Retraction

 This will be short and sweet. Sometimes I do get things wrong, and as hard as it is to swallow crow, I try and admit my mistakes.

In my previous blog I made mention of an End of life meeting we had for today from Chuck's family Dr.  I stated she seemed excited etc. and apparently had all sort of goodies to offer for End of life. I have to retract my comments that were actually made in a rather nasty frame of mind I have been dealing with for some time. I was actually terrified of this meeting, as I think most of you will understand. My emotions are pretty raw and there is very little covering them at this time, and I made a mistake of directing my anger, stress, and frustration unfairly.

The meeting was rather pleasant. Our youngest came with us, more in support of myself than wanting to be a part of this, and it was appreciated. The Dr. actually did have something to offer us, if NEEDED, because of the way the wheels work in cases such as we find ourselves in, it is best defence to starts things in motion before, or if , they will be needed. There is palliative care offered, just a nurse who specializes in these cases, that will pop out (after notifying us of a visit) and check in to see if we are in need of anything medically. This nurse will have direct communication with the Dr. so if pain meds are necessary they will inform her, etc etc. This is great, because where we live, often an appointment will be a month, if not months after a request, so huge bonus! 

Talking about such a possibility is incredibly difficult, but we have been touched too many times by Cancer not to know it is necessary. We do speak, not alot, but we have covered what we feel are the main things, in fact it has offered me the ability to make my wishes known, as well. Now we are done! Sadly legal stuff is a part of this, and we still have a few things to get in order, but we have been procrastinating for decades in this regard, probably like many others. It is time to get off our butts and do what has to be done, so we can simply focus on extending life which is the road we have decided to take.

Today I realized that writing all of this down for everyone and their dog to read, is a hundred times easier than speaking about it. So I guess I am grateful I made this decision, as this part of Cancer is a reality and a big part of the journey. I am actually somewhat relieved making my wishes known, as I have aged, the fear of spending my last days in some long term care home alone is now not a worry. Funny, although not faced with a dreadful disease,I think many of us (oldies) do give thoughts to this, we just don't speak it out loud. We've just sort of been backed into a corner so we can't really ignore it. One more thing that we have ticked off the to-do list. 

So again, to this Dr. who today showed concern, and compassion, I apologize. It was actually a pleasure to speak with someone professional who cared, something very lacking in this journey!

The Swiss Cheese Cancer Care Syndrome

I honestly didn't know if I would be able to sit down and write this "story". It occurred at 9AM and basically blew us out of the water.

Now you will recall my previous blog explaining we had an appointment on the 19th for him to have an IV treatment. We were unsure if we should go to this, but I made a point of listing it in the questions I wanted answers to on our Friday appt in PG, We were told by both the Nurse who spoke to us on the Wed. and the Cancer GP that spoke to us Friday that is was still on his chart, therefore we had best make the appointment.

As it is about 1.5 hrs from our house to Smithers we left at 7:15, keep in mind Chuck has been prescribed some pretty harsh steroids to reduce swelling on his brain, and he does not sleep very well on these. Most mornings he is up about 4AM and then has a nap about 8:30 -9 he is always tired. Getting out the door at this hour was not pleasant, but off we went. I think I might have gone a little over the speed limit, as we got there 40 minutes early. 

Now I am not sure how other "Satellite" Cancer Clinic are set up, but here, it is upstairs and is completely separate from the rest of the hospital, so patients must pick up a phone and call to tell reception they have arrived. Chuck did this..only to have the person on the other end say he was NOT on the list!!She was very pleasant, and told him she would have to check things out. She came outside into the waiting area and sat down with us (well I stood, I was pi$$ed) She explained to us that one of the Cancer GPs had put his treatment on hold, he had to wait for an echocardiogram that was scheduled for the 11th, and then a CTscan we had not received a date for. So clearly we had spent time and money driving all the way out to Smithers for absolutely NOTHING!! Apparently, technology does not include the phone, because both of us have cell phones, both numbers are on file, and neither of us got a call informing us he was not getting an IV. 

We have been dealing with this system for almost a year now, and we are well aware those folks who often end up dealing with most of the crap that happens in this incredibly dysfunctional system, are those who are not part of the medical profession, just like this poor woman who had to give us this news. Maybe this is a plan, they have no part in the mistakes, so folks don't want to blow up on them, we certainly don't, however, they have to face us, and hear our frustration those who have a part in it, are never around. They don't need to face any responsibility, and we don't get any apologies for thoughtlessness, and no communication. 

