Archive for the ‘lu-177 CLEMENT study’ Category

New Developments

Thursday, December 9th, 2010

Hi all,

Well, we have had to deal with several new developments in the past month or so.

On the 19th of November I suddenly had a temperature spike, and because I was on Interferon, we immediately headed over to the Emergency Department (ED) at the local hospital in Busselton. They kept me overnight and diagnosed a UTI as a result of my suppressed immune system. My oncologist was contacted and I was instructed to discontinue the Interferon treatment until he and met as scheduled the next week. My GP sent me home with a script for oral anti-biotics and that seemed to fairly quickly begin to control the UTI.

I had an MRI of the abdomin and pelvis on the 23rd of November in Fremantle, followed two days later with a meeting with my oncologist Dr. Phil Claringbold. Unfortunately, there was very little he could tell us at the point, since he was missing the previous scans (Gallium 88 PET) from September. He continued to keep me off restarting the Interferon treatment until we had more data from the scans. We immediately overnight express posted the CDs of the September scans to him when we got home that afternoon, and he finally called back on Tuesday the 30th. He told me that the scans showed that there was apparrently more diffinition of the tumours in the liver and it appreared the Interferon was not doing much of anything at all to help. So he discontinued any further Interferon Treatments. He also told me there as very little else available in the public health sector that he could do for me. I wasn’t eligible for the current LU177 study because of the use of Capecetabine (an allergy for me). When I asked what might be available in the private health sector, he said there were several treatments readily available. I then placed a call to my original surgeon to see what he might suggest as a course of action since I had no one else that seemed interested in managing my case and Harsha Chandraratna has always taken an interest. I have to say that going off the Interferon was a great relief. It was only after going off it I realised how poorly it was making me feel. Without it I felt very normal, energetic and positive about things.

Unfortunately all that changed that same afternoon (Friday, 26 November) when that same afternoon I had an even higher temperature spike than the previous one and we immediately went and checked into the ED at Busselton Hospital. This time they kept me in for two nights as they diaganosed that the UTI had spread to a different infection, Epididymo-Orchitis. This was extreamly uncomfortable to day the least and the fever stayed up. Eventually, once they felt oral anti-biotics could handle it, they sent me home Sunday morning. Harsha called me back Saturday afternoon whilst I was still in the hospital and immediately to referred me to, who he feels is the best oncologist in Perth for my situation, Dr. Andrew Dean. I called Dr. Deans office first thing Monday morning. He is out of town but they made me an appointment for the first day he is back, 20 December.

Everything then was going quite normally with the infection slowly reducing, until Tuesday afternoon, when I began developing a shocking pain in my left eye and upper sinus over a period of a few short hours. I had this type of pain irregularly over the past 2-3 weeks, but with a little paracedamol and a couple hours eye rest it went away and was fine. This time it was different, the pain just kept increasing and the pain meds I had weren’t touching it. This was a real concern to us, because the Septemper scans had shown a gallium focus in this area of the left eye, indicating possible tumour(s). So after a quick call to the my GP’s surgery, we were off to ED at the hospital again. This time primarily for pain control and initial diagnosis. The next couple of days had the doctors getting the pain levels lowered to tolerable (mostly using morphine) and a new CT scan of the left eye. As we suspected, there are two tumours in the area, an 11mm involving the left eye inferior rectus muscle and a 7mm at the inferiorlateral margin of the left orbital globe. My GP then attempted to contact Dr. Dean and Dr. Chandraratna, and was able to arrange an appointment with Dr Jerome Freund at Perth Radiation Oncology. They feel that this specific site is best treated with radiation and usually responds very well to radiation treatment. In the meantime I am on fairly heavy doses of oxycondone hydrochloride for pain control and dexamethasone (sterioids) for reducing the inflamation.

So as you can also see, ’tis been quite a busy start to the Christmas season. I did feel well enough last night to go to our annual Moon Haven Company Christmas Dinner, which I greatly enjoyed as did everyone there, to see me!

I’ll be keeping everyone up to date as things develop over the next few weeks.

Until next time, take care of yourselves and each other, I certainly have an angel taking care of me and her name is Leonie!

Blessing to you all,

Eric

Sometimes You Don’t Get What You Want or Think You Need

Tuesday, September 21st, 2010

Hello All,

Just spent the day driving to Perth and back to see my oncologist, Dr Phillip Claringbold. We had hoped he would be able to tell us that I would be to start a series of treatments with LU177 in the near term. Unfortunately, while the next trial is November, it is using Capecitabine as one of the drugs in the trial. I had a severe reaction to that drug during the previous clinical trials and had to continue the trial without the Capecitabine. So even though Dr Claringbold would have been ready to put me in this next trial, he can’t because of my allergic reaction.

