General Chat

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Marilyn is the ten days classed as urgent at your hospital, did they give you any idea when they examined you , these ten days will go before you know it you just keep chatting to us ok all my love xxx you must be so scared but i have learned that people who have cancer do feel any other pain is the cancer spreading and you would do keep chatting xxxxx

Hi Marilyn fingers crossed for you wish i could hold your hand and tell you its all good news, what Ive learnt is that when people have cancer, every pain or ache anywhere on there body my step dad says its spread and i understand when that's being said it most be awful thinking that way but it cant be helped wish you all the luck in the world Marylin xxxx
Hi Wend, yes where are the men, we hope you are having a good feel or get your partner to NOW xx

Hi Sylvia Daff is a very knowledgeable and has cancer , I'm sure she will add soon when she sees this xxxx

Marilyn and all those undergoing treatment,I am thinking of you and if this thread is helping you to unload all your thoughts that you can't tell those closest to you...well that can only be good.
A few years ago,I offered to head a support group at the hospital,but they refused.It wasn't for giving medical advice,but just to give hope and help people to cope with this disease,as I'm sure with the right attitude it can help so much.
Keep smiling and enjoy each day.
Thanks for starting this thread Puss.
Brenda x

your welcome Marilyn yes me to, helped friends and family through it. never thought it would happen to me, but hey I am still here and dont intend going anywhere for a long time yet, to much to live for oh but then again I am going to book a hol abroad soon lol

Thank you Sylvia & Wend for your kind words.......funny though its usually me that tries to sooth out other people's misfortune in this terrible disease , you don't think you might need it yourself..................but you do .

So sorry, Marilyn with the sweet face, posted before I'd read yours. Thinking about you lots. xxx

Lpc has daff got medical experience in cancer, she seems very knowledgable.
Marilyn I understand how you are feeling , the waiting is worse. I have sat for hours in a waiting room for results, stomach churning etc.Hopefully they are just being cautious which is good , I will be thinking of you.

Bless you too, Puss, for starting this thread. So many fantastic people have posted and I'm dumbstruck by the positive attitude all of them have. Such an inspiration and help to anyone who is anxious and worried at the moment. No men, though, where are you? - you sometimes have concerns too, I'm sure. I know my boy does and I keep a regular check on him :-)

I had Cervical Cancer 3 years and had all treatments Chemo & Radio plus internal treatment, I thought I was doing well, really well until a few weeks ago when I had the most excruciating pain in my lower abdomen , went to doctors and got refer' d back to Oncology dept ,
My appointment was this afternoon..........news !! more MRI Scans and CT scans .
Its hit me a bit ........I know they are just covering everything for me, but you cant help thinking has it come back ???????

I got to think straight for 10days until the scans .....don't know if I can..!!

BUT I WILL ........

Sylvia i know what you mean, i have spoken to daff on here bless her because i needed to know what whats and what to expect then Ive been able to support my mum instead of breaking down with her poor woman lost her first husband aged 32 he is no loss to me but the thought of her losing my step dad had really broke her but through positivity its amazing what you can do , and yes speaking on here for people who are suffering im really glad it helps, i know what you mean about talking to relatives they ask you how are you but do we really answer the truth, but at least on this we can say and feel what we want xxxx love to you all xxx

Lpc god bless your dad, and everyone who has told us of their fights with cancer. Stay positive and enjoy your lives .I think this site is brilliant, I have found it good to talk of my experiences to you lovely ppl who I dont even know. Sometimes I dont like to talk about it to much to family as I dont like to upset any of them. xxx sylvia

God bless you all for adding your stories , lets all stick together and help each other on here, and so much so that explaining treatments and diagnosis and prognosis will help us all understand.
My dad is home now he is having to get use to using the loo like a lady and is still very sore, he has to go back in 7 days xx

Need to add i know i haven't replied using names but i have read every story and think your all wonderful and brave xxx

I was diagnosed with Leukaemia on 19 Feb 2009.

I didn't even know that I was ill. I had a toothache and thought a filling had fallen out so made an appt at the dentist. Went to the appt and had a new filling done. About a week later it was still really sore and I looked in my mouth at the tooth and saw a distinct line in it which I found to be a crack. So made another appt at the dentist. He said that I could have a crown done and a few other bits and pieces to repair the tooth. I told him whats the point as it will deteriorate anyway and told him to remove the tooth. Have had a tooth out before so knew what to expect with regard to blood loss. Well this one bled for 13 hours. I had no sleep and was up all night spitting out blood.