The system is full of holes like swiss cheese. No one contacts anyone else, things do not pass from one department to another, if they are ever sent, they are never received. One hand never knows what the other hand is doing, or has done, departments assume information has been given where it is needed, but this seldom happens, it simply disappears into the twilight zone, never to be seen again, and then mistakes happen, serious mistakes, life and death mistakes, criminal mistakes! Problem is, because these things are floating about in limbo, there is nothing resembling a "paper trail", is this on purpose? I have to wonder. I have requested Chuck's medical files from both Northern Health and the Cancer Clinic, the amount of correspondence is minimal, which is frightening, because this is someone who has been dealing with Stage 4 Cancer for a year now, where is all the communication between the Cancer GPs and the Oncologist ? Trust me there are reports after each CTscan, with the Oncologists name cc'd, but nothing really from him to the GPs, in fact not even a medical record of the meeting we had in December. Is this right? I can't think this is proper. In fact, when he had his last scan that showed there was a pretty high likelihood the Cancer had returned somewhere in his body, the oncologist apparently simply wanted to continue the same treatment, and wait 3 months to do another CTscan? WTF!!! I am not a Dr. I am not even very intelligent, however, I am smart enough to realize that a fast growing cancer, such as he has, will grow pretty frigging big and move incredibly quickly if left 3 months! And then BINGO he is retired, and we are left holding the bag, no where to go except, yep you guessed it, to ER to find out those nasty little lymph nodes were indeed screaming cancer not in his chest or abdomen, which was the limit of the CTscan, but in his frigging brain!! Trust me folks, this is not something I would ever wish on my worst enemy, let alone the man who has been beside me for 39 years. 

Oh this is a long one, sorry, just have to vent it all out. When we got home, Chuck was just as Pi$$ed as I was. He had been told over and over, how the Drs, could not request any tests, could not change any treatment etc etc. without the specialist (Oncologist) ordering them. However today, to us, it appeared this Dr. had made the decision to stop treatment. It took us all day to find out the facts. We called our trusty councilor, who has had to listen to our complaints over and over, and has always tried to find answers for us. She was NOT surprised, our issue happens often. NO communication! Clearly something had happened and someone forgot the main characters in the show (Us). She promised to try and dig out what had happened. The Cancer Agency listened to Chuck and promised to get him answers. Hours later we did get the answer. Apparently his new Oncologist, who we are to meet October 2nd. had been in contact with the Cancer GP in Smithers, and they had decided to stop the present treatment, as clearly it wasn't working and we will hear what the new course will be when we have our meeting. I am guessing one assumed the other would have contacted us, but that didn't happen. 

I am also going to tell you about another royal F*ckup. I might have mentioned over 2 months ago, he had been to the optometrist in Smithers (Chemo patients often have damage to their eyes, so exams are needed upon completion). During the exam, it seems they found something concerning, and sent a referral to the neuro opthamologist inTerrace. He was told it may take up to 2 months to get a call. I emailed the optometrist the other day, telling him the system was broken as he had already been diagnosed with brain cancer and we still had not received a call. Yesterday, as we were shopping in the local health food store my cell rang. It was the optometrist. He explained he had indeed written the referral that afternoon, but....wait for it...It never arrived in Terrace!! He apologized, and actually told me he had suspected the cancer had moved to his brain!! Now the concerning exam was indeed mentioned during a Dr, appt. but must not have rang any bells. The optometrist apparently did not think the concern was enough to actually pick up a phone and call the neuro-ophthalmologist instead he sent a fax or something that never arrived. See this shit is everywhere folks!!

So tomorrow, we get to go to the family Dr. who appears to be very excited to have us in for an END OF LIFE meeting. She clearly got the latest CTscan report and wants to make sure we are all set up for the worse possible scenario, because clearly the medical system has all sort of goodies to offer us in this regard.  

Now our complaint has been sent, originally it was sent to Northern Health, because...many of the papers have this stamped all over them, their reply was quick about 24 hrs. stating they were NOT responsible, our issues were with the provincial Health agency, so off it went to them. They actually had the balls to say perhaps we should sue the Drs. involved????Again WTF!! These Drs. are not private clinics, they operate under the British Columbia Cancer Agency, this is who pays them, therefore the Drs. operate under their "umbrella". It is not easy dealing with complaints and cancer treatment therefore we have given a trusted friend authority to act on Chuck's behalf, because we need to concentrate on him getting better. I think this is why more folks do not complain, as they are so focused on the Cancer and the criminals continue to murder innocent folks with their lack of ethics, morals and professionalism. Thanks go out to Caroline for taking this task on for us, I say again, my goal is to stop this criminal activity, so others never have to deal with what we are going through now, and what my beloved sister in law went through with her family, and what my Quesnel friend is going through now, and what Dear Shelley, long passed went through. With an election on the horizon, I ask everyone to think very carefully before you vote, who is going to fix this mess? I can tell you it is NOT NDP, they have created a nightmare for all of British Columbia, and like us, you never know when you might be in our shoes..time for a change!!

Cancer disillusion

 Today was emotionally draining, as have been most days lately.  It started on a high, my Kordyban lodge buddy had an appointment at the CClinic this afternoon so we arranged a quick coffee visit.