The next trial, using a different group of drugs with LU177 isn’t scheduled until March 2011. This is not particularly good timing for me, in that it would appear the sudden increase in Carcinoid activity may indicate that is is taking a slightly more aggressive form. So I certainly don’t want to wait around for it to do its thing.

Based on the recommedations of Dr Claringbold, he feels our best bet is for me to start on using Interferon as a stop gap measure. This is what I have chosen to do. So we will continue the monthly 90 mg Lanreotide injections, and beginning the end of next week, I will start self-injecting Interferon 5 days a week. We will do a blood/urine workup this week, then a followup again 4 weeks after starting the Interferon. Then at two months do bloods again plus an abdominal CT scan to track what is happening, particularly in the liver. I can expect to be on the Interferon for about six months.

There have been some fairly reasonable results in using these two drugs in combination, so hopefully I will amongst that group. I can expect some fatigue and flu like symptoms as the usual side effect and of course I will be watching what happens with great curiosity and anticipation.

It is unfortunate in its timing (isn’t it always), in that we are looking at a potentially really heavy workload at the shop. However, we will find a way to deal with that and soldier on.

I wish I had better news for everyone, but those of you who know, know this is one tough disease and we aren’t given easy choices in fighting it. But we will fight it and we will overcome it!

Everyone take care of yourselves and each other…

Bestest, Eric

It’s Back

Monday, September 13th, 2010

Hi All…

Well it took an extra week or so to get my initial report from the scans done last month, and the news is not that good. In a brief letter from my surgeon to my oncologist, he notes the latest octrotide scan shows a reoccurence of my carcinoid tumours and they seem to be in my lymph nodes and they are evidently not suitable for surgical intervention. This is not a particular surprising report in that we knew the carcinoid had gone active, just from the reoccurance of the symptoms, but the apparent lymph node involvement was a small shock.

I’m not altogether sure of the entire significance of the report, in that I haven’t spoken to Harsha (my surgeon) directly (I will call him tomorrow) and I will be calling my oconologist in a day or so, to make an appointment. I have a sense that I’ve proabably got a series of LU177 treatments in front of me plus more scans and tests. However, we will deal with it, and as we have in the past, we will get on top of it again.

I will post updates as information becomes available and treatment plans begin to firm up.

Take care of yourselves and each other!!

Eric

The Journey Continues

Saturday, May 23rd, 2009

Here it is end of May already. Winter has arrived with a roar this past week. Heaps of rain, and blowing a gale! We really needed the rain and there has been plenty in these systems.

It’s been a bit over a year now since I completed my last CLEMENT Study treatment. Everything is fine, no symptoms and no signs of any tumour activity. I need to call Fremantle Hospital to see when my next follow-up is scheduled. Leonie and I just got back from a 2-1/2 week trip to Guangzhou, China and Hong Kong. A tough trip, all business and almost no play time. However, I had no problem keeping up with a lot of travel and long, very long days. Huge amounts of walking while visiting all the trade fairs.

I finished my eye surgery with a bit of laser treatment a week ago. Everything went really well and I am still getting used to seeing so well. My driving has been a lot safer too (according to my main passenger! LOL).

My newest issue is a small basal cell carcinoma has been found on the side of my nose. Actually I have had it for quite some time and suspected BCC, but given everything else going on, I kept putting off seeing the Doc and getting a biopsy. It is large enough to require a bit of plastic surgery when it is removed to rebuild the side of my nose. It should all happen in the next month or so. It isn’t any big deal though, I’ve had a couple BCCs before which were removed without a problem. The spoils of my ill spent youth on the beaches of Southern California!

That’s all that happened recently.

You all take care of yourselves and each other!

Regards, Eric

New Medical Adventure

Tuesday, January 13th, 2009

Since things are seemingly quiet on all other medical fronts… that is the carcinoids are staying inactive, my Bali bike injuries are virtually healed and I am on a serious weight loss program (8½ kg in the first month)… I decided now was a good time to take care of that pesky cataract in my left eye. Vision in that eye has seriously deteriorated over the past 18-24 months and my optometrist felt is was time to do something about it. I had an IOL (Interocular Lens) implanted in my right eye several years ago, but its vision was never as bad as the left eye is now. This afternoon I have an appointment with my eye surgeon, to review my case and hopefully set a surgery date. It is no big deal, having had it done once, I know the process and it is realatively quick, done without general anaesthesia and the results are pretty much instantaneous.

I know my brain will have to adjust, it has been using the left eye for close work and the right eye for distance for several years now and it will have to readapt to using both eyes for distance. New glasses will take care of the close work. I am so looking forward to having “normal” vision again.

