If you are not a registered member of our community, please click here to register...

 Home Message Boards Health Guide Join for Free Testimonials About Us
Search
   
  


PDA

View Full Version : ???? Lyrica for nerve pain


 

 

 
scbmxmom
04-20-2006, 12:58 PM
Hi everyone! :wave:
I'm new to this particular board. I'm usually on the back problem board. I had a fusion (L3/L4) and have been having pain going through my hip and down my leg before the surgery and now after. I was taking Neurontin (1800 mg) a day. Yesterday my doctor switched me to Lyrica 150 mg twice a day. Since takin it I have been sooooo sleepy. :yawn: Yesterday I slept off on on from 3:ooPM until 7:00AM this morining. Today it is taking all I have to keep my eyes open. Does anyone have experiences they can share about taking Lyrica?

Sponsor
 



mondaymorning
04-22-2006, 05:50 PM
When my doctor changed me to Lyrica I had similiar experiences in the beginning with sleepiness, but I only started with 50mg 2x day. So I can imagine with the 150mg 2x day you must really be sleepy. It took me about 2 weeks to get over the big tiredness. My doctor put me on 50mg to start for 1 month then increased it to 75mg 2x day. Just to get accustomed to the drug. I'm due to increase again. It hasn't helped much yet for my pain but I'm hoping once we get to the whatever mg? it may help.
I hope it helps you with your pain as my wife has back problems and her pain meds do nothing for her pain.

scbmxmom
04-23-2006, 10:19 AM
:wave: mondaymorning
Thanks for the response!! I'm starting to adjust to the sleepiness. At first I didn't think it was helping much but now it is helping. I don't notice where it is any different than the Neurontin other than I only have to take it twice a day instead of three. My doctor said it has less side effects. I don't know if it's the meds. or just me but I do have a HUGE appetite. I can't get full. I hope that goes away because I can't afford anymore weight gain. I've already gained 30lbs since all this. :eek: I start PT next week so hopefully that will help. Again, thanks!! :wave:

justfine
04-23-2006, 05:17 PM
When I was taking Lyrica I fell asleep at the dinner table while eating. Family got a big laugh from it. but yes made me very tried.

Sharon/B
05-03-2006, 06:01 PM
Hi
Am new to this and have only posted once on the pain site but decided to look here today. I started taking Lyrica 5 days ago at only 25mg a day. I asked for the very lowest dose as the Neurontin which I tried 3 years ago made me feel so bad I had to stop taking it at once. I felt a bit sleepy the last few days but otherwise alright. The bit question is whether it will have any effect on my nerve pain, wait and see until the dose is higher but I am going to do that very slowly. Good to hear of other people's experiences. Good luck to you. My nerve pain is mostly lower back but on bad days spreads down my legs to my feet and have had times when I can't even bear to have the duvet ontop of me at night. Am at a bit better place at the moment after the GP prescribed stronger pain medications (am on 3 different ones) and am now trying out the Lyrica.

Hope you get a good result and know that there are more of us out here in the same situation.
Sharon

scbmxmom
05-04-2006, 02:18 PM
Sharon :wave:
Thanks for sharing your experiences. It has been so helpful to hear what others have experienced. So far I'm doing much better. I know the Lyrica is helping because about an hour before my next dose, boy do I start feeling it. :eek: I haven't had to take the muscle relaxer or Vicodin as often. I started PT :bouncing: and that is really making me sore. :eek: I know it will eventually help. I have been doing really well but today has been bad. I think I overdid it this week. I been walking, house cleaning (mopping, scrubbing toilets, laundry), and PT. I guess as this goes on I will learn how much to do or not do. The meds. make is easy yo overdo it because I don't feel the pain at the time.