Chuck's Radiation treatment was for 1030, things must have been swinging in there this morning, as he was in and done before 1030. Then we have a nurse appointment. This is basically a visit with a nurse who checks his symptoms, "any nausea", "any seizures", "any headaches", etc etc. The poor woman, she was very new, and of course I started with 20 questions,because...she is the only medical person we have had a meeting with since last Friday. I wanted to know what was next after his last treatment on Friday. Here it is folks, we were suppose to get a call from a medical Oncologist Oct 2, actually we were suppose to go to Smithers to the Clinic there and have a zoom meeting in one of their rooms! By now, you will know, Zoom meetings are NOT acceptable to us. Cancer is NOT impetigo, it is something that deserves a face to face appointment, one in which perhaps a physical check is needed? I just do not understand why they think this is acceptable, it was basically put in place to help  folks who need to travel, so instead of our government providing patients the ability to actually meet the person in charge of their lives, they can simply sit in front of a computer getting less than those who live close to medical facilities . The lovely lady did not know how to go about putting the meeting in gear but she is going to find out how. We will get a call from the radiation Oncologist about the week after the medical Oncologist. See, you do not have to travel this road very far to see, communication is a massive issue! In places that do a great deal of Cancer care, they speak of Cancer Teams, because this disease requires a group of different medical specialties working together to fight this nightmare. It does not work well when no one seems to know what the other is saying or doing.In between treatments there are large spaces where things are missed, and because no one sits down with a full file on a patient, they are unaware of many things. This has become clear on far too many occasions, and it is extremely disturbing. I feel very bad asking people like this nurse questions that she has no real answers to. She simply has a computer screen with some stuff that she can access, such as the ability to click about to see when we can expect calls from Oncologists, but there is very little she can speak about. One question I had was,"what do we do in regards to the scheduled IV cycle on the 19th of this month, in Smithers?" Ahh there is an "answer" On August 27th there is a note from the Smithers Cancer Dr, stating he is to continue his regular cycle,, well that was 2 days before the head CT was done, and 2 days before we were informed he had brain cancer!! It appears we will head off to Smithers on the 19th to do something that clearly is not working anymore, since there is nothing else on the list. Again, absolutely NO communication..just a bunch of different folks with no clue what to do in regard to what is happening now. 

He has 2 more treatments, we have tomorrow's listed with no extra note such as a meeting with a radiology oncologist, so guess that is it for us. Head home after Fridays treatment , drive to Smithers on the 19th for IV,and likely have to listen to someone there tell us their take on things (more doom and gloom), the same people who told us the total opposite of what 2 specialists told us should have happened when he got the brain cancer diagnosis the floor below the Cancer care place . So trust me, questioning everything becomes impossible to stop, no trust in anyone anymore! 

Now we go into the next mental twister! Yesterday he got a call from our local hospital informing him his family Dr. wanted a phone call today with him. It was suppose to be 10 to 12, so Nurse appointment over at 11:30 and he decided to stay at the Cancer center and wait for the call instead of getting our cab back to the hotel. We waited 20 minutes, nothing, so I called the cab, yep, you know it, the call comes as the cab pulls up. He could not put it on speaker (thank heavens) so he did the call in the cab and I could not hear. It was all about what the Cancer business seems to relish..END OF LIFE!! this seems to be what the whole lot of them just do up big time. He needs to get things in order, we need to plan home care, plan if he is to die at home or in the hospital, they must arrange someone to come to the house to ensure he takes his medication, etc etc. Now my Lodge buddy is going through exactly the same thing, seems to be so much in place for end of life, but so little in place for extending life. His Dr. has not seen him in months, she has no clue what he appears like physically, as he said, he is not sitting on the edge of the bed drooling he is ready to start on his next treatment in hopes it extends his life m but you get all this shit that one wonders is to have you simply give up and crawl into a corner, or maybe..take that lovely MAID offering, and let them put you to sleep.

It was after this call, my lodge buddy and her family showed up for the visit. I went down to meet her without Chuck, he was just getting up from his lunch. She was my lifeline, The hug was what I needed, we have shared so much over these last months, I think we have kept each other semi sane, neither of us have come through this cluster F*ck without major damage. We have both become totally disillusioned with this useless system, and the lack of any consideration at all. She was here to see the pain management team, she had still not heard from her Dr, after reading her test results herself on Health Gate last week. She said what we think, she believes this was all decided way back in December for both of them. The word Palliative in Chuck's case seems to have limited him to certain procedures that likely would have caught the spread of cancer to his brain (like a simple CTscan that went beyond his chest area), maybe an MRI, or a PETscan, his specific cancer has a 50% chance of moving to the brain, but some research papers I have read state they don't check for this because they feel it has no bearing on morbidity. I have also read that HERS2 brain cancer responds to specific chemo treatments better than other cancers, so ????

He is NOT ready to hand in the towel, his headaches have all but disappeared with the steroids, his speech has corrected itself since radiation treatment #1, he feels his balance is better, his appetite is unchanged, he is more tired than normal, however that is to be expected with radiation, we just have to hope that the medical system has not simply put a line through his name. So we know radiation did amazing things to his esophageal tumour, far more than expected by everyone, he has beat cancer in his liver in his lung, so lets give him a chance to do the same, or at least keep the tumours at bay, before we send home care to our door!

I feel so very sorry for those who have stepped onto this road. It is nothing one expects, do not be frightened to open your mouth, you HAVE to speak up, otherwise you are forgotten. Yell if you need to,I have! Just the most emotionally draining system one could imagine.

Cancer Rollercoaster

Well, here we are ..2 days into radiation.  I am so hoping this is helping someone, as it is one of the most difficult things I have done, way out of my comfort zone. I have already come to realize keeping the record of our experiences has been good in one way, and that is the fact I can reread every step of the way. I can understand that our disgust, our discomfort, and our lack of trust in the system has bearing, lots of bearing! My need to question absolutely everything has been with reason, we have not been difficult we have simply expected the best of care, and found the care lacking in so  many ways.

