Hey guys, remember me?
Well, my 3 month adventure in Brussels is over!
I had planned on keeping this up to date for the duration, but well obviously, I failed miserably at that. Things got quite hectic and busy and hard and good and lots of things actually. Too much to mention it all now. But I think I did more in those last 3 months than I have in last 3 years! That pretty much sums it up til I get a chance to do a proper round up of it, if I ever do!
I thought I got to week 3 but It seems now looking at my last post, I only made it to end of week 1! Oh dear!
Anyway, my last IV treatment was last Wednesday (ironically also marked the day I got sick 3 years and my world/life/future fell apart), well better to get the treatment late than never , but I hate to think of the irreversible damage done in all that wasted time doing nothing, that it took 3 years to the day to finish 1st round of treatment is crazy. I flew home on Thursday, and since then I have been resting from trip, and unpacking and washing lots and lots of clothes.
My consultation with the Professor was the week before, so week 11. It went ok, but while he was not in a bad mood, he wasn't very informative etc, we felt no further on with info or advise etc after we left the meeting. To all our questions, his answers were mainly along the lines, 'No, not now', 'Later', 'Too early' etc. Just vague! I was a bit stumped coming out of it, but I don't think it was a bad thing really. I am a little different to others, and some serious issues to consider that he is not used to. So he needed to think on it.
So had the consult Wednesday week 11, but he couldn't tell us at that point what next step was, which I was eager to find out , and also to start planning pharmacy ordering and collection and price comparisons too. I asked if it would be orals or herbals. he did not say then, but on Monday week 12, we collected the prescription from Ira.
(I had also asked if LDN would help lower my cytokines which were crazy high, IL8 especially at 20,000 ish, in last /follow up appointment, he was very concerned over this and said it was v damaging. So myself and my mum were anxious to get this down obviously, and I had heard other patients were on it, and it could lower cytokines too. He said no, too soon to bring them down , needs more time at treatment.? )
Anyway, back to the prescription, he eventually went with 2 months of doxy and clarithromycin (not sure how to spell it), as well as continuing the original so called pre-treatment. Now, we got no instructions or info or advise on these two new ones. And since we didn't get to find this out til after the consultation, we could ask or inquire etc from the main man himself. Jan was on holidays and still is now this week. So I can't ask him either.
So I am looking for a lil advise in the mean time. When is best time to take them, or avoid other meds or foods, etc
I was not told either when to start them , straight away or take a break. So I am making that one up on my own. I decided not to start on Thursday straight away cos I was flying and stressy with packing and such. I had planned to start on Monday instead. Give me the weekend to rest etc. I still not started them, so gotta start today, I guess, but slept really bad and deeply and disturbed, bad headache etc.
I don't want to put it off starting orals, cos my next appointment is exactly 8 weeks away so need to start now.But with no info, it is hard. The instructions for clarithromycin is in french, flemish and german and maybe something else. Not English anyway. And the doxy was made up pure by pharmacy from scratch and i think see any leaflet provided . I guess they assumed the doctor would do it.