Posts filed under ‘Congenital Heart Defect’

Happy 4th Birthday

cakeAnother year is here. You would be four years old. I can’t believe it’s been this long and yet it still only feels like yesterday. It has been building up for days now and my anxiety and sadness is at it’s peak. My journey in grief is still only in it’s early stages. But I know your day will be nice since we will be focusing on your day as a holiday from school to be filled with thoughts of you and celebration. We will be missing daddy though as he is off in Washington, DC, fighting for your cause. It will be the first that we are not together today and I hope it will be the only time. I was reluctant to let him go, but mostly due to selfish reasons. I did not want to have to wake up and face today with the other kids alone on my hardest day of the year. I know it will be hard on daddy too, since he is so far away and alone. We don’t have each other to lean on to make it through the day. Luckily daddy’s day will be filled with you and our battle to save lives. He is lucky. He gets to be on the frontline for you. I get jealous sometimes since I have to be in the background supporting him and taking care of our family. I wish I could be up there with him talking about wonderful you and helping to prevent more deaths. But I am slowly accepting the fact that my place is taking care of your siblings and encouraging daddy to fight the good fight. Without me backing him up, could he do this?

After four years, are we any further ahead? Some days I think not. Daniel wound up in the hospital again and the pediatrician offerred him medication to help stop his vomiting so he could rehydrate. She had no plans on giving him an IV. She decided on a drug. And even though we brought up drug risks, she went and got it anyway. She could have gone quickly to the computer and googled the drug to see that it is contraindicated in children under 3 and to not give it if the patient has electrolyte imbalance such as in dehydration. Or the other warnings Health Canada has put on it. Instead she came back and gave it to him. A few people have told us we had the right to refuse the drug. And yes we did. But how do you refuse a drug that she took out of it’s package as she came to our bed and then just shoved it in his mouth? Coming home and researching the drug, we would have definitely told her no. The study on it had shown that it is no better than placebo in children and in fact caused the vomiting children in the study to get diarreah. So I have to ask myself, how do these things get on the market? And then give it to my child under 2 with a heart defect? And the answer we get from the hospital? Those warnings have to be put there but don’t really need to be followed. All our work and this happens again? At least at the end, we were told that the hospital now monitors all newborn for their first 48 hours if they were exposed to antidepressants. That sounds like progress, only we didn’t see any proof. We’ve been jerked around so much, I am reluctant to believe them. And I question them if they even ask the women coming in if they are on them. I only pray that what they said is true and they are in fact doing this. Babies can be saved and maybe they’ll begin to notice how these exposed babies are reacting. That is a right step in the right direction. But I am still waiting for our case to be taken care of. I no longer want your death swept under the rug and pretend you never happened.

So again, I face your day with sadness. I will get through it. I will enjoy it. We have so much planned today that it should be quite happy. The kids have been so excited for today. They picked your cake and balloons and plan to spend the afternoon decorating the kitchen and your wish lanterns. It will be so nice to send those off this year and I’m optimistic since it’s much warmer compared to last year. Will you be watching? WIll you be waiting for your balloons and lanterns? I wish I could begin to imagine what you would look like now and sound like. I dream of that often. As you watch us celebrate from heaven, please say a little prayer for daddy so he doesn’t feel so alone and for your siblings so they always remember you. Happy BIrthday little man. Mommy loves you so much.

February 21, 2013 at 7:23 am 2 comments

Merry Christmas little guys.

boysAnother year without you. That makes it 4 now. It is still difficult. Knowing that you won’t be here in the frenzied morning ripping open your presents like the other kids. But you are far from forgotten. You two are stil included in our Christmas. You two have your stockings, but in a special place. We have ours and the childrens on our mantel, but you boys have yours held by an angel. As much as I wish they were hung with the others, I just can’t bring myself to have two empty stockings looking sad intermingled with the other full stockings. Your angel is dutifully keeping you two prominent and we look at her often as she stands guard with those socks. She even moves around the room, and occassionally dances around the room as Daniel likes to carry her around. I like to pretend he is playing with the two of you. I guess whatever I can make up to make myself feel better is never too bad a thing. So to my two angels, Matthew and Simon; Merry Christmas! We love you so much.