This whole experience has been a mental rollercoaster, with tiny little highs, and deep,dark lows . It has been mentally and physically exhausting, we have changed, along with our whole family.  I have been lucky to reach out to the woman who was given the job of personal counciller to Chuck, and thankfully myself as his partner. I have abused my friends with calls full of break downs, I have cried in front of more people than my entire life before this.  When I tell you this journey is one of the lonliest ever, I am not exaggerating. Those who hold all control are not our friends, nor our families, they have no connection to us besides their pay cheques. We are simply a couple that has entered their area, like thousands of others, and they do their small part of Cancer Care, and go onto the next. 

Is it just us that have fallen into this horror show? No! This past week has seen my Kordyban Lodge friend read her most recent test results on the Health Gate app. They were less than positive. No medical professional who has dealt with her case bothered to call with some pretty damn serious news, she had to find this out all on her own, amidst phone calls explaining how to deal with advanced care, how to talk to her family, how to have a end of life plan. So much help flying through the phone and mail at her, after sitting at home waiting for a call from those in charge of her care, that just didn't come. This is NOT acceptable!! Can any of you imagine this scenario? Thankfully the two of us will meet up here in PG tomorrow, as she has an appt. after the fact. We were all to meet up when herself and Chuck had managed to beat this F#cking thing, abd celebrate. We won't be celebrating tomorrow, but you know what? We will just regroup , we will share our strength, and hope, and fill each other with enough power to kick Cancer's butt.

Two radiation treatments done, 3 to go. He has taken them well. Tumour pressure does strange things to the brain. He has balance issues, much like those suffered by stroke victims, same with speech, and of course intense headaches. The headaches disappeared quickly with steroids, as they reduce swelling rapidly. The speech seems to have improved as well, he says the balance is better, but he has a ways to go with that. What today brought, was the intense tiredness. He came back to the hotel after treatment, he ate,and has been in bed since except for a quick walk down the block for supper. This is a repeat from before, basically expected by us. As this is 1/2 the treatments as last time, we are not sure how long this will last, but exhaustion with radiation is almost a given, it will take weeks maybe months for him to get his energy back, sad, as he was almost there when this hit us.

Tomorrow he has an earlier appointment, 1030 radiation and an appointment with a nurse who will discuss his side effects etc at 11AM.So glad our dear friends from Hudson's Hope were here yesterday and this morning, as he was able to enjoy their company before this exhaustion kicked in. 

Hoping we get an meeting with his Oncologist  before going home, but we understand it takes a very long time for the effects of radiation to end. we were told this sometimes goes on for about 2 weeks after the last treatment, so updates to follow.

Thank you to all those who are in our corner. Your words and thoughts are appreciated, even if I don't always comment. 

Day of Desperation

Tuesday, the beginning of absolute desperation.

Now as you know the brain cancer diagnosis happened on the Thursday. Try and imagine getting that type of news, and then going home with no idea what was to happen. Then waiting the Friday before a long weekend, with no call from anyone. Of course Cancer takes the long weekend off, so you sit for 3 more days, just hanging onto a string for Tuesday to arrive. Tuesday, you know someone is going to call and let you know what they are going to do to help. Surprise Folks!!! No call, no one, no Cancer care team who you know got this information the very day it happened from the floor below them, no call from your family Dr. who had also been sent the information, no call from the Cancer agency (but that was never ever expected). I gave them plenty of time, and by the afternoon, I was going insane. 

Many suggestions ,some from the wonderful Locum we saw, yes I called Tuesday morning for an appointment at the walk in his headaches were keeping him awake, he was in pain, and his walking was becoming very unbalanced, something was needed. We had an 11:20 appointment, I sat hoping someone would call before this, but nope. The Dr. was extremely caring and compassionate, and very understanding of the lack of communication from the Cancer agency. He prescribed some pretty potent painkillers for Chuck, something to help him sleep and something to help him relax, and then asked if he could hug us.  Now I am pretty good at holding it together for short periods, but the hugs..well they just open up the flood gates.Felt pretty good leaving there, simply because we had spent time with someone who cared (that is so important at this time).

Back home we go. He was not interested to take anything immediately, because he was set on butchering our meat birds. Things he felt he had to do..however we did talk him into it. Off to bed he went.

\Now sleeping was continual he would get up have a coffee with his eyes closed because of the pain, and head off to bed right after, I would be lucky to get him to eat some breakfast. We were all so worried and hated watching him suffering.

I decided to contact one of the few people with the Cancer Agency in Prince George that had been in our corner the last go round in PG. She had listened to our complaints, and stepped up to the plate to take our concerns to the folks who were in charge. She was pretty much answering our concerns on a steady basis, as if you remember back in December we had so many issues, and as the Aboriginal Liason ....AND  personal Councillor to pretty much everyone (I think there is one other councillor at the PG Cancer Clinic), she is stretched to the limit, but somehow always there.I can't remember if I gave her Kudos in the past, but,she gets a truck load now. See I was absolutely desperate, no one seemed to give a shit..here it was 5 days after a horrific diagnosis, and no one was calling. I was in tears, and figured why not send her an email just asking for a moment, maybe she would read it the next day and get back to us?

