Jump to content
RemedySpot.com

Re: UG stopping mtx

Rate this topic


Guest guest

Recommended Posts

I have a lot of fatigue and only just recently found out (from this

group) that mtx can cause fatigue. I had no idea. Anyway, I vote

for less pain and swelling because the pain and swelling will likely

lead to more joint destruction. I don't think fatigue can do that.

Although someone recently posted a study that joint damage can occur

even without obvious RA symptoms, but for now I'm going with the

theory that if I have little pain and no swelling, I'm in good shape

RA wise.

It's hard to accept the give and take of all this. I have bone loss

from the prednisone and someone asked me why they'd put my on the

drug that can do that. I said because for one, the risk of bone loss

was low (I'm just lucky I guess) and the alternative was way way way

worse.

Jennie

--- In , " dreamer_plus " <dreamer_plus@w...>

wrote:

> I did notice, however that while I have LOTS more pain and

swelling, I also have LOTS more awake time and less fatigue- at least

for the moment---

> Now I am wondering gosh- do I live with the pain and swelling or go

with the less awake time and more energy?

Link to comment
Share on other sites

I have a lot of fatigue and only just recently found out (from this

group) that mtx can cause fatigue. I had no idea. Anyway, I vote

for less pain and swelling because the pain and swelling will likely

lead to more joint destruction. I don't think fatigue can do that.

Although someone recently posted a study that joint damage can occur

even without obvious RA symptoms, but for now I'm going with the

theory that if I have little pain and no swelling, I'm in good shape

RA wise.

It's hard to accept the give and take of all this. I have bone loss

from the prednisone and someone asked me why they'd put my on the

drug that can do that. I said because for one, the risk of bone loss

was low (I'm just lucky I guess) and the alternative was way way way

worse.

Jennie

> I did notice, however that while I have LOTS more pain and

swelling, I also have LOTS more awake time and less fatigue- at least

for the moment---

> Now I am wondering gosh- do I live with the pain and swelling or go

with the less awake time and more energy?

Link to comment
Share on other sites

I think I have an attitude problem. LOL. I was SO sick no money to be under

docs care when I first got sick with all of this- and I was extremely sick,

bedbound. SCREAMING. It was awful. I had to wait for Medicare to kick in and

then I had to wait to save up for labwork- hard choices with 2 of our 3 kids

also disabled and also my husband---

By the time I finally got to be on mtx, I was SO grateful to have so much less

pain. BUT all my life I worked 2-3 jobs...It is hard for me to choose between

pain or this level of fatigue. You would think I could just accept it and be

glad I do not have that kind of pain. I guess I want it all? Quality of life?

We have talked here a little about family and people outside of our homes

judging us....I know people talk about me.... I am " lazy " I think sometimes

that gets to me. At my most ill, noone saw me except my kids and hubby. Noone

at all. This illness just seems to do all kinds of strange things to me and how

I view things.

No, I no longer work, not even 1 job. Most days, tho, I am glad to have this

time with my family, hubby and kids, I mean. SO, there is a positive side here.

Had I not gotten so sick I have no doubts I would still be working 100 hours a

week.

- In , " Jennie G " <xponder70@y...> wrote:

> I have a lot of fatigue and only just recently found out (from this

> group) that mtx can cause fatigue. I had no idea. Anyway, I vote

> for less pain and swelling because the pain and swelling will likely

> lead to more joint destruction. I don't think fatigue can do that.

> Although someone recently posted a study that joint damage can occur

> even without obvious RA symptoms, but for now I'm going with the

> theory that if I have little pain and no swelling, I'm in good shape

> RA wise.

>

> It's hard to accept the give and take of all this. I have bone loss

> from the prednisone and someone asked me why they'd put my on the

> drug that can do that. I said because for one, the risk of bone loss

> was low (I'm just lucky I guess) and the alternative was way way way

> worse.

>

> Jennie

>

>

> > I did notice, however that while I have LOTS more pain and

> swelling, I also have LOTS more awake time and less fatigue- at least

> for the moment---

> > Now I am wondering gosh- do I live with the pain and swelling or go

> with the less awake time and more energy?

Link to comment
Share on other sites

I think I have an attitude problem. LOL. I was SO sick no money to be under

docs care when I first got sick with all of this- and I was extremely sick,

bedbound. SCREAMING. It was awful. I had to wait for Medicare to kick in and

then I had to wait to save up for labwork- hard choices with 2 of our 3 kids

also disabled and also my husband---

By the time I finally got to be on mtx, I was SO grateful to have so much less

pain. BUT all my life I worked 2-3 jobs...It is hard for me to choose between

pain or this level of fatigue. You would think I could just accept it and be

glad I do not have that kind of pain. I guess I want it all? Quality of life?