December 25, 2012 at 7:11 am Leave a comment

Happy 3rd Birthday Son

Happy Birthday Matthew. I can’t believe that it is almost 3 years to the minute since we said goodbye. We barely even got to say Hello. 3 years and it feels like just yesterday. 3 years and it feels like an eternity sometimes as well. Every year, every day is a stark reminder of what we will never get with you. This is your 3rd Birthday. What will your 13th or your 30th be like?

This is not natural son. Mommy and I are not supposed to be celebrating your birthday without you. 3 is that age where kids really start to understand the magic of a Birthday Party. I hope you can see it. We’ve got balloons, decorations, even a Dairy Queen Ice Cream Cake picked out just for you. You would love it so much. It’s a really special day this year. Your baby brother Daniel will get to destroy a piece of your Birthday cake.

We’re working on change son. Just this past week we met some of the great people that have helped us to get your story told. Each one of them is a hero of mine in their own right. Yes, because they are fighting to help us make sure this doesn’t happen to other families, but more so because they remember you by name and you are important to them as well. It is that remembrance that keeps you alive.

3 years and still nothing major has changed though son. Sure they’re talking about implementing change, but until that happens, other babies and their mommies are in danger just like you.

Not a day goes by that I don’t ache to hold you once more. That day will come again. But we still have lots of work to do here, okay. I will never stop loving you. I will never stop missing you.

All my love,

 

Daddy

February 21, 2012 at 7:37 am 1 comment

Changes, they are a comin’!

If only the title of this blog were a true indication of how I am feeling about the latest developments in Matthew’s case and with psychotropic medication prescribing in general.

Certainly we are making progress; if you can call a cautionary position statement being issued by the Canadian Pediatric Society, after having Health Canada warnings around for over half a decade progress. The position statement can be found here: http://www.cps.ca/english/statements/FN/fn11-02.htm

Experts in the fields of neo-natology and drug exposure during pregnancy have been advocating for over a decade that babies exposed to SSRI’s and SNRI’s must be monitored for adverse events at birth. Even the drug company shill Gideon Koren at the Motherisk Program in Toronto has gone on record as far back as 2008 saying that we should at least be monitoring babies exposed to antidepressant drugs. So, the position statement being issued by the Canadian Pediatric Society is best summed up in the words of our good friend and ally Barbara Mintzes from the Therapeutics Initiative at the University of British Columbia. She stated the following to me after reading it:

I just looked at the CPS position statement and agree that this is bad advice – essentially supports SSRI use in pregnancy. For paroxetine the only recommendation is lowering the dose or maybe switching antidepressants. All of the evidence on harm from SSRI use in pregnancy is treated with a heavy dose of doubt, concern about methods etc., but the benefits of antidepressants in pregnancy are taken at face value. I didn’t see any recommendation for first-line use of non-drug treatments in pregnancy, for example, and SSRIs are seen as necessary for ‘moderate to severe depression’ despite their poor record of effectiveness.  There are no direct recommendations to avoid antidepressant use if possible, to look at other options.

I and most others not on a drug company payroll would tend to concur, Barbara. What the CPS position statement fails to mention is that each of the authors of said statement either have pharmaceutical company conflicts or are heavily influenced by those that do. You can look it up for yourself.

As it has been quite some time since I last blogged, we have had some very exciting developments happen as of late. Recently we have had a wonderful woman come in to our lives, Dr. Gerarda Cronin. She is the new Medical Director for Perinatal and Child Health for the Interior Health Authority of BC. Apparently, her job was created in the wake of Matthew’s death, and we are extremely grateful for her. In her capacity as the Regional Medical Director, Dr. Cronin also has a considerable amount of influence with not only Provincial Health standards, but also those at a national level as well.

This past week, Dr. Cronin forwarded to me the following edict from Perinatal Services BC. I take great pride knowing that it has been our hard work and diligence and the media pressure that has been continually applied by our good friends locally as well as at a national level by the CBC, that indeed is causing the necessary governmental bodies to act.

As the advisory states, we have been asked to be part of the Provincial working group that it alludes to. I guess these people understand that we won’t be silenced and that we in fact have some important things to say.

