CanPKU, News

PKU Advocacy Training Seminar

For the past 2 days I have had the honour of attending an invite only, CanPKU advocacy seminar.

I am so very fortune for this opportunity and I have learnt so much. The seminar has been so informative and I have really learnt a lot. I really feel like I have taken away new knowledge and tools I can use to apply in our mission. We are so lucky to have had these professional consultants and experts to dedicate their time to us and to train us in media and government relations.

I have walked away from the seminar today feeling inspired and empowered.  For the first time in a very long time I am hopeful and excited for PKU. With the changes in the government and with our new health minister Terry Lake and deputy minister Steve Brown. I have hope and I am excited to work with this advocacy team. I really believe and feel this is the start to the end and we WILL make this happen.

I am currently in the truck right now on our way home to Kamloops , reflecting on the past few days and all that I have learnt. Taking it in an absorbing it. I had planned to take time, to plan out my blog post and then publish it when I got home. However, I have so much information swirling around in my brain that I cannot relax or focus on anything else. So I have pulled out my lap top, pillows and blanket and set up myself off line to write this down.

We had 3 Professional consulting teams at the event

Cohn and Wolf- Who work with media relations. We had work shops and roll playing on how to prepare for interviews, what to expect, What type of questions we may be asked and how to answer.  They taught us how to focus on 3 key messages and how best to get them across to the interviewer. Also what to say and what not to say.

Global Public affairs – They educated us on the Government, how it works,  what the rolls of the ministers are and the differences between politicians and beurocratics. They taught us about government relations and how to advocate in government efficiently.

Also we had the pleasure and expertise of Ryan from Advocacy solutions –  Who  educated us on being strong and efficient advocates, How to get our message out and how to speak or talk , to articulate and what language to use. Ryan worked with us on our personal stories and developing our messages.  Ryan even gave us homework!

Then of course we had Nicole Pallone, Vice president of CanPKU and John Adams President of CanPKU and our advocates. Including myself,  there was 3 PKU patients  ( 2 adults and 1 teenager) , Nicoles mother in law, 2 fathers, and 3 mothers

Our team has really grown since we started advocating 3 years ago.  Over the weekend we discussed our campaign in depth, what we are really asking for, the brain protection strategy plan in depth.  We exchanged information, experiences and debated issues, and topics on how to be best consistent and united in our cause.

I  learnt a lot of new information in the past few days that its a little overwhelming. I learnt new   facts regarding  treatments and new developments in PKU , as well as more details about our campaign.

This was our first sit down as a team and first face to face. We have had plenty of conference calls but all sitting down together like this around the conference table was amazing and valuable experience.

Since beginning this journey CanPKU has met with our government over 40 times. Only to have been told NO, to be ignored and to be disappointed.

BC really is the worst place to have PKU and our mission is to bring BC from worst to first!  Recently Ontario has approved KUVAN and is funding it,  they even have un restricted access to the medically necessary low protein  foods. It is not capped off or dependant on income.  It is unrestricted!!!

Saskatchewan is also close to signing a deal to approve KUVAN .  Joining many other countries around the world such as : France , Italy, Greece, and the Netherlands.  Just to name a few.

BC was offered the same price for these treatments at the “table” with Ontario and Saskatchewan,  and is the only province to walk away with a definite NO! Even with the same evidence, facts and education as the other provinces. Ontario and Saskatchewan had the same information and they made the completely different and right decision. It irks me that BC cannot do the same!

When Nicole and John have gone to parliament in Victoria to meet with legislation and discuss coverage of our medical foods and KUVAN they have been dismissed many times from MLAs and ministers who say that is not their legislation. Well in fact, we learnt that there is no one in the BC government who has legislation regarding medical foods.

The government has even gone as far to release statements in the media with wrong information and facts regarding KUVAN the cost and efficiency in the media. Stating is not government responsibility to cover food and that KUVAN is not proven to be efficient and too costly. KUVAN has been proven to be efficient in managing PKU, not only has it been approved by Health Canada but it is also being used and prescribed by doctors. In fact Doctors have spoken up in favour of KUVAN.

