Saturday 31st October 09
Only three days to go....... BUT bad news my hair is coming out in handfuls it's horrible i was crying my eyes out last night. Those STUPID Keppra pills i have to take they are doing it i HATE them..........
Sat 24th October
10 days to go!!!
Okay here is my half term...... Monday: My best friend Chelsea from riding and dancing is coming to play and I am really excited cus she has never been to my house before. Tues: I am going to Olivia Hazeltons house to play with her and I can see her baby brother Jack. Wed: I am going out with my great aunt Gillie if my blood test on Tues is okay. Thurs: I am having Sophia Furber on a sleepover and we are going on a pony day at debbie varleys. Fri; .... nothing Sat: Dancing in the village, dog agility ,riding. Sun: Jonses 4 lunch!!!!!
Okay here is my half term...... Monday: My best friend Chelsea from riding and dancing is coming to play and I am really excited cus she has never been to my house before. Tues: I am going to Olivia Hazeltons house to play with her and I can see her baby brother Jack. Wed: I am going out with my great aunt Gillie if my blood test on Tues is okay. Thurs: I am having Sophia Furber on a sleepover and we are going on a pony day at debbie varleys. Fri; .... nothing Sat: Dancing in the village, dog agility ,riding. Sun: Jonses 4 lunch!!!!!
Sunday 18th October 2009
ONLY 16 DAYS TO GO UNTIL I FINISH TREATMENT!!!
We are all getting very excited and counting down the days now until I finish treatment for Leukaemia. I have had my last lumbar puncture for ITMTX, my last vin and christine was last Wednesday. I am finishing my last steroids tonight and then it will just be a final lumbar puncture and bone marrow aspirate on November 3rd with daily chemo, weekly chemo and antibiotics every weekend up until then.
I have to tell you though that I have been back in to hospital for a couple of days because I had another seizure at school on Thursday two weeks ago. The Neurologist has decided to put me on some anti-seizure tablets now and I have to have them for 2 years!!!!!!(They called it epilepsy) I don't mind though if it means I don't have any more seizures. The last one really frightened me and I was at school, so even worse.
I am now counting down every day and we are going out for lunch today and I am really excited. I am going to ring Daddy at 12.00 because that is the time we should be meeting him at the restuarant.
P.S just because I have a name for all my seizures it doesn't mean that you should treat me any differently than before I was diagnosed with epilepsy. I am still just the same old Mima and you shouldn't be scared of me.
love mima xxx
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