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mabri"When I was diagnosed about 18 months ago with fibromyalgia, I didn't know where to turn. I got on my computer and looked for a support group where I could talk to other people with the same disease and get some help...Information, suggestions, mostly just what I can do now that I have this.....disorder/disease/syndrome...I didn't even know what to call it. I found MDJ, and yes, there was a support group for fibro. I started a post, and figured I would never get an answer. However, very quickly I was welcomed in, and became really involved in the group. I received help, support, friendship and the feeling of being truly cared about by these strangers who had become like family to me. Now, I have been here for about a year and a half...I have become a group leader, and love every minute of it. It is so wonderful to be able to help others. I still receive help and answers from the members in this group. The fibromyalgia is where I go to help, support, listen, care and even laugh. I don't know what I would do without this group." (mabri)

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Rheumatoid ForumsGeneral & SupportRhuemy changed meds
04/26/2012 04:01 PM
lakelady
lakelady
 
Posts: 140
Member

My rhuemy does blood work every 2 to 3 weeks.
Reply

04/26/2012 05:13 PM  Top
movn
Posts: 306
Member

Trying to read all I can about all the different meds from you all before my appointment on Wed. With the mtx, you say you only take it once a week. If taken on Friday night would the side effects be gone by Monday in time to go to work? Do they normally last a couple days. Not how I would want to spend every weekend, but guess you have to do what ya have to do.

I really love my job, and can not even think about what would happen if I had to step down from my position or quit because of this


04/26/2012 05:38 PM  Top
JoLoBa
 
Posts: 325
Member

I had the same trouble with MTX. (I'm not very experienced--just had my 3rd dose this weekend.) For the first 2 doses, I took it in the morning. I'd be fine for almost 2 hours, then was miserable, just as you describe, lakelady. It wiped me out all day and I started feeling better around bedtime. Somewhere on this forum, I saw that others are taking it in the evening. I figured it was worth a try--at least I'd be out at night and maybe able to function the next day. So, I called my rheumy who said I could move the dose forward to the previous evening.

I don't know if my body's getting used to the mtx or if it was the timing change, but it was an amazing difference. I don't even know if the overwhelming fatigue hit me--if it did, I was sleeping through it. And, since I have insomnia with the prednisone, I'm actually looking forward to the next MTX dose!

Joann

04/26/2012 09:49 PM  Top
PauleR
PauleR
 
Posts: 1550
Group Leader

My doctor told me to take it Friday evening around supper time and I should be better by Monday. I did not have overwhelming fatigue and I know how lucky I am.

The Mtx might have kicked in early for you, or taking it in the evening is the answer. I'm just thankful that you are seeing results.

Paulette

I am not a doctor and my advice is purely my opion which should be regarded as such!

God grant me the SERENITY to accept the things I cannot change
The COURAGE to change the things I can & the WISDOM to know the difference.

The best and most beautiful things in the world cannot be seen or even touched - they must be felt with the heart.
Helen Keller

04/26/2012 09:51 PM  Top
PauleR
PauleR
 
Posts: 1550
Group Leader

When I was going through a terrible time with fibro, many years ago, I explained the fatigue as being bone deep, indescribable. I don't know if that is what helped others to understand or the fact that I looked like hell. Lol
Paulette

I am not a doctor and my advice is purely my opion which should be regarded as such!

God grant me the SERENITY to accept the things I cannot change
The COURAGE to change the things I can & the WISDOM to know the difference.

The best and most beautiful things in the world cannot be seen or even touched - they must be felt with the heart.
Helen Keller

11/21/2012 09:28 AM  Top
badgurrrl
badgurrrl
 
Posts: 103
Member

i take GENGRAF (modified) ...100 mg cuz of my liver too... at first the fatique was paralizing...now its jus tiredness so i rest n feel refreshed and do wat i can at watever rate i go...if its sloooo OOOOOoooOOO well...i'll get there ontime... cuz i'll leave sooner... But overall i feel comfortable in my own skin finally after 30 years of suffering... No more predisone...i quit takin it i hate how i felt when it was wearin off...No more swollen face either~ yea!
~bad_guRRRl~


~he forgives ALL of my sins and HEALS all of my diseases~ PSALM 103:3



~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ I am not a Dr. but i make lots of trips to their offices...i am very in tune with my body and symptoms and all of my own info or opinions are just that...and what has worked for me~...
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
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