Mucus membranes symptoms and conditions

Wow! So glad and sad to find other sufferers. I wish our doctors would listen to us and take us seriously! Why are they stuck on forcing Synthroid on us? At this point, I think I'd rather not take any Synthroid. I stumbled upon this site while looking for something I might take to counteract the effects of Synthroid. I had to halve my 112 mg pills because of the side effects: frequents headaches, bloating, weight gain, irritability and anxiety, dry mucus membranes (eyes, nose, throat, etc.), allergies, muscle fatigue, achy joints. Of course, my doctor is slowly upping the dosage again, because my TSH is chronically high, but I feel like sh*t, physically and mentally. I used to feel so much more normal and like myself before I was diagnosed and "forced" to take Synthroid.

Nausea, vomiting, headache, dizziness, acid stomach, dry mouth, dry throat, tight breathing.

I'm taking 200 mg doxycycline, twice a day. I'm 6 weeks into a 9 week regimen for suspected but unconfirmed lyme disease (no memory of tick bite and no positive tests), and in conjunction with permanent Ceftin 500 mg twice daily as a prophylactic against strep which triggered an apparent and ongoing Rheumatic Fever. (I think my doctor is more confused than I am.)

I've gotten nausea and acid stomach, but both of these are lessened if I drink a large glass of water with the doxycycline. 200 mg can be hard to keep down.

I vomited once but only after taking it with other medicines which my doctor assured me wouldn't interfere. So I spaced them apart by 2 hours and started eating some food prior to the doxycycline, and the result was no more nausea or vomiting, and a much easier time.

Headache & dizziness are reduced when I take the doxycycline with food, and then it seems not to hit me as fast or as hard, and so I tolerate it much better.

At first I thought the doxycylline was helping relieve some kind of bronchial infection, but it was actually just drying out my mucus membranes. Now I wake up early with dry mouth, dry throat, and even my lungs get dry which is causing mild difficulty breathing. The bronchitis I thought it was helping was actually not an infection but an autoimmune symptom of the Rheumatic Fever, and it wasn't really helping with that, it just made it drier. Now instead of coughing up fluid, I get this unproductive dry pain when I cough, and my cough sometimes tastes like blood. I feel the dry pain in my lungs all the time now. I'd rather have the fluid.

3 weeks left on this regimen, which seems like an eternity, but I'll try to stay the course since I want to rule out lyme disease. All these high-dose powerful antibiotics and doctors don't even know what I have. They don't seem to be helping me much.