Addison's Disease Support Group
Addison's disease (also known as chronic adrenal insufficiency, or hypocortisolism) is a rare endocrine disorder. It is estimated that it affects about 1 to 2 in 100,000 people. It occurs when the adrenal glands, seated above the kidneys, fail to produce enough of the hormone cortisol and, sometimes, the hormone aldosterone

I have tried homeopathic things for the swelling and nothing is working. Does anyone know how to balance getting enough HC and not swelling, or is there something natural I can take for the swelling that I have overlooked? Also, does HC cause any of you to have a really overactive bladder where you just get running to the bathroom to urinate all day and all night long?
I still have nausea, everyday. My migraines and nausea go away by my 3 rd dose of HC. Then I do it all again tomorrow, lol. Although it isn't a fun way to start your day. But I just remind myself that I'm lucky to have the meds and doctors so I don't feel bad all day, and comfortable bed, my iPad, etc. I would hate to have a serious condition in a third world country. It's already hard enough.
There HAS to be a better way of dosing that will allow you to feel better.
Also, Lynn, please read up on Circadian Rhythm and Addison's Disease. (google it all together) I think you need to try getting bright light in the morning, either by sunlight (cheapest) or light box. If you are like me and are dragging in the morning and by night time you feel so much better, your circadian rhythm is flipped. If you can straighten that out, not only witll your AD do much better , but I think those horrible a.m. symptoms may improve. That is what I am currently working on -- getting my circadian rhytm straightened out. We have had so much rain that ti's been hard to get into the sunshine in the am. but I am determined to fix this problem.
I've had migraines since I was about 21, but only maybe 1 a week. Leading up to my dxd I started having multiple migraines. Once I had Addison the headaches were 24/7. Lack of cortisol and not being dxd with celiac for another 10 years. Still have them daily, but they aren't nearly as bad as they were.
Thanks for thinking of me.
Yes, I think you are right. I have to find a dosage that is just perfect for me. But I do find that changing my dose to 5 am and again at 10 am works well for me.
Yes, Darla, you can change your circadian rhythm which is often 'off' or backwards with AD people. Google "Addison's Disease and Circadian Rhytm" and also "Adrenal fatigue and circadian rhythm". Because I had a lot of eye surgery, I wore sunglasses continuously for several years. My poor eyes never saw sunshine. This flipped my circadian rhythm so that my body wanted to sleep in the am and party all night. It is so important also for depression among other things to get out daily in sunight without any glsses or contacts on our eyes and let the sunshine strike our pineal gland. You can gogole that too. It sure has helped me. No more sunglasses for me!lol