\I felt a tiny bit better knowing I had actually done something that might work, but again, the twilight zone of just sitting at home with nothing happening, and no one there for us, drove me nuts. I picked up the phone and called Laura. I figured I would leave a message as well as the email, to my surprise she answered! You know that feeling when a weight is lifted off your body? It was instant, I knew I was talking to someone who cared. She must have a ton of folks she helps throughout this nightmare, but somehow she remembered us , in fact, she was just about to call me! How can it be that a person who is dealing with the massive number of folks from Northern B.C. who are sent to PG,can be so quick, and everything else takes a lifetime?If that place had 3 more Laura's , patient care would improve 100% from what it is now!

She listened to Chuck's story, she knew his past story, somehow, she started to ball rolling within minutes. She was going to contact an Oncologist for us, she was going to look into things for us, and basically, open the door to the walls of silence. She promised to call us back on Thursday with all the news. Honest to goodness folks, again, sometimes I do not realize how heavy a weight I carry around all day, every day, dealing with this Agency, and of course my beloved's cancer. I don't think I have even mentioned what was happening in our world before the Thursday. Maybe I will put that piece of personal life in, so understanding the pressure may become a little clearer.

Chuck and I have been together about 39 years, in fact we started to live together in September 1985. When all this began, we needed something to brighten things a wee bit, and also to give the kids something to look forwards to. We (he said I) decided to actually commit, and September 7th was to be our wedding day. It was going to be small. Just our immediate family, with their children and grand children, and some dear friends, some of which were going to travel quite a distance to share our day. I was actually stressing about this when he was in his IV treatment, as there was so much still to do, and he had been so short tempered, and so tired, I didn't even want to ask him to do anything(brain cancer does some pretty serious shit with personalities). When he was told the CTscan results, and I kind of lost my temper in the ER because I could not believe after 11 months of treatment and Ctscans, no one had even considered doing a scan beyond the original area, even though they were telling us the lymph nodes were hollering the cancer was back somewhere, I told him we would cancel the wedding. He was insistent we continue on with the plans. One day of enjoying time with those important to us, a day to laugh and remember. So...I agreed. 

That brings us to Tuesday afternoon, I can't remember what time, but the phone rang. It was the specialist from PG. He asked Chuck if anyone had spoke to him about the scan, yes, the ER Dr. had explained the results, so....he mentioned something about Vancouver, we thought he was saying he could have Chuck in Vancouver the next day, but it was a misunderstanding. he was explaining the Oncologist was in Vancouver and would be calling us at 9AM the next day, I asked the specialist how quickly Chuck would be getting treatment his answer was "very quickly". Ahhh a little breath of relief was beginning. 

Wednesday morning the girls were with us when the phone call came right at 9AM. The Dr. asked Chuck a whole whack of questions on his symptoms, explaining that he had 3 large tumours and each of those tumours caused different disabilities. Apparently, SHOCK, one of these tumours is situated right in the area he had a massive sub dural bleed many years ago causing him to have 2 burr holes drilled into his skull to drain the bleed off. I am NOT a medical professional, but would that perhaps be a weak spot for this evil disease to take up a home? He explained that there were 2 options for radiation, one was the new clinical trial (I had actually read about the previous night, knowing the Oncologists name) that was a one time heavy dose of radiation, it was untested, and the effects had a fairly large amount of risk to it, the other was the tried and true one of 5 doses of radiation to the brain, this one was proven to help stop more tumours from growing, as well as shrinking the ones there. Radiation was not going to kill these suckers off, that will once again be Chemo's job, but this treatment was going to help him regain 50% of what he has lost so far within a month or so. Now there are side effects, his memory may very well be affected, not sure how, but it is likely. There are other risks and side effects as well, but we have been given a handfull of hope ...Then he tells Chuck he wants him in PG that afternoon, treatment to start the next day!! Holy crap, folks...Big rush up the stairs to start packing, organize everything else with the kids, thankfully they are there . Grandson in charge of all the poultry. Just insanity but joyful insanity, this was what we wanted.  I was honestly just coming down the stairs when the phone rang. Chuck answered and put it on speaker. It was the PG Cancer Agency...That is when the day turned into the absolute worst since we began. The woman informed Chuck that she knew his Dr. wanted him out there that day, however...she did not have a spot for him, they did not have a Dr. so..he would have to wait until Sept. 11th!! That was pretty much the end of me, and Chuck. All the air in our bodies just exhaled, we were completely deflated. My legs were like rubber, my back bent, my head dropped, and there was absolutely nothing left inside me. I might have said some things in the background while he was on the phone that were not nice. I had to leave the house as I have never had a panic attack before, but I knew that was what was happening. I feel bad now just going out the door and leaving Chuck,but I could not do anything at that moment to help, I had lost it! I did some serious crying, this appeared to be a repeat of the last bout with the Cancer agency that took 11 weeks for him to even see anyone! I calmed a wee bit called a friend, did more crying, and my girls called our Liason, Laura and left a message with the specialist in PG. I don't think we have felt so crushed before, like he did not matter in the least, and we were out of luck. 

