Bit of a bombshell..

4 minute read time.
Yesterday was a lot of information to take in, I had a meeting with my case consultant and my specialist nurse, finally raised all the lifestyle and safety stuff that I'd wanted spelt out for me. The first thing I spoke to Jill (my specialist nurse) about was my parents. Obviously I want them to be involved in everything, otherwise they're just going to worry and with all the good will in the world I don't think they would trust me 100% trust me to tell them absolutely everything. So Jill says she can do regular phone appointments with my parents and let them know everything that's going on, I think that would put their minds at ease to have a direct line to somebody like that. I don't want to have to worry about them worrying if you see what you mean! Plus Jill said that Jenny (my consultant) could always ring them now and then to let them know exactly how treatments going as well. So that was all positive. What else... I spoke to her a lot about lifestyle stuff and exactly how strict I'm going to have to be about going out in to crowded places and all that kind of thing. To be honest I knew what she was going to say, I just really needed it spelt out for me. In fairness she did say that if I wanted to plan a trip or a day out I should just keep an eye on my blood counts and see how I feel but for the most part it was pretty much a resounding 'you cannot take part in social situations'.... Now I'm 21. I don't go out loads. But my age group goes out to clubs, bars and gigs. To be fair, out of all of me and my mates I probably go out the least and I had been starting to get real bored of going out to the same shitty clubs in Bristol... but still, to be told point blank how careful and aware you've got to be about it was pretty devastating. With all my best mates spread across the country at different Uni's I'm pretty gutted that I don't have the freedom to just jump in the car and go see them whenever I want, primarily because I can't be too far from the hospital... I'm not looking forward to saying to people "sorry I can't do that... I have no immune system", that's gonna sound great.. Even just thinking what I'm going to do when my parents come down today is difficult, I'm not really supposed to go to the cinema, though if it was a quiet showing it would probably be fairly safe. I did ask her about gigging and that, obviously going all the way to Brighton to do gigs is pretty much out of the question (gutted...) but I think again if I keep an eye on my counts and I'm feeling good there's no reason we couldn't keep gigging now and then. Might have to skip the sound check and just turn up for the gig, get George and Ben to set everything up... be a fucking pain in the ass but better than giving it all up surely. I mentioned exercise as well, Jill really just told me to do whatever I want, obviously I'm going to be knackered a fair bit, so just do what you can. So after talking to Jill I got to speak to Jenny about the next stage of my treatment. Although it is all pretty dependent on the results of my bone marrow test at the end of this cycle, it looks like I'm going to be in hospital every single day. Monday's will be a 4 hour drip and an intrathecal... which is a quite a lot, but then the rest of the week is just quick injections so hopefully overall I'll be spending less time in the hospital overall. Looks like I'll be off the steroids fairly soon as well, which is a relief because I hate not being able to sleep properly. At the moment it's looking like I'm not going to need the bone marrow transplant, although really it depends on the results of the MRD bone marrow test at the end of this regime. I'm really hoping I don't need it, it would definitely be a weight off my mind. Also I've got somebody coming to talk to me about Radiotherapy, which is likely to start after the second regime of treatment. I'm pretty worried about that, to be honest, mainly because I know nothing about it I suppose but still it just sounds a hell of a lot scarier than being pumped full of drugs. So that's where I'm at really, it was a lot to take in, and a lot of it is pretty shocking. I think I'd partly kidded myself that I was going to be able to swan in to hospital a few hours a week, have some drugs, feel a bit shit now and then, and eventually get better. Lot to take on board.
Anonymous
  • FormerMember
    FormerMember

    Hello,

    yes, what a lot you do have to take in and it sounds like your team are doing an excellent job keeping you informed.

    I just wanted to say that, for me anyway, radio therapy was a real easy experience. Not scary at all. You lie on a large stretcher type bed and the machine just rotates around you, not claustrophobic at all.After the first session to line you up with the equipment and they make little marks on your skin your further treatments should only take a few minutes. The only side effect I had was a bit of tiredness.

    It would be good to know how you progress.

    Very best wishes

    Angela

  • FormerMember
    FormerMember

    Hi Will. Hope I didn't scare you with any of my replies to your earlier blogs. Your radiation will probably be different to most treatments. With ALL they give you full body radiation. With mine I had to sit on a bench for an hour and a half for six treatments (morning and night for three days) without moving a muscle. They had to set everything up before every treatment and give me a ten minute blast on one side then repeat the setup for the other side. It's not too bad really as long as you have a good cushion. Maybe they do it differently over there. I didn't notice any bad side effects till about ten days after the radiation and that was easily managed with pain killers. It's not so bad and you'll probably sail through it. Have a good one. Craig

  • FormerMember
    FormerMember

    Hi Angela,

    Thank you for your insight in to the radiotherapy, I'm not really sure why I was so worried about it, just the idea of radiation to your brain I suppose is rather daunting.

    It won't be for a month or so yet, but I'll be sure to let you know how it goes.

    Will,

  • FormerMember
    FormerMember

    Hi Craig,

    Don't worry about scaring me mate, I really appreciate your honesty, you've been a big help to me already. I'm just not sure how to reply sometimes you know seeing as I'm new to all this.

    I'm glad the radiotherapy isn't as bad as I thought, just when they told me it would be cranial and mentioned possible memory loss I was getting pretty concerned.

    I'll let you know what it goes.

    Will,

  • FormerMember
    FormerMember

    Hi,

    Just joined this website but have been keeping up to date with your blogs. I just want to wish you well as I have a - just turned 20 - year old son at university and don't think he could have coped as well as you with everything that you have been through - you sound very positive with everything that is thrown at you.  Life is tough enough sometimes without having this hanging over you.  I'm not on radiotherapy, just chemotherapy but I hope that it all works out well for you with the minimal side effects and you can find time to fit in a bit of a social life too - I know how important that is from what my son has told me.  

    Marie x