Anyway, thanks and hope you are doing well.

meandautumn
05-09-2006, 07:42 PM
Hi friends with nueropathy. I have had it in my feet for several month and it is mostly awfull numbness, which makes it difficult to walk. I am now using a crutch and cane. I am on 300 mg of Lyrica and it does nothing so far for this numbness. awfully sleepy!!! anyone???N

Silvio
05-16-2006, 03:49 PM
Hi everyone! :wave:
I'm new to this particular board. I'm usually on the back problem board. I had a fusion (L3/L4) and have been having pain going through my hip and down my leg before the surgery and now after. I was taking Neurontin (1800 mg) a day. Yesterday my doctor switched me to Lyrica 150 mg twice a day. Since takin it I have been sooooo sleepy. :yawn: Yesterday I slept off on on from 3:ooPM until 7:00AM this morining. Today it is taking all I have to keep my eyes open. Does anyone have experiences they can share about taking Lyrica?

Silvio
05-16-2006, 03:54 PM
:yawn: Hi everyone! :wave:
I'm new to this particular board. I'm usually on the back problem board. I had a fusion (L3/L4) and have been having pain going through my hip and down my leg before the surgery and now after. I was taking Neurontin (1800 mg) a day. Yesterday my doctor switched me to Lyrica 150 mg twice a day. Since takin it I have been sooooo sleepy. :yawn: Yesterday I slept off on on from 3:ooPM until 7:00AM this morining. Today it is taking all I have to keep my eyes open. Does anyone have experiences they can share about taking Lyrica?

Silvio
05-16-2006, 03:55 PM
Hi everyone! :wave:
I'm new to this particular board. I'm usually on the back problem board. I had a fusion (L3/L4) and have been having pain going through my hip and down my leg before the surgery and now after. I was taking Neurontin (1800 mg) a day. Yesterday my doctor switched me to Lyrica 150 mg twice a day. Since takin it I have been sooooo sleepy. :yawn: Yesterday I slept off on on from 3:ooPM until 7:00AM this morining. Today it is taking all I have to keep my eyes open. Does anyone have experiences they can share about taking Lyrica?

Silvio
05-16-2006, 04:17 PM
SCBMXMOM , I can understand why you are so sleepy. Thats a hefty dose. I started out with 75mgs 2x day, then 100 mgs 2x day, and am now on 100 mgs 3x day and was converted from neurontin 3oomgs at bedtime. Every time my dose is increased i am sleepy but not for long. It also relaxes me and I need that !!!. In Europe it is used for anxiety so it helps more than one area. Any person in chronic pain needs that. I had been on and off neurontin for approx. 8 yrs and Lyrica doesnt give me the spacey,amnesic,or memory problems associated with neurontin. :yawn: So that's my exp. with lyrica and lovin it. Silvio :angel:

scbmxmom
05-29-2006, 04:42 PM
Silvio :wave:
Thanks for your response!! I haven't been on-line for a while. VERY BUSY!! The sleepiness HAS improved!! Thanks goodness. BUT, I'm having problems with my hands and feet swelling. That hasn't happened since I was pregnant. I'm trying to eat healthier in hopes of not gaining anymore weight. Thankfully I haven't gained anymore weight but I'm having a VERY HARD TIME LOSING weight! :eek:

The Lyrica does help the nerve pain shooting down my leg, but it does nothing for the numbness around my knee. But now my right hip and tailbone are killing me. The Lyrica doesn't take away the pain I'm having from this so I know it's not nerve related, but I wish I knew what it was. It's driving me CRAZY!!! :eek:

Anyway, thanks again!!!!!

Captain Colon
05-31-2006, 10:10 PM
Lyrica can cause swelling in the hands and feet...as far as I know this is supposed to be "normal." However, if you're experiencing muscle pain or tenderness that you didn't have before taking the lyrica, you should probably talk to your doctor.