I have no idea who worked the magic, but within an hour or so, the phone rang again, and surprise..it was PG Cancer agency, and they had found a spot for him for the next day!! I am going to say, this mental rollercoaster is cruel. It is one of the worst things to deal with, the ups and downs, the waiting game, the loss of control of every moment in our lives. \

We have made it to PG, our liason was waiting for us when we arrived at the clinic, we had a consultation with Dr. Jiang's fellow oncologist, a very pleasant woman, Dr. Cua who tested his loss of field vision, his balance etc, and told us that Dr. Jiang would be in from Vancouver soon to speak with Chuck. Feeling pretty good, He was taken in for his CTscan, and fitted the creepy goalie mask thing for his head. It is much like a 3D goalie mask except it is a plastic mesh, they heat it up and then mold it to his head to ensure no movements during radiation. First treatment is tomorrow at 3 in the afternoon. So we have tried to spend the last 2 days just relaxing and resting up for the week to come.

LOL the easiest past of all this was the decision to cancel our wedding. It was not a hard choice. We were , of course, looking forwards to having our family and friend together for a nice visit and lots of laughs, and I felt badly telling those folks who mean a lot to us that they would have to cancel all their plans, those traveling long distances, those cake bakers, those brother's who were going to walk beside me (that is singular and he is the best brother ever!) those kids who had planned everything, those friends who were going to stand beside Chuckie, Cindy Lynn and Archie, doing up those lovely wedding cups that will now need a new date, Caroline, who is gearing up to do battle for us, Ginny for her offer, Nick for his de-maleing our little piggies, Joe for all he did,and for simply being his normal calm self,Lizelle for her help and smiles, Jordan for doing bird duty, Kayle for all she did, Naida for the beautiful memory box that we look forwards to sharing with folks in the future. Dawn Kyle and I think Paul? for doing the meat bird end of days finale for us.This would be twice as hard without those dear to us and our kids who keep telling me to stop saying thank you..but I am not going to stop.

So you are all up to date on things, I know I have a bunch to thank still and I will continue as I go along. We shall see what tomorrow brings, I have a happy moment to look forwards to as our friends are going to visit from HHope, and it has been far too long since the two old bats sat down for some coffee and laughs.

I pray no one ever has to follow in our footsteps, and I will do all I can to try and have those cracks filled in this cluster f#ck of a health care system. I hope when the time comes, and it will , we will not be alone in our hope to stop this insanity!!

So this has brought things pretty much up to date, I will keep the blog going, and hope it has a happy story , because so far, we have been thrown in the lions den over and over...Fingers crossed a change is on the way.

The Business of Cancer

I did not want to be back so soon, I certainly did not want to fall into the pit of despair, and,  if I didn't feel the overwhelming need to put this down fresh as only hours ago, I would not be here.

Now you remember, it was only Tuesday, 2 days ago, we had our Dr. appointment. Concern about the swollen lymph nodes was the main focus, along with the "any trouble swallowing"question that had me asking why it was asked. Apparently the last CT showed some swelling in the esophagus, but they were assuming that was scar tissue. Again folks, it is exhausting grabbing onto every word spoken, to ensure what is being said is understood. We were told they were simply going to continue on with the same treatment, until such time as he got another Oncologist, no time mentioned when that would be, however because of the swollen nodes, it may be time to try another medication, perhaps this one was not working?

Well here we are on Thursday, did I mention he has had some pretty harsh headaches lately? Today the head ache was bad. Years ago he had a sub dural bleed that was pretty serious, he had to have neurosurgery to drill 2 holes in his skull , the headaches were as bad as they had been when this happened. I tried to get him in to see his family Dr. sadly, he would have to wait until October for that, even after speaking to the assistant, it was suggested he go to the ER. He wasn't having that. So off to the treatment in Smithers. Now folks, this is when I wondered WTF was going on. 

The nurse did the regular questions (been through 12 treatments before this) but once again "any problems swallowing?" So I tell her, his esophagus has been cleared of cancer he swallows fine and dandy. Hummm..she answers that is NOT what Dr. Saltzman had in his notes, the esophagus is not cancer free. I was pretty touchy today, so I blurted out we would not know what was in his notes as we saw him once in December, and he never bothered to call, zoom or even put his notes in the papers we requested from Northern Health, we were told different!We were told his liver is cancer free as well!!Again sometimes I get ticked, and this ticked me off. If that was true, then someone has been lying to us all along, and we know it was certainly not the surgeon who did the bloody biopsies, then she proceeds to ask Chuck if he needs a counciller to speak with, the Cancer Clinic in PG offers personal councilling.Of course Chuck tells her, I am the one who needs someone to speak with about all of this, so she gets me a card, now we are 11 months into this, why the offer?. He tells her about his headaches, she suggest we head down to ER after the treatment. FYI because I am sure you folks do not know this, The Cancer Clinic does not do anything beyond deal with the Cancer issue, any other issues must be dealt with by Family Drs. or ERs, totally separate and apart. I can tell his head is really bothering him, so once the treatment is done, down stairs we go to ER. 

As far as wait times go, it moved very quickly. He was seen by the ER Dr. who was very nice, he mentioned the head aches, mentioned the previous bleed, CTscan was arranged and done. All we had to do was wait for the report. 