I’ll Keep you all posted as things progress. Take care and be good!

Eric

Six Months Post Treatment – No Issues

Sunday, December 21st, 2008

Hi Everyone,

Sorry I haven’t updated lately.  I had a bit of a motorbike accident in Bali in November which layed me up for a while, so I have mostly been dealing with recovering from those injuries.  All is much better now, broken collarbone is healing well, other injuries have healed but an internal infection in the left ankle is still giving me some grief.  I just got back to the shop for the first time in almost 7 weeks last Thursday.

In October, just before the Bali holiday, I had my 6 month post-treatment MRI scan with a follow-up with Dr Harvey Turner at the end of November.  Our visit with Dr Turner was all positive, all reports are good with no indications of tumour activity or growth.  Dr Turner expects that based on the study results thus far, they we can expect at least 18 to 24 months without reoccurance.  Thus far, in all his cases, he has only had to do a retreatment on two patients.  I will continue to have 6 month interval follow-ups for the foreseeable future to track any possible developments.

One of the interesting developments in patient care is a move by the Western Australian Department of Health to create a Centre-of-Excellence for Carcinoid Cancer for  Western Australia.  It will be run out the three teaching hostpitals in Perth where a standing board consisting of experts in the treatment of Carcinoid Cancer will review the care of all Carcinoid patients in the state and develop individual treatment plans for each patient according to established treatment protocols.  WA has already established its world reputation in the area Cardinoid treatment due to the efforts of people like Dr Harvey Turner, Dr Phil Claringbold and surgons like Harsha Chandraratna and many others.  For me it represents assurity if I require more ongoing treatment in the future, I am in excellent hands.

My focus now is accident recovery and weight loss.  I am on a serious program of weight loss control for a serious problem of overweight.  Thus far I am having excellent results, but I have a long way to go to get to my most desired weight (like 25-30 kg!).

All my wishes to all of you for a joyous and festive holiday season and a happy, healthy New Year!

Eric

Months on and no change (that’s good!!)

Friday, September 26th, 2008

Hi everyone,

Sorry I have been so quiet recently.  Actually I have been far from quiet, but I also have been at times far from my computer or far from time to edit anything.  It really has been months since I posted.  In the meantime, Leonie and I have travelled to Turkey, Italy and Singapore on a mixed business and pleasure trip, did a major gift fair/show in Melbourne in August and Lee has just come back from a large fair/show in Sydney (I stayed home for that one, too much to do here!!),

I guess one could surmise that life has been a bit frantic for us since mid-May.  At last we think things will start calming for a bit, at least for the next few weeks.  Of course, that is just as we start coming into our busiest retail season.  Lee has some tentative plans for a return trip to Turkey in December, back to Sydney in February and now she is talking about attending some shows in Guandong Province, China in April.  I don’t really know how I keep up with her, it is a real challenge sometimes.  Fortunately for me, the Carcinoid is not an issue right now.

Everything has been great for many months now, I feel great, I do not really suffer from any of the normal symptoms, although we know there are still several small tumors in the liver.  I am scheduled for my definitive MRI next month at Fremantle Hospital to determine the overall efffectiveness of the study treatment.  I will be very interested in the results of that scan (if I can fit it in my schedule…hahahah  like I wouldn’t miss it!!).

Anyway I just wanted to let everyone know I am feeling very good, I am very busy and life is good, exciting and still fun!!.  I still run the junior staff into the ground any given day and I really do need at least 27 hours days, if any are available, to fit it all in.

Take care,  God speed, and good health to all.  I promise not to be so sporadic in keeping my blog up to date in the future (God willing and the clock slows down a little!)

Love and blessings to all…

Eric

I

The Crunch is Here

Friday, May 16th, 2008

Blessings to Prof. Turner and Fremantle Hospital! It’s a good thing that the Lu-177 Clement Study has been as beneficial to me as it has been, and had no lasting side effects. I seem to be fully recovered and have a very sustainable energy supply. That is essential givern that we are being buried in business commitments and there is really no time to stop for the next several months. Our plans for travel to Istanbul at the beginning of June are set, and our Distributors there are eagerly awaiting our arrival. Products for the EuroAsia show are in transit and with the exception of a couple of minor items to be done in the next couple of weeks, we are ready.

My brother Tony has been in touch, and he and Anne are on their way to Florence where we will meet up with them in mid-June for a long overdue holiday and family visit. So looking forward to that.

