Hi All,
Just registered as having been reading all the messages on here and thought I would share my experiences too.
I had a complete MP in Nov 2012, it was our first attempt at pregnancy so was all a bit of a shock to the system. I had the ERPC 2 days later and then my levels were monitored. I was contacted about them going up and had to go in to Charing Cross to start Methotrexate injections on Christmas Eve. It sounds rubbish being in hospital over christmas but the TV on kept me entertained! :)
My first key bit of advice would be to check if you have private healthcare that covers you, say that it is a cancer and is not a pregnancy-related condition otherwise most won't cover you. If you do then you will be on the 15th floor in your own room (assuming they have a bed available).
It is a scary process until you meet the team at Charing Cross. They are the most supportive and understanding group of medical people I have ever dealt with. Being told you are going to have chemo is scary...it's a big word and you will probably find that parents will struggle with it the most, mainly due to the fact that in their generation cancer means something completely different and much more scary. Just keep in your mind that it's curable and the treatment is simply a process you have to go through to get rid of tissues that shouldn't be there.
My levels dropped well on MTX but then started to rise again so I was then moved to the higher dose chemo. That was a bigger fish to fry! The concept of losing my hair took a bit of adjusting to but once I got my head round it (no pun intended) I was OK with it. I had a good 4 inches cut off my hair to a chin length bob to make it less of a transition.
The worst part of the high dose chemo is having the IV drip overnight. Mainly as it stopped me sleeping. Next key bit of advice....TAKE EAR PLUGS!!! With the machine whirring away it can keep you awake, if you block it out it's easier to sleep.
My body responded very quickly to this treatment (I am apparently a freak of science). However my hair did thin alot. I decided to shave it off when I had 1 treatment left. The main reason being that I thought I looked more like a cancer patient with thin hair that I would if I just embraced the bald! :) It was the best decision I made as it was the only thing I could control. My hair continued to thin for 4 weeks after I finished treatment but I'm also pleased to say that now 8 weeks after treatment I have had my first hair cut. :)
You are given the option to not work whilst you are receiving this treatment, this wasn't an option for me. I'm lucky enough to really enjoy my work and the people I work with are very supportive. I went down to working 5 hours a day either in the office or at home. The days when I had IV chemo I didn't go into the office. Working gave me the sense that I still had some normality in my life, that I was still me and not the 'cancer patient'.
This message is much longer than I was intending it to be but just wanted to share my experiences and hope that it settles a few peoples nerves about what they are going through or potentially facing.
Listen to the advice you are given by the medical team, take it easy when you feel tired and stay as positive as you can. I'm a big believer that a positive attitude helped my husband and I get through this and has made us stronger and even more determined to be parents when the time is right.
I'm now waiting to have an AVM sorted, once this is done then hopefully that should be the end of a period of our lives that has been challenging but at the same time (bizarrely) enriching in many ways. :)