Now I have shared all our private shit on here, against my nature and his, but I did it in the hopes that it may help others, and maybe , just maybe somehow get out to the world, how disgusting the whole system is. It is simply a business, money is poured into it, folks get the feel good feeling when they donate, numbers of donations are put up for the province to see, and no one really knows where all that money goes. As I said last time, Big Pharma is rolling in mega billions with the business of Cancer, CEO's are making major dollars running "charities" yes research is funded, but Pharma funds most research. Those folks who are suppose to be keeping an eye on your case only have a minimum amount of time for you, so....things just slip through the massive cracks, huge wait times allow cancer to grow, and if it is a fast growing one, weeks can make a huge difference, and we know that, big time. Procedures are missed, holidays mean treatment stops, Staff shortgages mean wait times. Treatments are doled out over periods of months and months, with checks continuing on as limited as possible. Chuck's checks are every 3 months a CTscan, well, today we realized they simply scan the same area, over and over again, not checking beyond the original problem area with Stage 4 Cancer, (that means it is moving around, folks! )This same old routine is a huge mistake, and today we found out how huge it can be. 

The report came back, and it was beyond what we ever imagined. Chuck now has cancer in his brain!! Not one CT scan of his head in almost a year, not one body scan, not one MRI, not one PETscan, and now, not one, but multiple metastasis.. 

So..we have an ER Dr. having to give us this absolutely devastating news, I pretty much lost it in the ER, and sadly took it out on someone who had done their job properly, I ranted about the Cancer Clinic and I was loud, I ranted the fact that in all this time, those people never looked beyond his chest area, I had to walk out of the room because I was so livid. I did return and apologize to the Dr. and the nurse, I told them I knew this was not on them. The Dr, had checked his file during this time, to see if they had ever done the head CT, and they had not. Now, we go right back into the nightmare of the Cancer Agency, the results are sent by the ER Dr. to PG, and she hopes that she will be put in touch with the Oncology department (remember he does NOT have an Oncologist) and we will once again have to wait until they contact us, remember 11 weeks last time! This agency is criminal, as I said before they murder people. They weld all the power over this disease, it has been given to them, ordinary Family Drs. ER Drs, folks who attempt to cure, have no part in this. It is a medical hierarchy with inadequate staff, and piss poor service. The longer you wait (a file marked urgent sits for 11 weeks) the more time that deadly cancer grows. 

I am hanging onto my anger, it has only been a short time since I watched my sister in law fall through the Cancer Care cracks, and lost her, now those cracks are swallowing another, and we have absolutely no control over the insanity that surrounds this system. This power has got to be taken from them, they are not capable of doing their business, they remove certain procedures from specific stages of the disease, not allowing all to have the same, giving them the same chances. They play God, and answer to no one, leaving grief in their wake. These people must be held to account because they are indeed killing people, perhaps not with weapons, but definitely with absolute lack of care and consideration. I have to make this my focus, I abhor the thought of other  families suffering through this nightmare . 

Sadly the ER Dr. believes a specialist will call us tomorrow, I have very strong doubts this will happen. But maybe I am wrong? 

Cuckoo's Nest

Well, as promised, I am keeping the world up to date on the latest happening, along our journey through British Columbia's Cancer system. I am somewhat grateful I decided to make this public, as some days I simply cannot figure out WTF is going on! Now is one of those times.

First, let me tell you all, we have decided to grab hold of anything and everything out there offering any possibility of destroying cancer cells. Both of us spend hours on-line researching and checking out Mother Nature's medicines, along with, yes, the famous "Horse" medication. At this point Chuckie has his very own pharmacy to swallow down capsules, tinctures, etc. No, we are not stopping his actual medication, but check to see if any of the other stuff counteracts with the IV medication he is given every 3 weeks. 

The past few months, we have been questioning his diagnosis, and, of course this whole process, which has pretty much baffled us. Since I have let you all follow this from the beginning, perhaps you can offer us some answers, as something so life altering should come with specifics, and one would certainly hope due care and consideration. 

So, as you will remember, in September last year (yes, it is almost a year, but seems like forever) Chuck was diagnosed with an enormous tumour in his esophagus, so big, he was unable to swallow without water to assist food down. We had no doubt this was indeed cancer, as his surgeon did biopsies, along with a CTscan. Please keep this infamous CTscan in mind as I continue. The Ctscan also showed other spots , some on his liver, some on his back, some along his lower side. This was classed as Stage 4 esophageal cancer. Scary, yes, but as I have mentioned before , the surgeon who explained all of this to us, offered us the statement, Chuck had a very long road ahead of him. When speaking about Cancer, a very long road, actually sounds pretty positive, he spoke of radiation to shrink the massive tumour, and surgery to remove it, and then of course, Chemo afterwards. 

Following my blog, you will remember the length of time it took to begin any course of treatment,  late November he started, 10 days radiation, and December he began Chemo. We had a meeting with the Oncologist in December in PG before starting chemo cycles in Smithers, we were told this Oncologist would call us 1/2 way through the cycles. 

In March I became very concerned , as no one called for a CTscan after the first in September, it became clear then, no one was actually reading his medical file, as the professionals had not caught this fact. This error caused a baseline to be pushed back much farther than it should have been, it was impossible to tell exactly what improvement the radiation had done, and what almost 3 months of Chemo had done. The CTscan was done in March, before this scan he had been to see his surgeon who did a Gastroscopy, and was thrilled, the tumour had disappeared, the biopsies he took were all negative, but then the CTscan. Apparently he had spots on his liver, and suddenly a spot on his right lung, this is when we were told it was simply a matter of time when the Cancer cells explode and take over his whole system, there was no chance of remission etc etc. 