I have come to a stark realization this past week, that we in fact are treading on uncharted ground. If I am not mistaken, no jurisdiction in North America, perhaps even the world, has taken steps to formally address the dangers that psychotropic drugs pose to developing and newborn babies. If we are remembered for nothing else, and if Matthew is remembered for nothing else, his life was lost so that countless others may be saved. Although the pain can be unbearable at times, we know our angel is cheering us on. We will not be silenced, we will not give up.

November 28, 2011 at 12:21 am Leave a comment

Sometimes Moving Forward, Means Letting Some Things Go.

Amery and I had a discussion last night that ended in silence on my part. Silence as I realized we have moved in different directions. Silence since no matter how we talk about it, or fight about it, we can’t do anything differently. The past is gone. We have only today. So I believe my thinking has to change to accomodate that. We were watching a video posted by a friend on BC Children’s hospital. In it they are talking about allowing BCCH to do organ transplants. The mother of a 10 year old girl who had a heart transplant as an infant, in Toronto, Ontario. It was the hospital she needed to be to have this transplant, and her family had to live in a hotel for 6 months. The news story interviewd Dr. Ghandi, the doctor who repaired Daniel’s heart. He has improved heart surgery dramatically since he arrived at BCCH and we were blessed to have him operate on Daniel. Daniel’s surgery and recovery time was quicker than it had been 6 months prior to his surgery, because of Dr. Ghandi. I applaud the efforts of this family and Dr. Ghandi to open up BCCH to allow organ transplants and pray they accomplish their goal.
How does organ transplants affect Amery and I? Daniel had a repair and did not require a transplant. It came down to the fact that any infant recieving a transplant is due to another infant dying. We had wished we could have donated Matthew’s organs as he was in perfect condition. To know another child got to go home to their family even though we lost our child. To give a family the chance we never had. But in BC any person under the age of 18 who dies, no matter what, must have a mandatory autopsy. At first this upset both of us. We wanted to save other children through our loss. We were quite angry as we know personally, people who could have benefitted from transplants had our province had the availability for surgery, and the organs. It seemed we lost our chance to see our son “live-on” in another child.
After watching this video last night, we started a discussion that had to be ended before it got heated. Although I am still hurt by not being able to share our child, I have taken a different outlook than Amery. I can’t dwell on the fact his organs couldn’t be used. That is the past and I have to move on to the now or I will go absolutely crazy. He is still quite angry about it and doesn’t see why I am no longer angry and actually glad we did have that automatic autopsy. Without Matthew’s automatic autopsy, his death would have been documented as “natural” and we would have had to accept that, since we would have never really known. We wouldn’t have recieved the pathology report that documented that he had Effexor in his system and that it was a contributing factor. Without that information, we would have been in limbo with his cause of death. Unanswered questions, which I find disturbing in a circumstance with a healthy child. Healthy babies don’t just die. Like with Jacob, we would have had to accept the so-called “answers” to why that happened to him. I would have never seen that Effexor was a culprit. I never would have researched. I would have never found other families that have lost their child because of antidepressants. We would have never learned of the dangers, side-effects, and FDA warnings that were issued. I would probably still be on my Effexor as I would have never had the reason to look at my medication. More importantly, as I was on for 8 years and getting worse on them. I could possibly be dead today.
So I’ve mourned the fact we lost our chance to save other children through organ donation. But I’ve learned so much more. Because of his autopsy, I weaned my medication. I’ve saved my own life. My future children’s lives. And any future child who’s mother has listened to what I’ve had to say and has either weaned or not started antidpressants during their child-bearing age, if ever now. And unlike organ donation, I will never know how many lives Matthew saves. But I take comfort in knowing he has the potential to save many more lives than had we used his organs. I only wish it had been possible to do both.
I understand that moving forward means letting things go. I will NOT let his death as deemed “natural” go as it would be an injustice to my son and any future exposed children. But I can let the organ donation go since there is nothing I can ever do to change that and I don’t want to spiral into that darkness of “if onlys”. And since I can’t change it, I must accept what has been given to me. And like the saying goes, God’s plan is always the best plan.

September 9, 2011 at 6:20 pm 1 comment

Under Pressure

The following is an email that I received the day before our story ran in the paper.

Good afternoon Mr. Schultz:

Thank you for taking the time to return my call this afternoon.

