Hello! For over two years, I have stumbled upon this forum and have read (many times over) your dilemmas and responses in hopes of coming to terms with my Crohn's diagnosis.
I am 50 (diagnosed at 48) with mild-to-moderate Crohn's (the consto kind) and still have so many wonderings about
what and how I am feeling. My gastro dr is amazing, and he is so easy to talk with. But I have found myself seeking your "companionship
" over the past few years to understand more of what is going on with my body.
I am a VERY "type-A" personality, and this diagnosis has kicked my butt more than I realized. I think I really had major flares for a while (just pushing through my hard-headed life) until I finally ended up in the emergency room two Christmases ago.
My first question is: How do you know when you are having an authentic flare? Mine seem to be high-abdominal pain, constipation, extreme lethargy, severe mood swings, and basic "I don't give a hoot mentality." My gastro dr has me on Entocort and my colonoscopy shows no signs of scarring as of last test. Barium test confirmed Crohn's, but MRI with contrast was "normal." I'm just confused.
Second question: For an episode two weeks ago, my gastro dr called in prednisone for inflammation (I have follow-up appointment in 4 weeks). Took my last dose this morning. Had to go to dentist for a cleaning, and my BP was through-the-roof. I have always had characteristically low pressure; so, I was shocked. The dentist offered to call an ambulance. Is the prednisone possibly what caused that? It's 9:00 at night now, and I still feel weird. My husband took my BP and it was 180/100. This is not me!!!!
I'm just looking for folks to share ideas with. In these two years, I have grown to respect people with chronic health issues so much as I have (from the outside) read, learned, and grown from your strength.
Looking forward to chatting.
J