Here here Mavis!! 🙂

And thanks to all you guys who post on here…it keeps me on the straight and narrow! 🙂

Have a great weekend, and well done Mavis, long may your remission continue!

Vicki and Colin x

Oh bugger Helen

I really thought your last post was so positive and that may be it was a blip!. How come they have changed their tune so quickly. As Tom said entitled to some soul searching and then bat that damn thing right back into oblivion!!

Its such a blow for you:-(

Love and hugs

Vicki and COlin xx

Hi Mandy

Colin had his SCT in November 2011. Like you he had a really rough ride during his induction treatment. He was in and out of hospital with infections and temperatures, virtually every month for 7 months. Antibitoics etc etc. It was a really long haul. However that said the trial was worth it and he got to SCT and remission!. He also…[Read more]

Hi jacqui,

Yes we go to EJU, and we are now moved to a Wednesday afternoon clinic. All good today and they want to see us again in two months. Colin's back is still bad so thinking what to do next, but they are referring to back specialist. :-). Glad Geoff is seeing Nicky. Colin sometimes says its like a dream (nightmare more like :-(), being…[Read more]

Dear sue,

Our thoughts are with you and Keith. He is a man of great strength and fortitude, who has and is a great comfort. Should this be a final journey, peace and tranquility will await x

Vicki and Colin

Oh jacqui, what a dilemma! But if that is what Geoff wants, go with it!

Colin was very very emotional leading up to sct….and like Geoff, although he wouldn't admit it, his nerves were bad too. He had some terrible panic attacks. He saw the clinical psychologist before he went in for sct. Colin was very anti that before but I persuaded him…[Read more]

Hi Ali,

Glad to hear your mums out of hospital! 🙂 its difficult isn't it knowing who to contact. I asked the consultant when we had our first visit after sct and she said continue to contact them for now. So last week when Colin was really really tired we phoned the chemo helpline and went in for blood test. We felt a bit guilty as they are…[Read more]

Hi jacqui and jeff

How are things? Did you get some reassurance?

Vicki and Colin x

Tom,

Good luck. It's strange, but when Colin got,told we were going to,sct it was a huge boost but scary too. It's what had been worked for but when it came to,it we were scared. You can do it as you've got this far 🙂

Vicki and Colin x

Hi Helen,

Yes colin has started to take it easier, a little less tired but is sleeping when he needs to. Got back pain at the moment, he's reduced his meds due to it being morphine based and the pain specialist is going to give him another drug which is not morphine based and can be Taken long term. I do worry about any pain as I always link to…[Read more]

Eve,

Translate attitude for leaving no stone unturned to make sure slim gets the right results. I don't care either…..bet the hospital staff think I am mrs 20(no 100) questions but that helps me to help Colin. Hope you and slim are getting some good nights sleep.

That helps so much, take care both 🙂

Vicki and Colin x

Mary and Charlie,

Relax!!! Just be thorough with cleaning like normal but taking care of handles and surfaces as they are where bugs get transmitted most. Neutrophils are the immune system getting stronger and normally hospitals say 0.5 and patient can go home. It's just like when you are having treatment, the neutrophils go up and down. When…[Read more]

No more need for a onesie then Tom ha ha

Vicki and Colin x

Hi Ali,

How's your mum doing? Hope she is feeling a lot better. Isn't she due to go on holiday soon?

Best wishes….Colin less tired but now his back is playing up. He is cutting down on painkillers due to pain specialist advice due to being morphine based, they are planning to put him on something else. He says its muscle pain…..but I…[Read more]

Ann

As you can see a huge support on this site….wishing you all the best with your treatment 🙂 Colin has never said why me but it does make you wonder, but then why anyone. You and your husband have had a tough time, so you ae due some good times now!

Ann and Pete, glad you guys are doing well. Hope Peter is making a slow but sure…[Read more]

Hey Tom

Hope you are feeling a lot better, can't get the imagine of the onesie out of my mind :-)you and Cheryl cold both would have one!!

Vicki and Colin x

Good luck on your 100 day assessment and well done for doing so well, so far 🙂

Vicki and Colin x

Hi Ann

Welcome to the forum, yes it's unbelievable! My partner Colin 56 was diagnosed in October 2011. In that year he did ski-Nig in the January, weeks golfing holiday in march (had shingles). May we went to Mexico for 2 weeks (kayaking, volleyball, tennis etc), July walking holiday to Cornwall…..back pain started early August and then…[Read more]

Hey Helen,

Focussing on all the ups…plateauing and only a few plasma cells…..that's got to be good. This could be a blip after all. You know what parking at work, a bloody nightmare….can't you get a medical bay space? Especially if you are in a lot of pain and walking a long way is an issue? No imminent change of treatment….that's good…[Read more]

Terry

I've just posted on your other thread. As the others have said…..give up if you feel you can and want to. I would say don't give up something to do nothing. If the classic cars are your idea of enjoyment go for it, keep focussed and absorbed. I'm a firm believer that someone having a purpose helps!!

Go for it

Vicki and Colin…