It has been
an emotion-filled past 2 weeks for me on both the work front and health
status.
Recent
results on potassium level showed that the level is back to normal range.
I asked whether I should continue with Micardis since my blood pressure during
the period I stopped the medication is perfectly normal. I somewhat suspect
that diagnosis of hypertension way before the diagnosis of SLE could be lupus
related. And since I have my lupus under-control now, whether it would be
mean that I can stop the hypertension medication. The answer from doc is to
continue to take the Micardis (even though it may elevate potassium level). His
reason - I have evidence of renal inflammation (in medical term - it is called
nephritis) in the initial stage of my SLE and mild protein in the urine.
Micardis is useful to help control renal disease and therefore I should
continue to take 40mg daily. I suppose that means I also need to watch my diet
and not to take too much high potassium foods.
Just
recently, I wake up with pain on the big toe joint. I thought it was a
sprained joint from walking too much the day before. Didn't think too much
about and thought it would heal after a day or so with some massage. The
next day, the pain became worse and I noticed the foot has become
swollen. It then daunted on me that it might be gout - though I has never
had it before. I read up about gout on the internet and learned that gout
is due to uric acid accumulating at joints and cause it to be inflamed (commonly
occurred at the big toe - a condition called podagra). A diet of too much
protein may cause too much uric acid for the kidney to excrete it, especially
if the kidney function is not efficient - perhaps like mine. while I waited for
the next day to see a doc, I also decided to self-medicate with Naproxen Sodium
(Synflex) - a NSAID that I used sparingly for margarine or severe menses
cramps. While this medicine is effective for pain and inflammation and
also can be used for gout, it is harsh on kidney thus I used it only when
necessary or in low dose. I had one tablet in the night and by next
morning - the pain and the swell have both subsided. The doc visit was
abandoned since I reckoned that the doc would prescribe the same medicine or if
not, give me prednisolone that I would be reluctant to start.
On
reflection, I wonder why my health is being hit by one thing by another
recently. Stress could be a trigger since I have dealing with difficult
work matters in recent weeks and some involve personnel issues which is
emotional straining for me. Diet could be another factor - but now I am
in a fix - I actually do not know how to eat anymore since I need to exclude
potassium rich food and also protein rich food... I really do not know how have
a balance diet then. Think I am giving up on this front and just continue
to eat everything in moderation and don't care about their potassium or protein
level. Maybe that will make it happier and also help in my health!
Sharing of my journey with systemic lupus erythematosus. I know I am not alone in this journey and hope this would help to lend support to others who have this same condition.
Saturday, April 20, 2013
Friday, April 12, 2013
Lupus, Kidney Function and Potassium
Living with lupus is like living with a time bomb that you never know when it will explode. Regular doc follow up, blood and urine tests are essential routines that I adhere to so that I will have some early warning signs to prevent the time bomb from going off. For people with SLE like me, it is always a worry that lupus flares might cause organs damage to kidney, liver, heart, etc, no matter how responsible I am towards health.
Recent blood test shows that my potassium level is high - a sign that my kidney function may not be functioning properly (since it cannot eliminate excess potassium effectively), although most other indications like ds-DNA are stable. Doc has asked that I stopped my high blood pressure medicine (Micardis) temporary and also avoid food with high potassium like bananas. I will repeat the test in a week time. I read up information on the Internet and realize that high blood pressure medicines might cause high potassium level (apparently potassium helps to lower blood pressure). Found that some food/drinks like potatoes and orange juices have high potassium level. High potassium level can be dangerous as it might affect the heart condition and stop heart beating. Since I stopped Micardis, I also have been diligently measuring my blood pressure. It has been at the healthy range so far. Some time I also wonder that my high blood pressure is caused by lupus and now that I have my lupus under control, I also have blood pressure under control, then I should not need to take medicine for high blood pressure. But medicine reference always says once you are diagnosed with high blood pressure, it is something that cannot be cured.... but what happened if the diagnosis is wrong in the first place? Anyone can shed light on this area?
Though I remain quietly confident that my potassium level will go down during my repeated test next week, I wonder how to achieve the dedicate balance in controlling the different medical conditions and the side effects of medications. Micardis helps to control high blood pressure but yet it can be harmful to the kidney. Plaquenil controls lupus but yet it can be harmful to the eyes. Doc will say it depends on whether the beneficial effects of the medicine exceed the cons at the time of treatment.
Anyway, no point worrying too much and I will just take one thing at a time. I strive to live each day fully since I do not know what will happen next. Good luck to the my next test results.
Recent blood test shows that my potassium level is high - a sign that my kidney function may not be functioning properly (since it cannot eliminate excess potassium effectively), although most other indications like ds-DNA are stable. Doc has asked that I stopped my high blood pressure medicine (Micardis) temporary and also avoid food with high potassium like bananas. I will repeat the test in a week time. I read up information on the Internet and realize that high blood pressure medicines might cause high potassium level (apparently potassium helps to lower blood pressure). Found that some food/drinks like potatoes and orange juices have high potassium level. High potassium level can be dangerous as it might affect the heart condition and stop heart beating. Since I stopped Micardis, I also have been diligently measuring my blood pressure. It has been at the healthy range so far. Some time I also wonder that my high blood pressure is caused by lupus and now that I have my lupus under control, I also have blood pressure under control, then I should not need to take medicine for high blood pressure. But medicine reference always says once you are diagnosed with high blood pressure, it is something that cannot be cured.... but what happened if the diagnosis is wrong in the first place? Anyone can shed light on this area?
Though I remain quietly confident that my potassium level will go down during my repeated test next week, I wonder how to achieve the dedicate balance in controlling the different medical conditions and the side effects of medications. Micardis helps to control high blood pressure but yet it can be harmful to the kidney. Plaquenil controls lupus but yet it can be harmful to the eyes. Doc will say it depends on whether the beneficial effects of the medicine exceed the cons at the time of treatment.
Anyway, no point worrying too much and I will just take one thing at a time. I strive to live each day fully since I do not know what will happen next. Good luck to the my next test results.
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