Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS)


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Old 02-09-2007, 09:05 PM #1
InHisHands InHisHands is offline
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Question Amitriptyline... no results?

Anyone taken Amitriptyline and got NO results? I am taking it for sleep, and it doesn't seem to be doing a THING. So much for thinking it was going to zombie/ knock me out.

Any experience??
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Old 02-09-2007, 09:58 PM #2
debbiehub debbiehub is offline
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Default Hi

I take Pamalar which is similar and no- I dont think it does anything...as usual

Deb
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Old 02-09-2007, 11:22 PM #3
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Default elavil

Hi,
This can depend on the dosage.
Are you on 10 mg, 25, 50 or 100 mg. Ten may not helpm
your doc may need to up the dosage.
Same with the Pamelor, which is very much like the amitryp...aka elavil.
There are supposed to be less side effects with the Pamelor.

I take Trazodone. It is given instead of what you take. It helps me sleep,
it is cheap and it has pain relieving qualities.

So check with your doc. Hope this helps;
blessings,
hope
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Old 02-11-2007, 01:11 PM #4
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Thanks, Hope! That helps me... I am only on 10 mg right now. Maybe increasing the dose is what needs to be done. I know the Dr started me on a really low dose because of my strange reactions to different meds., so if she sees I'm okay with the low dose she might increase it.

Thanks again.
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Old 02-11-2007, 01:15 PM #5
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Originally Posted by HopeLivesHere View Post
I take Trazodone. It is given instead of what you take. It helps me sleep, it is cheap and it has pain relieving qualities.
My Dr. didn't want to start me on Trazadone because she thought Amitriptyline would be better as she said it has a pain relieving effect as well as sleep. I didn't realize Trazodone has pain relieving qualities as well. Either way, I'm on Amitriptyline for now. Thanks for your reply and ideas.
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Old 02-11-2007, 01:52 PM #6
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Default been on both..

Hi there..

I was put on amitriptyline around 3 months into RSD, good pain relief and I finaly got some sleep, it was upped to 30mg by the same time a year later when they switched me to trazadone.

I cant remember wheather the A took a while to start working origionaly but there were 4 days of realy bad pain again (8+), between drugs when I was switched to T and then it was as if I was still on the A sleep and pain wise for me.

I was switched because the A was making me gain too much weight..

I had gained over 30 lbs, but I gained no more with the T and actualy I had lost 5 lbs in the 8 months following, I since have lost another almost 15 lbs in the month of dec 2006 due to bein in hospital so long (nasty food *yuck twey*) and I am keeping it off it seems so far.

The weight was realy making the pain worse as my RSD is predominantly in my right ankle.

I found no diffrence pain relief wise between these two drugs over the long term, they are what has kept me sane I think.

I hope this helps and I hope that you are having low pain days,
Sandra
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Old 02-12-2007, 05:36 PM #7
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I am also taking Amitrip. My primary physician put me on 10mg and also lorazepam for spasms. His idea was that I needed to get sleep 'cause pain is so tiring and he wanted me to sleep through the night. It does seem to work for me along with the 50mg lyrica too. I don't have any real opinion about the lyrica, but I do sleep so I guess they're doing something.

I hope "In His Hands' that your pain with decrease and you will have some relief SOON!

Never heard of trazadone...think I'll look that up!

You're all swell and I will keep you all in my thoughts. Peaceful night to you all.
Cathy
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Old 03-25-2007, 06:32 PM #8
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Just wanted to update this~ I am now taking 80 mg of amitriptyline before bed and I am only waking once-twice during the night, unless it is a bad pain night (then I'll wake 5 or so times)! I am so happy that I am finally sleeping, and it really helps with tolerating the pain and coping!

Of course sleeping makes the pain easier to bear- every little thing will make your pain worse or appear worse (being exhausted, hungry or thirsty will even do it)...


Now the thing is- I hope this affect doesn't wear off. With me, after taking a medication for a while, my body builds up a tolerance to it, and it'll stop working like it used to. Does anyone else deal with that? What do you do?
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Old 03-30-2007, 05:03 PM #9
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Hello, I have rsd in my left ankle ;-( was just diagnosed and it has been rough ...how long have you had it..I also was wondering about the pain clinic they want to give me these blocks 2 a week for 3 weeks ?? Dont know to much about them and they really scared me they dont comunicate with my Dr ans I flet thrown out to the dogs with a number??? I still have movement but tingling and the redness and pain is starting to come at night dont know what to do??? Take care
Tammy
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Old 03-30-2007, 11:39 PM #10
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Quote:
Originally Posted by tmrsfitz1967 View Post
Hello, I have rsd in my left ankle ;-( was just diagnosed and it has been rough ...how long have you had it..I also was wondering about the pain clinic they want to give me these blocks 2 a week for 3 weeks ?? Dont know to much about them and they really scared me they dont comunicate with my Dr ans I flet thrown out to the dogs with a number??? I still have movement but tingling and the redness and pain is starting to come at night dont know what to do??? Take care
Tammy
In the posts I have read, I am blessed to have found out so soon. I was injured Dec 2, 06. RSD is in my Rht Knee. However, I have shooting pain up and down my whole leg sometimes. It has taken four months but I found a doctor (the 5th one) through outside referral through my health insurance that said "this is what it is and we need to aggressively treat it so it doesn't become worse." He immediately set me up for water therapy. This was this past Wednesday and PT was today. It hurt like hell. I even said to him "this is going to hurt later huh?" and he responded with "yes, this will definitely hurt later." I was crying while walking in the pool. I will also be calling the doc that referred me out to request a referral to a neurologist for help with pain.

I have found that googling helps with the different terms and definitions and side effects. That would be a good route. I would also search the forums here and find other posters who have gone through it so you can get firsthand accounts.

Hugs - you can make it.
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