As I mentioned, your letter to the Honourable Christy Clark makes reference to your correspondence to Ms. Lapointe dated on or around May 20, 2011.  I was away from the office at this time and I would greatly appreciate it if you could e-mail me a copy of this correspondence.  I do apologize for any inconvenience this may cause you but I am very appreciative of your help.  I understand you are away at the moment and I look forward to receiving your e-mail at your earliest opportunity.

Kind regards,

Claire

 

Claire R. Leek | Executive Administrative Assistant to the Chief Coroner

Metrotower II, Suite 800 – 4720 Kingsway, Burnaby BC  V5H 4N2
Phone: (604) 660-8219 | Blackberry: (604) 992-9323 | FAX: (604) 660-7766

 http://www.pssg.gov.bc.ca/coroners

 

 What does this mean exactly? Did someone actually receive my letter or not? It’s interesting how the Coroner’s Secretary says,”I was away from the office at this time”. Sounds to me like a nice way to say we lost your letter and nobody is going to ever accept responsibility for it.

Then our story hit the paper and the TV and what do you know? I recieved the next email from the Coroner’s office.

Good afternoon Mr. Schultz:

 Please accept my apologies for the delay in replying to your e-mail dated August 2, 2011.  I have spoken with my colleague, Ms. Kellie Kilpatrick, Director of the Child Death Review Unit and sought the information you requested.  Kellie has asked me to share the following with you.

 The child death review methodology includes the following:

  • The case reviewer examines the Coroner’s file;
  • She determines if there is additional information that may inform the review – this may require seizing records and files held by other agencies;
  • In most cases, a letter is sent to parents advising of the review, explaining what it means, how their child’s information will be used, and inviting them to participate in sharing their perspective, experiences, concerns, and helping us understand who their child was in life;
  • All child deaths are then presented and reviewed by the CDRU multi-disciplinary team;
  • Protective factors, risk factors and other observations are considered and a determination is made re: preventability;
  • Recommendations are researched, considered and made to improve the health and well-being of children.

Matthew’s case was assigned to Paediatric Medical Case Reviewer Tansey Ramanzin and her initial review was completed on June 3.  Matthew’s case has been identified as one where a letter will be sent to you.  You will likely receive the letter next week.

Should you choose to meet with Tansey it is possible to meet in person (on the lower mainland), talk on the phone or correspond in writing – this will be dependent upon your wishes. Many of our courageous parents share what they have learned and their views on prevention with the hope that other families do not have to experience the unthinkable  – the loss of their child.  

Matthew’s death is scheduled for review by the multi-disciplinary team on September 20, 2011. The deliberations of the multi-disciplinary team are protected under the legislation but any action items or recommendations arising would be shared with you.

Kellie has also asked that I extend the deepest condolences of her Unit to you and Matthew’s family.

I hope you find this information useful Mr. Schultz. 

Yours truly,

Claire

 

Claire R. Leek | Executive Administrative Assistant to the Chief Coroner

Metrotower II, Suite 800 – 4720 Kingsway, Burnaby BC  V5H 4N2
Phone: (604) 660-8219 | Blackberry: (604) 992-9323 | FAX: (604) 660-7766

 http://www.pssg.gov.bc.ca/coroners

Amazing how people are moved to action when the media is breathing down their neck. Two dead babies whose parents are screaming for justice; Who gives a shit?  Media discussing how inept your Ministry is; We’ll move you to the front of the line Mr. and Mrs. Schultz.

The Child Death Review Unit is just not good enough though. I have little faith that they are anymore than a simple extension of the rest of the bumbling Coroner’s Service. We’re not even allowed to sit in on the deliberations. Why? Are you afraid that I may call you all fucking idiots?

So, Since the Chief Coroner’s Office lost my original request for a Jury Inquest, I obligingly sent a revamped, updated version of it to Chief Coroner Lapointe’s attention. Here it is in its entirety.

