UTI and Rheumy

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Regular Member

Date Joined Mar 2005
Total Posts : 401
   Posted 7/5/2007 12:20 PM (GMT -6)   
Does anyone here contact their Rheumatologist for a UTI? Or not... just wondering... seems like he has treated so many of my problems because of meds and stuff that I am on I would think to call him but I dont know.. He treated me for bronchitis a few months ago...
5 seperate skin Biopsies 01/05
Diagnosed SLE, Lupus Anticoagulant & Lupus Nephritis 02/05
Kidney Biopsy 2005
Hospitalized 2005 for Transverse Sinus Thrombosis (Blood Clots in my Brain)
Hospitalized 2005 for Rectus Sheath Hematoma and Supratherapeutic Anticoagulation.
08/2006 Back Surgery for Herniated Disk, Right L4-5 Hemilaminotomy & Microdiskectomy
Spinal Stenosis and Arthritis in my back
Fibro and Insomnia
The list goes on and on and on..... and on
Current Meds: Prednisone, Cellcept, Coumadin, Lisinopril & Ativan

Veteran Member

Date Joined May 2005
Total Posts : 7720
   Posted 7/5/2007 12:31 PM (GMT -6)   
My rheumy would probably tell me to see my PCP...but I don't know what he'd do w/bronchitis. Can you call the rheumy & ask the nurse?

Lynnwood, Co-Moderator: Lupus Forum
SLE(’00), Sjogren's Syndrome, Raynaud's Syndrome, SAD, Depression, Herpes Simplex 1
Piroxicam, Plaquenil, Cellcept, Prednisone, Xanax, Trazodone, Fosamax, Wellbrutrin SR, Valtrex
Click: DIAGNOSING LUPUS (4 of 11), LUPUS INFORMATION, LUPUS RESOURCES, Donate to HealingWell, Drug Interactions

Veteran Member

Date Joined Mar 2006
Total Posts : 2608
   Posted 7/5/2007 1:16 PM (GMT -6)   
I agree with Lynnwood that mine would tell me to contact my PCP. I believe it's important to have a good PCP to be in charge of my overall health and it's critical that my PCP have a working relationship with my rheumy. I go to the rheumy for AI problems, monthly blood work to monitor my cellcept, etc., and she forwards all my labs on to my PCP. My PCP is the hub of the wheel and gets lab results and doctor reports from any specialists I see, such as my rheumy, dermatologist, neurologist, sleep specialists, gastro, etc. When my rheumy changes my meds, she sends a report to my PCP, therefore my PCP knows everything about my medical care, including every med I'm taking. That's probably more than you wanted to know, but it's the reason I'd go to my PCP for a UTI.

I've never had a UTI but I understand that it can make you feel awful. I hope you recover from it real soon.
Lupus, Rheumatoid Arthritis, Sjogren's, osteoarthritis, fibro, ibs, renauds, restless leg, hiatal hernia, double vision.

cellcept 1,000mg, neurontin 1,200 mg, prednisone 5mg, plaquenil 400mg, synthroid .15mg, triamterene 37.5mg, tramadol prn, lunesta 6 mg, actonel, tri-est (compounded estrogen) 7.5 mg 2xmultivitamin, calcium w vit D, fish oil, aspirin

Barbara Lee
Veteran Member

Date Joined Sep 2003
Total Posts : 2889
   Posted 7/5/2007 7:14 PM (GMT -6)   
I normally see my PCP for various infections and problems. She can contact my Rheumy if she feels he needs to be contacted. Since my rheumy doesn't do a heck of a lot of stuff for me I only see my rheumy every 4 months or so. I do however, see my PCP every 4 weeks or sooner if necessary. Hope your uti gets cleared up quickly.


dx fibro, SLE, glaucoma, cateracts, bells palsy, depression, migraine headaches, gastreopaersis, chronic anemia, MDS (Blood Cancer). Mediport and tons of meds.

Veteran Member

Date Joined Dec 2006
Total Posts : 2818
   Posted 7/7/2007 9:44 AM (GMT -6)   
My pcp does almost everything that has to do with my normal health problems. I would think that a rheumy could do most anything if they wanted to. They still have to train as a regular doctor before they do a specialty. The bad thing with a rheumy is unless you are already there when somthing comes up it's pretty hard to get in normally and they charge a lot more money.
God Bless
Lupus, possible Crest, COPD, Cervical Cancer survivor. Osteoporosis
Prednisone 5mg, Plaquanil 800mg,Evista60mg, Effexor 150mg, HCTZ25/Triamterene37.5mg,Xanax.5mg
When things are really dark look up. You can see the stars.

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