When it comes to our medical foods, the BC government has many different positions but they do not understand the fundamental differences between these medically necessary foods and “ foods” they hear the word food and automatically say no!

The Difference is these medically necessary foods are not regulated by the Canadian food inspection agency, who governs the foods you see in the grocery store. Our medical foods are regulated by Health Canada and are kept out of grocery stores because they are potentially dangerous to “normal” people.  We cannot just go out and buy these foods. They have to be ordered and imported into our distribution centers and then shipped to us.

What the government has not grasped is that regular food, and PHE is a neuro toxin to us. IT is poison!

This is the sole reasoning for our campaign and our efforts from getting BC from worst to first in PKU care. It is also the reasoning for our seminar.

Our Seminar began yesterday afternoon, with going around the table and sharing our advocacy efforts with the team, what we have accomplished, where stand currently and how we feel about our progress.  Many of us worked hard during the election to engage our MLAs and the media. We fought hard to build these relationships and essentially get on the MLA’s radar.

As I stated in an earlier blog post I was finally able to connect with Terry Lake . I had a wonderful meeting with him and now he is our Health minister!

Many of our other advocates have established relations with their MLAS and many of them have now become cabinet ministers. I believe this will certainly have a positive effect on our efforts in the coming months as we reconnect with them and as they come into their new rolls in parliament.

I found it very helpful to review the government and learn about the rolls. I am and have never been understanding of how the government works and how they do the things that they do.

I learnt about the political parties , the politicians and then the beaurocrats.

The political make up the Ministers. They are governed by the Crown. They are made up of political staffers and are elected.  Their sole purpose is to serve the government. They have transitory positions. So example, Terry Lake use to be the environmental Minister. He is now the Health Minister.  He was appointed by Premier Christy Clark.

The Beurocratics are the deputy’s, they are not elected.  They are appointed by the ministries and the government. Beaurocrats are a hireococy and their careers are as civil servants whose sole purpose is to serve the people or the public.

The Beuoroctaric positions are permit and are not transitory. They are not motivated by government but the minster will try to impose his views.

When Ministers are appointed to a new department, they usually no nothing about that sector and this is by design. The Beuocrats educate and brief them on the sector. Then the Ministers filter the information and use it to make decisions.

I find this all very interesting and fascinating.  I still have much to learn and rap my head around this but it’s a very exciting time , having a new health minister and a new deputy health minister since our last one was very direct  and non-supportive of our mission.

It is as if the stars are aligning and things are coming together. It’s a very exciting and hopeful time in the community.

This is the time to make change.  A mandate is the time in which a party is in power.  We just had our election in May and now when the parliament comes into session, we may have a short spring election if the bi election for Christy Clark in westside Kelowna wraps up in time, otherwise we will defiantly have a fall session.  Once the session begins the first and second year of the mandate is very important and where the changes will be made.  This is the time where the government is the most powerful.

After the first and second year, the power tends to wane down and the power shifts more to the beurocrats.  The ministers are beginning to focus on the next election and not wanting to “rock the boat “ as it were.

It was very interesting and mostly new information to me.  Understanding the process will really help me utilize my knowledge and my skill set to be more efficient in communicating and advocating for PKU.  But with knowledge comes responsibility .

So to understand this responsibility, we also learnt about the “curse of knowledge” and how that can affect our message.  The Curse of Knowledge I am defiantly at fault for. It can be broken down into 2 parts.

1 : the reflex need to explain the whole issue. I do this a lot.  I feel so passionately and that the whole issue is important and want to give as much information as I can, I want to educate and its hard for me to think that if someone has all the information then why would they not want to help us? But sometimes by giving to much information and spending to much time on the whole issue can take away from your message and you can lose the attention or focus of whom you are speaking too.

