I have hadd Lupus for 9 years and I have had everything under the sun or so it seems to have happend to me that could happen. Now I am having my hair falling out they said it isnt the meds and I am on two different types of chemo treatments but they say neither of those cause d this it was the lupus. I am wondering if anyone else is going through this or has gone through this/ I need some words of encouragement :) I am getting a little depressed about this even though I have a wig I can wear, it bugs me that I have to go through this and will it get better? Please lend some advice.
Posts You May Be Interested In
Hi all! This is for those of you that have or have had the same neurologist for 4 years or more. I have been with mine now since 2009. He is one of the best movement disorder secialists in the midwest. I know he is extremely busy on the lecture circuit now and in fact not taking new patients there is a huge waiting list for him. BUT.... I feel like my visits are not what they use to be. He...
theatre and I are there already. I'm having a very berry tea with crackers, cheese and cherry tomatoes and she's having a joint with some beer and we're both on really comfy recliners on thick pile carpet. we need some help with the decor if anyone is around??