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my understanding is that the inflamed synovial fluid begins to gel, thus

causing the stiffness. As you move around, it thins out. That's my

understanding for what it's worth.

Mark

rheumatic Stiffness

> From: Anihan@...

>

> Has anyone gotten an answer from a Doctor as to why RA causes such

stiffness

> during sleep, and prolonged periods of inactivity? I have asked 3 Drs.

and

> none have an answer only saying it is a symptom of the RA. I never had it

in

> the early years of my RA or during 13 and 1/2 years on Mtx but since

quitting

> it my stiffness is horrendous.

>

> Could it be the Fibromyalgia that came on later?

>

> Anita

> RA 26 years, Fibro, AP 17 months.

>

> ---------------------------

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  • 2 weeks later...
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In a message dated 7/18/99 10:29:44 AM Eastern Daylight Time,

LCARROLL@... writes:

<< I am scared to death over this . I feel the doxi must be accelerating this

disease since I have never had any night stiffness or day stiffness before

the AP.

>>

Hi ,

I too have experienced stiffness for the first time after going on the AP.

Also I have joints involved that have never been inflamed in 26 years with

RA. I now have inflammation and deformity in the knees. Stiffness and pain

in the elbows, hips and ankles. Hips could be deformed but who can see the

hips joints? (LOL.) I am not as stiff as I was 2 months ago. My steps are a

bit faster than Tim Conways now in the mornings.

Shoulders, hands and wrists have been my pain nemesis all these years. I am

seeking a new Dr. (end of August) and am hoping she will work with me and the

AP. I apparently need IV's or minocycline killers already. The Minocin is

not doing it.

Take care, and let's both hope we all get better SOON. I do mean ALL of us.

Hugs, Anita

RA 26 years, Fibro, AP 17 months

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In a message dated 7/18/99 2:47:18 PM Eastern Daylight Time,

jkirsten@... writes:

<< Perhaps even the fact that

our bodies do their healing at night has something to do with it. >>

Hi Jan,

Boy the above statement is a new one for me. Never heard that before. What

I have heard, is that everything slows down at night, even our endorfins are

not as active at night, hence the pain. Wonder why a baby always cries at

night and wakes up Mom? LOL

Anita

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In a message dated 7/18/99 3:34:20 PM Eastern Daylight Time,

jkirsten@... writes:

<< Specifically, tissue repair occurs during a particular phase of our sleep.

Stage

II has some, Stage III has more, and Stage IV is when it's maximized. >>

If that's REM sleep, well I'm not getting any. How about all of us? Don't

suppose any of us are with the pain we're in. No wonder we hurt, huh?

Thanks, Jan,

Hugs, Anita

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Hi ,

About the only thing I can tell you is that I have been through phases like

this and likely will again. I'm not going to claim to be in remission, but I am

in a vastly improved state at the moment. And before I got here a couple of

weeks ago I was having reasonably good days and nights just like you're

describing. Waking every couple of hours completely locked up in my joints and

back and just flaming pain through them, in my case my heels, elbows and

shoulders. I haven't really puzzled any kind of a theory about it. Perhaps its

a time when the body's doing some major kicking of the bugs. Maybe it's just a

time of unusual high accumulation of the toxins or dead bugs in the joints

since we aren't moving or flushing them with water. Perhaps even the fact that

our bodies do their healing at night has something to do with it. The hope I

can give you is that it did come to an end and over the course of a week or two

the night pain and sleep problems went away too.

Best - Jan K

M Carroll wrote:

> From: M Carroll <LCARROLL@...>

>

> Hello all,

>

> I would like to address a question to those who feel they are in remission

> or close to remission or just to anyone who is going through this.

>

> THough my day pain has vastly improved, my nights have become sheer terror.

> Before the doxi I never had any stiffness or pain when sleeping ( or

> stiffness during the day either) Now when I wake in the middle of the

> night, my elbows, shoulders, and knees ( especilly the knees) feel like

> they are cemented together. When I try to straighten my knees or bend them,

> they are " stuck " . I almost can not move them. When I do get them to move,

> the pain is so great I feel as if I am going to pass out.

