Do our bodies get used to our meds? - Cure Parkinson's

Cure Parkinson's

26,572 members27,877 posts

Do our bodies get used to our meds?

Court profile image
6 Replies

I have already commented on the fact that my meds are not doing their job at the moment. This has happened to me before and usually rights itself. I have a hospital appointment soon, if it does not.

I was wondering if I am getting used to taking the same meds - Stalevo and Requip XL, as I have been taking these for about 3 years. It could be that these need increasing, or that my condition is progressing, although my physiotherapist said that I am stable at the moment.

I am now wondering if my body, or my brain, is getting used to the same combination of meds, but as they usually do the job, am not sure I want to rock the boat by changing them.

Has anyone else had this problem and come up with a suitable answer, please.

Written by
Court profile image
Court
To view profiles and participate in discussions please or .
Read more about...
6 Replies
honeycombe3 profile image
honeycombe3

Hi Sue, Better today - I think this does happen I've been on Requipxl 16mg for many years & started Sinemet last November. I'm having terrible pain in my left side again, bad tremor & clawing - also dizziness, fatigue & bad headaches. Nothing seems to shift it. I've just started tingling in the extremities, feeling cold & the internal tremors. Anyone for tennis?

Court profile image
Court in reply tohoneycombe3

Well, I suppose things can only get better. Not been too bad myself today, but could all change when next tablets are due as evenings are my worst time.

Good job we can laugh at ourselves and stay strong as this Parkinsons would try the patience of a saint.

PatV profile image
PatV

No . I think there should be a rehab facility to go through titrating PD meds. A pleasant place with gardens, classes and massage :D

Court profile image
Court in reply toPatV

Sounds wonderful. Count me in. :-)

Iron1 profile image
Iron1

yup to ALl the abo ve,,, Sinemet seems to do less "movin and shakin

and Yikes U really find that that the evenings are tough and it is truly the worst time of day. . But, the optimism shown by the comments here help tide me over until : Tomorrow Tomorrow, I luv ya Tomorrow......

and PatV and Honeycombe3

Court profile image
Court in reply toIron1

Yes, I agree the evenings are tough and are also the worst time of the day for me. I often have go to to bed really early with a hot water bottle to survive them. I have very little social life of an evening as you can imagine. Even changing times of my meds does not help.

But tomorrow is another day and who knows ..........

Not what you're looking for?

You may also like...

Chewing my meds to make them work faster

I recently started chewing my meds to try to shorten my dreaded off periods. I take Stalivo (150MG)...

To fall asleep when you do not want

I have some time falling asleep when I don't really want it. It has been on the job and there...
MrDay profile image

Meds to take with Carbo/Leva

My husband takes Carbo/Leva 25/100 three times a day at 1 1/2 pill first thing in the morning and...
tbirchf profile image

What criteria was used to diagnose you had PD?

I am interested in knowing how people were diagnosed. I accept that I have PD but have only ever...
Court profile image

Really struggling to know what to do

Hi all. I've not yet officially been diagnosed with Parkinson's because I've never had the typical...

Moderation team

See all
CPT_Aleksandra profile image
CPT_AleksandraAdministrator
CPT_Anaya profile image
CPT_AnayaAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.