Experiences with

Sleep disorders

The study compared the efficacy of different non-pharmacological interventions for sleep disorders in patients with PD, and results suggest that massage therapy may be the preferred non-pharmacological intervention for improving sleep disorders in PD, followed by music therapy and treadmill training

He practices at the Center for Sleep Medicine Kempenhaeghe in the Netherlands, a leading institution dedicated to diagnosing and treating sleep disorders.

It's not specific to RLS but does mention sleep disorders generally. https://www.mdpi.com/2072-6643/16/14/2259#:~:text=Consequently%2C%20it%20is%20proposed%20that,prolonging%20sleep%20duration%20%5B51%5D.

About 3 /4 nights i the week I am awake u till about 4.30 in the morning which makes me exhausted the next day. Also if I do sleep I have disturbing nightmares. I think the problem is drug related but Doctorsnot interested. I take Gliclazide,trajenta, carvadilol, amiodarone and losartan Does anyone

I forgot to mention Rivaroxiban and Amiodarone

I was looking at Dementech Neurosciences in London who have a number of doctors specialising in sleep disorders, including RLS , which I suffer from. Has anyone used any of these?

I was looking at Dementech Neurosciences in London who have a number of doctors specialising in sleep disorders, including RLS , which I suffer from. Has anyone used any of these?

Hiya all. As a support for getting to sleep when my PLMD is problematic , (rather than using Zopiclone), my GP has suggested Promethazine. aka Avomine, Phenergan, or Sominex. Has anyone had any experience of this, or does anyone have any insights? Thanks for your thoughts.

I'm not feeling well today , face dropping and difficult to get my words out stuttering, I'm so tired even after 9 hours sleep.I've done the normal checks that its not a stroke everything seems OK. Going to have a sleep. Talk soon .

Two weeks off requip.... gone on for a sleep study, no results yet. Contacted Dr. Andrew Berkowski. He can't see me until next week. Will cost close to 1000 $ but worth it if I get help. My symptoms have gotten worse. Legs start within 10 minutes of laying down. Mostly my left leg. Gone from just jerking

Have you been advised to have an ablation and know what it is? An ablation is a long term, effective procedure with a high success rate for atrial fibrillation and atrial flutter. It is completely natural to feel anxious about a procedure, so preparation is key. Our information sheet 'Preparing for

Is it possible that CPAP may improve PD symptoms? https://www.medicalnewstoday.com/articles/cpap-for-sleep-apnea-may-help-lower-parkinsons-risk People with obstructive sleep apnea may have a higher risk of developing Parkinson’s disease, but early use of continuous positive airway pressure (CPAP) therapy

After several years on Belbuca (buprenorphine) and developing mixed apnea during that time, I am wondering—suspecting—that the cause of the apnea is the breathing suppressant in the semi-ipioid. Belbuca works wonderfully to tame my difficult-to-treat RLS of over 50 years now. However, I need oxygen above

For those living with syncope in the US and the UK. We are working with Duke Clinical Research Institute, North Carolina, USA as they undertaking a research project to better understand what is most important to people living with and experiencing frequent episodes of loss of consciousness (syncope/

I’m off to the first appointment with cardio consultant today I think to discuss ablation. I was very concerned last year as very symptomatic but since being diagnosed with sleep apnea and starting with the CPAP I’m feeling so much better even though still getting episodes. Last week. 9% the week before

For those living with syncope in the US and the UK. We are working with Duke Clinical Research Institute, North Carolina, USA as they undertaking a research project to better understand what is most important to people living with and experiencing frequent episodes of loss of consciousness (syncope/

Hello everyone, I am a 42-year-old man experiencing persistent symptoms, including joint pain, skin rashes, insomnia, and chronic fatigue. Despite completely avoiding food from my home, these symptoms persist, and new ones occasionally appear, making the situation even more difficult to understand.

For those living with syncope in the US and the UK. We are working with Duke Clinical Research Institute, North Carolina, USA as they undertaking a research project to better understand what is most important to people living with and experiencing frequent episodes of loss of consciousness (syncope/

Hi, I'm starting to think that I have perimenopause induced narcolepsy or something form of sleep disorder as I'm 43 and for the last few years I have suffered from sleep problems which are becoming so severe that I can't function. I can generally manage day 5 - 17 of my cycle but from day 17 to 5 I

I was diagnosed with PD 8 yrs ago. I have strength and fatigue issues and would like to know if anyone has experienced improvement with Ivermectin and if so what is the dosage protocol for? Thank you.