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Hello everyone,

I am new to the list, and newly diagnosed with RA as of June 2010, although

every single blood test I have taken comes back completely normal - which

is confusing and strange. It was a bit of a cluster to get to the

diagnosis, but once I went to the Rheumatologist, I was diagnosed almost

immediately with an Ultrasound of my hands/wrists. I had a lot of swelling in

my

hands/fingers/wrists - I have not been able to get my wedding ring on since

March. This started basically overnight - from nothing at all to wham! I

initially thought I had a pinched nerve or something! I am 43 years old and

the mother of 7, so it was very frustrating for me to be in constant pain

and not know what my problem was.

My Rheumatologist has me on Methotrexate, Prednisone and Folic Acid - I am

beginning to reduce the Prednisone slowly, I have been on 10mg for a couple

of months and just took it down to 7.5 and am supposed to reduce 2.5 mg

every couple of weeks. As soon as I went to 7.5 I can feel just a little

more soreness in my hands and wrists, but no synovial swelling so far. Not

sure if the Methotrexate is doing anything at all - I am only on 10mg (4

pills) once a week, which I was told is the lowest dose and it will probably

get

increased (oh goodie). I know the prednisone works, because I have been

on it a few times now since this started and as soon as I stop it,

everything comes back.

The one weird thing that has recently started is muscle twitching around my

eyes. Does anyone know if this could be a side effect of one of the

medications, or is it a symptom of RA? I have noticed a tendency to have

muscle

cramps in my legs/feet at night, but this eye twitching is new and

annoying. I don't go back to the doctor until next month - is this worth

calling

about?

I am so glad there is a e-mail list like this!

thanks for any input!

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Hi - welcome to the group. I am new here too I guess. I also have been

recently diagnosed with RA which came on suddenly. I also take Methotrexate and

Pred ( 20 mgs each ).

 

I dunno about th eye thing, but for the leg/feet cramps, my old Rheumy had me

sip Tonic water w/ Quinine in it mixed 50/50 with whatever I wanted to drink

with it. I just sipped it throughout the day and my cramps vanished. You prolly

should consult w/ your Rheumy first since I dunno about the DMARD and the

Quinine- it was before I was diagnosed, so I wasn't on the drugs yet. You just

never know.

 

I hope you learn as much as I have on here. I am not the brightest bulb in the

box, but can understand parts of the technical lingo they toss around in here.

If you ask, they will explain. Nice folks.

 

Welcome, and may your days be pain free.

 

in SC

 

Hello everyone,

I am new to the list, and newly diagnosed with RA as of June 2010,

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Hi , Welcome. I read mostly on this site but wanted to welcome you. You

sound similar to me. Seems like it came on kinda fast and my wrists, fingers

swelling, stiffness and pain. My neck hurts, hips, knees and feet. But as like

you. All bloodwork comes out perfect. I too use to get muscle cramps at night

in bed pretty bad and I looked it up and started taking magnesium sulfate

vitamin and 1 month after all stopped. I have to believe it may have helped. I

continue taking it because it can only help and isn't bad for you. I also am

osteoporosis and it helps absorb calcium.

I have been on plaquenil for almost 3 months and to my knowledge no significant

help. Too bad too I was hoping. Plus, my nails are starting to get white

blemishes under nailbed and I noticed today they are lifting!!!! I need to call

my RA dr. on Monday. Good luck.

>

>

> Hello everyone,

>

> I am new to the list, and newly diagnosed with RA as of June 2010, although

> every single blood test I have taken comes back completely normal - which

> is confusing and strange. It was a bit of a cluster to get to the

> diagnosis, but once I went to the Rheumatologist, I was diagnosed almost

> immediately with an Ultrasound of my hands/wrists. I had a lot of swelling

in my

> hands/fingers/wrists - I have not been able to get my wedding ring on since

> March. This started basically overnight - from nothing at all to wham! I

> initially thought I had a pinched nerve or something! I am 43 years old and

> the mother of 7, so it was very frustrating for me to be in constant pain

> and not know what my problem was.

>

> My Rheumatologist has me on Methotrexate, Prednisone and Folic Acid - I am

> beginning to reduce the Prednisone slowly, I have been on 10mg for a couple

> of months and just took it down to 7.5 and am supposed to reduce 2.5 mg

> every couple of weeks. As soon as I went to 7.5 I can feel just a little

> more soreness in my hands and wrists, but no synovial swelling so far. Not

> sure if the Methotrexate is doing anything at all - I am only on 10mg (4

> pills) once a week, which I was told is the lowest dose and it will probably

get

> increased (oh goodie). I know the prednisone works, because I have been

> on it a few times now since this started and as soon as I stop it,

> everything comes back.

>

> The one weird thing that has recently started is muscle twitching around my

> eyes. Does anyone know if this could be a side effect of one of the

> medications, or is it a symptom of RA? I have noticed a tendency to have

muscle

> cramps in my legs/feet at night, but this eye twitching is new and

> annoying. I don't go back to the doctor until next month - is this worth

calling

> about?

>

> I am so glad there is a e-mail list like this!

>

> thanks for any input!

>

>

>

>

>

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Thanks for writing -- I will look into the magnesium sulfate

vitamins - I am already taking Biotin because I'm a freak about my hair -- if it

starts falling out all bets are off with the Methotrexate. Although my

doctor said if that happened they could give me something -- isn't happening

yet, actually no side effects other than fatigue that I have noticed.

Unless of course it causes muscle spasms.

Isn't it odd to have obvious visible inflammation -- the ultrasound showed

it and it was severe -- but have completely normal blood work??? The

doctor who performed the ultrasound said it looks aggressive -- but a normal sed

rate?? Makes no sense to me, but what do I know. I do know the

prednisone works like a charm - at least at 10mg -- we shall see about the lower

dosages.

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