Now technology is incredible, but in some cases not incredible enough, as we learned in the beginning when the cancer in his spine, was actually explained as old fractures showing the same as cancer (he did NOT have cancer in his spine). So, could these other spots be something else, as well? At this point in time, we are beginning to believe this is indeed true. Clearly as he is listed as Stage 4, some things within the Cancer system in British Columbia are no longer available to him. CT's, blood work that gives tumour marker numbers, and maintenance medication are basically what he is offered. No MRI's, no PETscans, no biopsies, his stage 4 is based on one CTscan back in September and we must simply accept that any and all spots are indeed cancer. 

So since March his esophagus is cancer free, but we have been following his CTscans that he gets every 3 months, and up until yesterday, they all mentioned spots on his liver. Now, that spot on his lung the nodule that had us so concerned, well that disappeared a few CT's ago (big relief). Yesterday, there was a student Dr. in the room for the appointment so we had a much longer time to ask questions. I asked about the liver cancer, because I was going to see if they would consider a biopsy to confirm it was indeed Cancer. SURPRISE!! We were told that had disappeared, no spots on his liver, apparently that had happened a couple of CT's ago????However, he had some enlarged lymph nodes they were concerned about in his chest. We had decided before this appointment we would request a second opinion, as pushed into the twilight zone of just existing waiting for the inevitable time when the medication stopped working and faced with the end, we wanted a clear evaluation not based on the medical report of Dr. Padma who clearly lied and did not do a credible reading of the CTscan all this has been based on. So Chuck asked about a second opinion. This was when we learned this Dr. had never gone through his file! She explained she was not the one who initiated him, therefore she had not seen Dr. Padma's report , or in fact anything before he began chemo. Does that worry anyone? Sure made us sit up and wonder. We were told Chuck does NOT have an oncologist yet, his retired July 31st, so at this point the clinic is simply going to continue this maintenance therapy until such time as they find one for him????? That will constitute a second opinion, right? WRONG!! That will simply be more of the same we have been getting, someone who simply picks up the file and begins where we are at right now. 

This folks, is how deadly mistakes happen. When a person listed as Stage 4 is put on a treatment plan that is Palliative. (of a medicine or form of medical care) relieving symptoms without dealing with the cause of the condition.

"palliative drugs"  .  

What they have decided is, there is no hope, but they are doing what they can do to offer more time and comfort. No one is going to attempt to actually biopsy, remove, radiate,or chemo, just continue on with medications until they no longer work. Again, all based on a CTscan read by a radiation Oncologist who did not do her job properly! Then put on the desk of a medical Oncologist who never once checked in with us, and has since retired. At this point, this means that from now on, no one will/ actually have a clue about the history of this file (besides the surgeon and his family Dr. who have absolutely no say with the Cancer clinic).We do indeed have someone professional on our side who is going to attempt to get us a second opinion, but with our medical system I imagine they will have a very difficult time doing this. 

So, we are going the route of non pharmacy. We have researched natural remedies that fight cancer cells, we have products that regenerate good cells , we have products that kill off parasites, cleanse the liver (seems to have helped with those spots) we have products that increase energy levels, what harm can this do? Yes, we totally understand that these may not cure cancer, but in some cases they have indeed done so, perhaps they will do the same with Chuck? When you have been placed in the position that medically you have been diagnosed as no longer offered a solution to your condition because you have reached a specific stage, you have to try that that science has not researched because Big Pharma doesn't make an enormous profit from what Mother Nature provides. 

For folks who end up in this nightmare I have pity, I understand this becomes your whole world (like us) your focus, your battle, like us, you walk in believing the specialists have your best interest in mind. Sadly it does not take very long to understand, you are simply a number, not worthy of a full read through your file, not given any more time or effort than a big stack of others in the same boat as yourself. Your voice is your only weapon, never stay quiet, always question, and never forget, you are NOT their family, you are NOT their loved one, you will possibly be momentarily missed on an appointment day, but you will quickly be replaced by another, that is the reality. They simply deal with you for a short period of time, and then they go onto the next. This is their job, they see you as a statistic, you get to a place that they decide you are no longer worth giving extra effort to, and you are on your own. It is a very tough lesson to learn, you can simply give up, or you can speak up. Science is ever changing, Cancer is a huge business, no matter how you look at it, yes it is a disease, but it is a disease that is making many extremely wealthy , cures for some cancers have indeed been found, but at the rate we are going, business will continue for decades into the future. When specific medications that cost very little suddenly become extremely difficult to access, one has to question facts. They are not dangerous medications, no where near as toxic as Chemo drugs(you would be blown away at the costs of some chemo medications) but governments have made them difficult to access, why? Again, we continue with the medically prescribed stuff, we took the pause from all the vitamins he was taking, as requested during radiation and chemo, because NO studies had been done in regards to effects of the vitamins during treatment. One wonders why this is so? All we were told was they were antioxidants and he had to stop taking them. So again, clearly he has reached the end of medically proven cures (apparently) so we are heading down another road with renewed faith and hope, something we have lost with the Cancer Care system!