Half way house

Treatment today will be halfway through the Rituximab. All going well, and gut now settling down with new regime of laxatives

Piriton

As part of each Rituximab maintenance therapy they give me a steroid and an antihistamine. The Rituximab and the steroid are fine, but the antihistamine makes me very drowsy. I drowsed all afternoon during the treatment, too sleepy to read my book, and it was too noisy to actually sleep. It's nearly bedtime now, and I'm just about starting to feel more awake!

This treatment will be the half-way point of the maintenance therapy. It's a little scary to think about when it finishes and I will have to stay in remission on my own. I know I managed for 25 years before, but not sure how long it will be this time!

My hair, as predicted, has grown back curly! I've had it cut short and layered and am experimenting with it, but seem to be good at getting it looking frizzy, not so good at the loose curls I was hoping for!

More results

I met with the gastroenterologist on Monday and the tests have all come back clear. He thinks I have a 'sluggish' gut and that is causing the constipation and then the diarrhea. He had prescribed a selection of laxatives last time, but they didn't seem to make much difference. He has prescribed a slightly different selection for me to try, assuring me that they are safe to take in large quantities (not sure I like the sound of that!)

I've been researching this a little myself and am going to include a probiotic (Yakult) in my diet to see if that helps. In addition, I'm going to try a home-made mixture of prunes/figs/dates/currants as well!

Hopefully, with my normal healthy diet and exercise, my gut will start to settle down and get back to normal.

Review

Review at the hospital today and I was able to talk about the problems with my gut. They assured me that the endoscopy was to rule out anything serious, but they are sure there's nothing serious. My blood counts are improving - white blood count nearly normal!

Prep Day

To prepare for the colon procedure I had to follow a very strict regimen. I had to eat a limited 'low residue' diet and take some strong laxatives. The diet sheet included several things I don't normally eat, so had to go shopping specially for cornflakes and white bread. The laxative is taken twice, once in the morning and once mid afternoon, after which you don't eat until the morning of the procedure. By the end of the day it was apparent that I am resistant to laxatives! Not really good news. The procedure was fairly painless, but my colon wasn't clear enough for a full test. Saw some fascinating pictures of the inside of my colon! Results in a few weeks.

A surprise!

I had my appointment with the gastroenterologist this week and I was rather surprised by his possible diagnosis. I've been having bouts of diarrhea that left me feeling very weak and poorly, sometimes for several days. The consultant said that he thinks I am chronically constipated, probably brought on by the treatment - not what I associated with diarrhea! A very good diagnosis, though, as easily treatable! I have to go for an endoscopy at the end of August to check the bowel and I'm not really looking forwards to that!

The cancer talk at the university earlier this year reminded me to consider the environmental causes of cancer, so I've taken the decision to go vegetarian (kind of - I still eat fish and occasionally chicken) because red meat and processed meats are known to be associated with cancers. There has also been some research on the use of hair dyes and NHL that suggested there might be a connection, so after a bit of research, have used Henna to colour my hair back to dark brown. It's quite a change after all these years of being blond!

Spring at last...

It's now a year since I went to my GP with my swollen lymph, and here we are again with May blossom!

I had the 3rd maintenance last week and all seemed to go fairly well except for a bout of tiredness: my blood doesn't seem to get back to normal between treatments and the levels are quite low. In addition, my gut doesn't seem to have recovered yet from the chemotherapy and I've had a couple of episodes of feeling very unwell. Sometimes it's tricky to know if something is related to my NHL or the treatment or something new, so I've been to my GP. She doesn't want us to miss anything, so I've been referred to the gastro-consultant at the hospital and have an appointment at the end of July. Hopefully, it will have all settled down by then anyway.

Running going well, and I've taken up a new (very mad!) hobby and made some lovely new friends - see below for pictures! Must be something in the spring sunshine....