Of course Simon then wanted a re-test. They tried to convince him to just do it by sending random people (medical ones) in to talk to him about it, but he insisted on doing the tests again. He's certainly not opposed to having a transfusion if he needs it, but when the risks of having one - although small, outweigh the risks of not having one (when his counts are 70 and above) then he doesn't see the point of having one! He was feeling fine, and didn't have any of the symptoms they thought he should if they were so low. Meanwhile I called mum and asked her to be praying that they would be above 70.
Within an hour the results were back and they were 80. Interesting.
It seemed like yesterday there were alot of things that made it not great for him! Earlier in the morning a doctor had told him his potassium levels were really low again, 2.9 and that he would need supplements. He waited and waited, but didn't actually get any. Later on in the afternoon he mentioned it to the nurse, so she went and asked a doctor and finally he got some.
Also his methatrexate counts were still pretty high (13.something) compared to what they would normally be at this stage. Half an hour after his folenic acid (helps clear the methatrexate from his body) was due the nurse came in and started giving various tablets but not the folenic acid. Simon mentioned he was due for it and that he thought it was more important than these other tablets, but she wouldn't do it. Finally 45 minutes after it was due, he got the folenic acid. The nurse went and spoke to the head nurse about it because Simon was pretty insistent and she had to come back and apologise, he had been right.
At 2pm when the next lot was due she came in and did something then said (in a friendly way)she would leave him alone now for a while, he suggested that she wouldn't because his folenic acid was due again now! It just seems crazy that he is having to be like this and I can't help thinking of all of the patients who wouldn't feel well enough or think it necessary to be watching things so (crazily) carefully.
Often he will be told something by someone then the complete opposite by someone else there. He was also moved to a pretty depressing room, he thinks because he caught them out on so many things, but I'm pretty sure there was some poor person really unwell who needed a room alone.
Last night he was feeling pretty down about it all and exhausted from feeling like he needs to make sure there are no mistakes made. Again, it just makes the end of it all so much more exciting, but I didn't know how he was going to cope. After I got off the phone from my poor sad husband I went and prayed, not really knowing what to ask for that would help the next few days not seem so hard. 10 minutes later David, my brother came in visiting Simon and stayed for 5 hours (this was a really good thing!). They also met a really nice family on the ward and just amazingly had a really nice night. My cousins also phoned him and said they would be coming in for dinner the next night and all of a sudden his days didn't seem so daunting.
This week he has also found it a bit harder being on a different ward than he has been on all year and not having a relationship with any of the nurses there. Yesterday they seemed to be coming and lecturing him on things that he already knew because he had been doing this all year, then they would go and forget what they were supposed to be doing or something and he felt like they should be looking after themselves rather than lecturing him like he didn't know what was happening!
Sometimes this blog may seem like we think there aren't any good doctors or nurses there, which isn't true, there are many amazing and wonderful people there and we are soooooo thankful for the treatment he's been able to have. And I know I haven't written about all of the times when they did things right! There just seem to have been many mistakes made which make this all a bit harder to deal with!
Excitingly I just found out his methatrexate levels from last night were 1.6! Not long now!
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