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Hello Araminta and welcome ...I am sure you will get alot of input on

MTX from this group as quite a few are on it...I started taking it

about 2 months ago and I am still waiting for results...I did have a

problem with running to the bathroom at first but that is about it...

: Welcome and I think you will find this is a great group and

the moderators are always great at finding informative answers to most

questions.....has anyone suggested Blue Stuff...my friend had fibro

and she swears by it....you can find it on the net although it is

expensive

Kapzu: Welcome and I think Al gave a great answer from a mans

perspective...I will say it is not uncommon for anyone with autoimmune

diseases to go through denial some take longer than others....I am

sorry it is so tough on you....but until he decides to take the steps

to deal with some of it ...your road will probably be rough....I know

my spouse had a hard time when I was first diagnosed but I couldnt see

his pain I was centered on mine for awhile.....

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I have been on MTX for about a year and have found it has made a big diff

for me...along with the combo of other meds, my flares are less frequent and

shorter in duration...doc has started discussing rem and we will make some

decision in Oct...but the mtx has certainly made a diff for me. I've tried

the blue stuff too...I think it gives some relief...I don't use it often

because of the cost...but some of the nights I can't seem to get to sleep it

seems to help...welcome to the new folks..marge

[ ] RE: Welcome newbies

> Hello Araminta and welcome ...I am sure you will get alot of input on

> MTX from this group as quite a few are on it...I started taking it

> about 2 months ago and I am still waiting for results...I did have a

> problem with running to the bathroom at first but that is about it...

>

> : Welcome and I think you will find this is a great group and

> the moderators are always great at finding informative answers to most

> questions.....has anyone suggested Blue Stuff...my friend had fibro

> and she swears by it....you can find it on the net although it is

> expensive

>

> Kapzu: Welcome and I think Al gave a great answer from a mans

> perspective...I will say it is not uncommon for anyone with autoimmune

> diseases to go through denial some take longer than others....I am

> sorry it is so tough on you....but until he decides to take the steps

> to deal with some of it ...your road will probably be rough....I know

> my spouse had a hard time when I was first diagnosed but I couldnt see

> his pain I was centered on mine for awhile.....

>

>

>

>

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Araminta, running to the bathroom because of bowel

problems...I have lost weight but I cant say it is

because of the MTX....as of yet I really havent

noticed anything else , except I have more energy for

about 4 days after taking my dose which I take on

Sunday, but by Thursday I am in slow motion

again...Kathi in OK

--- Araminta Ditch <binky@...> wrote:

> Hello iamladybird,

>

> > Hello Araminta and welcome ...I am sure you will

> get alot of input on

> > MTX from this group as quite a few are on it...I

> started taking it

> > about 2 months ago and I am still waiting for

> results...I did have a

> > problem with running to the bathroom at first but

> that is about it...

>

> When you say that you were " running to the

> bathroom " , do you mean that you

> had bowel problems, or bladder problems, or both??

>

> Did you experience any weight gain?? Any other side

> effects that I should

> know about??

>

> Araminta

>

>

>

__________________________________________________

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Welcome Araminta...the only side effect I had to Meth was when I took it in

pill form, I spent most of my time with an upset stomach and

vomiting...lost about 35 lbs....bt the hard way! I changed to injections

and my stomach is fine....watch being out in hot sun too much...the

improvement made it all worthwhile...shorter flares and much more mobility.

after a year...I'm finding my feet swelling frequently..and stiffness...but

the pain is definately much better...glad you are here...when did you

startthe mtx...marge

[ ] Welcome newbies

> Hello iamladybird,

>

> > Hello Araminta and welcome ...I am sure you will get alot of input on

> > MTX from this group as quite a few are on it...I started taking it

> > about 2 months ago and I am still waiting for results...I did have a

> > problem with running to the bathroom at first but that is about it...

>

> When you say that you were " running to the bathroom " , do you mean that you

> had bowel problems, or bladder problems, or both??

>

> Did you experience any weight gain?? Any other side effects that I should

> know about??

>

> Araminta

>

>

>

>

>

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  • 4 years later...
Guest guest

Welcome newbies!!! Sorry you have to join this list but glad that it is here

for you. I am 31, living in Braintree, MA with my son and husband. I was dx in

Oct of 05.

:}

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  • 1 year later...

Hi Vicki,

It does help so much to have support from someone, who DOES know how you

feel. So, your never alone here. At your lowest moment, someone here,

can get you back where you need to be.

With chronic illness, there is always pain, but some are worse then

others. Just take one day at a time, and the days you can get around a

little better, take advantage of it.

I have a cane, and its helpful at times. I do have some trouble with

it, because I have bad wrists. Using my wrist bands help quite a bit.

I am on Medicare, and they do pay for all that stuff, so I've heard.

The cane I bought was real cheap, so I didn't mess with it.

I have been thinking about getting some crutches or boot, with my heel

spur. I'm walking on the front of my foot, and now I'm making that part

painful. I already have SO much pain in my feet anyway from the RA. I

was already to talk to the foot doc about what I might use. I'm on a

freecycle group, and guess what, I got a boot!!

If some don't know what freecyle is, I'll explain. Its a group,

and there is one usually in every town. People give stuff away they

don't want, and you can do the same thing. You can also post for

something, and usually you will get it. So, its helping the

environment, but also everyone. Its all free!

You can go on www.freecycle.org <http://www.freecycle.org> or you can

go to group, and type in your town, st. Its really fun, and if

your looking for something rare, you can ask for it, and you just might

get it.

Sorry about getting off the topic, but wanted to share. I'm so happy to

get that boot, I heard its kind of expensive.

I'm usually here somewhere, if you need someone to talk to. I am so

glad your here, we can all help each other, Tawny

>

> Thank you for the welcome Tawny. It is comforting to know we are not

alone. With all of the meds I currently take I just wonder if there is

anything else I can do to get through the rougher times. Today was more

of limbo land day. Painful, but I was able to get some things done as

well. Whereas yesterday was a day I didn't even bother to get out of

bed. The pain and over all sick feeling was not tolerable.

>

> Someone mentioned buying a cane. I am not sure if the members here

realize it but if you get a prescription written out by your doctor your

insurance will re-imburse you. I have gotten ankle braces, knee braces a

walker and a cane that way.Just a bit of info that may help some of you.

>

> I look forward to hearing from each of you, on both the bad days and

the good.

>

> Vicki

> Iowa

>

>

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