change your Internet passwords as each site informs you that they've fixed this security problem - Update your HealthUnlocked password NOW - they've patched their servers 3) For at least the next week, keep an eye on any
AussieNeil
Partner
in
CLL Support
10 years ago
A helpful medication for anyone who suffers from sleep apnea caused by PSP.
I'll try to give a brief:) summary regarding how my apnea came about...My Neuro recommended a sleep study to confirm or toss out this diagnosis. I thought he was nuts. Believed I slept fine. In fact, I take a sleep-aid at bedtime. Also, I'm a slender person. Believed this mainly affected persons who
I'll try to give a brief:) summary regarding how my apnea came about...My Neuro recommended a sleep study to confirm or toss out this diagnosis. I thought he was nuts. Believed I slept fine. In fact, I take a sleep-aid at bedtime. Also, I'm a slender person. Believed this mainly affected persons who
JudyJ
in
PSP Association
10 years ago
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PLMD and reasonable accomodation. I am being treated for PLMD and recently started taking.25 Mirapex. It is working well, but I still am
having trouble sleeping, and somedays feel like a worn out dishrag. There is a work meeting coming up in a couple of months that will last 3 days from 8 to 5. If i am having a dishrag day, i won't be able to deal with a day long meeting. Currently, i work at home, so i can nap if i need to during the
having trouble sleeping, and somedays feel like a worn out dishrag. There is a work meeting coming up in a couple of months that will last 3 days from 8 to 5. If i am having a dishrag day, i won't be able to deal with a day long meeting. Currently, i work at home, so i can nap if i need to during the
Cynicgirl24
in
Restless Legs Syndrome
10 years ago
i m male 59 my Fbs ranged 77-88 and pps 180 after 2hrs my liver,kidney prostrate glands , blodder,pancreas are normal functioning.
Microurea 20% and in electrolite Na++ nd K+ normal range and chloride is little high 0.12 than the normal range Medication Glynase 5mg morning and 2.5mg at night NerveupOD daily night.. HB1Ac-5.7..I feel more weekness while walking thigh muscle pain and feet pain ..regular walking in Treadmil .25 mints
Microurea 20% and in electrolite Na++ nd K+ normal range and chloride is little high 0.12 than the normal range Medication Glynase 5mg morning and 2.5mg at night NerveupOD daily night.. HB1Ac-5.7..I feel more weekness while walking thigh muscle pain and feet pain ..regular walking in Treadmil .25 mints
kadavul
in
Diabetes India
10 years ago
What should I do next?
I was recently told that I should go in for Cognitive Behavioral Therapy and Biofeedback because of my FND. The consoles let me know point blank that they see no need for me to be in therapy. I am going in anyway. Because the original diagnoses was Guillian-Barre, then Conversion Disorder and now FND
I was recently told that I should go in for Cognitive Behavioral Therapy and Biofeedback because of my FND. The consoles let me know point blank that they see no need for me to be in therapy. I am going in anyway. Because the original diagnoses was Guillian-Barre, then Conversion Disorder and now FND
Allyw
in
Functional Neurological Disorder - FND Hope
10 years ago
Just a few amusing Quotes
Some of the best Quote Sometimes I think the surest sign that intelligent life exists elsewhere in the universe is that none of it has tried to contact us. It may be that your sole purpose in life is simply to serve as a warning to others. If you think you are too small to be effective, you have never
Some of the best Quote Sometimes I think the surest sign that intelligent life exists elsewhere in the universe is that none of it has tried to contact us. It may be that your sole purpose in life is simply to serve as a warning to others. If you think you are too small to be effective, you have never
tettridge
in
Fibromyalgia Action UK
10 years ago
What to do about dosage??
Recently had my thyroxine increased from 150 to 175. Felt the best id felt in a long time. My gp just rang to day I need to go back to 150 as my blood result say tsh 0.06 and t3 is 31.4. I feel the best ive felt in a year. What should I do?
Recently had my thyroxine increased from 150 to 175. Felt the best id felt in a long time. My gp just rang to day I need to go back to 150 as my blood result say tsh 0.06 and t3 is 31.4. I feel the best ive felt in a year. What should I do?
bucklemyshoe
in
Thyroid UK
10 years ago
Sleep paralysis? Anyone with fibro find this a problem?
Hi guys, does anyone else find that when they sleep they feel like they are sort of in a paralysed state.. Eg hearing what's going on, needing the loo, hearing (or not hearing more frequently) loud noises that would wake the dead but being physically unable to move or get up? Eg, I hear my husband
Hi guys, does anyone else find that when they sleep they feel like they are sort of in a paralysed state.. Eg hearing what's going on, needing the loo, hearing (or not hearing more frequently) loud noises that would wake the dead but being physically unable to move or get up? Eg, I hear my husband
Rhiann230
in
Fibromyalgia Action UK
10 years ago
i started .25 mg mirapex for plmd. That amount seems to have stopped the nighttime jerkiness, but i still wake up frequently.
I have trouble getting back to sleep. Do any of you take something else to sleep? The doc said i could increase the mirapex to .5, but i am afraid it will make me less sleepy.
