I had my appt. Monday with my neurologist and she of course wanted another MRI with contrast which I get done at another place rather than hospital I had it. She thought the resolution of the pictures was awful!! She seemed more concerned about
my lupus than what may or may NOT be there
So my rhuemy said continue on with the MTX so I was wondering since I was off for a week of the 6 pills do you all think I should take the 6 at once or 3 tonight and 3 tomorrow night
My rhuemy's office was closed today so I couldn't ask. How do most of you on MTX do the dosing??
Now I hope I get along with MRI contrast since I'm allergic to CT contrast.
Thanks so much for being supportive!!!
Diagnosed dystonia 1982,COPD 1995,SLE(Lupus)2005,Subclinical hyperthyrod 2005,neuropathy 2004,mild spinal stenosis 2005, and the list goes on and on.....Raynauds March 2006, Bollous of SLE Jan 2006,chronic pain for many years, chronic pancreatitis, cysts on liver
Meds Sectral 200 mg 1 x day, Methotrexate 15mg per week, Xanax .5 4 x day,Hydrocodone 7.5/500 every 6 hrs as needed, SVN treatments as needed,Folic Acid 2-400mccg per day