We were on a much needed holiday when we got our first clue that all was not well. Bert had had Bronchitis all through our holiday and against his better judgement he went to see the Dr the day we were due to fly home. The Dr in Turkey was amazing done loads of tests and told us after only 45 mins we were told that his white cell count was really low at 1.2 and that we were to see a Dr on our arrival home. He was admitted on the 15th of September and we were given the diagnosis on the 18th the day after his 56th birthday. His count dropped rapidly to 0.1 in a couple of days but then stopped at that. The Dr had told us that his chemo would start the following week. However she changed her mind, and sent him home after 2 weeks of antibiotics, antifungals and antivirals, which was just as well as I developed Laryngitis and a chest infection. I was amazed that he never got any infection. We went to the out patient clinic 2 weeks later and were told he was stable to come back in 2 weeks. on our return we were told he had to be admitted on Mon 2nd Nov despite the fact that his blood was still stable and he was to be starten on Chemo on Tue 3rd. The 1st lot of chemo mad him look dreadful I was not expecting that. However, he did look a little better the next day although he was very breathless and had tracking up his arm where the chemo had been put in. But all of that turned out to be ok. Here we are on day 4 gutted to find out that his brothers are not match for Bone Marrow, that left him feeling very upset and down in the dumps. So we will see what tomorrow brings Goodnight
Anonymous
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  • <p>Im new to this site, not sure what we are facing yet and have a meeting tomorrow afternoon, Hubby is a bag of nerves as am i, he has had a Endoscopy and a CT scan, we went through a very worrying time with my Daughter some years ago after she was diagnosed with Breast cancer, she died 2 years later after deciding not to have treatment and trying alternative treatment, i really came on here to see if i could see how others have coped and look for support  too, im in awe at how brave you all are and it has given me hope and strength too,thank you in time i hope i will be able to pass on hope too.

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  • Time goes fast now that Bert is home, C Diff has finally settled as has the bronchitis. He is still not very mobile and tires very easily but I suppose that's a small price to pay. He has peripheral neuropathy in his feet so now has to get something for the pain. still attending Physio for muscle wastage in his shoulder. Other than all of that he is fine

    Love Teri

  • Sorry I haven't been on the site for a while I was having real problems accessing the forum. But we seem to have got things sorted. Hope you are both well

    Kirsty x