Secondly, the curse of knowledge can be when one does recognize if the person you are advocating for  knows anything about the subject you are talking about.  Example using a lot of wording  such as  “scientific or “nursing” language in your message.  We learnt how to focus our message, make it personal, use emotion and keep it short.

Ryan spent time educating to us  what true advocating is and how to be efficient.

Simply put, Advocacy means, “ Telling your story to someone through various means in the express interest of telling them to do or not do something”

Advocacy is a process and it takes time.  When advocating to be efficient and to get your message across you need to ground it into something tangible , make it personal and use emotion.

To focus on our One ask! Not a list of what we want.  That less is more.

Our homework last night was to write our personal story. To use emotion and to have 3 key messages. What is the problem? What is the impact of the problem and what the consequences are if not solved vs. solved.

To summarize what has happened to us and how it relates to the issue.  Our perspective based on our experience and how the government’s inaction or policy has impacted your life.  Your personal story must include your name, age, occupation, where you are from, challenges faces, why you believe they should help and how you personally feel.

The challenge with this homework was to keep this hole personal story under 1 minute!!  Well!! I have so much trouble with that. There is soooo much I want to say and to get across.

I changed my story so much last night and went over it and over it.  I am still not satisfied with it but I have decided to share my version with you.

This is my personal story I wrote for the seminar:

“Hi, My name is Amanda. I live in Kamloops BC. I am turning 27 in a few weeks. I work  as a pratical nurse. I have classical PKU. As an adult and a women with PKU I face many challenges, but to me personally my biggest challenge is maternal PKU. MPKU means that whatever the blood phe levels in my body are , they are double in my uterus and are potentially toxic in my uterus. Which can cause dangerous side effects to my future child. Such as deformities, and mental retardation.

The only way for me to have a successful and healthy pregnancy is to have an even more restricted diet , and even lower phe levels. Currently I am unable to do this because of the limited acess I have to the necessary medical treatments. There is nothing I want more in this world than to me a mother . The idea that they may never happen for me is both devastating and terrifying.

I believe the BC Government needs to commit to improving the care of PKU by investing 2.8 million dollars , a 0.016 % of the health care budget to bring BC up to the rest of Canada’s standards. We need this commitment because, Our brains, our bodies and our dreams are worth protecting. “

I presented this in just a few seconds over 60 seconds. That’s pretty good for me. I have real difficulty condensing my message and what I want to get across.

After this seminar I feel more confident on articulating my story and being efficient at communicating key messages.

The work shops and the roll playing really helped me . I have taken a lot away from this event and so far all I have told you about is only from our first day!

The organizers of this seminar really need to be recognized for their incredible job putting this together for us. Not only for our time but for the efficiency and time utilized, the information and the education but also the services. You see the event was catered. We were in a meeting room at the Raddison hotel and we had so much ground to cover, it was broken down into 2 days.

I actually had worked over night Saturday night and left for Vancouver as soon as I got home from work. We arrived in Vancouver at 1 and the seminar started at 2 pm and went till 9 pm last night. We didn’t have to go anywhere,  it was very convenient having the meeting room at the hotel but as well our meals where catered to us in the seminar , including PKU meals. I had so many new foods this weekend! I made sure to try everything to see if I liked it and if it would be something I may try to incorporate in my life. I was so amazed and impressed with the effort.  Last night for dinner I had pizza by cambrooke, and then the day today started off at 830 with breakfast and diving right into the discussion and presenting our home work. I was so surpassed when I took my seat and the waitress brought my my PKU labeled meal. When I removed the cover I was so taken back to see LOW PROTEIN EGGS!!  2 cambrugers, a onion bagel,  some fried potatoes and fruit! I have never in my life had EGGS! Even low protein eggs! This was a total first for me, They tasted kind of like thin pancakes or crepes. They where very good and I will defiantly try them together . I think when I order them I will add veggies and try to make my first ever omelette.