If you had the pain before taking the lyrica, why not just ask your doctor for some traditional painkillers? I found that in addition to helping tons with muscle and bone pain (my neuropathy is the result of a fractured femur wreaking havoc on the nerve about halfway down the thigh) and even a little for my nerve pain, my hydrocodone went a long way towards keeping my mood up. Now if only I could get any of my doctors to give me more than 40 tablets at a time, considering it's only been a month and a half since my accident/surgery and most of the area still hurts :(

PlaXibo
06-03-2006, 04:21 PM
I take 300mg of lyrica 2 times a day. And yes when I started taking it it made me a little tired. But that could also be from the other pain meds I take. I use fentanyl 50mcg patch changing it every two days and up to 6 darvocet a day. I still have pain and honestly can say that the lyrica is helping. It seems to help my other pain killers to work better. But I guess its different for everyone.

Mark B

Too Sweet 74
06-09-2006, 03:32 PM
I was just wondering if there was anyone that wasn't helped at all from Lyrica at any dosage? I started taking it yesterday 75MG 2xday and have been really tired. The first dose caused a feeling like I had been drinking .I felt unsteady. I'm hoping this drug is what finally helps me.Been dealing with a nerve injury for almost two years in my riight arm and chronic headaches from a bilateral EMG done for diagnosing the arm for a year and three months. I've had alot of steroids,epidurals ect.Nothing is helping yet.I am on tramadol now and that helps to take the edge off so I function a little better. I'm crossing my fingers that Lyrica will finally be what really helps me.

pattihabs
06-09-2006, 10:29 PM
hi, welcome to the boards. i've taken lyrica and was having other problems and now i'm on neuronton and have the sleepy problem. most people i've talked to say they like the lyrica better, give it a wirl and see if it helps u. lots of luck, patti :wave:

~Kaelie
06-10-2006, 01:56 PM
I've been on Lyrica for about 4 months now

Started out slow at 75, 3 times a day = 225mg That lasted about a month before I got in to see my Neurologist. From there the dosage has been slowly skyrocketing.

I am now on 300, 2 times a day = 600mg (!!!) They take away the pain of the PN along my leg, but not the pop-can sized lump on my hip, so I think my neuro will continue to increase the dosage (which scares the bejesus outta me)

Side effects: (warning: not for the faint of heart)

- drunkenness - falling down drunk/dizzy, I doubt at this point I could pass a roadside sobriety test.
- vision changes - to the point that my optometrist will not give me a new prescription because the change has been "too drastic"
- constipation - went from 2 cups of coffee being enough for a BM each day, to now taking fiber supplements at 6x recommended dosages, plus stool softeners with laxatives daily, and still only go once every 6-8 days on average (yes, I drink plenty of water)
- sleepiness - I have yet to make it through an episode of CSI. It seems if I stop moving, i sleep.
- Interaction with opiods. For a cough i had some codine-type syrup. Made me so dang hyper I could not sleep.
- Weight gain... omg... I am living on a 900-1200 calorie diet with as much exercise as I can manage and still not losing weight. It is unreal!

Too Sweet 74
06-10-2006, 02:47 PM
Kaelie,
I was wondering what happened to you to bring all of this about ? I just started Lyrica a few days ago and I don't like the way it makes me feel but my doc wants me to give it a try for at least a week to see if have improvement. The side effects scare me too. It seems that ,with me at least,the docs are just throwing pills at my problems hoping to get something that MAY help without knowing the problem. I am hoping that you find the answers to your pain and feel better soon. Till then hang in there ,you are not alone......
Sherri K.

~Kaelie
06-10-2006, 03:34 PM
ugly story :(

Last April, while trying to get a referral for a new neurologist to prescribe me my epilepsy medication after my insurance company switched over and stopped covering my old neurologist, I decided to have a bothersome mole removed by my GP so as not to waste the visit simply for a referral. (I am such a pennypincher!)

The mole turned out to be malignant melanoma. The diagnosis came on my 4th wedding anniversary.

Surgery was performed on May 23rd. They removed lymph nodes, and a section of skin roughly 14 inches long and 4 inches wide (at the widest point). The very odd location of the melanoma left a very odd scar... Women will understand this description better than men, but here goes... the mole was situated on my hip/upper thigh/side, right where the three seams meet on the leg of "granny panties". LOL The surgery left a scar that is 14 inches long that goes from (picture yourself wearing tight jeans to imagine this) the lowest part of the front pocket, around the side where that underwear line would be, to the top of the back pocket. It looks horrible, but that is the least of my worries...

