symptoms and doctors

New Topic Post Reply Printable Version
[ << Previous Thread | Next Thread >> ]

New Member

Date Joined Aug 2007
Total Posts : 4
   Posted 8/13/2007 2:32 PM (GMT -6)   
Hi!  This whole thing is so new to me.  I have all these symptoms, and I'm not sure who I'm supposed to tell.  Do I tell the Rhuemotolgist (sp?), or do I just go to him for the pain, and go to my regular doctor for the lack of appetite, fatigue, and saddness I can't seem to shake?  This is so frustrating!!
I'd appreciate any advice I could get!!


Veteran Member

Date Joined May 2005
Total Posts : 7725
   Posted 8/13/2007 2:57 PM (GMT -6)   
My general rule of thumb is to tell every doctor as much information as I can. They are the experts on how diseases, medications, and symptoms are inter-connected; not me!

In my case, lack of appetite and fatigue were addressed by my rheumy as being part of lupus -- we changed medications around till we found a combination that works. While the rhuemy explored the sadness to some degree, he ultimately decided a psychiatrist was better prepared to address medications for long-term depression.

Some rheumies want to make sure anything being caused by a medication is addressed by the dr prescribing the medication, others want to pass some of these side-symptoms along to a PCP or other dr as needed. You just have to keep feeling out your drs and you will learn what should be addressed by whom -- since lupus is so different for each of us, there is no sure way of defining what drs will be needed or which ones will address which issues.

Hang in there,

Lynnwood, Co-Moderator: Lupus Forum
SLE(’00), Sjogren's Syndrome, SAD, Depression, Herpes Simplex 1
Piroxicam, Plaquenil, Cellcept, Prednisone, Trazodone, Fosamax, Wellbrutrin SR, Valtrex
Links: DIAGNOSING LUPUS(4of11), LUPUS INFORMATION, LUPUS RESOURCES, Donate to HealingWell, Drug Interactions

Regular Member

Date Joined Jul 2007
Total Posts : 261
   Posted 8/13/2007 8:08 PM (GMT -6)   
Hi, 3gifts. I'm with Lynnwood. I tell every doctor every thing. Of course, I have only been diagnosed for about a year and a half, so I'm never sure who to tell either. I have tried to make a "friend" out of a nurse at each doctors office, so there have been times I have called and run what's happening by them and sometimes that helps especially if there's a new med involved. I do try to keep my rhuemy involved all around though. Hope you can get the help you need. Keep us informed.
Always looking for the silver lining, Sharen

SLE '06, Sjogren's '06, Traumatic Head Injury '94
Prednisone 10mg and tapering, Caltrate 1200mg, Multi-vitamin, Prevacid 30 mg, Actonel 35mg

New Topic Post Reply Printable Version
Forum Information
Currently it is Tuesday, September 25, 2018 10:33 AM (GMT -6)
There are a total of 3,006,432 posts in 329,336 threads.
View Active Threads

Who's Online
This forum has 161833 registered members. Please welcome our newest member, LorrieL..
332 Guest(s), 13 Registered Member(s) are currently online.  Details
notsosicklygirl, mattamx, Kent M., physedgirl09, browntrout, Admin, Cashed Out, Jay79, Lynnwood, Fairwind, nakamura1967, Aerose91, paisan