Hello,
I was diagnosed with lupus… horrible thing. And I got this antibiotics, but I also gained 6 pounds!!! Besides this lupus, I am also fat now!!! Is this normal that lupus patients gain weight?
What can I do?
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Hey,
I am sorry for your lupus…
Weight gain is very common in lupus patient… weight gain is a side effect of those medications you are taking, but do not think of stop taking those pills because of weight gain- lupus is more dangerous than weight gain. I guess, the only solution is proper dieting- less bread, more fruit and vegetables.
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I'm just start a healthy diet so I hope I can lose some weight.
Brenda
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Hello,
I was diagnosed with lupus… horrible thing. And I got this antibiotics, but I also gained 6 pounds!!! Besides this lupus, I am also fat now!!! Is this normal that lupus patients gain weight?
What can I do?
HI! My name is Michelle, I also have SLE. I was diagnosed 5 years ago and have gained nearly 50 pds! The steroids are the main cause as well as the lack of excercise. I was a proffesional cheerleader, than went on to run a gym where I taught high impact step areobics and kick boxing. I now have a hard time just getting out of bed. Depression plays it's part in my weight gain as well. I am currently trying the Atkins diet, which means absolutley no carbs. My doctors say it is okay to do but for no longer than 2 months. I have lost 12 pds in 2 1/2 weeks. I'm hopeful that I can shed this horrible weight and get back my life. Fruit is okay, however you must choose the proper ones. Well good luck to you, and to all with this horrible disease!!
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As for gaining weight, does the doctor have you on steroids? They are the largest cause of weight gain in lupus patients. The best offense is a good defense. Watch what you eat especially when on steroids so that your weight doesn't spiral out of control. Steroids muck with your blood sugar, they cause you to retain water and put on fat. Other drugs used on some lupus patients (like tricyclic antidepressants) also cause a sweet tooth.
I've had lupus for 21 years; it's a struggle. Good luck.
Tracy
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I'm now 26 years old and trust me, I've gone through alot
because of the Lupus. I have gained and lost weight for
years now and I do not think the Atkins diet is a good thing
for you to do. If you want to lose weight, just eat right (lots
of veggies and protien) dont starve or deprive yourself,
do pilates and/or yogi, aqua aerobics is also awesome and
easy on your joints. Also, make sure you take it slow and dont
over work yourself, get plenty of sleep and drink lots of water.
Other then that stay positive and take it day by day. God Bless.
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Hello,
I am a 35 yr. old male that is (as of yet) undiagnosed. I have the buterfly face rash, small round sores on my lower legs and forearms that will not heal. I also have been complaining of extreme fatigue/triedness for years. As of 6 months ago (which is the same time my rashes and sores appeared) I am now expierencing horrible pains in my joints. My father is a type 1 diabetic, my mother is a SLE survivor (she almost died from kidney failure in the early 90's before her doctors realise it was lupus) and have recently discovered that I had a grandmother on both sides that died from unknown kidney failure in their ealier 60's. When I was 21 I gained 90 lbs in the corse of a year without any major changes to my diet or activity. My largest concern at this point, is that the joint pains are becoming unbearable (and the worse part, 1 day its my back, the next my hip, and today its my jaw....it seams that any of my joints can be hurting on any given day). What also worries me is sudden unexplained weight lost. When I finally went and ssen my doc in late march, he decided it was "suspected SLE" and decided to chart my physical stats on a weekly basis. At this time he has not commented on blood work other than "interesting" (I think its time to see a specialist), but he is concerned about my weight. I have lost 48 lbs in 4 weeks with no effort on my part to lose weight. The comment he made today was that it appears that if it is SLE, that my symptoms are begining to spiral out of control, and has actually suggested hopsitalazation is possible in the near future. Is this possible?!!? I thought Lupuus was a long decay of the body over the corse of years....so why are my symptoms coming on so fast and strong. FYI, yes I am under an extreme amount of stress at this time from other factors that are unfortunatly beyond my control. What has me scared the most, I cant help but feel that if this continues to progress at this rate...well....I guess it's more a question, Can Lupus be acute ending in a fatallity in a short period of time... or to put it another way, I don't know if I can hold out much longer. I am pushing for a diagnosis because I'm an auto technician by trade, and that job can be physically taxing. I dont know how much more work I have in me, but it isn't much...maybe a couple months at best. Do the treatments allievate the symptoms enough to continue a "normal" life? On the flip side of that, if not: is it possible to get social security disability for Lupus? I guess Im really reaching out for support. Im a husband, and father of 3 wonderful children, and I want to be the best "me" I can manage from here, but I'm in so much pain, and I feel like absolute c**p all the time...I just don't know how much longer I can carry on like this. So if anyone has the time to possibly share some of their time, I would appreciate some inside information froma Lupus patient as to what I can expect..or, what to do from here.
Thank you in advance.
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Thank you for reminding us to not beat ourselves up. I can't seem to get the 50 lbs. I gained off at all. I eat very healthy and barely anything. Typically, almonds for a morning snack, salad at lunch and skinless chicken with brocolli for supper. The best I can do is tell my self, it would be worse if I didn't do what I am doing. The amount of medications is amazing. Family and friends don't begin to understand how you feel on bad days. You have to put on your fake smile as you try to keep up with daily routine. I was on Methotrexate for 1.5 years. It was wretched for me gave me horrible flu like symptoms and body aches. I told the doctor it was like a body migraine. I hope it works well for you. Plaquinel works for me much better.
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What were the signs when you were diagnosed with Lupus. The reason I am asking is because first of all I have fibromyalgia and lately I am very exhaused no energy. also the past 2 weeks I developed a rash on my arm just about where you fold your arm in and it itches terribly. I thought it was a heat rash. I know my Uncle had Lupus. I hope I do ot have it.
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