Guest guest Posted July 9, 2004 Report Share Posted July 9, 2004 - I myself have been wondering if there is anything to the hormones. Due to my past med history I was trying to corrolate something to this disease. I have had to deal with ovarian cysts; 2 on r ovary w/ the second one bursting and having to have ovary removed, then when symptoms of panc started (fullness in abdomen, nausea, and pain in back in pancreas region) I had cyst on l ovary. They thought my amylase levels being mod. elevated (this is only clue to a possible pancreas prob w/ me) were due to that cyst, so I had a surgery to drain cyst. It never changed my amylase or the pain that was starting to be constant in the back. After this it was gallbladder out and several ERCP's to see if stenting would help me. A year and several tests later without any resolve in my pain besides pain meds, I was deemed possible chronic pancreatitis. Never ill in my life before except for those cysts. About 4 months ago another CT scan and another ovarian cyst. At first they were just going to watch it because your body naturally produces a cyst every month and mine was about that size, but last month it grew too large. Doc thought it would be in my best interest too have the ovary removed. With no ovary there would be no sense in keeping the rest so I had a hysterectomy. Interestingly enough during the time frame this cyst had grown about 1 1/2 weeks I had NO pain. I was singing halleluia and all that jazz! I was finally better. To wake up because it was time and not due to pain, it was heaven for me. I would wake up real cautious and slow like then go, " Okay this is amazing " I was so excited. While I was in the hospital overnight they gave me meds that set my panc off, but after coming home I wasn't in the constant pain I had been in this whole year. It was about 1 1/2 weeks after my surgery I began questioning whether hormones really did play a part so started the research of the role hormones play in your body. It's really rather amazing how our body works, but discouraging too because there is so many anvenues to think of when trying to " cure " an illness. For instance if my out-of-balance hormones cause cysts, do other things not function correctly when your hormones are out of whack? One thing I did become convicted about after researching was supplementation and drinking lots of water. (If you don't get enough water in your system tries to overcompensate, work overtime, and it helps to release toxins in our body. With our systems already being comprised due to damage caused internally, but also what we put in it. Un " purified " water, pain killers, supplements that are made from sythetics. Make sure you know where they are manufacturing your vitamins before you dive in. They can do you more harm than good. Also let me know if you want to know what supplements are needed besides the antioxidants. Sorry about the lecture, I became very passionate about this after all that research!) Well as you may have experieced due to menopause I was having hot flashes and migranes, and just a feeling of not being well. I wasn't sure if I just wasn't feeling well due to withdrawals of drugs because I wasn't having to take them, the surgery, or it was my original panc probs, but anyhow Doc prescribed low dose of estrodiol patch though he was hoping I could give it a month or so to see if that was my panc problem. Mostly I just wasn't feeling good, not like an infection or stomach ache, just maybe like the flu sort of. Because I wasn't having any panc pain I was beginning to think my panc pain had been in my head this whole time because I wasn't really having any pain to speak of. So my decision to start the HT was because of migranes and hot flashes and not feeling well. (Unfortunately it was my naitivity from not having this illness for so long.) And two days ago I began feeling that nagging in my back and below my ribs. Was it that Twin Bing I decided I could eat? Or the hormones I am on? Or just the nature of the beast? I am not sure but I do know it is definitely panc pain again. I can go off the hormones and I may try that after I get healed from my surgery. Also another thing I was wondering does someone from a pancreas research place subscribe to these digests to see if there is any corelation to their research or maybe they could play off these ideas everyone puts forth? Thanks for always asking the questions ! Angie B Message: 25 Date: Fri, 09 Jul 2004 14:40:08 -0000 From: " she_remembers " > Subject: Hormones I'm just wondering if there is a hormonal component to CP. The reasons I wonder are quite simple and probably don't have anything to do with it. However, I've noted (at least on this board) that the people most often afflicted are women. Some have said that they have no pain while pregnant which may just be the positioning of the uterus although I would think that would cause more pain with the pressure of the growing uterus. Then there are some that like me who are either in natural menopause or surgical menopause (which is the case with me) and are taking HRT, etc. I can't really explain the hormone theory involving the men but wonder then too if it has something to do with say testosterone levels. I don't know...probably a bunch of hooey but just trying to think out of the box I guess. Anyone with any input to this or know of any studies, etc.? Just curious...... Quote Link to comment Share on other sites More sharing options...
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