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Medical Forum / Diseases and Disorders / Lupus / April 2008

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Good day everyone, I want to ask a Lupus for life question..........

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Steveo - 10 Mar 2008 21:05 GMT
I have not posted in a long time.  Mostly because I have been in
fairly good health and then there is so busy aspect.....  I have
always tried to push myself as much as I can since the Lupus likes to
try and limit me.  however I am now realizing that the constant
fatigue and joint pain is making me slow down a lot.  I now find
myself completely wiped out after just 8-9hrs of reqular work, I work
full time as a Server administrator.  I also own my own maint business
and honestly it is beging to be affected by my fatigue.
    My question is this.  How many people on this board still work
40+ hrs a week?  And if you do how do you juggle the fatigue and then
the time with the family?  I am so tired these days all I want to do
is sleep.  I have backed out on going to the movies and or dinner with
my family because I am so dang tired.  MY side business is being put
off until I feel awake enough to go do the work or I can get my
partner to do it.  Eitherway the response times are getting longer.
Now my day job is becoming more of a chore as well.  Any testimonals
out there?
ironjustice@aol.com - 10 Mar 2008 21:55 GMT
On Mar 10, 1:05 pm, Steveo <sjarr...@optonline.net> wrote: fatigue and
joint pain <<

The hallmark symptom of iron overload is fatigue.
Arthritis is not too far behind.
Lupus has been closely linked to myelodysplasic disease.
Myelodysplasic disease manifests hemolytic anemia / red blood cell
destruction which is KNOWN to lead to iron overload.

Think about getting a competent doctor who is **able** to assess the
state of oxidation / iron overload in your body.

Imho ..

Hemolytic Anemia: A Blood Disorder
Causes of hemolytic anemia include infection, certain medications,
autoimmune disorders (such as Lupus), and inherited disorders. ...
http://www.itzarion.com/lupusanemia.html

Who loves ya.
Tom

Jesus Was A Vegetarian!
http://jesuswasavegetarian.7h.com

Man Is A Herbivore!
http://tinyurl.com/a3cc3

DEAD PEOPLE WALKING
http://tinyurl.com/zk9fk

>      I have not posted in a long time.  Mostly because I have been in
> fairly good health and then there is so busy aspect.....  I have
[quoted text clipped - 13 lines]
> Now my day job is becoming more of a chore as well.  Any testimonals
> out there?
Steveo - 12 Mar 2008 20:05 GMT
Thanks for the info.  I did have mild anemia but it has passed.  My
iron levels are normal.  My Rhumy and Kidney doc are very highly rated
in their respective fields.  My Rhumy is a clinical Professor at Yale,
I am completely confident in both of them.  I have been complaining
about fatigue for a few years now and as far as I can tell that is
pretty normal with Lupus.  My post wasn't so much a request for
possible other afflictions but rather I am looking for insight into
what I can expect.  Since you were nice enough to share that
information with me I will indeed ask my doctor about it.  Thank you
for your response.

-steve
Ruth Tay - 15 Mar 2008 19:05 GMT
In article
<06200f7e-af31-42d9-a3bc-bb713c3c6a0b@y77g2000hsy.googlegroups.com>,

> Thanks for the info.  I did have mild anemia but it has passed.  My
> iron levels are normal.  My Rhumy and Kidney doc are very highly rated
[quoted text clipped - 8 lines]
>
> -steve

Hi

Having lupus for 25 years gives my body the chance to dictate how to
live.  I have worked steadily except for the times that lupus sent me
to the hospital and kept me in bed.  From a 50 hour week to a 36 hour
week  seems to keep me on my feet.  Luckily I do accounting and
human resources  that  is located on the same acreage  as our home.
I am blessed to have a husband that can take over the duties when I
have a lupus attack.....First of all you need to recognize that your
body is going to call the shots for the rest of your life.  Having
two jobs should be in your past.  When  Lupus first struck me
I tried to ignore it but after a few trips to the emergency room and
an extended stay in the hospital that damaged my heart  I learned...

Men seem to have more severe symptoms than women.........You
can still have a very good life   but take more time to smell the
roses.................ruth
Ruth Tay - 17 Mar 2008 00:25 GMT
For Steveo   Just re read my response to your question and feel like a
pompous a.s.  The advice given was really advice to my self.  It
should have been just go by what your body allows you to do.  Thru
the years of not listening  I continued working  and depended on
others to pick up and continue work that needed to be done..The stress of
trying to meet expenses can be tough.  You are wise to be tackling
Lupus  head on.  good luck     ruth
Steveo - 17 Mar 2008 15:55 GMT
> In article <ruthtay-1CF545.11053415032...@corp-news.dsltransport.net>,
>
[quoted text clipped - 5 lines]
> trying to meet expenses can be tough.  You are wise to be tackling
> Lupus  head on.  good luck     ruth

Ruth, thank you for the insight.  Please do not feel bad, I appriciate
any and all insight.  I have be DX'd for about 4 years now and I am
still learning my way through all of this.  All the people here with
the years of experience, you girls and guy are a lot of help to those
of us that are new to dealing with this.  Thank you again.

-Steve
kodama - 19 Mar 2008 17:35 GMT
Hi Steve,

Fortunately for me, my husband makes enough money that I don't have to
work.  Frankly right now I don't think I could work full-time but
maybe part-time if I had to.  At this point I really don't have the
endurance to live a "normal" life.

I think if I had to work I would have to be creative.  Do you have to
work at a set time?  I find there are certain times of the day when I
am most tired (for me usually 3-6:30 PM)  Can you break up your work
day so you avoid your worst time of day and could rest or have a short
nap.  A short nap really can make a huge difference in how you feel.
Also for me, is making sure I go to bed before midnight.  If I got
after that my body pays for days.  Controlling my bedtime is about the
one thing I feel that I do have control of with my lupus.

Jeanne
luster - 08 Apr 2008 08:55 GMT
Hi, I am Server and network administrator and I have Lupus.
Most of the day tired and I've got alopecia arealis, so I am feelng bad and
I lood bad.
I don't know if my family use to see me OK.
But, there is no exit - only try to supres illnes and live on.
Maybe my job is too stress for me?

>     I have not posted in a long time.  Mostly because I have been in
> fairly good health and then there is so busy aspect.....  I have
[quoted text clipped - 13 lines]
> Now my day job is becoming more of a chore as well.  Any testimonals
> out there?
shana - 11 Apr 2008 23:30 GMT
> Hi, I am Server and network administrator and I haveLupus.
> Most of the day tired and I've got alopecia arealis, so I am feelng bad and
[quoted text clipped - 22 lines]
>
> - Show quoted text -

Hi I have been having lupus for 15 years now. I be so stress out with
my play sister. I tried to stay from the house to
where I won't get sick
 
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