Then as a mid-morning snack I had pitas with salsa. I loved them!  Lunch was a boxed lunch so you had the option to take it with you if you had to leave. My lunch was a low protein sandwich made with cambrooke home-style bread, 2 butterscotch cookies, a cup of salad and apple juice. I have never had a lunch like this. Or found a bread I can eat un toasted that didn’t taste awful or crumble and hard as rock. I was very impressed. It was a great lunc and very filling. Something I could defiantly see myself taking to work with me on a night shift.

I have posted photos of my special meals from today on my facebook fan page.

Today’s second half of the seminar focused on media, our petition , interviews and discussion around our brain protection strategy plan we submitted to the government  before they dissolved . We discussed more in depth and touched on our key messages, our ask and our strategy for our campaign.

upon leaving today and walking away I have had time to absorb the information from the past few days and I know for me personally this was probably the most valuable session I have and I am so grateful for the support of the experts .

I appreciate them putting this together and am very impressed with how efficient and well done it was.

I really do feel excited. Like I said when I started this blog post, I feel very empowered and supported by the consultants and by CanPKU. I am confident we are a strong force and will not be taking NO as an answer. We will Bring BC from worst to first in PKU care.

But we cannot do it alone; we need and always welcome more advocates.  If I have learnt anything at all it is that you can really make a difference. No voice is to small. I never thought I could make change or have any effect on anyone. I didn’t think anyone would listen to what I had to say. I do feel like what I say and the things that I do like my blog and my fan page are important but I just didn’t grasp that someone else would listen to it or take away from it. I have learnt with working as an advocate for PKU how valuable my voice is and how valuable all voices are.  So do not think that you wont make a difference. Be the change you want to be and stand up! Alone we are rare, together we strong.  PKU Strong!

If anyone takes away from this post and is inspired or would like to learn more about advocating or wants to get involved in our campaign please do not hesitate and please contact me. I will support you and help any way that I can. Even if it means just putting you in touch with others who can help you get started.

The more voices they stand with us the better.

I really hope you will consider getting involved, but if you do not want to take such an active roll as I have , there are other ways you can help. Like signing our petition or using the email tools on the CanPKU website to send a letter to the premier and the health minister about PKU.  You can also support us by making a donation online to canPKU , Buying merchandise from the site or by attending an event!

Be sure to stay tuned in to my blog for more updates and our progress over the next few months !

Thank you to anyone who has read this post in its entirely. I know its probably one of my longest posts as it has taken me almost the whole drive home to write. Also now approaching 3400 words!!

So, until next time,

Amanda!

 

News

The votes are in.

Yesterday was our provincial election. The Liberals one with a majority.

For my region, My Local MLA Terry Lake was re-elected. I look forward to working with him to further improve the quality of life for PKU patients in BC.  I am hoping to meet with Terry Lake in the next 3 months to follow up and discuss our advocacy efforts in CanPKU and the community.

I am hoping Terry Lake will be able to make it out to the “Kamloops Walk for PKU” so I need your help! I want to show Terry Lake the support the community has for PKU and I want him to meet many families and patients. so please help me spread the word and invitations to the walk a thon , please tell all your  friends and family and lets have a strong turn out!

Don’t forget we are taking donations for CanPKU any amount counts! Including our “Pennies for PKU” penny drive.  when you register on the  CanPKU website for the walk you will receive a ledge form to collect donations and sponsors.  Sure hope to see you there!

 

 

News

Today is your day to vote!

BC Residents today is the 2013 provincial election and polls have not closed. I hope you all exersized your right to vote . The right our ancestors fought and died for, and for all the women who gave spent their lives working towards us having the right now to vote.  as well as for all the countries who do not have the same right as us. We need to protect our right and use it. We only have to do it every 4 years and even though you can never be sure what politicians tell you,  Please be sure to vote. Dont not vote because you dont like the leaders, vote for the MLAs in your community who you believe would most benift you and your life and your community.  vote for who can do the most good and be your voice and your advocate. For those who support your beliefs and your values.  Who will help your career and your future and for your familys future.

