Dose anyone here have a lupus without face rush/butterfly rush?
Just remember that Lupus and fibromyalgia have so many overlapping symptoms. I was tested 3 times by different doctors because they were sure I had it. All 3 tests came back negative . Try not to worry...I know it's easier said than done! π
@A MyFibroTeam Member, I am same as you constantly thinking what of if something else more serious, I suffer from horrible anxiety and panic attacks because of my health. My son is only who is giving me strength and I know I have to fight as much as i can. He is only 13 y old. Only thing that helps me little bit is anti-anxiety pill and mental health therapist. I wish that I can find a way to make this illnesses easier but look like older i get things getting worst. Stay strong as much as you can and take care . Hugs to you
@A MyFibroTeam Member, yes I leave in Saint Clair Shores MI, sorry to hear that your daughter has to deal with so many health issues since she was a child I can't imagine how you felt through all that. I pray for her and you to finde strength and relief to get better π we just have to fight all this. Take a care and hugs to you. Thank you for adding me to your team I added you to my as well
My daughter as Lupus SLE Class III and Lupus Nephritsis since the age of 9yrs. She will be 32 Aug. 29th she never had the butterfly rash.
Oh you poor dear...but you sound like you have an amazing, positive attitude. My husband says I obsess over every symptom and make them worse. He is probably right!! I am a "what if" person! I pray constantly, but do you have any advice on how to stay focused during all the storms?