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DrivetimeYou are in: London > Radio > 94.9 Presenters > Drivetime > Hodgkin's Lymphoma diary Eddie, with his wife, in hospital Hodgkin's Lymphoma diary91热爆 London presenter Eddie Nestor was diagnosed with Hodgkin's Lymphoma - cells in the lymph nodes that have become cancerous - in February this year. Here he writes about his diagnosis, treatment and recovery. Final WeekI've been putting this last diary entry off for at least a fortnight now and it is not hard to know why. I have written as much of the truth as I possibly could over the last few months. Trying to be as candid as I can about a condition, which may well affect many of you reading this one day in your life but also one which may still one day kill me. I have become very fond of the outlet and I am not keen to let it go. What ever was going on, however bad I felt, I had to get myself together to write my diary. It has been a few weeks since my last treatment and I have had much time to reflect; physically I am fine. I think the fact that I was healthily preparing for the marathon when I found out must have helped. Mentally I am an absolute mess.
If this diary was not read by the people who employ me I might be tempted to be more forthcoming but I think I will have to hold that back for the book. I really do hope to write one very soon and to give any money to one of the cancer charities which are doing so much to help people live with what is (whatever the outcome) a life changing condition. But I will say this, if the knot in my chest doesn't subside soon I may have to go and see someone. I only leave the house to go to work. I am only 30 but cancer has put at least twelve years on me. Kath Melandri and Eddie Nestor in 2003 I have been doing drivetime on my own for the last couple of weeks because Kath is in Australia on a well earned break. And I had forgotten how hard it is doing it solo. I think it has been good for my confidence but I will be glad when Kath is back. It is so weird talking about confidence. Before this, it was something I had never thought about, yet look at me now. I have earned my living entertaining people for a very long time now and I am struggling (even temporarily) to get used to the "new" me. Next big date for me is October 29th. I am told that it will take at least 3-5 years before you can say with any confidence that the Big 'C' has gone so it is going to be a long wait and I had better learn to try to get on with it otherwise I will become very boring indeed. We are trying to book a holiday for our anniversary at the end of November but that may well depend on what the insurance situation is. We have had one quote which has already indicated that things may well be very different from now on. Thank you for reading this diary. Thank you for allowing me to write it. Hope I am strong and brave enough not to let cancer define me but simply to make it something I went through for a while in my life. Week 18My last night before my last chemo and I am terrified. Everyone around me presumes I am happy because barring an absolute catastrophe this will mean an end to the poison coursing through my veins. An end to the dreaded chemo head. And an end to the blood thinning injections I have had every single day since June 2nd. Why am I scared then? Maybe it鈥檚 the fact that we are now embarking on a new adventure. Now the cancer is gone how long before something in me stops waiting for it to come back. Last week Kath and I celebrated four years together on air. Wow, who would have thought Drivetime with Eddie and Kath would be four years old? The partnership and thankfully the audience has grown and I can truly say that she has done as much as anyone to get me through the most difficult period in my life and I will forever be grateful. The show has really acted as a pick me up and she has literally carried me through on air. Last Saturday I went out with the wife to a charity ball for the African Caribbean Leukaemia Trust. It鈥檚 nice to go out. It lifts your spirits, makes you feel alive. I intend to do a lot more of it. It is an annual do and I usually host a table and do my best to make sure people have a good time but this time what with my present predicament it was just a little different. The message of getting people to sign up to a register of donors seemed all the more poignant. It's, must be like buying a car and suddenly seeing the same model everywhere, cancer is all around me. Trying to finish off my diary with chemo head is never easy but always worth a try. It is Monday October 1st and I am watching the clock, it moves so slowly when I am ill and so quickly as I start to recover. I just lie there trying not to feel too sorry for myself, it is after all the last one. I am like a child asking its parents 鈥淎re we there yet? Have learnt to do the time thing in bits. First it is the injection in the morning, then seeing my wife off to work. Then I have a tea and a daydream. Long and slow shower is followed by sleep and an element of self motivation, contemplation and I am sad to say, self pity. Then my wife comes home after her three calls to make sure I am well. It gets dark, we have dinner, I daydream, then it is time for bed again. Hey, why does this sound so down beat? I have had 12 chemo sessions over 24 weeks and it is all over isn鈥檛 it? Week 17Just recovering from the affects of another chemo session and the positive head is saying 鈥渏ust one more to go鈥. I am ignoring the negative head at the moment it is taking up far too much of my time and energy. I probably only have two or three of these diaries left and that will be strange. The end of my documentation, the completion of one of the most difficult phases of my life. If you are reading this then you have been on, at least part of, the journey with me and with so many people surviving and living with the condition then I sincerely hope it has been eye opening and informative. It certainly has been for me. And needless to say I haven鈥檛 liked all that I have seen. I would have hoped to have been braver, more resilient, not so needy and a lot more upbeat. I talked to the doctors at Whipps about what was to come and they told me that I would not need another scan as they were happy with the first one and that there were worries that the scans themselves could be causing cancer. My last chemo session will be on September 28th and then monthly checks to see how my body is coping. I am told that the clear-up rate with Hodgkin鈥檚 is really good but that the first six months will be crucial. After that the checks would be less frequent. Say every six months, then hopefully every year and so on and so on until one day it will all be just a distant memory - I hope. My McMillan nurse has gone on maternity leave and has not been replaced. I miss the little reassuring chats. It is not that the other nurses do not give freely of their time but that was what Karen was there for and I am sure many other sufferers at the hospital miss her too. One of the things we talked about was sex. Not that it has been right at the top of the agenda recently but before the treatment started way back in April my wife and I were trying to have a baby. We had left it till the time was right, till we were married, till we were sure and now I wish we had done it years ago. No one knows what life will bring. And now the conversations with my wife are strained and unsure. I may now be infertile and if I am not then how long will it take to get to those little 鈥淓ddies鈥 being kept in a laboratory somewhere in Central London. And even when you get to those, I am 30 and though she would kill me if I told you her true age on these pages lets just say the clock is ticking for my wife. last updated: 10/04/2008 at 15:36 Have Your Say
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