%-) %-) >:( >:( :'( o.O
Gall bladder runs in my family on my mother's family. My gall bladder we removed in 1984. Over the years I have told my doctor that I still feel the pain in liver/gallbladder area. The pain has escalated, I am feel the same level pain as I was before the original gall bladder surgery. My primary care doctor could not see me that day and asked me I was willing to see a differnt doctor, because he did not want me to wait.
This doctor that I was referred to examained me and wrote orders for blood work, as well as schedule ultra sound. He also thought that this was in a fibromyalgia flare (I was diagnosed with this disease in 1997), I disagree. The results of the ultra sound did not show a clear abdominal picture due to gas. But, the ultasound did show a slightly enlarge liver. After my test I made an appointment with my primary care doctor. My primry care doctor did not agree that Fibromyalgia diagnosis from the doctorm he referred me to. My primary care referred me to a surgeon
The surgeon, was a very level headed person with a good bedside manner. He discussed that he needed for informatioin in order to come up with a plan. He schedule a CT and endoscopy as soon as possible. I agree with his caution to take this one step at a time. In the meantime my pain level is through the roof. I do have Vicodin but it takes the edge off. in on diet is bland when I can eat. I am finding that it is harder and harder to eat and drink. My bowels are loose and, (Pardon this part) they are baby sh*t yellow.
The complicated part of this is the celiac sprue disease as well as Fibromyalgia diagnosed in 1997, meaning I am on a gluten free diet (no wheat, Rye and barley). I abide be this diet religiously. Any information or questions you might have would be appreciated
Gall bladder runs in my family on my mother's family. My gall bladder we removed in 1984. Over the years I have told my doctor that I still feel the pain in liver/gallbladder area. The pain has escalated, I am feel the same level pain as I was before the original gall bladder surgery. My primary care doctor could not see me that day and asked me I was willing to see a differnt doctor, because he did not want me to wait.
This doctor that I was referred to examained me and wrote orders for blood work, as well as schedule ultra sound. He also thought that this was in a fibromyalgia flare (I was diagnosed with this disease in 1997), I disagree. The results of the ultra sound did not show a clear abdominal picture due to gas. But, the ultasound did show a slightly enlarge liver. After my test I made an appointment with my primary care doctor. My primry care doctor did not agree that Fibromyalgia diagnosis from the doctorm he referred me to. My primary care referred me to a surgeon
The surgeon, was a very level headed person with a good bedside manner. He discussed that he needed for informatioin in order to come up with a plan. He schedule a CT and endoscopy as soon as possible. I agree with his caution to take this one step at a time. In the meantime my pain level is through the roof. I do have Vicodin but it takes the edge off. in on diet is bland when I can eat. I am finding that it is harder and harder to eat and drink. My bowels are loose and, (Pardon this part) they are baby sh*t yellow.
The complicated part of this is the celiac sprue disease as well as Fibromyalgia diagnosed in 1997, meaning I am on a gluten free diet (no wheat, Rye and barley). I abide be this diet religiously. Any information or questions you might have would be appreciated
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