Newbie here, and this is my first post to the forum.
I'm 29 and I've been having symptoms of an IBD for the past few weeks, though I think I might have been having more mild symptoms for a lot longer that I've just been ignoring. For the past 2+ weeks, I've been experiencing bloody and mucous-y stool, intense fatigue, dizziness, stomach pain, nausea, bouts of diarrhea, increased frequency of having to go, blurry vision, and just a general feeling of unwellness. I should have gone to the doctor sooner but just kept thinking that maybe it was a bad cold or something.
Oh, and my father had Crohns, so I also have a family history.
I finally saw a gastroenterologist yesterday and he suspects ulcerative collitis. I am waiting to hear back about the results if my bloodwork and stool sample. In the meantime, the GI gave me two antibiotics to take: cipro and another one (flaxyl maybe? I forget). I will probably be scheduled for a colonoscopy next week.
I have two questions for the more experienced members of the forum. First, is it typical to be given antibiotics before a diagnosis? I don't like taking antibiotics if I don't need them and I'm a bit confused about what exactly the antibiotics would do. Are antibiotics a typical early treatment for this sort of thing and do they help you feel better?
Second, I'm really struggling with the way that my spouse and family are reacting to this, which is basically downplaying the significance of me possibility having this disease. Basically, everyone's been like "oh, that's not such a big deal". But I'm feeling really really sick and it's having a major impact on my ability to function, to play with my kids, to work, etc, and I'm struggling to juxtapose my experience of these symptoms and stress about how this might change my life with their reactions to it. Granted, my father was also sick with pulmonary fibrosis, which eventually killed him, when he was diagnosed with Crohn's, so in that context my family didn't really pay all that much attention to it as an issue. But for me as a previously healthy person with young kids and my life ahead of me, I'm really struggling to accept this and to cope with these symptoms.
I think it's also hard for my husband and family to understand what I'm going through because there's no diagnosis yet. Any tips on how to deal with others not understanding and for getting through the dianosis period? I'm so stressed and I feel so crappy, but it's hard just not knowing what's really going on yet.
I'm 29 and I've been having symptoms of an IBD for the past few weeks, though I think I might have been having more mild symptoms for a lot longer that I've just been ignoring. For the past 2+ weeks, I've been experiencing bloody and mucous-y stool, intense fatigue, dizziness, stomach pain, nausea, bouts of diarrhea, increased frequency of having to go, blurry vision, and just a general feeling of unwellness. I should have gone to the doctor sooner but just kept thinking that maybe it was a bad cold or something.
Oh, and my father had Crohns, so I also have a family history.
I finally saw a gastroenterologist yesterday and he suspects ulcerative collitis. I am waiting to hear back about the results if my bloodwork and stool sample. In the meantime, the GI gave me two antibiotics to take: cipro and another one (flaxyl maybe? I forget). I will probably be scheduled for a colonoscopy next week.
I have two questions for the more experienced members of the forum. First, is it typical to be given antibiotics before a diagnosis? I don't like taking antibiotics if I don't need them and I'm a bit confused about what exactly the antibiotics would do. Are antibiotics a typical early treatment for this sort of thing and do they help you feel better?
Second, I'm really struggling with the way that my spouse and family are reacting to this, which is basically downplaying the significance of me possibility having this disease. Basically, everyone's been like "oh, that's not such a big deal". But I'm feeling really really sick and it's having a major impact on my ability to function, to play with my kids, to work, etc, and I'm struggling to juxtapose my experience of these symptoms and stress about how this might change my life with their reactions to it. Granted, my father was also sick with pulmonary fibrosis, which eventually killed him, when he was diagnosed with Crohn's, so in that context my family didn't really pay all that much attention to it as an issue. But for me as a previously healthy person with young kids and my life ahead of me, I'm really struggling to accept this and to cope with these symptoms.
I think it's also hard for my husband and family to understand what I'm going through because there's no diagnosis yet. Any tips on how to deal with others not understanding and for getting through the dianosis period? I'm so stressed and I feel so crappy, but it's hard just not knowing what's really going on yet.