Around late July after many visits back to the surgeon telling her that I was still unable to put any pressure on that side, i noticed that the previously "numb" section of skin was oddly sensitive. One particular instance I remember was when we were fooling around with cardboard "swords" while assembling a basketball goal and my son swatted my hip with no more force than one would swat a baby's bottom... but it brought me to my knees in tears. There was also a fairly large lump (about the size of a 12-oz can of soda) just below the scar.

I had been to the surgeon only a week before and been told "everything is fine. you have a little fluid build up, but that should go away." I knew it was time to visit my GP again.

I put it off a few weeks still thinking that it would get better on its own, and finally went in early september. He gave me cortisone shots into the scar. By a few hours later I was screaming at my husband to "DO SOMETHING!!!!" Poor guy never knew what hit him... I was in terrible pain. It felt like lightning striking my hip every few seconds. The next day I went back and got Lidocaine patches.. and so began my quest for relief

The GP sent me back to the same surgeon again in October for a second surgery. She removed another section of skin (4" x .5") and said that it was a "one-in-a-million thing" and that I should have no further problems now. She said that the nerves had become spiralled instead of growing back together properly.

WELL!

First visit post-surgery... all ok... still swollen really bad and I associated the pain with typical post-surgical pain.
Second visit.. The lightning-pain was beginning to return. the swelling had not gone down any. I reported everything to the surgeon.

In December I went for a CT scan. From that the surgeon determined that there was 30cc of fluid in the wound and drained it in a subsequent appointment. Her comment following the procedure made me so angry.... she said "the amount of fluid i drained is disproportionate with the amount of pain you say you are experiencing"

no ***** sherlock!

I felt like responding "well then you'd better stick that needle into my head and pull something out of there since that is where you think the pain is"...... but i didn't... i should have though!

She then started mumbling something about "pain management". She was writing me off... She had done everything surgically possible to fix me??? wth???

I went home with a "I'll show her... I'll show them all !!" attitude. I stopped using the patches, I stopped taking any pain pills. (I had a tonne of them stockpiled from the surgeries since i hate taking painpills) I spent 2 months in misery. In late January, my husband had had enough. my depression was out of hand, i was not sleeping, my day consisted of laying on the sofa exhausted and crying and there was nothing he could do. He finally convinced me that he thought my pain was real, and because he thought so, a doctor might think so too.

I went back to my GP. He gave me Lyrica, and a refillable script for Lidocaine patches. It was more of a relief to be believed. But, whaddya know, back on Jan 1st, insurance company changed again, and I never needed that original referral to a neurologist (which I never did get because of everything else) My GP told me to go back to my old neurologist and explain the story. I did, and was given refillable lyrica.

The neurologist also said I should go to pain management... i blatantly told her that I was not ready to be written off. She suggested that I research "diabetic neuropathy". weird. I am not diabetic. I know exactly what that is and this it ain't.

By this point, the pain is not just around the scar area... All the way down the back of my leg hurts now and halfway up my butt-cheek. I can't sit properly. The skin hurts to the point that clothes hurt. Air hurts. I hate when the kids are home... it means I have to get dressed.

Now, i'm none too happy about being on any pain meds at all to begin with. I hate taking anything! I feel so dopey... I used to have an IQ of 168... I don't feel that bright anymore. I'll ask the kids the same question 5-6 times within an hour and get the same answer each time... they think I'm trying to trip them up when in reality I just don't remember asking the question. It's maddening!

whew.. i really need to copy/paste this tale into a msword document so I don't have to re-type it each time!

