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Major rant and advice please...

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  • Major rant and advice please...

    My younger sister currently has Hodgkins Lymphoma (for the 2nd time) and was put forward for a new treatment at the Royal Free in London. The treatment is currently on trial, but between stages, however the hospital are willing to treat people in the meantime as ‘compassionate’ treatment. However, they require some funding from the PCT for this. The charge to the PCT is around £3k (personal funding would be around £18k, as it would include the specialist staff and room necessary for the treatment).

    My sister has waited over 13 weeks for a decision from the PCT and today has been refused funding for the treatment because the drug is unlicensed. The drug itself is licensed for use as an anti-rejection drug for transplants, however research has proven it has another use, hence the trial.

    The consultant at the Royal Free is looking into the appeals process, but has warned us that it could take just as long again.
    My sister is currently back on chemotherapy every two weeks, which technically isn’t working as she is still cancer-positive, in the hopes that it might keep the tumours from growing (they are getting visibly larger every day).

    She is lined up for a stem cell transplant, using my cells, once she is in remission, however Christies have warned that they have pretty much run out of options to get her into remission.

    We are really unsure what to do. Of course, people have said we should contact our MP (who apparently doesn’t have the time, with the forthcoming elections etc) or go to the local paper; however, I’m worried that this might prejudice our chances with the PCT if we get a chance to appeal.

    Should we let the process run its course (another 13 weeks or more!?) or should go down the whole publicity route and hope that we get the desired outcome??

  • #2
    Sh*t Shelley Talk about a rock and a hard place?!! Do you know anybody who can get you 'insider' type info on the PCT? Find out how they are likely to react to adverse publicity? Even your sister's GP might be helpful in that department.
    Also, the local paper might have past stories where they tell you what the outcome was?

    I have no idea what I'd do in the same situation. I think I'd be tempted to go to the paper anyway, and kick up additional fuss about the MP being more bothered about the election than real people!

    Whatever you decide to do, the best of luck. xx

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    • #3
      I would be shouting from the roof-tops. Get as much publicity as you can, embarrass the PCT into submission.

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      • #4
        How many members on the Vine? If we all chipped in/raised £10, would this help?

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        • #5
          That stinks!
          I have no idea what I would do in your place but I really feel for you.
          Sarz's advice sounds pretty good to me.
          Big hugs to you both, I really hope it gets sorted quickly!

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          • #6
            Originally posted by Polly Fouracre View Post
            How many members on the Vine? If we all chipped in/raised £10, would this help?
            THats a good idea

            Shelley, thats a horrible position to be in. Make lots and lots of noise, it has to be done. Maybe put a fundraising slant on the story, people may be moved by it and donate anyway

            Good luck xxx
            Kirsty b xx

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            • #7
              Shelley get a facebook campaign going.
              I'm with Polly Fouracre as well - count me in!
              Whooops - now what are the dogs getting up to?

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              • #8
                ...and me...
                All the best - Glutton 4 Punishment
                Freelance shrub butcher and weed removal operative.

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                • #9
                  *hand up too*
                  I don't roll on Shabbos

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                  • #10
                    As its a trial have you tried to contact the drug company they could well be very responsive

                    Best wishes for you and yours

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                    • #11
                      Originally posted by Pies View Post
                      As its a trial have you tried to contact the drug company they could well be very responsive

                      Best wishes for you and yours
                      I'm with pies on this one - I worked for a massive international pharmaceutical company who run said type of studies and it's massively important for the drug to be trialed correctly. Try them, they might well surprise you in a very positive way.

                      Also try speaking to public relations at N.I.C.E and M.H.R.A for help (google the acronyms) they might be able to help convince the PCT that the drug is fine - even though it's not licensed both government bodies will have given their approval for the drug to go to trail in the first place.

                      Massive hugs to you.

                      XXX

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                      • #12
                        This is going to sound very cynical but I think whilst they are waiting for a general election result all PCT's are going to deny test treatment until they know who their next set of bosses will be. In the meantime kick up as big a stink as you possibly can. I've seen no end of cases where the PCT's have folded due to negative publicity. If you can start a fund raising campaign as well that also looks good to the media as if you have the money to pay for the experimental treatment yet the PCT still say no then they have another reason to demonise them and whichever government backs the policy. It may take a while but if it means that your sister has a better chance it's got to be worth it (Don't worry that it might prejudice the PCT against you as they are far too busy trying to look caring to be prejudicial).

                        As both a blood donor and someone who is on the bone marrow donation list (I urge all members of GYO to be at least blood donors) I hope the transplant goes well for your sister and is as pain free as possible to you.

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                        • #13
                          Originally posted by Buleste View Post
                          As both a blood donor and someone who is on the bone marrow donation list (I urge all members of GYO to be at least blood donors) I hope the transplant goes well for your sister and is as pain free as possible to you.
                          Used to donate blood every time but since they brought this booking system in I've had real problems, unless I book about 6 months before I can never get a time I can make (and so they end up booking me in for a time outside the time I said I could make..........) and that far in advance I have no idea if I'll be working away etc so it's a waste of time. Tried just turning up and had to wait for over 2 hours before they told me that I should have booked. Really annoying and as a result only give blood about a quarter of the times I should

                          Some of us live in the past, always talking about back then. Some of us live in the future, always planning what we are going to do. And, then there are those, who neither look behind or ahead, but just enjoy the moment of right now.

                          Which one are you and is it how you want to be?

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                          • #14
                            {{{{{{{hugs}}}}}}} Shelley.

                            I don't have the first clue what you should do.My dopey brain would think maybe kicking up a media stink about your local MP being to busy campaigning to look after his constituants interests would be my first thoughts.


                            {{{{{{{more hugs}}}}}}}for both you and your sis.xx
                            the fates lead him who will;him who won't they drag.

                            Happiness is not having what you want,but wanting what you have.xx

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                            • #15
                              I would go for the publicity, shame them into paying. Count me in for any fundraising on here too!
                              WPC F Hobbit, Shire police

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