>

> Is this unusal or just part of the treatment? By day, I am doing pretty

> much anything I want to, but by night I am getting worse and worse.

>

> I am scared to death over this . I feel the doxi must be accelerating this

> disease since I have never had any night stiffness or day stiffness before

> the AP.

>

> Any thoughts are appreciated very much.

> Thanks!

>

>

>

> ---------------------------

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Hi Anita,

Specifically, tissue repair occurs during a particular phase of our sleep. Stage

II has some, Stage III has more, and Stage IV is when it's maximized. I haven't

a clue if it's related to the discussion, but that's the bottom line of the

research I found when I was investigating fibromyalgia. It's why the lack of

sleep so common in fibro is believed to leave folks in so much pain. The daily

maintenance of cellular repair and replacement supposedly aren't taking place,

causing increasing pain as the lack of sleep continues. At least that's my take

on it, more or less, without looking it all up again. Liz may have something

more specific to say about it.

HTH - Jan K

Anihan@... wrote:

> In a message dated 7/18/99 2:47:18 PM Eastern Daylight Time,

> jkirsten@... writes:

>

> << Perhaps even the fact that

> our bodies do their healing at night has something to do with it. >>

>

> Hi Jan,

>

> Boy the above statement is a new one for me. Never heard that before. What

> I have heard, is that everything slows down at night, even our endorfins are

> not as active at night, hence the pain. Wonder why a baby always cries at

> night and wakes up Mom? LOL

>

> Anita

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http://www.geocities.com/HotSprings/6028/drugs.htm

Here's a link that talks about stage 4 sleep and drugs which may

interfere with it. Although there are many theories as to what is the cause

of fibromyalgia, and what can help it from what I've read so far, the one

thing that most all seem to agree on is that sleep disturbance is a major

factor. For me, sleep disturbance has been a big part of RA flares also. I

have read that the same cytokines that are involved in inflammation can

affect sleep as well.

For me, stiffness has always been a sign of an impending RA flare. First

overwhelming fatigue and feverishness, then stiffness, then joint pain and

inflammation. Morning stifness was one of the first things to improve on the

AP for me. Maybe you need to think of trying another variation of the

antibiotic, or IV's now. I hope you both find something soon to help you. It

is so very frustrating to go through setbacks once you have had some

improvement, and have gotten a taste of the good life! Liz G

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" Liz G. " wrote:

>

> Here's a link that talks about stage 4 sleep and drugs which may

> interfere with it. Although there are many theories as to what is the cause

Interesting...

Anything on items which may enhance and/or prolong Stage IV sleep?

--

Regards, -----------------------

Geoff Crenshaw ** Usual Disclaimers **

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

Religion: Man's attempt to discover God

Christianity: God's offer to save humankind

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Hi ,

I too went down hill fast on Dioxy--try a different antibiotic ASAP. It put

me in a major setback. I know Dioxy works for great for some but for the rest

of us...it's bad news IMHO.

L

RA 9 yrs, 7 yrs antibio (currently Minocin and Biaxin--very slowly improving)

In a message dated 99-07-18 14:47:18 EDT, you write:

<< Hi ,

About the only thing I can tell you is that I have been through phases like

this and likely will again. I'm not going to claim to be in remission, but I

am

in a vastly improved state at the moment. And before I got here a couple of

weeks ago I was having reasonably good days and nights just like you're

describing. Waking every couple of hours completely locked up in my joints

and

back and just flaming pain through them, in my case my heels, elbows and

shoulders. I haven't really puzzled any kind of a theory about it. Perhaps

its

a time when the body's doing some major kicking of the bugs. Maybe it's just

a

time of unusual high accumulation of the toxins or dead bugs in the joints

since we aren't moving or flushing them with water. Perhaps even the fact

that

our bodies do their healing at night has something to do with it. The hope I

can give you is that it did come to an end and over the course of a week or

two

the night pain and sleep problems went away too.

