The Lupus Encyclopedia edition 2 Summary of Updates from Edition 1

Dr. Thomas describes the vast amount of updated information in The Lupus Encyclopedia: A Comprehensive Guide for Patients and Health Care Providers

Order The Lupus Encyclopedia, ed 2:

IF YOU ENJOYED MY BOOK, PLEASE REVIEW:

[veronicaashleygamez]

Thank you so much Doctor Thomas I was recently diagnosed with lupus in September 2023 and have been looking for a book and more practical info on my new life journey. I’m so excited and feel a lot more confident that this book is out there and available for us patients. God bless you and your family 💜🦋

[WFPB__Life]

How exciting!!! Congratulations Dr. Thomas! I preordered my copy a couple of weeks ago. I was diagnosed with SLE in 2012...the first edition of The Lupus Encyclopedia has been a game changer for me. My Rheumy is so busy and our appointments are never long enough for me to ask the many questions I have about labs, symptoms, etc. so the Lupus Encyclopedia has been my trusted reference for the past 11 years. The book is one of the absolute best investments I've made to help me thrive as a Lupus patient. I truly believe that every newly diagnosed Lupus patient should be encouraged to purchase a copy of your book. Thank you so much for all of your work. Nice to meet Gary too!

[lauralupusandsupport]

We appreciate all the information!! This book is a wonderful and helpful resource...timeless and classic!!

[lacasadelasflores]

Great for all of us with lupus. I just went to Amazon to see if I can buy it but it will be very expensive for a chiapaneca person (Chiapas Mexico). Even do, More then lupus have told us so many things inside the book. Thank you so much doctor.

[fotinachristopoulos]

Congratulations Dr Thomas on the 2nd edition. Looking forward to getting mine.

[rebeccawood]

I’m always worried about traveling! I was what the Lupus support group called a “unicorn” because I got approved in just 4 months for disability. I do also have Sjogrens, seronegative RA, have had 3 pulmonary emboli, 2 strokes. One thing that needs to be battled is medical insurance covering dentures/implants for Lupus and Sjogrens patients. I have your original encyclopedia and look forward to getting this one. Thank you for all your hard work and dedication!💜🦋

[hollycatania]

Congratulations, Dr. Thomas. Thank you so much for all the hard work you did on this book for all of us with lupus. I have the previous version. Can't wait to get my copy of the new one!

[bekkibuenviaje]

Wow. Amazing. Thx! I’m getting it. I’m going to see if I can get in with your recommendation here in Chapel Hill.

[lacasadelasflores]

¡¡¡¡Que hermoso gato!!! Parece un ocelote

[rebeccawood]

Oh! That’s another thing! I’m on Coumadin for life due to my hypercoagulability. I just went through menopause and all my Drs advised against HRT. Ugh.

[scores]

Dr Thomas greetings from nyc. I am not a kupus pt. I have ppms e5 yrs last winter strange leg rSh which my harvard trained derm couldnt identify! I have appt with rheum in 2 weeks. Anyway I will start by getting a preowned copy of your first ed.
I have read ms and lupus are rarely comorbid ( if that is right way to say it:) interested in everything since day 1. all the best to you both.