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Medical Forum / Diseases and Disorders / Arthritis / April 2006

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tingling in hands and feet

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Becky - 22 Apr 2006 04:51 GMT
How many people with RA suffer from tingling of the hands and feet and
around ankle and some in the calves, my doctor doesn't seem to think that is
part of RA but what I have read it seems like it could be.
Does anyone else have these problems and if so what has helped?
Thanks
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vickie b. - 22 Apr 2006 05:20 GMT
I have this too but it is always tracked down to a separate cause.  In
both cases it is due to pinched nerves.  In the hands it can be carpal
tunnel syndrome and in the feet it's tarsal tunnel syndrome.  I had
surgery last year on my right foot to relieve the pressure of the
tarsal tunnel just like the surgery for carpal tunnel.  This is not
really RA but a secondary effect of the RA.  

Take care,

Vickie B.
Becky - 22 Apr 2006 15:46 GMT
Vickie,
Thanks for the info, I am sure part of it is the RA, when I get up in the
morning it is like before I took meds, ankles are still, hips joints ache,
wrists feel tight and neck can hardly bend , the doc had said he was going
to give me prednisone to try a couple days of to see how I would feel but
now since this mri was down he mostly is holding off on everything till I
see the neurologist except he raised the mtx.
Thanks again
Becky
>I have this too but it is always tracked down to a separate cause.  In
> both cases it is due to pinched nerves.  In the hands it can be carpal
[quoted text clipped - 6 lines]
>
> Vickie B.
Nann Bell - 22 Apr 2006 15:17 GMT
My dad had tingling and pain in his feet.  A podiatrist tracked it down ot an
inflammed tendon in his ankle and fixed him up with a couple of pred shots in
the ankle.  Daddy had RA and I've always assumed the inflammation was
connected.  YMMV

Also, there is a fairly high incidence of carpal tunnel problems in folks
with inflammatory arthritis, presumably because we have greater inflammation
in our wrists than the general public.  I've been there and had great success
with the surgeries.

If you suspect something like that is going on with your hands and feet, you
might ask the neurologist if it would be worth doing EMGs to check out the
nerve conduction in those areas.  I warn you though, some of us have found
the testing painful.

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Thumper - 22 Apr 2006 16:39 GMT
>My dad had tingling and pain in his feet.  A podiatrist tracked it down ot an
>inflammed tendon in his ankle and fixed him up with a couple of pred shots in
[quoted text clipped - 5 lines]
>in our wrists than the general public.  I've been there and had great success
>with the surgeries.

I have Carpal in one hand due to RA but I won't have surgery.  The
inflammation will go elsewhere eventually and the tingling will stop
as it has in the past.  Sometimes it takes a few months but icing and
resting the wrist seems to work.
Thumper
>If you suspect something like that is going on with your hands and feet, you
>might ask the neurologist if it would be worth doing EMGs to check out the
>nerve conduction in those areas.  I warn you though, some of us have found
>the testing painful.
Cindy - 22 Apr 2006 19:17 GMT
Becky, I don't have RA, but when the doctor put me on Topomax for my
migrains...this has been a side effect of that medication...
So maybe some of the medications that are given for RA can cause the
tingling...Just a thought...
Hope you find some answers...
Hugs Cindy
> How many people with RA suffer from tingling of the hands and feet and
> around ankle and some in the calves, my doctor doesn't seem to think that
[quoted text clipped - 4 lines]
>      ­­
>      ­
Becky - 23 Apr 2006 01:17 GMT
Thanks Cindy,
I have asked about meds and the doctor and pharmcy guys say no.  I just got
back form being gone for 6 hours, and my poor feet are killing me, I wore
the tennis shoes and the orthodcis, the ones I worse for a long time, the
new ones are to big, anyway I am more convinced then ever it is the stupid
orhtoidcs, my back is killing me and my the right side of my ankles fill
like a knife is going thru them, that can't be the RA in the back, who knows
but it has been over a year now that I have had this and I am so SICK and
tired of each doctor having a new version and you try and and nothing, I go
back to the podiartist on Monday and he already said gee my martharon
runners wear those orthodics so don't see why you can't, gee I don't think I
am a marathon runner, they are made out of hard plastic and my arches and
heels are very sensitive and don't need to walk upon cement!! Sorry to be so
grouchy just plain tired of it all, they tried to make me a softer pair but
they were so bulky they were ridiculous!!  I tired on Birkenstocks today
also, but the erosions in the bottom of my big toe and side of foot made it
painful and they are not the right size the 39 is a little to small and the
40 is a little to big!
It is going to be an evening of a big pity party, please forgive me!
Thanks
Becky
> Becky, I don't have RA, but when the doctor put me on Topomax for my
> migrains...this has been a side effect of that medication...
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DianeW - 23 Apr 2006 19:28 GMT
Becky - I've worn orthotics for years. Since I was 16 in fact. Over a
year ago, I went and had new ones made. They were supposed to be the
cadilacs of orthotics. Cost a small fortune. It was the first pair I
reallly ever had to adhere to a break in schedule. After 10 months of
my feet and back hurting worse and worse I decided that it just might
be the orthotics. They were just too damn hard. I went to a local shoe
store called Foot Solutions at the advice of a friend. The man there
fitted me with a pair of off the rack orthotics well, actually -
inserts - that are made of a moldable material. As you walk they
conform to your foot and become what you need. They run about $60 if I
remember correctly. There were about 6 different styles depending on
your need which was analysed by a computerized mat that you stand on.
Within days of wearing them, the killing pain in my feet went away. I
know it's time to get new ones when the pain comes back. They did help
the low back pain some as well. I've been told that with diabetes and
also with RA, we can loose the naturally occuring fat pads on the
bottom of the foot and if you combine that with other problems I have -
FMS, MS and peripheral neuropathy - it would be hard to say exactly
which was causing the pain. The bottom like is that the new "inserts"
worked much better than the expensive dr made ones did and I'm not
stuffing my face with a new pill. If you want to try pills, neurontin
or B6 have worked for me in the past for this same problem but that's
another story.  Let me know if you want the brand name and I'll look
for the box. DiW
Chris Malcolm - 23 Apr 2006 10:20 GMT
> How many people with RA suffer from tingling of the hands and feet and
> around ankle and some in the calves, my doctor doesn't seem to think that is
> part of RA but what I have read it seems like it could be.
> Does anyone else have these problems and if so what has helped?

