Hi everyone is there anyone on this site that has Parkinson’s disease with resting tremor as only symptoms and what medication is good for resting tremor because ime reading everything i know about my disease and not fully understanding the outcome in real time
Welcome Calv1960. When I was diagnosed in 2005, I found my resting tremor becam worse when under pressure at work. This was treated with Beta Blockers, which worked for 2 years before I needed Parkinson’s specific drugs.
One thing quite a few people forget to do is inform the DVLA. A note of caution though, if you rush to tell them before you have begun to take any drugs or know how they affect you. The DVLA have be known to suspend driving licences for Parkinson’s, while making enquiries with your doctors. There’s a Parkinson’s Driving questioinaire on the DVLA website that gives you insight into what they are concerned about
If you haven’t already been put in touch with your local Parkinson’s Nurse, ask for a referral. I have found mine to be invaluable.
The best treatment by far though is: exercise that gets your heart rate up. But don’t overdo it if taking beta blockers. At least until you know how they affect you.
As your symtoms progress and more medications are discussed, take care to read about and look out for side effects. Parkinson’s has many symptoms and drugs with a corresponding number of side effects.
Hello kendo i have informed the dvla that was done xmas i now have a 3yr medical driving licence, ime trying to find out on here how many people started with resting tremor as this is something ime interested in and Parkinson’s treatment, side effects whats good for 1 person and why
Hello again what beta blockers were u on and was it a resting tremor you had or another type of tremor
Propanalol 40mg twice a day. Helped control my resting tremor. When I move my arms the tremor goes away as expected. I took them for 5 years. For the last 10, I’ve been on more conventional Parkinsons drugs.
I have also benefitted from being one of the 42 on the phase 2 GDNF trial and for the past 18 months Deep Brain Stimulation
Sorry to trouble you again my resting tremor goes when i fall a sleep so my partner tells me does this happen to you by any chance, also my tremor is between my thumb and my elbow
Mine does go to sleep when the drugs are working and I can finally fall asleep. When the drugs wear off though, the tremor from my elbow to my fingertips is what wakes me. Started on left side only and over 5 years the right arm and legs joined in to a lesser extent.
Another not often talked about impact of a resting tremor is the difficulties it can create in public toilets unless a cubicle is quickly available. Not just in toilets as well. Since it goes when you voluntarily move your arm you develop habits that involve regular normal style movements. This can be exhausting on it’s own.
Hi Calv1960 I’ve had Resting Tremor for the last 10yrs now-my right arm and hand,and sometimes my right leg. I have always taken the same dose of Sinemet Plus and Propanalol. If my tremor starts I often try to put my brain on another course! ie Taking the dog out,going on the pc etc.My final resort is trying to sleep to shut things down. (I think of my brain a bit like a pc-where if there is a default you need to reboot!) I also use Mindfulness and can often stop the tremors. I usually find they last between 20-60mins. My PD has got better rather than worse over the years!
I’m guessing you’ve already read our information about tremor? https://www.parkinsons.org.uk/information-and-support/tremor
You can always call and speak to a Nurse Adviser on the helpline about symptoms - 0808 800 0303
Tash - Moderation Team
I noticed a resting tremor in my right hand well before I got a diagnosis. Looking back there were other early symptoms but it was the tremor I noticed first.
Hi all i am taking co careldopa 12.5/50 no change what so ever after a week of taking meds so looks like this med is not good for me at this strength wots the next step ? Increase the dose or leave well alone
If you’ve just started on medication for Parkinson’s, it can sometimes take a while for you and your clinic to find the dosage and frequency that works for you. Do have a read of the Drug Treatments section of our website, which includes some of the following advice…
Every person with Parkinson’s has a different experience of the condition so your specialist, Parkinson’s nurse or pharmacist will work with you to find the best combination of treatment that is best for you as an individual.
Finding the best drug, dose and timing won’t happen straight away. Your treatment regime will usually need adapting as your Parkinson’s symptoms change over time.
Which medication you take depends on how much your symptoms affect you and other factors such as, your age and your lifestyle. Most people find they tolerate their treatment well and will return to clinic after six to eight weeks to review their response. This is when your specialist or Parkinson’s nurse will increase or decrease the doses, the frequency, or add new drugs until your symptoms are as controlled as possible.
It’s really important not to stop or change your medication without specialist advice, do contact your Parkinson’s clinic if you have any questions or concerns about your treatment, and as Tash mentioned, you can also call and speak to a Nurse Adviser on the helpline about symptoms - 0808 800 0303
David - Moderation Team