Guest guest Posted April 22, 2003 Report Share Posted April 22, 2003 Hi y'all, For the past several days I've been experiencing a lot of pain from my pseudocysts. I think the stress and apprehension of " not knowing " is taking it's toll. Anyone who says stress doesn't affect the pain is a nit whit, IMHO! I've been working on my SSDI application and trying to lay low, but still having continual problems with the local pain and now the back pain has started up again. This pain is quite different from the earlier CP pain. It is more localized and precisely in the two areas where the cysts are located. I have had to start back on my pain medications, the duragesic patch with percocet for breakthrough, but the percocet just isn't cutting it this time. I was supposed to do a three day test this week for my CDE by keeping a record of my blood sugars before and after each meal, injecting calculated insulin based on the carbs for each meal, and noting the post prandial results...but indulging in absolutely NO EXERCISE for the three day test period. Exercise lowers blood glucose, and they wanted to see the affect that the insulin had to lower my blood glucose without any other contributing factors. Well....I haven't been able to finish this test because I haven't been able to eat the scheduled three meals a day and snacks because I just don't have any appetitie with this blasted pseudocyst pain. It's too bad, because at least I'm able to fulfill the NO EXERCISE part of the test........I haven't felt like doing much of anything...he, he, he! Thursday I meet with my new gastroenterologist and find out what the results of the ultrasound are, and what he proposes to do about the pseudocysts. I'm getting tired and stressed out about " not knowing " and just hope that whatever is decided, we can go ahead and make some definite plans. Speaking of plans.....I'm really pouting and feeling sorry for myself because my husband, grandson and I were supposed to go to the Adirondacks for a week in May for our annual timeshare vacation and visit to see my dad, and anyway you look at it I don't think we'll be able to go this year because of this impending surgery. We'll either have to use the vacation time for surgery or use it for recooperation, because I understand the recoop time is weeks to months long. I'm so disappointed to miss this trip again, (second time we've missed it because of my CP), and my poor dad hasn't seen his only great-grandchild in three years now. And I feel really guilty that my husband should have to use his long awaited vacation time to hover over me in some hospital bed, or worse, stuck at home hovering and having to do be in charge of all the home responsibilities. Well, I got that all off my chest, and I do appreciate anybody who listened. I just had to let go of my self-pity and air my complaints so I can turn my day around. I'll try to go find something to occupy me that will turn my pout ... :-( ....into a smile again.....:-) Thanks for listening. With hope and prayers, Heidi Heidi H. Griffeth South Carolina Southeastern Representative PAI, Intl. Note: All comments or advice is personal opinion only, and should not be substituted by professional medical consultation. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2003 Report Share Posted April 22, 2003 Heidi: If anyone has deserved the right to " pout " you have! So pout! A good ole feel sorry for myself day is certainly in order! As far as SSD, from what I have seen, I can't think of anything else you could possibly do. Try not to worry, easier said than done I know. Be good to yourself! Kaye Quote Link to comment Share on other sites More sharing options...
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