It could be lots of things. In my case it was peripheral neuropathy as
a result of diabetes, i.e. a result of blood sugar often being too
high for too long. Once I got my blood sugars low it started to go
away slowly, and is now all gone except for a mild residue in one
foot.

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IPAB,  Informatics,  JCMB, King's Buildings, Edinburgh, EH9 3JZ, UK
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Diane - 23 Apr 2006 14:49 GMT
becky, i've had off and on tingling in hands and feet for years. also
occasionally on one side of my face (for more than a decade),
particularly if i rub that side of my face--then i'll have a few
moments of tingling. i went through so many tests i don't remember them
all. the only thing that was discovered was a problem with the c5-6
discs in my neck, which would not cause the symptoms in both hands and
feet. my rheumy was at first concerned it was ms because i was on
enbrel when it started, but the mri was fine and i've had no
progression. as a matter of fact, the tingling's much rarer these days.
i did a lot of research on it and discovered there are a zillion
possible reasons, some benign, others not. so all this is to say, i've
had the tingling too. good luck, and i hope yours turns out to be
nothing serious.

diane
carolyn - 25 Apr 2006 09:02 GMT
Hello Becky,
I suffer with Rhuematoid and Osteo Arthritis and have the same problem with
tingling of my hands and feet.
My Rhuematologist sent me to another specialist as he thought that I may
have had the start of MS.
Thank goodness that was not the case, so I continue with the pins and
needles.
Still puzzled WHY !..........if you have any luck and find out what it is,
could you please let me know !

Best regards,
Carolyn  (from Aussie)
____________________________________________________________________________
_______________________________
> How many people with RA suffer from tingling of the hands and feet and
> around ankle and some in the calves, my doctor doesn't seem to think that is
[quoted text clipped - 4 lines]
>       ­­
>       ­
Dawn - 25 Apr 2006 12:00 GMT
Becky,
 Have you been checked for Fibromyalgia?
The sensation of pins and needles or as some people refer to it as burning
is a symptom of it.
Just a thought
Dawn
> Hello Becky,
> I suffer with Rhuematoid and Osteo Arthritis and have the same problem with
[quoted text clipped - 8 lines]
> Best regards,
> Carolyn  (from Aussie)

____________________________________________________________________________
> _______________________________
> > How many people with RA suffer from tingling of the hands and feet and
[quoted text clipped - 6 lines]
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> >       ­
Navy1 - 25 Apr 2006 22:05 GMT
I had that  so badly, I would just rub my legs.  My GP put me on 300mg
four times a day.  No problems.  I tried to cut back one pill and my
legs started burning again.  It works for me.  I haven't noticed any
side effects from it.  He called it neuropathy.  

Loujean

>Becky,
>  Have you been checked for Fibromyalgia?
[quoted text clipped - 28 lines]
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Navy1 - 27 Apr 2006 01:44 GMT
Sorry - forgot to put the medicine - Neurontin.

Loujean :-(

>I had that  so badly, I would just rub my legs.  My GP put me on 300mg
>four times a day.  No problems.  I tried to cut back one pill and my
[quoted text clipped - 35 lines]
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