Best - Jan K

M Carroll wrote:

> From: M Carroll <LCARROLL@...>

>

> Hello all,

>

> I would like to address a question to those who feel they are in remission

> or close to remission or just to anyone who is going through this.

>

> THough my day pain has vastly improved, my nights have become sheer terror.

> Before the doxi I never had any stiffness or pain when sleeping ( or

> stiffness during the day either) Now when I wake in the middle of the

> night, my elbows, shoulders, and knees ( especilly the knees) feel like

> they are cemented together. When I try to straighten my knees or bend them,

> they are " stuck " . I almost can not move them. When I do get them to move,

> the pain is so great I feel as if I am going to pass out.

>

> Is this unusal or just part of the treatment? By day, I am doing pretty

> much anything I want to, but by night I am getting worse and worse.

>

> I am scared to death over this . I feel the doxi must be accelerating this

> disease since I have never had any night stiffness or day stiffness before

> the AP.

>

> Any thoughts are appreciated very much.

> Thanks!

>

>

> >>

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>Anything on items which may enhance and/or prolong Stage IV sleep?

Many fibro. patients use low-dose anti-depressants to assist with stage IV

sleep. The same inflammatory reactions that cause swelling can also affect

sleep, so if you can get the general state of inflammation down in the body

it should help as well. Sleep disturbance, which has been a lifelong problem

for me, improved a great deal when I started to respond to the AP. Liz G

PS Ambien, a non benzodiazepine sedative-hypnotic seems to be one which is

mentioned over on alt.med.fibromyalgia a lot as one which is especially good

for sleep disturbance, and amitriptyline, an anti-depressant is also often

used.

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  • 2 months later...

what form of arthritis were you diagnosed with? Must not have been RA,

cause morning stiffness and stiffness after sitting is pretty much a major

trait of that particular form of arthritis.

Mark

rheumatic stiffness

> From: M Carroll <LCARROLL@...>

>

> Hello group,

>

> There have been many wonderful improvements since starting the protocal

but

> I have one thing that did not happen before antibioitics that is happening

> now...STIFFNESS!I never had morning stiffness or sleeping stiffness until

I

> started Doxicycline. I evne get stiff if I take a short nap.

>

> While I sleep the joints in my knees seem to cement together and it takes

> all my might to move them and when I do it feels like they have been hit

by

> a hammer!

> My shoulders are stiff, and the elbows but to " unstiffen " them doesn't

> require this much effort or pain.

>

> Is there damage being done unbending the knees to have such horrible and

> excrutiating pain? It make me feel as if I am going to pass out!

> Does anyone else experience this? Thanks!

>

> I did stop prednisone this weekend and I haven't seemed to have had any

> more stiffness or pain than usual. But I guess 1 mg wasn't doing all that

> much anyway.

> Any suggestions or input would be mucho appreciated!

>

>

>

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,

Skip's first symptom of the RA was stiffness. It got so bad in 1988 that we set

the alarm to go off 2 hours before she had to leave for work so she could try to

get loosened up enough to work the gas pedal and brake pedal on the car. For a

while she woke me up to help her to the bathroom if she needed to go in the

night. Then the Dr. prescribed the Prednisone. The very next morning she woke me

up at 4 a.m. to show me how she could dance around the bedroom. It had to be a

miracle drug we thought. After a couple of years of high doses of prednisone we

discovered a lot more about the drug and she slowly weaned herself off it and to

this day will have nothing more to do with it. As she got off it, the stiffness

returned. She still has the morning stiffness, although not nearly as bad as in

'88, and after a couple of hours of riding in the car takes a while to loosen

up. We figured that the stiffness was one of the first signs of the RA and will

probably be one of the last to go. The stiffness you have was probably masked by

the prednisone. We don't know if it will ever disappear completely but she is

very much improved. Especially in the endurance area. The last month has been a

real trial for her ( her brother had a triple bypass and her mother has severe

back problems) and she has physically held up better than we had ever hoped for.

Maybe someone else in the group can answer the question about the stiffness

disappearing as the AP does its job. We can only pray for that to happen. Hang

in there.