I have trouble getting back to sleep. Do any of you take something else to sleep? The doc said i could increase the mirapex to .5, but i am afraid it will make me less sleepy.
Cynicgirl24
in
Restless Legs Syndrome
10 years ago
Does anyone with only RLS (not PD as well) and who takes Mirapex / Mirapexin / Sifrol / Pramipexoole also have blurred and or double vision?
Pete-1
in
Restless Legs Syndrome
10 years ago
ENZYMES!!!!!
Enzyme lecture very informative...if interested in learning more, go to www.thewolfeclinic.com. This site is not affiliated with the lecture I just attended. That was a different company (which by the way is planning on having a class in the UK sometime in the future)....for those interested in aiding
Enzyme lecture very informative...if interested in learning more, go to www.thewolfeclinic.com. This site is not affiliated with the lecture I just attended. That was a different company (which by the way is planning on having a class in the UK sometime in the future)....for those interested in aiding
Natura
in
LUPUS UK
10 years ago
fibromyalgia and sleep
Hello Fibro Friends, Has anybody out there had any sleep studies, tried anti-snoring devices, tried sleep meds or anything else sleep-related which has resulted in a definite improvement in symptoms? I know that many days when I have fibro flare-ups are directly related to a poor quality sleep the
Hello Fibro Friends, Has anybody out there had any sleep studies, tried anti-snoring devices, tried sleep meds or anything else sleep-related which has resulted in a definite improvement in symptoms? I know that many days when I have fibro flare-ups are directly related to a poor quality sleep the
omshanti12
in
Fibromyalgia Action UK
10 years ago
Does modafinil cause weight loss?also do you build tolerance to it? How can i take it so i dont bcum tolerant ?
Modafinil ,provigil ,weightloss
Modafinil ,provigil ,weightloss
limited
in
Fibromyalgia Action UK
10 years ago
Has anyone taken modafinil and msm together?msm is an organic sulfur btw
MSM is homeopathic . I take 20000 mg MSM n 1000mg of vitc and 100mg modafinil .it causes insomnia like maaaaaaaad:/but i was wondering if taken together would it cause a rash or something worser ?
MSM is homeopathic . I take 20000 mg MSM n 1000mg of vitc and 100mg modafinil .it causes insomnia like maaaaaaaad:/but i was wondering if taken together would it cause a rash or something worser ?
limited
in
Fibromyalgia Action UK
10 years ago
Has anybody had problems with a natural chemical called tyramine which is in certain foods and can cause atrial fibrillation.
Also suffer from underactive thyroid and hayfever
Also suffer from underactive thyroid and hayfever
craftyanne
in
Gluten Free Guerrillas
10 years ago
Tests for ACTH deficiency
Other than the short SynACTHen, can anyone recommend any tests for secondary adrenal insufficiency? As a much removed pituitary patient and persistence of symptoms despite T3 (which has definitely helped but not cured) I'm beginning to think of it as a possible culprit. As all find, it takes a good 3
Other than the short SynACTHen, can anyone recommend any tests for secondary adrenal insufficiency? As a much removed pituitary patient and persistence of symptoms despite T3 (which has definitely helped but not cured) I'm beginning to think of it as a possible culprit. As all find, it takes a good 3
mumcat2
in
Thyroid UK
10 years ago
Partial Update
So I did that last sleep study with the PES (long story short, they put a tube up your nose, down your throat, and into your chest and inflate a balloon at the end of it to measure air pressure) and it didn't show UARS (upper airway restriction syndrome), but it did show obstructed sleep apnea. So I
So I did that last sleep study with the PES (long story short, they put a tube up your nose, down your throat, and into your chest and inflate a balloon at the end of it to measure air pressure) and it didn't show UARS (upper airway restriction syndrome), but it did show obstructed sleep apnea. So I
ookla
in
Restless Legs Syndrome
10 years ago
Feeling so down
been feeling so low out burst of tears at times and not sleeping just feel though im falling down this deep black hole and not being able to climb back out I'm on medication Mirtazapine and diazapan but now fell they are not helping me sleep im feeling as though now i want to just give up. im realy
been feeling so low out burst of tears at times and not sleeping just feel though im falling down this deep black hole and not being able to climb back out I'm on medication Mirtazapine and diazapan but now fell they are not helping me sleep im feeling as though now i want to just give up. im realy
don-rob
in
Mental Health Support
10 years ago
FIBROMYALGIA AND SLEEP Something to take a look at :)
HI EVERYONE Emma's poll got me thinking about how we all strive for a good nights sleep and the answers show a varing number of differences between us all. This link discusses how to deal with sleep problems and Fibromylgia. I hope that some of you find it useful :) http://www.webmd.boots.com/pain-management
HI EVERYONE Emma's poll got me thinking about how we all strive for a good nights sleep and the answers show a varing number of differences between us all. This link discusses how to deal with sleep problems and Fibromylgia. I hope that some of you find it useful :) http://www.webmd.boots.com/pain-management
Hidden
in
Fibromyalgia Action UK
10 years ago
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