Has anyone with RLS, while sitting and laying down, BUT HAD NO PROBLEMS GOING TO SLEEP, OR STAYING ASLEEP?
It seems all the posts are from people saying the RLS prevents them from going to sleep, or staying asleep. NOT ME, AM I WEIRD??
Has anyone with RLS, while sitting and laying down, BUT HAD NO PROBLEMS GOING TO SLEEP, OR STAYING ASLEEP?
It seems all the posts are from people saying the RLS prevents them from going to sleep, or staying asleep. NOT ME, AM I WEIRD??
Just a little unusual.
What are your exact symptoms of rls?
Symptoms are my legs continously shake, when I sit and laydown. Day and night. I can sleep at night no problem. Thanks for replying.
Do you have to keep moving them? Do you have a very strong urge to move feeling /sensation that you can't ignore? Do you have to kick your legs about? Do you voluntarily move your legs or do they shake by themselves? Do you have to get out of bed and walk about? C
Hi,
Yes to all your questions, but I don't have to walk around. I'm so confused,
I am glad you are going to see your doctor. We are called Nightwalkers for a that reason. When the dopamine drops at night time, the RLS ramps up. So, if you are never getting that at night time ever, it may not be RLS that you have. But, we do not know you well enough yet to make a guess. Anyone with RLS would kill for the sleep you are getting. The diagnostic criteria, all 5 listed, states "you MUST have the urge to move that you cannot ignore" . irlssg.org These are the people who set the diagnostic criteria and I am very familiar with them and their work.
As Pippin's above.
I'm thinking this is more likely some neuropathic issue. Has anyone diagnosed you with rls?
Most people with rls would be utterly delighted to get the sleep you describe.
I'm sure the shaking all day is very distressing, I know friends who have severe Parkinson's and it is truly awful.
I hope you get relief.
Long may it continue 😊
Hi Kel
You mention in another posting that your RLS symptoms only started a few months ago. What happened/changed in your life around that time?
The only change I can think of is the addition of hydrOXYzine for anxiety. I only take maybe once a week.
Just a thought. See Medications to Avoid in this link. rls-uk.org/treatment/
Antihistamines are listed in this link, to avoid if possible, but not specifically Hydroxysine but it is an antihistamine as well as used in the short-term to treat anxiety.
Anything that ends in "zine" can be a trigger for RLS, most antidepressants are triggers for RLS. That may be your answer there. Kaarina is right. Look at the list of Drugs to avoid. Antihistamines can be evil for us, and also stay away from any over the counter med with Diphenhydramine in it. 99.9% of us cannot take most antihistamines at all.
Thank you. Where can I find "the list of drugs to avoid"?
I found the list and am taking it to my neurologist appt. Thank you.
You're welcome. Pleased that you found the list of Medications to Avoid in the link I posted for you. An excellent idea to take this list with you to your neuro appointment. The RLS-UK website provides some very helpful information. rls-uk.org
Thank you. I have an appt. with the neurologist in a couple weeks. My nighttime shaking is worse than the daytime shaking. Do not have a strange pulsating feeling. Just urge to shake my leg.
and there it is, the "Urge to shake your leg". That is what I was looking for. The URGE to move. Look it up on here for the RLS criteria. irlssg.org They set the criteria for diagnosis. And the URGE has to be there. You may have a milder case that lets you get more sleep. Can I ask you approximate age? RLS is progressive as get older.
The only reason l didnt think it was RLS is because your symtomes didnt sound like RLS but everyone is different. Only a medical person can advise you properly
The fact they don't keep you awake certainly doesn't sound like rls. Shaking or not.
Does moving the legs give respite? That is the crucial point.
I dont understand, "Does moving the legs give respite?". I have to constantly shake my legs. It's involuntary.
Then , I would say it's definitely not rls.
But really, this is all quite pointless- trying to define whether, what you are experiencing, is rls or not.
You have what you have.
The real question is, what can help you?
It's quite likely that most rls medications, such as Pramipexol or opiates, will quieten your movements, but only a neurologist can really decide. You are not in pain, as such,- just need to stop the involuntary shaking.
Hopefully, your visit to that eminence, will help you get some peace.
All the best.
I'm adding a link that may help you , before you go to the specialist.
mayoclinic.org/diseases-con...
I hope this will give you some ideas.
Cheers.
Kel, the urge to move is voluntary, we HAVE to move our legs its a urge we cant resist, its not involuntary. By moving our legs it gives some relief, thats why we pace. But as Madlegs said we can discuss it til the cows come home. Just make sure the neuro knows what the RLS criteria is for you to be diagnosed. Good luck.
irlssg.org/diagnostic-crite... This is the criteria for RLS, all must be met,
Did the muscle relaxers stop the shaking????
Hi kel
I’m new to this forum and reading you msg sounds a lot like what I’ve been going through since I was 15. I’m now 34 and still nowhere with the doctors, I’m now being referred to guys hospital to discuss about rls as I’ve been told it’s not arthritis and I’ve had key hole surgery. Could you tell me if you’re knees are painful especially after walking or standing/ sitting for a period of 5 maybe 10 mins at a time. Also when I sit down driving or just at my work bench during the day I get the urge to moving my legs and when I walk the knee slips forward. Are you getting any of these symptoms.
Thanks Tony
Ok thanks for the reply
Hello.
Glad to know someone else is like me. I have RLS I am told in my foot and in pain all day every day but - as soon as I am settled and comfortable at night - it does not bother me. Very experienced people on this forum say that if that's the case then it is not RLS but possibly some form of peripheral neuropathy. Seeing consultant at end of August to get results of MRI scan so will see what happens after that. All very interesting though.