We have talked here a little about family and people outside of our homes

judging us....I know people talk about me.... I am " lazy " I think sometimes

that gets to me. At my most ill, noone saw me except my kids and hubby. Noone

at all. This illness just seems to do all kinds of strange things to me and how

I view things.

No, I no longer work, not even 1 job. Most days, tho, I am glad to have this

time with my family, hubby and kids, I mean. SO, there is a positive side here.

Had I not gotten so sick I have no doubts I would still be working 100 hours a

week.

- In , " Jennie G " <xponder70@y...> wrote:

> I have a lot of fatigue and only just recently found out (from this

> group) that mtx can cause fatigue. I had no idea. Anyway, I vote

> for less pain and swelling because the pain and swelling will likely

> lead to more joint destruction. I don't think fatigue can do that.

> Although someone recently posted a study that joint damage can occur

> even without obvious RA symptoms, but for now I'm going with the

> theory that if I have little pain and no swelling, I'm in good shape

> RA wise.

>

> It's hard to accept the give and take of all this. I have bone loss

> from the prednisone and someone asked me why they'd put my on the

> drug that can do that. I said because for one, the risk of bone loss

> was low (I'm just lucky I guess) and the alternative was way way way

> worse.

>

> Jennie

>

>

> > I did notice, however that while I have LOTS more pain and

> swelling, I also have LOTS more awake time and less fatigue- at least

> for the moment---

> > Now I am wondering gosh- do I live with the pain and swelling or go

> with the less awake time and more energy?

Link to comment
Share on other sites

That is the bright spot for me. Although I didn't have to stop

working, getting RA made me choose to change just about everything in

my life. I was so far ahead of the game knowing exactly what this

disease was because of my mom, and knowing what the drugs were and

what they did. I got to skip most of the process of " accepting " my

having RA because in the back of my mind I knew that possibility was

always there. When the symptoms started and my mom and I both knew

it was going to be RA, I realized that I had to start taking better

care of myself and slow down. I have made so many changes since that

time (most in the last year) that my life doesn't even resemble what

it did then. I am so much happier, healthier (despite RA) and I know

I am a better mother to my daughter.

Jennie

--- In , " dreamer_plus " <dreamer_plus@w...>

wrote:

Most days, tho, I am glad to have this time with my family, hubby and

kids, I mean. SO, there is a positive side here. Had I not gotten

so sick I have no doubts I would still be working 100 hours a week.

>

>

>

Link to comment
Share on other sites

That is the bright spot for me. Although I didn't have to stop

working, getting RA made me choose to change just about everything in

my life. I was so far ahead of the game knowing exactly what this

disease was because of my mom, and knowing what the drugs were and

what they did. I got to skip most of the process of " accepting " my

having RA because in the back of my mind I knew that possibility was

always there. When the symptoms started and my mom and I both knew

it was going to be RA, I realized that I had to start taking better

care of myself and slow down. I have made so many changes since that

time (most in the last year) that my life doesn't even resemble what

it did then. I am so much happier, healthier (despite RA) and I know

I am a better mother to my daughter.

Jennie

Most days, tho, I am glad to have this time with my family, hubby and

kids, I mean. SO, there is a positive side here. Had I not gotten

so sick I have no doubts I would still be working 100 hours a week.

>

>

>

Link to comment
Share on other sites

> I have a lot of fatigue and only just recently found out (from this

> group) that mtx can cause fatigue.

I have found that something as simple as a regular 10 p.m. bedtime

helps a lot.

S

Link to comment
Share on other sites

> I have a lot of fatigue and only just recently found out (from this

> group) that mtx can cause fatigue.

I have found that something as simple as a regular 10 p.m. bedtime

helps a lot.

S

Link to comment
Share on other sites

I have made so many changes since that

> time (most in the last year) that my life doesn't even resemble

what

> it did then. I am so much happier, healthier (despite RA)

Me, too! In many ways it has been a gift. What are some of the

changes you've made?

S

Link to comment
Share on other sites

I have made so many changes since that

> time (most in the last year) that my life doesn't even resemble

what

> it did then. I am so much happier, healthier (despite RA)

Me, too! In many ways it has been a gift. What are some of the

changes you've made?

S

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...