Joined: 26 Dec 2005 Posts: 10 Location: Liberty Lake, WA
Diagnosed On May 11, 2005 Posted: 12-26-05 22:03pm
I can't get into remission! I'm on
methotrexate, prozac, folic acid as well
as vitamins. I'm not experiencing so
much fatigue as much as I am muscle and
joint pain. The other day I had some
margaritas and by morning I felt like I
had been beaten over night! Another
concern of mine is getting back to jogging
and weight lifting but i'm too scared to
suffer the consequences! Any ideas would
be great!
Gena
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brenda49
New User, Becoming EHEALTHy
Joined: 24 Nov 2005 Posts: 6 Location: greenville,n.c.
Joint Pain Muscle Aches Posted: 12-27-05 03:30am
Gena
I too have lupus for many yrs. I am
on prednisone, plaquenil, and ecoated
asprin, lorecet plus, I also taked
vitimans. Mine are calcuim.Magnisum and
zinc,c and e. My lupus Dr. Also has me
on vitamin d 50,ooo units monday and
friday only. This is just a few. I have
been on plaquenil for many yrs. It is for
fatuque,jiont pain and muscles aches. The
only thing about this med you have to have
your eyes ch. Every 6 mos. My doctor
will not renew your give me a refill
untill this is done. It takes 3mos for it
to get totally into your system. I took
myself off of it a few yrs back after 1
month I was haveing joint pain, my skin
hurt to rub it and I was tired. I attened
a lupus support group and 1 woman had done
the same thing and experence the same
systoms that I had to come back. I
started back on plaquenil and within 1
month I felt better. First of all dont
ever stop a med without the permission of
your Dr. This helps me the plaqunil it
comes in different strenghts you might
want to discuss this with your Dr.
Good luck!!!!!!!!! And also talk with
him about your exercising.
Brenda foreman
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genaceresero
New User, Becoming EHEALTHy
Joined: 26 Dec 2005 Posts: 10 Location: Liberty Lake, WA
Posted: 12-27-05 23:34pm
Hi brenda and thanks for replying!!! I'm
so glad that I finally joined this forum.
Reading all the topics have been so
informative. Well, when I was
diagnosed....The first med they put me on
was a generic of plaquenil called
hydrochloroquine. It worked well but
then I was having hair loss and mood
swings. So, they switched me to
methotrexate.....It hasn't helped as well
and now again....I'm losing hair. So,
not sure what's going on. I'm probably
losing hair due to the lupus and not meds
or from stress. I might go back to the
hydrochloroquine or try the iv therapy.
I'm not sure what kind of meds go through
the iv yet, i'll have to find that out.
Since the beginning, I have refused
prednisone. I do not want the side
effects especially the swelling and weight
gain. I may change my mind if I get
enough people to talk me into it saying
it's worth it. But, at this point....No
way!!! Well, hope to hear from you and
others soon! Thanks again!! Gena
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BlakkStarr1
New User, Becoming EHEALTHy
Joined: 27 Dec 2005 Posts: 12
Posted: 01-02-06 20:40pm
genaceresero
wrote:
hi brenda and thanks for
replying!!! I'm so glad that I finally
joined this forum. Reading all the
topics have been so informative. Well,
when I was diagnosed....The first med they
put me on was a generic of plaquenil
called hydrochloroquine. It worked well
but then I was having hair loss and mood
swings. So, they switched me to
methotrexate.....It hasn't helped as well
and now again....I'm losing hair. So,
not sure what's going on. I'm probably
losing hair due to the lupus and not meds
or from stress. I might go back to the
hydrochloroquine or try the iv therapy.
I'm not sure what kind of meds go through
the iv yet, i'll have to find that out.
Since the beginning, I have refused
prednisone. I do not want the side
effects especially the swelling and weight
gain. I may change my mind if I get
enough people to talk me into it saying
it's worth it. But, at this point....No
way!!! Well, hope to hear from you and
others soon! Thanks again!!
Gena
i, too, have mood swings and some hair
loss, but I thought they were due to the
presnisone. I have been on prednisone
since 10/05, and plaquenil (generic), for
about 1 month. Although the prednisone
kills me, I need it for other symptoms of
sle. Hope I will lose the weight I
gained once I am off of it. Hope this
info is of some help.
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mamak3849
New User, Becoming EHEALTHy
Joined: 10 Jan 2006 Posts: 12 Location: Buchanan, Michigan
Hair Loss Posted: 01-24-06 23:00pm
Gena i'm losing hair too a lot of it did
they tell you anything special to do about
it?????
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mamak3849
New User, Becoming EHEALTHy
Joined: 10 Jan 2006 Posts: 12 Location: Buchanan, Michigan
Hair Loss Posted: 01-24-06 23:06pm
Gena i'm losing hair too a lot of it did
they tell you anything special to do about
it?????
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genaceresero
New User, Becoming EHEALTHy
Joined: 26 Dec 2005 Posts: 10 Location: Liberty Lake, WA
Hair Loss Posted: 02-02-06 01:25am
Hi and sorry to hear that you're
experiencing this stupid hair loss thing.
Just remember that it happens to the best
of us right? Well, i've spoken to my Dr.
And he said that if your hair loss is
overall 'thinning' it's more than likely a
side effect from your meds. If it's in
'patches' then it's from lupus. If your
patches scar, then more than likely your
hair will not grown back there. I was
told that I shouldn't perm or color as the
chemicals can be more damaging to your
hair and cause more breakage or hair loss.
Cutting your hair shorter can help as
well. The longer it is the heavier which
can cause breakage. Plus, the more
tangles you fight with which causes
breakage. Make sense? My hair was down
past my bra line and I just cut it to
above my shoulders! What a difference
it made! Hope this helps, it's all I
know! Take care, gena
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mamak3849
New User, Becoming EHEALTHy
Joined: 10 Jan 2006 Posts: 12 Location: Buchanan, Michigan
Posted: 02-03-06 17:43pm
Thanks gena that really helps the thinning
is on the top of my head its just getting
so thin no matter how I cut it you can
still see my scalp, but I guess its just
something I have to live with like
everything else that goes with lupus
thanks for replying.