Hi,
i am so sorry to hear about all that you are going through. Currently at the age of 31, I can truly say that being diagnosed two years ago was not an easy task. I suffered with joint pain for about 3 years prior to my diagnosis. The doctor said that I had migratory arthritis at first (about 1 year). Then after having a lip biopsy done, he said it was sjogrens syndrome (about 2 years). Then finally lupus. Later a kidney biopsy was to follow along with a terrible stint with blood clots (dvt's), a 3.5 week hospitalization in which I contracted a staf infection and lost 40 pounds, gall bladder removal, found fibroid tumors on my uterus, pancreatitis, adhesions, another dvt hospitalization and the list goes on and on. Lupus is a very tricky disease in that it mimics so many other diseases. Numerous er trips for a swollen/bloated belly that was so painful to breathe, lay down, sit up (or anything) until I was in tears and only a shot of morphine could bring the pain under control....
I know the feeling of going to the doctor, telling them about your 100 symptoms you've experienced since you last saw them and it seems to fall on deaf ears or they want to slap you on some depression medication. I still find it hard to share all of my symptoms with my doctors (cause first of all I have too many - primary/family, rheumy, nephrologist, obgyn, cardiologist, and other specialist as needed). I know I shouldn't feel that way, but it really does put you through a mind game because today it's one thing and tomorrow it's another. Then one morning you wake up feeling semi-decent and then two hours later your knee, or your finger, or the top of your foot begins to swell and ache..... I know what you are going through because it seems unreal how you feel on a daily basis and what you go through on a daily basis....
I haven't had any children yet and lord knows I love them and want some. I haven't tried yet. With the lupus and fibriod issue it may become trying for me, but I will keep my strong faith and believe that it will happen. Perserverance is everything!
Work with your doctors and be very diligent. Do your own research, request that certain tests be done. Make a list, starting today, of your symptoms, when they start, the severity, and how long they last, and share it with you doctor on your next visit. Request to see a rheumy, and work with them closely. Anytime you feel something different or the pain or severity is magnified schedule an appointment and go see your doctor. Also, share how you personally feel with your doctor. Letting them know that you feel that if you share all of your issues with them that they might start to question your sanity as you, like me, probably have already.
Just know that I can relate.
I hope this helps.