 

Be educated, be informed and read the platforms. But most of all please please vote! its our privilage and if we dont use it we could loose it!

 

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News

My Telephone Call with NDP Candidate Kathy Kendall.

I am happy to say I have finally connect with our local NDP Candidate Kathy Kendall to discuss the up and coming election and PKU. I would first off like to thank both Terry Lake and Kathy Kendall for taking time away from there campaigning and busy schedules to listen to my message and my concerns. I also want to thank party leader Adrian Dix for responding to my emails. I am very grateful for the support I have seen from both parties. Of course now I am faced with making my final decision for the vote on Tuesday. 

However let me for now put that aside and tell you about my call with Kathy. 

Kathy and I connected by email on friday, however I was sleeping from night shift and missed her email. I responded to her email in the early hours of saturday morning . Kathys team had looked up my home adress and she had planned to stop by but was unable to find a listed phone number for me. I do not have a house line so I only have a cell phone and of course those are not listed. Due to the shorten time frame and the election just around the corner we set up a meeting to speak on the phone. 

Kathy called me at home tonight at 8:30 and introduced her self to me. We spoke again mostly on PKU. I explained my concerns with how our last year of campaigning had been met in the liberal goverment and how BC is the worse place to have PKU do to their lack of support and treatment coverage. Kathy listened intently and asked how BC was behind the rest of Canada . We talked about the Comprehensive brain stradagey plan by CanPKU and what our requests where. She requested a copy of the plan after the election. We also talked about my desire to be a mother and our personal reasons for holding off. How we where scared and waiting for better aces to treatments and more support for adults. I talked about my past experiences and how my diet and my levels are directly linked to my income as a causal nurse. I felt as a women Kathy could relate to my desire to be a mom, and kathy  has a back ground as a legal aide lawyer and has made it a point to support lower income families and advocates for more supports for services to the lower class. Such as access to food. I felt that my message was herd by Kathy and was happy to hear that if she was elected she would continue to work with me and meet with me be an advocate for me and for PKU. I invited her to the Kamloops walk for PKU and told her about a few more families in her riding about PKU and some if the issues they face. both as adults, families and children. 

After discussing PKU we briefly talked about LPN’s, the future of health care and why the NDP voted against bill 18.  

Our call was cut short and it was getting late but Kathy invited me to continue to email her if I had anything else to discuss or had any more questions.  

So now we wait, after the votes or casted and the final tallies are in, I will be watching intensely and plan on following up as soon as possible with my elected MLA. 

 

I wish all parties the best of luck and look forward to working with either Terry Lake or Kathy Kendall. 

 

To everyone else, please go out and vote!! please please please. It is our democratic right and we need to exersize that right so that one day it is not taken away from us! 

 

 

 

 

News

2013 Provincial Election and PKU

As I said in my previous post, this election I am taking a more involved approach to voting.  For the first time I am focusing my energy on making the best informed decision and have been continuing my hunt for information and support for PKU.

you all know by now , that I emailed all the candidate in my riding as well as the party leaders regarding my concerns and questions regarding their platforms, as well as if they will support PKU and our campaign for coverage and support.   I had quiet the success with my meeting with Liberal MLA Terry Lake , that I reported on in my last post. However it has not carried over to the other parties.  However I have replied a reply from the NDP and from the Conservatives.   Though I cant say I am interly impressed.

The Conservatives only referred me to there website to review their platform. They did not take the personal time to reply to my questions or explain anything.

I was however surprised to reply a personal email from NDP Party Leader Adrain Dix.

Here is what Mr. Dix had to say,

” Thank you for sharing your experiences as a Phenylketonuria patient, and of the work you have been doing as an advocate in the community with CanPKU. I am sorry to hear that you have yet to receive a reply to A Comprehensive Brain Protection Strategy for People with PKU. We endeavour to respond to all correspondence in a timely fashion. However, depending on the nature of the submission, a reply might require extra time to prepare.

