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Pain?

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Hi,

How many of you suffer from physical pain? What are the causes of your pain?

What do you think would be the top common causes among us SMA'rs? How many

of you have some pain almost as a daily occurrence? Where and when do most

of you experience your worst pain?

I have pain in both legs at night and lower back and many nights my right

arm from elbow to knuckles depending on which position I sleep in. It can be

very painful. I wondered if it could be pinched nerves, but then I also have

some early to moderate osteo-arthritis. I find that if I lie on my left

side and put my knees together that I get pain in my left knee which then

spreads down the leg into the foot. It's almost like the pain is caused by

the weight of one knee resting on the other? Has anyone else experienced

this? Could it be caused by lack of muscle causing the nerves to be closer

to the surface? I also wake up during the night with strong pain in my right

arm if I lie on my back. This pain starts in my elbow and runs down the top

of my arm to the knuckles. The pain is so bad that I can barely bend and

straighten my arm.

Just curious. I am hoping to see a neurologist soon!! But, he knows less

about SMA than I do!!

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The pain I experience seems to come in two different forms.

First, I have pain from getting stiff, sitting all day in my

wheelchair. If I accidently bump my toes against something and get my

feet 'out of alignment', I get an ache in my knees especially. I

often 'reposition' my feet throughout the day by catching the toe of

my shoe on something to either turn my feet in or out. Sometimes my

legs also get slight spasms if they are in the wrong position for too

long. My lower back also gets stiff when I switch from a sitting to

supine position.

Second, I get nerve pain. There have been a couple times I have

pinched a nerve in my lower back/upper left leg. It was

*excruciating* to switch from a sitting to lying position or visa

versa! (I actually was prescribed a muscle relaxant for this

condition once, if you can imagine.) I often hurt nerves by resting

elbows or knees on surfaces that are too hard for too long. If this

happens, the affected limb starts to 'fall asleep' and then shooting

pains flash up and down it until I reposition.

Jenn

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I am in a lot of pain, all the time. i have chronic abdominal pain on my

left side since 99. they arent sure why but relate it to my scolosis and slow

motility in my intestines. i take narocotics for this pain, that is how severe

it is. i have not heard of many smaers with my type of pain. i also have bad

neck, leg, arm, and back pain. i did not have spinal fusion or rods put in

my back so i am very contracted and curved. right now i am having problems

w/my left side mostly falling asleep, paralyzing, and cramping up. this is in

my

hand and left side of face. sometimes it gets so severe my eye twitches, my

left hand will not open and hurts, and my mouth does not open well and i can

not speak well. we arent sure if this is from an electrolyte imbalance. if

anyone else experiences this please contact me. thanks.

kimi

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Guest guest

Kimi -

I wouldn't say it is a chronic situation with me, but I have from time

to time experienced crushing abdominal pain. I have rods on my spine,

but if I'm leaning totally incorrectly in my wheelchair when eating,

it almost feels like the food I'm trying to digest " gets stuck " . No

amount of antacids or the like seems to even touch the pain. I just

have to sit in pain until it goes away, and no matter how I'm sitting

or laying down, I'm practically writhing in agony!

I also get symptoms like these with the stomach flu sometimes. It

gets so bad, I'll pray to barf just to relieve some of the pressure.

But I never can. I think I've lost the muscles to barf. Weird, huh?

Jenn

> I am in a lot of pain, all the time. i have chronic abdominal pain

on my

> left side since 99. they arent sure why but relate it to my

scolosis and slow

> motility in my intestines. i take narocotics for this pain, that is

how severe

> it is. i have not heard of many smaers with my type of pain.

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Guest guest

Have you tried antigas pills? Sometimes gas pain, is just that very painful

and doesn't always pass very well especially for mobility impaired

individuals. You may also want to discuss with the docs the possibility of

other organs pushing on the gastro track which may also cause that " getting

stuck " feeling.

Beth T. the OT

Re: Pain?

Kimi -

I wouldn't say it is a chronic situation with me, but I have from time

to time experienced crushing abdominal pain. I have rods on my spine,

but if I'm leaning totally incorrectly in my wheelchair when eating,

it almost feels like the food I'm trying to digest " gets stuck " . No

amount of antacids or the like seems to even touch the pain. I just

have to sit in pain until it goes away, and no matter how I'm sitting

or laying down, I'm practically writhing in agony!

I also get symptoms like these with the stomach flu sometimes. It

gets so bad, I'll pray to barf just to relieve some of the pressure.

But I never can. I think I've lost the muscles to barf. Weird, huh?

Jenn

> I am in a lot of pain, all the time. i have chronic abdominal pain

on my

> left side since 99. they arent sure why but relate it to my

scolosis and slow

> motility in my intestines. i take narocotics for this pain, that is

how severe

> it is. i have not heard of many smaers with my type of pain.

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  • 6 years later...
Guest guest

Meg,

Please don't assume people are uncaring about your stuggle with pain.

I didn't respond because I have no experience with the drugs you were asking

about. I think pain is a common experience for many of us whether or not we

respond to your specific questions. Some people may choose to be private, while

others may not have discovered a solution worth sharing.

I hope you find relief soon.

Alana

>

> I guess since my post asking for advice regarding chronic pain medication

> got no response, I'm the only one suffering from pain.

>

>

>

> You guys are lucky.

>

>

>

> God Bless,

>

> Meg W.

>

>

>

>

>

>

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