Denny and Skip

RA-12yrs

AP-14months

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Thank you, . You reminded me that back in the " bad " old days Skip took

cyclopenzaprine (Flexaril) and it helped. The only complaint she had was of

feeling sort of out-of-it the next day. I will remind her when she calls,

tomorrow, about taking it for the stiffness again.

Denny

rheumatic RE:Stiffness

,

Skip's first symptom of the RA was stiffness. It got so bad in 1988 that

we set the alarm to go off 2 hours before she had to leave for work so she could

try to get loosened up enough to work the gas pedal and brake pedal on the car.

For a while she woke me up to help her to the bathroom if she needed to go in

the night. Then the Dr. prescribed the Prednisone. The very next morning she

woke me up at 4 a.m. to show me how she could dance around the bedroom. It had

to be a miracle drug we thought. After a couple of years of high doses of

prednisone we discovered a lot more about the drug and she slowly weaned herself

off it and to this day will have nothing more to do with it. As she got off it,

the stiffness returned. She still has the morning stiffness, although not nearly

as bad as in '88, and after a couple of hours of riding in the car takes a while

to loosen up. We figured that the stiffness was one of the first signs of the RA

and will probably be one of the last to go. The stiffness you have was probably

masked by the prednisone. We don't know if it will ever disappear completely but

she is very much improved. Especially in the endurance area. The last month has

been a real trial for her ( her brother had a triple bypass and her mother has

severe back problems) and she has physically held up better than we had ever

hoped for. Maybe someone else in the group can answer the question about the

stiffness disappearing as the AP does its job. We can only pray for that to

happen. Hang in there.

Denny and Skip

RA-12yrs

AP-14months

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  • 6 years later...
Guest guest

Hi All, I've been reading posts here for about 3 years (and occasionally

participating). Something caught my eye when I read Gayle's letter to the group.

It was about stiffness ....and even though stiffness is discussed

frequently... and I hope this hasn't been discussed at length also..(MS brain

you know)...

I'm wondering why stiffness would appear or increase due to taking

LDN..Endorphin production doesn't relate to stiffness does it ?

I've mentioned before that I happen to be someone who has continued to

take LDN only as a cost effective anti-depressant...since I seem to be one of

those few where it has not stopped my " progression " nor caused any positive

change in me except for mood (not a small thing).. At this point, I'm trying to

recall if the stiffness which is always with me, began when I began taking LDN.

(Note: a diary would be a great idea). Am considering going back to Prozac

after reading Gayle's letter. Any thoughts on this would be appreciated.

Take care,

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  • 4 years later...
Guest guest

How about fish oil?  I take 9000 mg daily and swear by it, even tho the docs

don't agree!

Terri LN Ireland

From: Cooky Stonkey <cookee1@...>

Subject: RE: rheumatic stiffness

rheumatic

Date: Friday, March 18, 2011, 5:07 PM

 

Not really. But thanks

Subject: Re: rheumatic stiffness

cooky, does hot tub or sauna help you? sally

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If you are not already taking Omega 3's, fish oil or krill oil you could try

that

Kinga

rheumatic stiffness

Anybody have a supplement or vitamin that is for stiffness? Right now my

body is so stiff (legs a lot more) and I stretch but it does no good.

cooky

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Just thought I would throw in here what I know about getting rid of Omega 6

(other than to give up everything you like eating)!

What you can do is to get more omega 3 into you to offset the fact that you have

too much omega 6, and distilled fish oil supplements provide the best source.

If they are distilled they will be free from any harmful toxins like the heavy

metals and PCB's found in fresh fish and be concentrated many times over in

omega 3. I used to use a supplement high in DHA (an important fatty acid), the

body converts it into a powerful anti-inflammatory chemical called Resolvin D2

to protect you from heart disease, lower cholesterol and relieve the symptoms of

arthritis. DHA is also the main fatty acid found in the brain and helps to

ensure proper functioning and research suggests it can help you to avoid

degenerative neurological conditions like Alzheimer's and Parkinson's.

Maz

PS : If you don't want to take a supplement 'cold-water oceanic fish oils' are

rich in DHA, so eat plenty of them!

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