I’ve been back from holiday for a whole, long week now. For those interested, it was amazing and it was great to have the opportunity to relax and not worry about anything whilst away. It was helpful to just enjoy a little break from everything and I felt a lot better for it.
I had to take my drugs on holiday with me and I was a bit concerned that trying to take a needle into the plane would be a bit of an ordeal. I had letters from my doctors confirming that I was undergoing treatment and that the needle’s purpose wasn’t malevolent in any shape or form. However, I didn’t have to worry about that at all as the bag went through check in without any problems and the needle even made the trip back home [as it needs to be disposed of in an appropriate manner] without any inconveniences whatsoever. So that was very good!
Now, back in the real world, I had my monthly appointment on Friday and it was, as it’s becoming the rule, a mix of good news and not-so-good news. The good news: My blood levels are all normal, my liver function is fluctuating but it’s still within reasonable levels under the circumstances, my body is reacting well to treatment and I now have to see the doctor in three months time [with a few blood tests along the way]. The bad news: As was expected, the interferon has not helped at all with my Hep B and it is now a distinct reality that at the end of this treatment [regardless of whether the interferon actually helps me rid myself of the Hep C virus], I will have to start yet another treatment for the Hep B. This treatment will be ‘very expensive’ apparently and I’ll have to apply for it on ‘compassionate grounds’ to see if I can get it subsidised by the NHS. So, as you can see, a mixture of good news and not-so-good news.
Anyway, I guess we’ll cross that bridge when we get there. In the meantime, I’m being very good with my current treatment and it seems to be working very well. The doctor is very happy with the progress and it all seems very positive overall.
On a personal level, I’m still as exhausted as I’ve been for the last three months and my muscles still ache all over but I’m still coping well with that. The people close to me have started to ask lately whether I’m ok [I’ve felt ok] so I’m hoping I’ve just been having a few days off and this is not the start of undesirable mood swings that I haven’t noticed. Hopefully that’s not it and I’ll be posting next week that my fears were unfounded.
Ok, I think I’ve taken enough of your time now. I’m signing off here but if you want to find out more, get in touch.
Peace!
I had to take my drugs on holiday with me and I was a bit concerned that trying to take a needle into the plane would be a bit of an ordeal. I had letters from my doctors confirming that I was undergoing treatment and that the needle’s purpose wasn’t malevolent in any shape or form. However, I didn’t have to worry about that at all as the bag went through check in without any problems and the needle even made the trip back home [as it needs to be disposed of in an appropriate manner] without any inconveniences whatsoever. So that was very good!
Now, back in the real world, I had my monthly appointment on Friday and it was, as it’s becoming the rule, a mix of good news and not-so-good news. The good news: My blood levels are all normal, my liver function is fluctuating but it’s still within reasonable levels under the circumstances, my body is reacting well to treatment and I now have to see the doctor in three months time [with a few blood tests along the way]. The bad news: As was expected, the interferon has not helped at all with my Hep B and it is now a distinct reality that at the end of this treatment [regardless of whether the interferon actually helps me rid myself of the Hep C virus], I will have to start yet another treatment for the Hep B. This treatment will be ‘very expensive’ apparently and I’ll have to apply for it on ‘compassionate grounds’ to see if I can get it subsidised by the NHS. So, as you can see, a mixture of good news and not-so-good news.
Anyway, I guess we’ll cross that bridge when we get there. In the meantime, I’m being very good with my current treatment and it seems to be working very well. The doctor is very happy with the progress and it all seems very positive overall.
On a personal level, I’m still as exhausted as I’ve been for the last three months and my muscles still ache all over but I’m still coping well with that. The people close to me have started to ask lately whether I’m ok [I’ve felt ok] so I’m hoping I’ve just been having a few days off and this is not the start of undesirable mood swings that I haven’t noticed. Hopefully that’s not it and I’ll be posting next week that my fears were unfounded.
Ok, I think I’ve taken enough of your time now. I’m signing off here but if you want to find out more, get in touch.
Peace!
1 comment:
Hi there, if you want some support thru your treatment, come and join the HepC Nomads.
www.hepcnomads.co.uk
We are a group of around 500 members that help support others with this virus , we also focus on the Social side of support thats needed for lots of people.....hopefully see you there..px
Post a Comment