I’ve had my second IUI, first one with injectables instead of Clomid. More on that in a minute.
I hate taking pills. Well, really, I just hate taking medication. I hate that today’s science labs have created something that I need to take in order to make me feel better, and that if I lived in an age where these drugs weren’t available I’d probably die, or something. I suppose I should be grateful. I’ll work on that. I hate my need for medication, most of all.
And apparently, I need a lot. I realized this today, while giving a rundown of my drugs to the nurse at my gyno office. Once upon a time I occasionally took 2 advil for period cramps, or 2 tylenol for a headache. And my birth control pill. I went from that, to this:
-Ranitidine (really Zantac) – not for ulcers, though I may give myself one over time, but for those pesky autoimmune hives. It’s an antihistamine.
-Claritin or Zyrtec – the other antihistamine, I take this with the ranitidine, twice a day.
-Synthroid – the one drug I don’t mind taking, it’s saved my thyroid.
-Probiotic – from RainbowLight, a friend said her stomach felt good on them, and she has a stomach similar to mine. I figured they can’t hurt. Twice a day.
-Psyllium Husk pill – twice a day. These are the only fiber supplements that seem to help with IBS. Again, another autoimmune disease, and Miralax doesn’t touch it.
-Multivitamin – one that actually feels great on the stomach. I wouldn’t mind that after dinner if it were by itself, but it’s joined by the probiotic, psyllium husk, and:
-Vitamin D – allergist said I was low and should take this, and I know it helps with thyroid function.
-Folic acid – multivitamin doesn’t have enough, but the gyno said I could stay on it if I added 400 mg more of it.
-Vitamin B6 – I’ve heard lengthens your LP. Mine was 9 days, and I decided to give it a try based on a friend’s recommendation. It works – went to an 11 day LP to a more recent 13 day LP.
That’s 6 pills with dinner, two with breakfast, two when I get up, two when I go to bed, and one at 5 am with a big drink of water. I HATE all these pills.
Well, after the rundown with the nurse at the gyno, the actual doctor came and did a culture on me, since I just had my third yeast infection in about as many months. Granted, I had that infection a week ago, and with the IUI last Sunday I wanted it cleared up by then, so a nurse at the RE’s office gave me the Diflucan, plus a prescription for 2 more, thank god. That pill is a miracle worker. Anyway, the culture today probably won’t show any yeast issues, because I’m sorry, I couldn’t wait a week to be tested. Not to mention, the results will probably be screwed up because I took my first dose of Crinone this morning, before the appointment.
After the culture, the doctor at the gyno really had no words of advice for why I get these yeast infections, and I was all prepared to battle against the typical, idiotic comments: Do you wear tight clothes? Shower after exercise? Take a probiotic?…blah, blah, blah. This isn’t my first rodeo. But she didn’t ask. Instead, she told me to start taking – wait for it – more pills.
-Cranberry pills, 2 of them, twice a day.
-Acidophilus – another probiotic, twice a day. I checked my current probiotic, not the same stuff in there, it’s different. Should I continue to take the one I already have, too?
Adding these to the cocktail will put me at 9 pills at dinner, 5 at breakfast…so on and so forth. Doesn’t this seem excessive? Yet, many are supplements, not hard drugs, and most were recommended by various doctors (which is a whole other story – I hate that I need 8,000 doctors. Whatever happened to going to my primary care when I had strep throat?)
I suppose I could stop certain pills, maybe. People who see me take out my pill container must think I’m nuts. But yet – my thyroid is perfect right now. Other than being 10 pounds overweight, I feel good. Hives are down, I’m attempting to get pregnant…I just don’t want to jinx it, basically. And I get the feeling that when you have autoimmune issues, you’re short on a bunch of vitamins. Supplements should be my friend.
Okay, on to the IUI. Like I said, it was Sunday morning. In my last post, I was worried about it, because of the yeast infection and the fact that we were using my husband’s frozen sperm. Add to the mix the fact that I had some sort of weird stomach bug….I felt fine until I ate or drank anything, even water…and then it all came out. This went on for 3 days. I barely ate. I just assume that such a weird thing will somehow manifest itself in my uterus.
And just as I thought, it was kind of sucky. My husband’s count before the freezing was 43 million, which was way down from 140 million last time, which is weird. But either way. After freezing and thawing, it was 7 million. Wow. That’s a big loss. She said they want to see it at least 5 million, so 7 million was fine. But still. We had no choice – we had to do it this way. My husband is always home, always. But a year ago he signed up for the Ironman race, it cost a lot of money – it was happening. My IUI was the day of his race. Nothing I could do about it. Not only did the count suck, but the Sunday nurse whom I had never seen before got me in a half hour late, when I was told I could be in a half hour early, and by the time it was done it was a good hour later than I had hoped, considering I was driving 4 hours to see my husband finish the race. And she sucked. Couldn’t match up the holes, or something, she said. It took a while to figure it out, and painful all the while. Thanks, lady.
She recommended we have sex that night, just to strengthen our chances. Well, my husband was coming off a 15-hour race, and we were staying in a tiny camper with his parents. Needless to say, sex was not an option. So, my second IUI, first with injectables, was done with the least amount of luck possible. Small count, no additional sex, a yeast infection, and a stomach bug.
Afterwards, I did drive 4 hours to see my husband finish his race, which he did at 10:30 at night. He started at 7 am. It was very cool, he did a great job, and it is quite an accomplishment.
And now, I’m in the TWW. My 4th time in a year. This time, I have no clue how things are looking, and I will continue to think nothing of it. I’m not temping (I haven’t since April, the last time I was in a TWW) – so I actually have no clue when I officially ovulated. I assume, being two days after the IUI, that I am 2 DPO, but who knows. I’m not checking any “symptoms” – they’re all in my head anyway. I’m already planning my next cycle. And I think we’ve reached our decision – I want to do another injectable with IUI. We have the option of going to IVF, and our insurance covers it, thank god. But I don’t think this IUI was given a fair chance. I want to do it right this time, with fresh sperm and sex, and I assume there will be less shots, now that the doctor knows what works and what didn’t. A second chance at the IUI, then IVF. That’s what I’m thinking right now.
The Crinone – ugh. You’ve warned me. It reminds me of those days of Monistat, before I knew about Diflucan. Gross, and I’m already itchy. Any side effects from this I should know about? And besides “cleaning house” up there every few days, is there anything else I should do to lessen the grossness? Does anyone actually have sex while they’re on this? And how long are you on this? Just the TWW?
Finally, the pregnancy test. I probably won’t even get to this point, because I plan on waiting a long-ass time to test. Maybe I’ll even try to surprise myself – “Oh, my, look at the date, I haven’t gotten my period on time!” Probably won’t happen. But I’ve heard the trigger shot skews results. The LAST thing I want is to get a false positive, the first time ever seeing one. How long until it’s out of your system?
I appreciate the words of advice you guys give me. I try to stay away from Google, and ask you instead. 🙂