1959 Sage Place

Merritt, BC  V1K 1G2

 

 August 5th, 2011                                        

 

 

Lisa Lapointe, Chief Coroner

Metrotower II Suite 800 – 4720 Kingsway

Burnaby, B.C. V5H 4N2

Dear Lisa;                                

On February 21, 2009, our son Matthew was born and died at Royal Inland Hospital in Kamloops, BC. At the time, we were left in utter shock as to what had transpired, and today we are still as shocked by how ineffectual and apathetic the BC Coroner’s Service has been with handling our case.

Beginning on the morning of Matthew’s death we have encountered ignorance, unprofessionalism, complacency and at times, utter incompetence in dealing with various members of the Coroner’s Service. Although I understand a good, thorough investigation can take time, I find it absolutely inexcusable that the investigation of Matthew’s death took 2 years to the day for Dr. Robert Saunders to issue his “Final Report”. Yes, we were issued the final report on his 2nd birthday/anniversary of his death. The irony was not lost on us.

The findings of this “exhaustive” investigation were lackluster at best. Although much information was shared with the various investigators involved with our case, each and every concern that was brought up was categorically discounted. Coroner Saunders relied heavily, almost exclusively on the medical opinion of Dr. Tim Oberlander, Professor of Developmental Pediatrics at UBC. Dr. Oberlander’s report is full of factual inaccuracies and even outright fallacy. One of the very bold statements that he made when reporting to Coroner Saunders was, “To date there have been no reported cases of SIDS following prenatal SRI exposure.” This statement in and of itself indicates to me that there was never any investigation done. Dr. Oberlander is a Clinical Researcher by profession, and yet I, as a layperson without any university education whatsoever, was able to find at least 3 cases on the Health Canada MedEffect Database, and no less than 8 cases on the US FDA equivalent, in about 20 minutes using my home computer.

Tim Oberlander seemed to be very understanding at the outset of our journey, even stating that he would be making recommendations about newborn monitoring after exposure to these drugs. By the end of the investigation he was singing a very different tune. I would be remiss if I didn’t mention that the very agencies that Dr. Oberlander works at, the Child and Family Research Institute at BC Children’s Hospital as well as UBC, receive heavy funding from Pfizer, the manufacturers of the drug Effexor which he was investigating. In fact, in December 2009, Pfizer made an extremely generous funding announcement of $9 Million to these agencies. I would never be able to prove it, but that certainly would be enough money to compel him to silence. Regardless, it represents a huge conflict of interest.

It was this discounting of evidence, incompetence of investigation and failure to make any recommendations that spurned me to request a formal inquest into Matthew’s death. This was done in the form of a letter sent to your office on or about May 20, 2011.

There were numerous aggravating factors that contributed to Matthew’s death. Any one of these factors by themselves should warrant a recommendation from a body whose mandate is to make “recommendations to improve public safety and prevent death in similar circumstances.” (emphasis added)

Officially, Coroner Saunders would like Matthew’s death to forever be enshrined in history as “consistent with a finding of SIDS” and “Natural”. However, there are a multitude of issues that render those findings obsolete. Some of those being:

–         Matthew’s exposure to the antidepressant Effexor which has a well known risk of adverse reactions in the neonatal period.

–         The narcotic Fentanyl was administered to my wife within 45 minutes of  delivery.

–         Failure to have a clear, well established protocol for administration of Fentanyl in Labour and Delivery unlike other jurisdictions in Canada, such as that from Nova Scotia found here: http://rcp.nshealth.ca/sites/default/files/clinical-practice-guidelines/fentanyl.pdf

This protocol states in unequivocal terms the following:

Neonates who DO NOT require naloxone at birth, but whose mothers receive

Fentanyl within four hours of delivery, must be observed for at least TWO hours post delivery in labour and delivery. (emphasis is from original protocol)

–         Failure to have a clear, well established protocol for monitoring of newborns exposed to psychotropic medications, like those set out in the Journal of Obstetrics and Gynecology Canada in April 2009 and other publications.

–          Both Effexor and Fentanyl use the same CYP450 enzyme pathways to metabolize and would definitely interact with each other, as well as previous codeine exposure. Although genetic testing for polymorphisms of these enzymes in both Matthew and my wife Christiane were recommended very early on, they were never completed and I demand that they do be completed.

–         Toxicology results were requested by myself, especially for Fenatnyl and those have never been forwarded to me, although I received the assertion they would be. If I am not mistaken a urine sample should have also been collected from Matthew and frozen. I would also like to have a complete toxicology done on this sample including for Fentanyl.