The next day I stayed home from work and was feeling rather ill due to blood loss so took myself off to the doctors. They did a blood test to see how much blood I had lost and the dr didn't seem to concerned at that point as the bleeding had slowed to an ooze and had almost stopped.

I went back to work the next morning and was getting myself a coffee and saw a missed call on my cell phone when I got back to my desk. It was the health centre. I rang them and the receptionist put me onto the telephone nurse and the nurse told me that the dr wanted to talk to me. Straight away I had a feeling that something was not right as I have never had a call after a blood test before. The dr told me an urgent appt had been made for me at the hospital and that I had to get there immediately to see a specialist.

Well that put me into hysterics. I went to the nearest team leader I could find and told him that I had to go to hospital and promptly broke down into tears. He managed to calm me down a little bit. He organised to come to the hospital with me.

When I saw the specialist she initially told me I had a condition called CML and I thought oh thats fine its a condition they will be able to treat that and then she said CML stands for Chronic Myeloid Leukaemia. I was so so distraught. I didn't know how I was going to cope. They rushed me in for a bone marrow test to confirm their diagnosis it all happened so fast I didn't have time to worry about the test.

18 mths later and there is no talk yet of remission. I am currently on Glivec which they are telling me I have to be on for the rest of my life, and if it is going to keep me alive then I will. I have to wait for my next blood test for my specialist to decide on the next course of action as there have been a few fluctuations in my leukaemia levels. The options I have been given is to keep my meds the same, increase the dosage of my current meds, changing to one of 2 other medications and down the track as a last resort would be bone marrow transplant.

Every day to me now is precious and I really believe that the visit to the dentist was a blessing. I still worry every day what my future will be and every day I don't want to go to work as I see that as a waste of my time when there are other much more important things in life that I could be doing.

Hopefully I can win the lotto and retire : )

Annie
xxxxxxx

I have had cancer of the womb, cancer of the ovaries and cancer of the breast. This over the period from age 47 to age66. Have been clear since then and am now 75 yrs old. Oh, had a triple by pass along the way! Think positive is my motto, but I always tell people about my experience when they are terrified of the diagnosis.

Having told you all about me,I have also got a d.i.l in Melbourne,that I have asked for positive thoughts for a few times.She had breast cancer 7 years ago,and had a double mastectomy.All went well for over 5 years,but since then has had it in her hip,and had a new joint.Then in her sternum,and now in her spine and lungs.
She is a fighter and is now on a course of Vit B 17,Vit C and ozone as well as radiotherapy.In fact my son says it is like a full time job as she has always got appointments somewhere.The Vitamin treatments are costing $20,000 dollars for 6 months.We are praying that this alternative therapy works.
We are praying for her to beat this. they are so far away and have a son of 10 and a girl of 9.
The hard work she is putting into keeping it at bay is amazing.She also runs a healing group at her local church.(she is a trained physio and acupuncturist).
I do believe in a positive attitude,and she certainly has it.

Brenda x

Thank you Puss for that. we never know do we. ? what will happened next. l lost my father a few years ago with Lung cancer a mother with breast cancer an Aunty and Grandmother with stomach cancer I have along list of cancers sufferers in the family.
They have come a long way in the fight against it now we must be gratful for what they have done and are doing. .


Rita

tina thankyou stories like this show its not just one particular cancer that can go on , mayby and mayby its been said we may inherit cancer genes, Daff is so well read on this will ask her to input
again well done and glad your being kept an eye on x x
fingers crossed for you rita hope you won't have too xxxxx

Brenda that is a beautiful story and gives hope too , so pleased for you, the hard work as we all know keeps us going xxxxx

l have lost many of my family to Cancer all types. I never thought it would happen to me. when I was rushed into hospital with a blood clot l was very ill. a few days afterwards when l thought l was going home. they did another scan and found I have cancer a spot on the kidney and one on my liver. they can not operate just try and keep it under control so for a year I was having to give myself injections. then l found it was stable l still attend the hospitals every three months for a scan then to see my consultant. that was 20 months ago. I have not had to do the injections for that last 16th months.but might have to start back again . l hope not.
l try not to think about it and live each day as it comes.

Rita

Brave gals on this thread, I reckon :-))