Tough Progress... but Progress it is!

I've been on Prednisone and Azathioprine both for 2 months, I can't wait til I get to taper prednisone! The second medicine I will have to stay on a bit longer since it takes longer to take effect.

I've been doing regular blood tests, make sure your doctor wants you to, as well! These expenses add up but even if you have bad insurance like me it will be worth it if remission is achieved. I'd rather be broke and healthy; able to go out even if I have no money to spend... haha.

I've lived outside the US a bit and although socialist healthcare has plenty of flaws itself (fewer sharp people want to be a doctor when they simply can't make as much money doing it, et al.) those $4 doctor visits are easy to get used to!

These meds effect my mood, make my skin break out, increase nausea and sometimes make it hard to sleep.
I am quite hungry almost all the time, which has made me gain weight.

But most importantly my UC has almost cleared up! These last 2 months have been quite difficult, with the first 2 or 3 weeks being the roughest. Feeling sick because of the Rx every day has not been pleasant. Now I'll go in to see the doctor and see what we can do to get complete remission. I assume it will include tapering Prednisone, since I've been on it too long and it's done almost all it can do, and stay on Azathioprine until I am completely well. I can see the light at the end of the tunnel!

Prednisone and Azathioprine Side Effects

So the good news is that my required blood test 2 weeks after I started prednisone and azathioprine came out fine. Your blood should really be checked, especially if you start taking a double whammy of immunosuppressive drugs like me.

I've become quite the pill popper. I now take Colazal with each meal. This makes sense, to constantly keep it running through my system. Before I was taking it just with breakfast and dinner. I suggest making sure your doctor prescribes it for you to take 3x a day.

This week I will call pharma companies that make 5-ASA drugs and see if they can help me cover the cost of my medication. I will have to take 5-ASAs indefinitely, and the cost of Colazal is simply too high to do so, especially with taking it more frequently than before. I'd then ask my doc to prescribe the drug I found the discount on. I will post if I have any luck.

I'm drinking ginger apple juice to fight the nausea and trying all kinds of dark berry juices for the possible cancer fighting properties. Ever since my GI told me about azathioprine and cancer I've been buying more juice.

So... the side effects. There are actually some positive side effects. I've got bad arthritis in some of my joints. Azathioprine is sometimes prescribed to fight arthritis, this drug has kept my swelling way down. My joints sometimes feel like they did when I was 20! Good for lifting... sorta. Ha. Prednisone can be prescribed for asthma, it is easier for me to breath now when I work out and I never get light headed anymore when I stand up. It is nice to have some positive side effects...

But the negatives outweigh the positive side effects... this can be handled because overall the meds seem to be helping! Colazal made me nauseous, these meds more so. Sometimes much more so, that I don't want to look at food. Colitis is kind of a cruel joke to me since I can be a mighty eater. I do not have the energy to work out as much as I am used to, but I am grateful to get in the gym at least a little.

My vision has gotten quite hazy twice. I am happy this has happened only two times since this bothers me more than feeling sick to my stomach. I often get a light headache and usually feel off most of the day due to the new meds. It is harder to focus, on reading a book for example.

I am having decent success just concentrating on what the goal is: remission. This helps me handle feeling a little sick or like I am hungover throughout the day. Then I just get tired at night. The drugs also don't let me sleep as well. I often wake up way too early, and am wide awake when I do so.

*Possible TMI incoming...
Thankfully I can deal with this because overall my condition is improving! Trips to the bathroom are less frequent, with less blood. I am 'evacuating' (sorry, I thought it was funny when my doc used that term) more completely. Yay, drugs.

My Next Step in UC Treatment

I saw my gastrointerologist this week. He said I've gone from what he considers mild to moderate UC.  =/
Since the 5-ASA drugs are not working for me (Asacol, Balsalazide, etc) I've moved on to the next step.

The good news is that the next step isn't as hard on the wallet as I feared it might be. It is just harder on the body apparently, with stronger side effects to go with the stronger medicine. He prescribed Azathioprine and Prednisone for me, the first to be taken indefinitely and the second for a month. I must take blood tests every 2 weeks and a followup visit with the doc in a month.

He told me Azathioprine could cause cancer, but of course the chances are much greater I'd have more problems with UC if I didn't take this medicine. Part of the doctors job is to weigh options and set out a plan, I have confidence in him. It only cost about $20! I started taking it today and feel nauseous... as I expected.

Prednisone is serious as well. At least this one only costs five bucks. I have to take it before 9AM each day so I will start it tomorrow. I'll post later about what kind of effects I feel from the new meds. I am kind of concerned about them but more concerned that my UC has become even more limiting to what I can do than before.

Interestingly, the doc said I should stay on the 5-ASA drug indefinitely as well. It helps control my symptoms a little, so it makes sense that I would stay on it. I just wish it wasn't so costly as my insurance Rx coverage is not the best. So this one has cost me thousands and will continue to do so. That brings the drugs I am on this month to 3.

The doctor said it was fine if I continued to take aloe vera gel pills and fish oil supplements in addition to these 3 meds. He did mention that the fish oil could cause loose stools... which is ironic since I think that is the least of my concerns right now, considering the kind of symptoms that are common with UC!   :p

Curious Cortifoam

I've been able to take Cortifoam, all I've noticed so far are the side effects.
I don't sleep as well, and feel bad for a while after I wake up.
I hope this works so I can stop taking it!
There are many other options out there for your doctor to Rx you, so I would recommend saving this for later if other things are not working.

Remission Impossible

Doc said I should be in remission after 6 weeks. It's been 6+ months, time to see a new doctor! Since I've started the medicine it has helped, but not enough. Even my old doctor agreed. I am headed for my 3rd insurance plan of the year, I am sure the ladies in the doctors office love me!

Balsalazide still makes me nauseous a little almost all the time, just like Asacol HD before it. Strange that I have had to adjust to and accept that feeling 24/7. The good news is that sleeping enough isn't as big a problem as when I first started UC meds.

Rowasa Side Effects

Taking Asacol HD every day made me a little nauseous but I got used to it. I took Rowasa regularly, and it was much worse. I'd get warm and it made me almost want to throw up a few times. I guess it is better than the alternative. I have run out of it now, but despite the strong side effects it seems to work the best.

I would continue taking it but it would cost over $500 a month out of pocket. I would actually recommend it, seems quite powerful. I will probably take it later if I can afford it, since I am aiming for 'remission' as the doctor calls it.

Asacol HD Discount Card

I am on Asacol HD. I am really getting sick, literally, of taking these big pills 3 times a day. They make me nauseous. Seems like I don't have any other good options.

Interestingly, once I get all my symptoms to go away the doc said I could continue taking only this medicine to keep symptoms away for good (hopefully).

If Asacol HD is too expensive for you, ask and search around for info on the discount card. This is a must and should make your costs more manageable if you are qualified.