–         Histological findings on Matthew’s autopsy were consistent with a diagnosis of Pulmonary Hypertension. Gail Holotuk argued with me that that was not the case. In the pathology report, Matthew’s lungs had “marked capillary congestion”. This is consistent with a diagnosis of Pulmonary Hypertension and I have the literature to prove it.

–         Misdiagnosis and discounting of obvious respiratory distress.

–         Matthew’s brain cell growth anomaly that is a confirmation of previous findings in rat models exposed to these drugs.

–         Understaffing on the maternity ward.

–         Repeated failure of hospital staff to listen to patient concerns.

–         Similar neonatal issues with 3 of our previous children exposed to the medication Effexor. Our 7 year old have been born 5 pounds at full term and suffering from Persistent Pulmonary Hypertension himself. To this day he still has autonomic regulatory issues.

–         Health Canada warnings issued in 2004 and 2006 regarding the potential for adverse reactions in newborns from all SSRI/SNRI medications that never made it to doctor’s hands. Effexor was not even listed as a risk factor in Matthew’s birth record, although it had been for some of our previous children.

As I stated already, any single one of these issues could have and should have resulted in the Coroner issuing a recommendation to prevent a tragedy like this from happening to another family. The pathologist who performed Matthew’s autopsy at BC Children’s Hospital, Dr. Angelica Oviedo, rendered the opinion that Effexor was likely the cause of Matthew’s death. In fact she felt so strongly about this that she made a report to Health Canada’s Canada Vigilance Adverse Reaction Online Database. In comments made to me in July 2010, shortly before the addendum was issued to Matthew’s autopsy, she told me, “His lungs didn’t make the switch.” Meaning that he was still suffering from what she referred to as “Persistent Fetal Circulation” or as is commonly referred Persistent Pulmonary Hypertension.

Yet, Coroner Saunders has chosen to do nothing. And the result of this has been another baby dying under very similar circumstances, the mother having dealt with the same hospital, same doctors, and same medication even. Alas, these are not isolated incidents; but for now I do not need to speak of the other cases I know of.

Greyson Rawkins, whose mother Nicole Rawkins also took this drug in a much higher dose throughout nursing and pregnancy, was born in January 2011 at Royal Inland Hospital in Kamloops, BC as well. Your office is also investigating his death. At present his brain is also being examined for anomalies, and I am quite optimistic that a similar anomaly will be found with his brain. Something I have found very interesting, is the fact that in Greyson’s case his cause of death was deemed UNDETERMINED although there is compelling published evidence that even exposure to Effexor via breastmilk is highly toxic to a baby and can cause serious respiratory distress. Yet in Matthew’s case, his death was deemed NATURAL. Is it really the position of the BC Coroner’s Service that it is perfectly natural for a 2 hour old baby to die in a hospital setting? Especially after the family fought with hospital staff over his color and breathing difficulty, only to be downplayed and at one point kicked back in our room because we were “disturbing other patients”. Especially after being exposed to not one, but two medications that have the very common side effect of causing respiratory distress in newborns.

Successive coroners failed to listen to us. Matthew was in distress immediately at birth, and he was until he died. We fought with Dr. Poelzer and the nursing staff over this. Yet this fact was continually ignored by Coroners Holotuk and Saunders even in to the final Coroner’s Report.  We have pictures that show his cyanosis and how briefly after he received 100% oxygen his color pinked up a little, yet we were continually told that he had facial bruising and that his symptoms were normal. I guess death is normal as well. No one from the Coroner’s Service has ever looked at these pictures.

In April 2009 when speaking with Gail Holotuk via telephone, I had a heated exchange with her over the fact that we argued with hospital staff over Matthew’s breathing. This telephone conversation culminated in her saying to me, and I quote, “Why didn’t you say something about his breathing?” I was floored. Not only had I told her on numerous occasions that we were complaining about Matthew’s breathing, the tone of her voice was shifting blame to me. I called her a stupid bitch and hung up the phone. Dr. Oviedo the pathologist gave heed to these concerns somewhat and issued the autopsy addendum in July 2010. But it still seems that respiratory distress was not an objective finding of any coroner investigating Matthew’s death.

