Oh Kieth
Bl****dy hell I am so sorry I know it comes to us all but we just hope for a little bit longer, go away and enjoy your holiday and good luck for the next treatments this might be the one for you
Love Jo xx

Hi Jen

Welcome to the forum but also sorry you had to join:-( well I cant add anything to what has already been said apart from take one day at a time and go with the flow watch out for raised temp and infection's (gosh av said a lot) and get your Dad to rest when he feels tired.

Good Luck to you and your Dad in the MM Journey.

Tom…[Read more]

Hey Keith well what to say?? you know I feeel for us all when it fails such a darned illness this bloomin MM but am sure you are strong enough to fight it off and get back into remission 🙂

Get yourself off on your Holls and if you can push the MM into the background for a time.

Tom "Onwards and Upwards"

Hi Andy well I am sorry the SCT hasn#t worked for you, this MM is a devil to work out everybody differant with the outcome to the treatment?.

I hope the new treatment works for you with no or little side effects.
Keep strong and well plus dont let the drought wet you hair 🙂

Tom "Onwards and Upwards"

Hi Eve and Slim

Yes its a bugger these infections, I have lost count of how many I have had.
As for the nurse even my grandchildren know the rule Blow Wipe and wash 🙂 and she should know better.

Good Luck and hope the biotics kick in sooner than later

Love and Hugs to you both

Tom "Onwards and Upwards" xx

Hi Jen

Sorry you have joined us but you have come to the best place.

First thing tomorrow ring Ellen she will be able to give you a quick run down and send you booklets.
Stop looking for a cause and and start learning as much as you can about the treatment,you are now on a journey and it is a big learning curve.
Myeloma is Staged and there…[Read more]

Oh Keith,
So sorry to hear that news….I can't imagine how you must feel about it.
On the positive, I'm glad you can wait till after your holidays, and if it helps, I never suffered badly with revlimid when I had it with dex (or without the dex now). The worst thing was the fact that everything tasted peculiar….not horrid, just weird!!!
Have…[Read more]

Hi Ann

My husband has just finished 1st week of CDT and he is saying that things taste different. The worse thing to him is the Water- and you know he has to drink a lot. Have bought bottled water to see if it made a difference. He says it doesn't taste as bad. Hope things improve

Love Jean x

Hi Jen

Sorry you have to join us but welcome. Like Alison I can't answer your questions but someone here will help you. My husband was diagnosed 6 years ago but only started on CDT last week. He has two lesions on his ribs. We saw radiotherapy consultant yesterday and she said that she didn't think that radiotherapy was necessary. Maybe…[Read more]

Hi Alison

I am replying to your post under treatment,it shows in my e mails but not on the board.When I looked into your profile it is not showing a posting,so I have used your last posting to reply.(does that make sense!!!!!)

I think the system is having it,s own blips as 2 of the headings have not been showing on my computer screen. Love Eve.

Well Thats great news dai, Its bad driving on moterways these days without the rain. I bet your both as proud as punch with each other for doing it together.

Good Luck on your next trip and I dont think the next one will be too far away.

Love to you Both

Tom "Onwards and Upwards"

Hi Eve and Slim

What good news that Slim is home – the other side of the SCT. After all the problems you have faced to get to this point, it is great to hear this. AS Dai says, there is a lot more hill to climb, BUT you are on the right side!

Very best wishes to you both.

Mavis x

Hi Paul

In spite of disappointing weather, I hope that you managed a break and that your legs are less jelly like!!! Knowing you, another couple of months and you will be bouncing about.

I'm also suffering with steroid round face – wouldn't mind, but people keep commenting on it – as if I didn't know!!!

Lots of love to you both.

Mavis…

Hi Andy

Just a note to say glad numbers are moving in the right direction, even if slowly. Enjoy your break, hope the weather is kind – and be encouraged that something is working for you.

Very, very best wishes.

Mavis x

Hi Eva

How is Sue getting on,although Slim is home we have spent 2 days going back and fourth to are local hospital,Slim has a problem with his platelets on Sunday they were 33 today down to 7,there is fine explanation under the Macmillan Site.Explaining some of the reasons why this does happen .

One explanation is having platelets from…[Read more]

Hi Gail
Eve again just realised I am loosing the plot called Howard,Henry,My excuse is i was up with Slim during the night and I have not caught up from all the travelling to the hospital.Sorry Eve

Na then Tery

I love the way you cope with it all I also feel that its a head as well as a body challenge kepp them both strong and you are on to a winner.

Keep strong and well

Tom "Onwards and Upwards"

Ps great photo. I must take my young Bride to Scotland one day soon x

And A Good Morning to you also jacqui, what great news to read today well done Girl and long may it continue 😀

I know itsa a little bit of a rough crossing but the more folk that say its worth the trip the more will take that trip with more ease and less uncertainty.

As for your low levels of energy mine came back to an acceptable level…[Read more]

Hi Gail

Sorry to hear henry is having a hard time,may be a little time in a hospice is what he needs.They will be able to get his symptoms under control and help with his anxiety this is what they do and a very fine job.

You said your self Henry,was behaving so out of character,I think we look on hospices as a place to die but they do so…[Read more]