"Donna G" wrote in message
news:20337-51...@storefull-3173.bay.webtv.net...
Trust me, any type of arthritis in the neck/spine can give numbness,
tingling, and affect a whole lot more than just the spine/neck.
I do trust you, Donna. I can believe it.
You have to remember that all the nerves in the body run through our
spinal column, so if there is inflammation, swelling, etc in the
spine/neck, it really can play havoc on just about any part of the body.
I understand. I've had the tingling and numbness for quite awhile now. the
oa wasn't bothering me until a few days ago, I mean in the neck and back.
The thing with arthritis, is that you never are fully without pain and
there will be flare ups and such from time to time that can leave you
fairly miserable. We all have different things that seem to help when
we are in a flare up.
Yes, I understand that too and that's what is so hard about having it.
For some, ice helps, for others, heat helps. Some do better with rest,
while others do better with moving a bit. A warm shower can help
relieve the muscles a bit from being so tight.
the warm shower seems to help, but this morning I hurt so bad that it didn't
do much. it hurt when I washed my hair, etc. any lifting up of the arms or
bending down was soooo painful. I know you already know that. I also tried
the heating pad on my neck, but the pad is so large and my hands and arms
hurt so much that I couldn't hold it there. anyway, called my pdoc crying
and he was going to see me at 4:15, but then a patient cancelled and his
recep called us earlier to come in. he is sooooo sweet. he gave me a
script for a pain med. just ate and took it and we'll see what happens. I
wrote two emails to my GP's office requesting an appt. ASAP. he'll return
this tues. so I'll see what happens. I'll always keep you updated. :-)
Not a lot can help with the numbness and tingling unfortunately.
I know that too. that's why we think there is more to this than oa. there
has to be!
We always tend to want immediate relief, and sadly, with arthritis there
often isn't any immediate relief. You learn as you go what things
trigger flare ups and what things seem to help flare ups for you. It's
such an individual thing often times.
Yes, I get that too. it's hit or miss, sort of. remember I told you way
back that I suddenly out of the blue became intolerable to sugar, sugar
subs., gluten, and lactose? some times I get a trigger from eating one of
those, but I can't help it. I am so skinny and weak that I have to eat.
the store near us (we walk - no car) has had gluten-free bread and muffins,
but for the last two weeks or more, they didn't get them in stock so I had
no choice but to eat a regular bread sandwich and regular muffins. so maybe
that combo gave me a flare up too. I just don't know anymore. I need more
tests and I will get them. my new, young GP will see to it, I'm sure. :-)
my new internist may do the same thing.
As far as peripheral neuropathy, that is a nasty thing to have and no
real treatments at all that work consistantly.
Yes, I believe that also. especially here in canada. if I were back home,
there *might* be a chance there'd be a med for me to help, but not here.
Hope your pain eases, Diane, and tomorrow brings a better day.
thank you so much donna. you are so sweet and kind. today was just awful,
but at this very minute, it is not so bad. maybe the pain med is starting
to kick in. so far, I've been able to type, which is a good thing. take
care of yourself too.
gentle hugs,
diane