Effexor or venlafaxine as it is generically called is a drug known as an SNRI (serotonin and norepinepherine reuptake inhibitor) which falls into the class of drug known popularly as antidepressants. Chemically, these drugs are not dissimilar from amphetamines or cocaine. Although the prescribing of antidepressant medications during pregnancy is not an indicated use, pregnant women are increasingly marketed to, and estimates put the number of women taking these drugs during pregnancy around 15-20%.

There is compelling evidence available that these drugs should not be prescribed to pregnant women. The strongest example of this was compiled in a study published January 2010, entitled “Are antidepressants safe in pregnancy? A focus on SSRIs”.  This study was compiled by the Therapeutics Initiative at the University of British Columbia and states clearly when specifically discussing the prescribing of antidepressants in pregnancy, the harms exceed the benefits in this setting”.  Again, it would seem the BC Coroner’s Service chooses to ignore information like this.

 

There are several things that I am seeking from you in your capacity of Chief Coroner. Firstly, based on the shortcomings, errors and even apparent conflict of interest on the part of the main expert consulted, I am seeking to have this case reopened and that a formal inquest be held. There is overwhelming evidence that Matthew’s death should be listed as ACCIDENTAL, and I am seeking that this be changed from the present finding of NATURAL.

Secondly, the genetic testing previously mentioned that has never been carried out. I request a full screen of all CYP450 enzymes on Matthew’s blood as well as my wife Christiane. This must be done, and I am well within my rights demanding it, as it was something we were told was going to be done. This is vital to the health of any of our children as well as pinpointing the causes of Matthew’s death.

At this time, as I have a need to consult with experts outside the sphere of influence of the BC Coroner’s Service, I would also request copies of any and all files related to the investigation of Matthew’s death. This would include test results, interviews, investigative notes, pictures (as graphic as they might be) etc. as well as an inventory of any biological samples of Matthew’s that might still be in the possession of the BC Coroner’s Service or any other agency .

I look forward to your response.

Sincerely and respectfully.

 

 Amery Schultz

1959 Sage Place

Merritt, BC V1K 1G2

250-315-5632  email: amery_s@telus.net

So,  after sending this email, I again receive an email from the Chief Coroner’s Secretary.

Good afternoon Mr. Schultz:

Thank you for your e-mail and attached letter to Chief Coroner Lapointe.  Chief Coroner Lapointe will respond to you in full in due course.

Yours truly,

Claire

 

Claire R. Leek | Executive Administrative Assistant to the Chief Coroner

Metrotower II, Suite 800 – 4720 Kingsway, Burnaby BC  V5H 4N2
Phone: (604) 660-8219 | Blackberry: (604) 992-9323 | FAX: (604) 660-7766

http://www.pssg.gov.bc.ca/coroners

 

She’s going to “respond to me in full in due course.”

WHAT THE HELL DOES THAT MEAN?!?!?!

Tomorrow? Next week? Next month? When she’s met with the Coroner’s who botched Matthew’s case and can formulate a good enough bullshit excuse as to why they don’t need to reopen the investigation?

The evidence seems pretty strong to me that Effexor by itself or in combination with Fentanyl caused Matthew’s oh so evident Respiratory Distress, that nobody seems to have a recollection of other than us, his parents.

Matthew’s death was not natural. Plain and simple. Any one of the points that I list in my most recent letter to the Chief Coroner confirms that statement.

 

August 9, 2011 at 9:11 am Leave a comment

Open Letter to Christy Clark, Premier of British Columbia

The attached is a letter that I am sending to Christy Clark, as well as various politicians and dignitaries who may have an interest in our case. I am alsio forwarding copies of this letter to various media outlets in hopes that they may also pressure some of these people for answers.

July 23, 2011 at 12:14 am 1 comment

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  • is scared to bond with this baby, just in case. 7 years ago
  • Happy 6 months today baby. I love you Matthew. 7 years ago
  • Living with loss, sucks. 7 years ago
  • Thinking I need to discuss plans for this baby soon or I will be having it in my doctors office. Where do I deliver? 7 years ago
Lilypie - Personal pictureLilypie Angel and Memorial tickers
July 2017
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