The BC NDP has not considered the issue of extending access to treatment and improving supports for PKU patients. However, our elected MLAs would be glad to meet with you after the election to discuss this issue.” 

 

Where as I am not as impressed as I was with Terry Lake, I am happy to have a reply from Adrian Dix. Its not as personal or as a face to face, I appreciated that he took the time from his campaign to actually reply to me. It is not the answer I wanted to here but I can work with it.  I did also email my NDP MLA Kathy Kendell but have not heard back from her. If elected I will continue to reach out to her and get a face to face meeting.

 

I have not received a reply from the Green Party or their leader Jane Sterk. We do not have a candidate in kamloops. I also emailed Premier Christy Clark.  Myself or CanPKU has not received any feed back or contact from her despite our best efforts.

 

I have voted NDP every year since I began voting, I never thought I would ever vote Liberal. However Cole had a good point, you dont vote for the leader, you vote for  the person in your area will help and benefit your life.  For that reason I will be voting for Mr. Terry Lake for the 2013 Provincial Election.  If the NDP wins the election I will continue my efforts to reach out to them and engage them in PKU.

 

 

 

News

My Meeting with local MLA Terry Lake.

If you are from British Columbia, you know we have a provincial election on May 14 th 2013. In 2 weeks. If you are like me, you really honestly don’t know who to vote for. Honestly until this Year I have never really focused on it to much or paid a lot of attention to politicians They always just seem to dance around issues, creating more confusion then help. So this year I set out on my own agenda to learn as much as I could to help me make my own personal, and informed decision  Based on factors that concerned me and would help me decide how to vote. Obviously one of those key factors was and is PKU. I want an MLA who will support me and help strength the voice of others like me. So on Tuesday morning I spent my day off researching campaign parties, and their platforms. As well as writing a list of questions I would ask if give the opportunity. I also emailed each party leader and each party candidate. My first reply came from the conservatives  it was no help at all and a generic response directing me to their website and “article 5 ” of there health care platform. This was not the answer I was looking for. i wanted to see if I got any personal responses. Who felt I was important enough to respond to and connect with.  To my surprise I got a personal email from our local kamloops MLA Terry Lake. I was sceptical as I had tried to engage him in the past with information on PKU and felt brushed off and un supported. However Mr. Lake extended an invitation to meet with me and discuss my concerns and questions . I did not know what to expect, if he would be fake? if he would lie to me and make me promises? if he would seem uninterested or supportive? needless to say I was anxious. I did not know what to expect. I set a meeting to meet with him today and began to prepare myself for a strong and factual exchange while taking the opportunity to educate Mr. Lake on PKU and share some of my life with him. I took a big bag of materials with me that included receipts of my medical foods, a blood dot card and sample, my food list book, my food tracking note book, samples of my food and formula, the CanPKU Comprehensive brain protection strategy plan , my petition and anything I could find to make this very real for him.

I met with Mr. Lake at 12:40 pm today and he was gracious enough to extend me an hour of his time. I found him to be responsive, interested  educated aware and supportive. Not what I was expecting , however I am very please. We had a lengthy conversation  I was able to get my voice herd from an adults perspective.  We talked about MPKU and my desire to have my own biological child , the side effects I have suffered, the experiences I have endured, my many hospital admissions, my struggles in school and holding a job, supporting myself and finical burden on my spouse and I .

Mr. Lake asked me a lot of questions and took a lot of notes. He did not see fake , he did not offer promises such as ” if im elected” he did not seem just out to get my vote. He was interested and concerned.  He was also realistic and understood the barricade of politics and funding, money and big drug companies. He kept all the materials I gave him. We of course discussed KUVAN and peg pal ,  the beneifts, the cost and how many patients in BC it would benfit. He did not close down that discussion and understood the benefits. We of course spent alot of time talking about the physiological side of PKU which was a point I really wanted to get across. It is not just all about treatment, we need supports. We talked in length about that and talked about some key points from the CanPKU brain protection strategy plan.  I did not feel rushed and that I only had a few minutes to have my message herd. I actually felt very relaxed and like we where just having a discussion. Exchanging facts.