Too Sweet 74
06-10-2006, 10:57 PM
Wow Kaelie you have really been thru the wringer !!! It is just amazing how one simple thing can lead to such dramatic events in our lives. I really pray the best for you and hope you somehow get better. I Was just put on Lyrica to see if it helps me. I too hate taking pills. I went from taking a tylenol once maybe a month maybe to tramadol and lyrica. I hate it. The docs seem to just throw pills at the problem in my case. There is no surgery to help the nerve damage I have in my arm but the EMG damage to my neck has to have an answer or treatment of some kind. I have headaces every darned day among other problems.Hard to concentrate alot of times. A good nights sleep just doesn't happen anymore . I understand the "in your head " thing completely. Been there too. Even got that from the women I worked with.One asked me if it wasn't from problems at home.LOL I have a visible lump from the EMG injury too. You can only hope for them to have a pain experience in their lives so they know how it feels.Nothing serious,just long enough to know what it's like. I miss being able to do everything for myself too. Like carrying the stuff for the garden,soil,mulch ect. It added satisfaction to the project somehow. Now I have to have someone with me to go shopping because I can't steer the cart by myself anymore. My five year old does that for me at times. I hate it.I'm amazed at what I've lost and the effect of my pain on my family and friends. I injured myself at work.I worked at a college near me. I was doing housekeeping part time. Not a great job but a way in to the college.If I could go full time I could go to school there at a huge discount and that is what I wanted more than anything.I wanted to get an art degree and possibly teach art to grade school children. My passion was painting and have lost that abaility. I tried since being injured and had too much pain. Like I said just one little event.....all I did was smack my elbow on a metal wall cabinet...... I had to laugh when I read the narrative my doctor wrote for my lawyer. It said I could maybe have a sedentary job with minimal arm use...LOL Any suggestions ? LOL

Kaelie Hope the best for you....You deserve it..... Take care......Sherri K

~Kaelie
06-11-2006, 08:05 AM
LOL

sedentary job with little arm use? hrmmmm...

how about one of those people we call for customer service at our insurance companies? I know they can't possibly be typing with more than 1 finger! And I bet you don't need more than a 2nd grade education to say "i'm sorry, we cannot help you with that". :D
It's good when you can keep your sense of humor intact through it all, Sherri... That is priceless... don't let them take that from you.

Forgive me but I'm not up on my acronyms... What does EMG stand for, and how did that cause a lump? My "lump" has no reason to be there according to every doc i've been to, and some don't even acknowledge its existance. It's high enough up on my thigh that I'm not the type person to show that much leg publicly I usually have a Lidocaine patch on it and that tames the pain a lot more than the Lyrica

We're hijacking this Lyrica thread y'know... LOL :nono:

I met my neighbor yesterday... happens that she is an RN and former headache sufferer. She was telling me that her neuro "just kept pushing pills at the problem" and that after she took her health into her own hands and a CT was finally done and a bone spur was discovered, surgically fixed and all headaches went away.

MORAL OF THE STORY: if you don't think you are getting the care you need/deserve, find a doctor that will give it to you.

Best to you Sherri, and to all lurking around here :wave:

