Jump to content
RemedySpot.com

Re: drug info

Rate this topic


Guest guest

Recommended Posts

Hi Jodi,

I have not talked to anyone who has had a terribly serious adverse

reaction to Sinimet, but I am new to the group. I know that it

usually stops working at some point, but my neurologist told me that

if you go back to it after a month or so the chances are that it will

work again.

All I know is that it works for me and I had terrible RLS ... maximum

doses of sleeping pills, anticonvulsants .... nothing worked like

Sinimet does for me. The one thing that I think Sinimet may do is

increase daytime RLS. It has a tendency to postpone the problem so

you can get to sleep but you may experience discomfort the next day.

I have noticed this (but I don't know if it's due to Sinimet or just

that my RLS is getting worse). I can deal with RLS better in the

daytime (compared to when I am trying to go to sleep and like most of

you cannot stay still for more than 15 seconds or so). The problem

comes up when I am in a long meeting, at the movies, where I cannot

get up and move around etc.

I also take Mirapex along with the Sinimet but I really don't think it

does much of anything. My neurologist (who is an expert in RLS) does

try and switch people from Sinimet to other medications or at least

decrease the Sinimet by using it in combination with another drug. My

understanding is that she does this because of the reasons above,

Sinimet loses its effectiveness over time and it tends to postpone

(rather than eliminate) the RLS until daytime.

janegf@...

---Jodi Judson wrote:

>

>

>

> I am forwarding this to the group, as it was sent to to old address.

>

> Jodi

>

> Subj: drug info

> Date: 2/5/99 6:04:33 PM Central Standard Time

> From: rstutt@... (Rigina Stuttkowski)

> To: RLSSupport@...

>

> Hi: I've just read some responses to my question on " drug info

please " .

>

> Question one to : You say you see a psychiatrist rather than a

> neurologist. So do

> I, but she says most anti-depressants will cause rls. What are you

on?

>

> To Jane: I've never heard of Sinimet, and from what I read in this

group

> alot of people

> don't like it or have adverse effects. Any comments?

>

> To E. Jude; thanks for the link, I will check it out.

>

> And for Donna: I am on amitriptyline for the fibromyalgia. I guess

it's

> the most

> commonly used drug here in Canada for FMS. They don't prescribe

enough for

> benefits for

> depression as it is mostly used in FMS patients as a sleep inducer.

> Doesn't really

> work though. It did in the beginning until I got this rls thing

happening

> and I'm still

> not sure if it was the Effexor for depression or something else that

gave it

> a kick

> start. Now though I wish it would go away cause I have enough with

the

> fibromyalgia.

>

> Thanks all for responding so quickly. Ah, before I forget, can

anyone out

> there

> associate temperature fluctuation with the rls. I've never played

with my

> thermostat as

> much as I have since the rls kicked in two weeks ago.???

>

>

>

------------------------------------------------------------------------

>

Link to comment
Share on other sites

Hi Jodi,

I have not talked to anyone who has had a terribly serious adverse

reaction to Sinimet, but I am new to the group. I know that it

usually stops working at some point, but my neurologist told me that

if you go back to it after a month or so the chances are that it will

work again.

All I know is that it works for me and I had terrible RLS ... maximum

doses of sleeping pills, anticonvulsants .... nothing worked like

Sinimet does for me. The one thing that I think Sinimet may do is

increase daytime RLS. It has a tendency to postpone the problem so

you can get to sleep but you may experience discomfort the next day.

I have noticed this (but I don't know if it's due to Sinimet or just

that my RLS is getting worse). I can deal with RLS better in the

daytime (compared to when I am trying to go to sleep and like most of

you cannot stay still for more than 15 seconds or so). The problem

comes up when I am in a long meeting, at the movies, where I cannot

get up and move around etc.

I also take Mirapex along with the Sinimet but I really don't think it

does much of anything. My neurologist (who is an expert in RLS) does

try and switch people from Sinimet to other medications or at least

decrease the Sinimet by using it in combination with another drug. My

understanding is that she does this because of the reasons above,

Sinimet loses its effectiveness over time and it tends to postpone

(rather than eliminate) the RLS until daytime.

janegf@...

---Jodi Judson wrote:

>

>

>

> I am forwarding this to the group, as it was sent to to old address.

>

> Jodi

>

> Subj: drug info

> Date: 2/5/99 6:04:33 PM Central Standard Time

> From: rstutt@... (Rigina Stuttkowski)

> To: RLSSupport@...

>

> Hi: I've just read some responses to my question on " drug info

please " .

>

> Question one to : You say you see a psychiatrist rather than a

> neurologist. So do

> I, but she says most anti-depressants will cause rls. What are you

on?

>

> To Jane: I've never heard of Sinimet, and from what I read in this

group

> alot of people

> don't like it or have adverse effects. Any comments?

>

> To E. Jude; thanks for the link, I will check it out.

>

> And for Donna: I am on amitriptyline for the fibromyalgia. I guess

it's

> the most

> commonly used drug here in Canada for FMS. They don't prescribe

enough for

> benefits for

> depression as it is mostly used in FMS patients as a sleep inducer.

> Doesn't really

> work though. It did in the beginning until I got this rls thing

happening

> and I'm still

> not sure if it was the Effexor for depression or something else that

gave it

> a kick

> start. Now though I wish it would go away cause I have enough with

the

> fibromyalgia.

>

> Thanks all for responding so quickly. Ah, before I forget, can

anyone out

> there

> associate temperature fluctuation with the rls. I've never played

with my

> thermostat as

> much as I have since the rls kicked in two weeks ago.???

>

>

>

------------------------------------------------------------------------

>

Link to comment
Share on other sites

Jane,

Just keep doing whatever works, for as long as it works! The sinamet

worked the longest and best for me for about 9 months. Then it gradually

stopped helping me at night, and the rebound during the day was

intolerable, so my neurologist prescribed the Mirapex. I've been taking

it for close to a year. It sure is not a cure - still don't sleep well

most nights, and still have some symptoms during the day, but I'll stick

with it for now. I know from past experience that things could be worse!

I have been tempted to try one of the benzos also, as so many in the

group have reported good results, when taken in combination with the

Parkinson's drugs. I'm really afraid to start with them however, due to

the fact that a close family member and a good friend experienced serious

addiction and withdrawal problems, not to mention diminished mental

abilities - loss of short term memory, inability to concentrate, etc..

This obviously doesn't apply to many, but addiction runs in my family,

and I am already addicted to cigarettes! Lack of sleep is no picnic

either, but I've been functioning for years without enough sleep. My

memory is no worse than others my age, and a lot better than some! Also,

I am able to focus and concentrate, and am rarely sick. I am envious of

those who can take the benzos and are able to sleep most nights as a

result - it would be nice!!

Good luck with whatever you choose,, and you are fortunate to have a

doctor who is knowledgeable.

ne, 59 (as of today- yikes!), Lawrenceville, NJ

___________________________________________________________________

You don't need to buy Internet access to use free Internet e-mail.

Get completely free e-mail from Juno at http://www.juno.com/getjuno.html

or call Juno at (800) 654-JUNO [654-5866]

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...