We have to be in Singapore by 2 July for the show there. Production is under way, and our son Chris will have to see that the shipment leaves on time in early June. Yesterday, I turned the whole manufacturing production for the day over to him and our stalwart Stacey. They did a fantastic job. There is still a lot to be done next week, but we are on track to get the production ready. I will cut short my participation at the Singapore show to get back to Western Australia to prepare for the Melbourne Gift Fair in August. Still tons of stuff to be done there. Displays to be designed and build, product production to arrange and make, and I am either building or having built a special pallet case to transport our show fittings, fixtures and products back and forth between here and the Eastern States. As soon as we get back from Sydney in late August we have to begin preparing for the Sydney Gift show in September. God, it is hard to keep track of it all, but we are using good planning tools to do it.

Along with all that there has been a surge in our wholesale business that is really keeping us hopping! You can see why I started out saying thank you to the Fremantle Hospital and Prof. Turner and his gang!

I’ll stay in touch as much as I can. Blessings to all

Eric

Full Speed Ahead

Friday, April 25th, 2008

Now that we are four weeks + post treatment, I find that I am back to some sort of normalcy for me. Which is very good considering the somewhat daunting tasks we have planned for this winter. All of June we will be in Turkey (for business) and Italy (for pleasure). July is Singapore for two weeks on business. August we’re in Melbourne on business and September we are off to Sydney on business again. Then comes the holiday rush after that!

Other than a low white cell and platelet count, all side effects of the treatments seem to have move on. We have been majorly busy getting a large shipment of soap and bath products off to Turkey these three past weeks, so I have hardly had time to think, let alone write anything. As potentially exhausting as that was, I stood up very well and had enough energy to spare to do a few things around the house that have been waiting for several months to get my attention. Emotionally, I think knowing all the treatments are behind me has certainly been a boost too. I will look with interest to the results of next November’s MRI scan, but my body says things are well under control right now.

We are back to the gym as well, but still not as often as we would like or as we need. Just too many demands for our time recently, but we are gradually increasing our presence there. It feels good and our intentions are good as well, we just have to make more time available for ourselves in this case.

My commitment to the study still requires five more weeks of blood samples, but that is a small burden compared to the benefits I have derived.

Bless you all, take care and keep well, …be back soon

Eric

All Over bar the Shouting

Friday, April 4th, 2008

Hi Everyone,

Well, it’s all over, for the most part…..

We’ve finished my last treatment of the clinical trial and the immediate follow-up scans. I do have blood work to be taken for the next 8 weeks, but other than that it’s done and over. How do I feel? Great! What’s my attitude? Positive and happy!

I had the normal, for me, side effects of mild occasional nausea, a bit of tiredness, (and a bit of ill temper as well) for the past week and a half, but I know from previous treatments, that by this weekend, everything should be back to pretty much normal. There were only two of us from the original four at the day clinic for treatment this time. Both of the missing participants had had recent surgery. One had a hernia correction unrelated to carcinoid, and his platelet count was too low; and the other had a bowel resection (we don’t know the cause, but assume it was carcinoid related).

Prof. Harvey and I discussed my initial results while reviewing the scans taken over the four treatment sessions since last July. There has definitely been a reduction in the uptake of octreotate on the smaller tumours (an indicator that they have been significantly reduced in size and activity) and with no growth on the others and no new tumours! They have appeared to have been hit quite hard by the treatment. A much more definitive MRI scan will be done in six months to determine the overall effectiveness of the trial. Possible ‘one shot’ future treatments with a single follow-up scan might be on the table if it is found necessary or the tumours appear to be becoming active again.

It is time for me to name names and thank the staff and doctors at Fremantle Hospital! Specifically and not in any order, Brenda and Jenny (Dr. Turner’s PA) at reception, Julianne and Sarah (Nuclear Technicians) who did my scans and kept me comfortable during those long scans; Paul and Phil, nuclear physicists; Jim, Bill and Jazz who managed and oversaw our day treatments; and most certainly Professor Harvey Turner! The dedication, warmth, sympathy and kindness shown by all the staff and doctors at Fremantle Hospital has been utterly fantastic. I can only say thank you and God bless you all!!

I’m off Sandostatin now, unless the symptoms show up again and so life is returning to normal. I’ve spoken to two of my daughters (Melanie and Allyson) in the last 48 hours (their birthdays are only two days apart) and they are naturally pleased and happy with the results and how I am feeling. I’ll call my third daughter (Cyndie) this weekend and see how she is getting on and fill her in on the latest (BTW it’s Cyndie you see in the background of the above picture while watching a sunset over the Indian Ocean).

Leonie has been very busy setting up a new website, Carcinoid Cancer Resources for Australians (www.carcinoid.com.au). It’s not fully functional yet, but it is getting there quickly and I expect she will be spending much of her time over the next three days getting it into order.

More to come (there always is…) Stay well, be good,

Eric