I have a few problems that I'd like to know if anyone else has had them and
how they dealt with them.
For a long time I have had lots of pain under the two toes next to the big
toe on both feet. I went to a podiatrist this week to have ingrown toenails
cut out and he xrayed my feet. He said I have arthritis in my big toes
(that's news?) and that it has affected the toes next to them and that
causes the pain under my toes when I mash there, and sometimes when I'm
walking it even goes down under the middle of my foot. His suggestion was
that I buy some SAS shoes that cost only $130 per pair, and they are lace
up. With my replaced hip that I have dislocated 4 times, I need slipons and
I don't have $130 for one pair of shoes!
Then I have pain on the front inside of my arms between shoulders and
elbows. My right shoulder hurts, but I have had injections in both
shoulders within the last six weeks and my RD gave me another in my right
shoulder Thursday. Any time I reach for something or pick up something with
my right hand, the right arm really hurts. He took xrays and said the right
rotater cuff repair has disintegrated some and it looked as if one of the
bones had been shaved. The bicep tendon was ruptured when I injured the
rotater cuff. He suggested that I check back with my orthopedic surgeon to
see what he thinks. But the orthopedic surgeon is the one who took xrays of
both shoulders when he injected them about 6 weeks ago and he should have
seen any problem, but didn't mention if if he did. And he is not the one
who operated on my right shoulder; that was done in Florida before Grayson
had Alzheimers and I moved us to Alabama.
Also, I have (the RD said) bursitis in my left hip on the back side.
Sometimes it doesn't hurt at all. Other times I will hear it pop when I'm
walking and it begins to hurt any way I move, and is very sore and hurts
when I sit down. He said since I'm on prednisone all the time and have had
the shoulders injected recently plus the right one by him, that he didn't
want me to have any more cortisone right now. Even now just sitting at the
computer, it hurts.
I'm beginning to feel so much stronger since I've been on B12 shots that I
guess I'm expecting other parts of my body to go along and feel better too.
Anyone have any suggestions?
Thanks. Gwen
vickie b. - 05 Jan 2008 21:01 GMT
Gwen, the shoes may be a good investment. They will last a long time
and you can have them resoled to added life. But if you still don't
have the money, I'd pick the best lace up shoes I could find. They do
make elastic shoe strings which you can then slide your feet in and
out. Payless Shoes sell this type of strings also Academy. My Rheumy
took me out of SAS because I needed more support. Are you diabetic?
if so, your insurance may pay for a pair of shoes every year.
My rotor cuffs are bothering me too. I can't take cortisone but my
rheumy uses something else and I took one just before Christmas and
received some relief.
(((((gwen)))))
Love and Prayers,
Vickie B.
sweetpickleNO@SPAMknology.net - 05 Jan 2008 21:06 GMT
Thanks Vickie. No, I am not diabetic. I wore orthotics at one time but my
insurance at first denied paying for them. The surgeon wrote them and then
they did pay. I'm afraid Medicare wouldn't be very easy to convince!
Gwen
> Gwen, the shoes may be a good investment. They will last a long time
> and you can have them resoled to added life. But if you still don't
[quoted text clipped - 13 lines]
>
> Vickie B.
d'huit - 06 Jan 2008 23:50 GMT
Thanks Vickie. No, I am not diabetic. I wore orthotics at one time but my
insurance at first denied paying for them. The surgeon wrote them and then
they did pay. I'm afraid Medicare wouldn't be very easy to convince!
Gwen
explain your limited income situation to and tell your doctors that this is
necessary for medicare reasons --ask your orthopod or podiatrist annnnd your
rheumatologist to write out prescriptions for the "specific" shoes, gwenie
("specific" is the key word here). it would be tough for medicare to deny
it when at least two specialists agree that you need these "specific" shoes
enough to prescribe them, for both arthritic and orthopaedic medical
conditions. i'm sure at least two of your doctors/specialists would agree
that you do.
kate
> Gwen, the shoes may be a good investment. They will last a long time
> and you can have them resoled to added life. But if you still don't
[quoted text clipped - 13 lines]
>
> Vickie B.
sweetpickleNO@SPAMknology.net - 07 Jan 2008 00:32 GMT
Hadn't thought of that Kate, but I'll sure try it. Thanks.
Gwen
> Thanks Vickie. No, I am not diabetic. I wore orthotics at one time but
> my
[quoted text clipped - 35 lines]
>>
>> Vickie B.
Paul T. Holland - 06 Jan 2008 21:42 GMT
one note - i wear a couple styles of the sas shoes, and like them very
much, BUT
not all of the models are made to be re-soled.
i do recommend them, but you must check if the model you like can be
done
"Vicki b." wrote:
> Gwen, the shoes may be a good investment. They will last a long time
> and you can have them resoled to added life. But if you still don't
[quoted text clipped - 13 lines]
>
> Vickie B.
