I wanted to post before I have a follow up w/ my cardiologist. I have had 8 heart caths since MAR 06, and have 5
stentsAbdomen - swollen
Brain herniation
Chronic persistent hepatitis
Coronary artery stent
Hyperemesis gravidarum
Lyme disease - chronic persistent
Stent in my LAD. I have had in-stent restenosis
twiceTwice-a-day in my LAD in bare metal
stentsAbdomen - swollen
Brain herniation
Chronic persistent hepatitis
Coronary artery stent
Hyperemesis gravidarum
Lyme disease - chronic persistent
Stent, but my doctor put a DES under the two bare
stentsAbdomen - swollen
Brain herniation
Chronic persistent hepatitis
Coronary artery stent
Hyperemesis gravidarum
Lyme disease - chronic persistent
Stent, and the last two caths were
clearClear by design
Clear eyes
Clear eyes acr
Clear eyes clr
Clear-atadine
Clear-atadine children's. But I still have chest
pressurePressure ulcer, pinching in my shoulder, discomfort in my back, and am very tired. Also, when running, my left arm goes numb a little bit. I have also had spells of dizziness and nausea lately, but could be my meds. I take Plavix, Lisinipril, Zetia, Metaprolol, Isosorbide Mononitrate, Cilostazel (Pletal), Lipitor, Niacin, Fish Oil, and an aspirin. What questions should I ask my cardiologist? What could be causing the continuing symptoms? The symptoms aren't as severe as earlier, but they are enough to cause me discomfort. Is it safe to continue to exercise? Are their any tests you recommend? And finally, when should I go to the hospital and when should I just "drive on". One of my biggest dilemmas is whether I need to go to the ER during strong bouts of symptoms. Any info you could provide would be very helpful, as I'm 40 with two little girls and would really like to get back to leading a normal life again. I have a strong family history of CAD (my dad has 9 stents and has had 19 caths/angio's) and do not smoke. I have already been tested for GERD and asthma, and both are negative. Thank you for supporting all of us through these posts.
I do not wish to interfere with your post but since our symptoms are so similar I would be eager to see the CCFMD's reply and see if there is anything new for this very common condition. Best wishes for recovery.
Chrisr