Too Sweet 74
06-11-2006, 12:38 PM
Hi Kaelie,
Sounds like you have met one of those wonderful(?) claim people.LOL I hope mine gets some poetic justice someday.LOL I have no idea how they can treat people that way. This is my first time dealing with comp and it has not been good .LOL
To answer your question about the EMG , it is a diagnosing tool for nerve damage. They stick these needles in you and wiggle them around to get a good signal from your nerves.Depending on that signal as to if your nerve is damaged or not.I went thru it twice :( . Once just one one side at the beginning of my adventure and again about six months later. The second was bilateral,didn't know it was going to be till I was on the table either.Bilateral means they do both sides. The firts time I had three needles in my neck, this time it was six. My damaged occurred when she hit something with one of these needles. She has to put pressure on these needles to get them in your neck where they need to be,not a surface test.It hurts tremendously. I about came of the table. Never experienced anything like that. Anyway after the nearly two hour procedure was done I was supposed to work for a few hours(on light duty already for arm).I went there and showed them what had happend,I had already developed the lump,it's about two and half inches long and over an inch wide.I went home and withina few more hours the headaches started. I figured that it was normal because of so many needles and what had happened,expected it to go away in a day or so.It didn't.I contacted the people that did the test,they said see the doctor who ordered the test,they took a week to get back to me.Then they say see your own doc !! They dropped me in her lap instead of taking care of their responsibility.That was a year and three months ago.An MRI was done on my neck a few months ago finally. It showed that I had cervical spondylosis but it was not causing the problem.No bone spurs or nerve impingment at all. It did show a mass where the damage is and they think it is possibly a muscle spasm. Been thru alot,muscle relaxers at first ,tens unit,trigger point injections,epidurals,lots of steroids( had problems from that).Nothing has helped.A therapist feels that the needle struck a nerve/muscle junction. The arm is getting worse and I just feel lost most of the time. You think I'm unhappy,hubby has gotten"Not tonight Honey I have a headache"for all this time.LOL I just miss the person I used to be before the pain. Feel sorry that I put my family and friends thru my moods ect too. I don't know about you but I get angry at how I feel. Angry for needing help to do things I did by myself . I am glad I have a doc who is not giving up on helping me. I pray for better days ahead not only for me but for everyone dealing with pain .
Thanks everyone for putting up with my rambling. :) .My heart feels a little lighter in finding a place where people understand what I am going thru..... Bless you all :angel:

Sherri K. :wave:

bdlorente
06-25-2006, 04:03 PM
Hi friends with nueropathy. I have had it in my feet for several month and it is mostly awfull numbness, which makes it difficult to walk. I am now using a crutch and cane. I am on 300 mg of Lyrica and it does nothing so far for this numbness. awfully sleepy!!! anyone???N

bdlorente
06-25-2006, 04:15 PM
Hi fellow Neuropathy sufferer, our symptoms are both in the feet. Mine started in a spot on the left side of my left foot, then spread to toes & then pad of foot & then into the middle of foot. Horrible sensation. Then it jumped & spread into the right foot but not as bad but yes, so difficult to walk and so painful. It started to spread to my right leg. Lyrica did not work for me and the doctor decided that if it didn't work that the older meds wouldn't either.

My primary doc is open to complimentary medicine & so he researched & put me on an extra strong B complex & an extra 200mg. of B6. I also take a good multi with B vitamins but he said that these B vits are for nerves. He said they might not correct any damage done but might prevent further spreading

Anyway it has been a life saver. My symptoms have lessoned. Symptoms have not spread farther & there is no pain. I can walk better now. I also do stretching with the feet in & out of the pool (YMCA).

These results have made me so happy, I just wanted to share it with you! God Bless, b

bdlorente
06-25-2006, 04:18 PM
Silvio :wave:
Thanks for your response!! I haven't been on-line for a while. VERY BUSY!! The sleepiness HAS improved!! Thanks goodness. BUT, I'm having problems with my hands and feet swelling. That hasn't happened since I was pregnant. I'm trying to eat healthier in hopes of not gaining anymore weight. Thankfully I haven't gained anymore weight but I'm having a VERY HARD TIME LOSING weight! :eek:

The Lyrica does help the nerve pain shooting down my leg, but it does nothing for the numbness around my knee. But now my right hip and tailbone are killing me. The Lyrica doesn't take away the pain I'm having from this so I know it's not nerve related, but I wish I knew what it was. It's driving me CRAZY!!! :eek:

Anyway, thanks again!!!!!

Shimz
06-27-2006, 05:16 PM
Today I got diagnosed with post herpetic Neuralgia. PHN and PN. I am having an emg and 2 more MRi's Thoracic and LS Spine I think it is spelled Thoracic unless I spelled it wrong. I was also given samples of Lidoderm patch and Lyrica pills.

I had shingles last june and just had them again this june. Reoccurence of shingles.

Anyone know what other test are there for MS? What else should i be tested for something is seriously wrong with me. I am searching for an answer





Site owned and operated by HealthBoards.com (TM)
Copyright and Terms of Use © 1998-2009 HealthBoards.com (TM) All rights reserved.
Do not copy or redistribute in any form!