Does anyone else experience tooth pain? All of my upper teeth just ache all the time.

I used to dye my roots only with Clairol root touch up. It’s time for me to cover those “few grays”, but I’m a little nervous to cause a bad reaction.

This is the third time my 5 year old has come to me about his concerns.....

My son and I are very close and open with each other. He asked me "what is going to happen if I die"? He does know
Mommy doesn't feel good a lot. He knows the name of mommys disease, Lupus. He is such a great helper to me. He is always helping, holding my hand,
to help me stand up and walking. He knows I don't walk very good and lose my balance. He is always giving me hugs and kisses!

We'll, last night he cried and… read more

I had my routine EMG testing on my upper and lower body. My neurologist said my legs are still getting worse. Left leg is really bad. My arms are not really
showing anything on the testing like he believes should be. Due to the weakness in my neck, arms and hands being pretty bad. So, he is requesting for me to have a biopsy done on my arms to check the tiny nerve cells on my arms. He thinks there is some underlying issue causing the EMG to not be able to get a reading. I do have Lupus… read more

I have a question and looking for advise.....

I'm am looking to purchase a home. I am on disability . So, to be able to qualify for more, i know we can earn an extra ...up to a 1,000/mo. I do own a business, but have never taken a pay check. What is the best way to go about doing this??

Thanks😊

I have been experiencing loss if balance for the past 5 years and the past few years loss of memory. As the years go by, the symptoms are slowly getting worse. My neurologist believes it's due to lupus sle. I can't even carry on a conversation anymore, because I can't remember simple words, what I was even talking about. It is do maddening. My family will fill in the blanks to help me out, but talking to anyone else is embarrassing. I'm due next month for another brain mri. My neurologist… read more

I went to my Dr to let her know that the Celexa she gave me us not working, I'm still in constant daily pain.... Instead of trying Lyrica or Gabapentin she prescribed Cymbalta.... 😟😞

Hello all, hope you are enjoying a peaceful Saturday. I have had low sodium/chloride on and off for over a year now. The last test that I had a few weeks ago, the levels were seriously low (low enough to be hospitalized). I did not have any obvious symptoms. I am confused as to why this is happening. I have both lupus and sjogren's. Sjogren's causes me to be very thirsty. I've been told conflicting things about hydration. I am now adding Propel once a day. Anybody have any thoughts about… read more

I want to try supplements to lose some pounds I’ve gained since I’ve been diagnosed. I don’t want to get too heavy, I know my rheumatologist told me to eat healthy but I feel like that’s not enough for me.

Ok, my cymbalta users. I am currently on celexa. I had a dr tell me I have Fibro and treatment is a different type of antidepressant, cymbalta, savella. I have an appt with PCP today and want to discuss. How has it helped you with your Fibro and any side effects, because I am the side effect queen, lol. Thanks