DeeDee - 05 Jan 2008 21:53 GMT
On Jan 5, 2:41�pm, <sweetpickl...@SPAMknology.net> wrote:
> I have a few problems that I'd like to know if anyone else has had them and
> how they dealt with them.
[quoted text clipped - 36 lines]
>
> Thanks. �Gwen
I am a lurker here off and on. The foot pain that you describe is
just like Morton's Neuroma. It is damaged nerve under the toes. You
can try shoes, orthotics etc and more than likely surgery to remove
the nerves is the only thing that will work. It is horrid pain.
Mine was in my left foot. I had even tried cortisone shots and that
did nothing. Another friend on Fibro board just had this surgery.
She described it as her doctor had no clue. Then she saw a podiatrist
and I told her to mention Morton's Neuroma (Google it) and he agreed
that was exactly what it was. Can be caused by too tight shoes,
stubbing your toes and even being on your feet many hours in a day.
Runners are bothered by this because of the pressure as they come down
on the ball of their foot.
DD
Kelly - 05 Jan 2008 23:40 GMT
Gwen,
What size shoe do you take???
Kelly
>I have a few problems that I'd like to know if anyone else has had them and
>how they dealt with them.
[quoted text clipped - 36 lines]
>
> Thanks. Gwen
sweetpickleNO@SPAMknology.net - 06 Jan 2008 03:27 GMT
Kelly, I wear a 7 B ( or medium).
Gwen
> Gwen,
> What size shoe do you take???
[quoted text clipped - 42 lines]
>>
>> Thanks. Gwen
Kelly - 06 Jan 2008 03:41 GMT
My New Balance haven't been worn (bought them just before my neuro problem)
but they are a 7.5 very wide. I thought if they would work they would be a
good supportive shoe and I would send them to you. The wider width in the
toe bed would allow you to put in cushioning or whatever in the toe area
(perhaps to seperate them - have seen orthotic off the shelf things to do
that). I have the elastic shoelaces that some wonderful person in this
group sent me and they are a godsend. I use my reacher to hold the tongue
of my shoe and just slip them in (sometimes need my long shoehorn too).
I wish they were the right size. Would be perfect. I also have a brand new
pair of Finn Comforts (at $240.00) but am keeping those in hopes that one
day soon I can wear them. Gradually the prednisone edema is coming out of
my feet.
Wish this had of worked. I just think these will be too big which is a
shame. They are the New Balance running shoes recommended for arthritis and
accomodate the orthotic.
Kelly
> Kelly, I wear a 7 B ( or medium).
> Gwen
[quoted text clipped - 45 lines]
>>>
>>> Thanks. Gwen
sweetpickleNO@SPAMknology.net - 07 Jan 2008 00:30 GMT
Kelly, I thank you very much anyway.
Gwen
> My New Balance haven't been worn (bought them just before my neuro
> problem) but they are a 7.5 very wide. I thought if they would work they
[quoted text clipped - 65 lines]
>>>>
>>>> Thanks. Gwen
jofirey - 06 Jan 2008 01:16 GMT
>I have a few problems that I'd like to know if anyone else has had them and
>how they dealt with them.
[quoted text clipped - 8 lines]
> lace up. With my replaced hip that I have dislocated 4 times, I need
> slipons and I don't have $130 for one pair of shoes!
OK, this I can help with. The SAS shoes are worth every dime. But look for
a sale or outlet. Or even try them on in the store and then buy online.
The good news is they wear like iron. Get a color you can wear year round
and they last nearly forever.
Then, either don't tie them all that tight, or get elastic laces and slip
those suckers on anyway. I can't get anywhere near mine to tie them while
they are on my feet.
They are the only shoes I can wear for any length of time. I like my Birks,
but they aren't that great if you have to walk or stand very long. And I
try to draw the line at Birks and socks.
Jo
Squirrely - 08 Jan 2008 07:40 GMT
Gwen,
I hope you get so much better soon with the OA.
I know at one point the dr told me if they don't get the exact spot they
need to get, the shots don't work sometimes. So maybe that is what happened
with you. Maybe he hit the wrong areas.
Oh ouch I feel for you with bursitis. Mine gets activated somehow when they
gave me a shot of solu-medrol. It sets it off big time.
I am so glad you are feeling so much stronger with the B12 shots. I hope the
other stuff gets to behaving itself too now for you.

Signature
Love and Hugs to all
Jo the squirrely one
I am nuts about you.
>I have a few problems that I'd like to know if anyone else has had them and
>how they dealt with them.
[quoted text clipped - 36 lines]
>
> Thanks. Gwen