We also talked about his life as a Veterinarian and his experiences with treating animals that had  renal failure with low protein food and how animals can have PKU too. He knew from those experiences how costly low protein food could be. He recognized its not the same thing, but it painted a picture. I met his daughter who is studying I think , a masters in science and health who had learnt a bit about PKU in her classes. Mr. Lake liked my idea of guest speaking at nursing classes about PKU to help extend the education. He also gave me some names of media contact who might be willing to help spread my story.

Mr.Lake understood the effects that a MPKU mothers levels could have on a unborn baby and the risk and expense that child would cost the government  as well as children who are already in the system from mothers who cannot look after then due to being off diet.

Mr.Lake noted the fact that we have a strong voice in the cabinet ministries from Bill Bennett and believes that the 2 of them together in the same corner can help us even more.

He has offered his support and has agreed to meet with me again and to continue to work with me.

Even though we spent the majority of our time speaking about PKU , He did take the time to answer my other questions regarding my professional interests as a LPN and my concerns with out health care. He even took the time to discuss our local economy and the potential of the AJAX mine here in kamloops, as well as environmental concerns and family issues. Even education.

Near the end of my meeting I walked him through a few days in my note book on what my meals looked liked, how restricted I was and what happens when I don’t have my food prepared and baked a head of time. He could understand just how much more that there is and that one does not consider that we go through on a daily basis.

I ended the meeting by extending him an invite to the “kamloops walk for PKU ” on june 1st. and even though its 2 weeks after the election and no one know where they will be at he said I could send him an invite via email and he wrote it down.

All in all, I feel very good after meeting with Terry Lake and I am so glad he took the time to meet with me. That he gave me the opportunity face to face to have my voice herd , specially during this busy time of campaigning. That personal connection will go a very long way when I take to the polls on May 14 th.

Either i am incredible naive and Mr. Lake is a very very good politician or He really is all that he portrays  Currently as of today, I am learning towards the latter ,And that makes me feel pretty at ease and confident that I have found a local allie in advocacy for PKU!

BC Residents and news, News

March 6th 2013

OK!!! so I know I have posted this before & here it is again. I want you all to sign your name to this letter to BC Premier Clark to get the coverage PKU patients need. It takes literally 2 seconds and it doesn’t matter where you live even if you live in the UK ;) ;) or Australia ;) ;) It doesn’t matter if you’ve done it before, do it again. Do it a hundred times if it can save a PKU patients brain. you can do it mupliple times from the same computer but we are trying for many diffrent people to email this in. The more names and more emails the premier gets the better. PLEASE PLEASE I am calling upon all of you my friends and family to please do this for me. I deserve the same qaulity of life as everyone else! This could really change my future, protect my brain and allow me to live my life to the fullest, not to mention.. many of you know how despertly I have always wanted my own child. I have put of that dream untill there is better treatments and support for PKU to ensure I can convince and carry a healthy baby to term. Please help me make my dream a reality. But dont do it just for me. Please help me save the next generations from facing the life and experiances I have had to endure. PKU has come a very long way since I was born but it has a even longer way to go! 

Every voice counts! every email sent counts. Please even if you have done it before please do it again. It takes 2 seconds!!

all you have to do is click the link.

http://www.canpku.org/email_premier/

 

 

 

Thank you so much, it really means alot to me!! 

 

Amanda 

News

February 24th 2013

– Funding solution aims to end three-year refusal to provide access to treatment and care –

VANCOUVER, Feb. 23, 2013 /CNW/ – After more than three years of being denied access to the care and treatment needed to protect the brains of 170 patients in B.C. with phenylketonuria (PKU), the Canadian PKU and Allied Disorders Inc. (CanPKU) is asking Premier Christy Clark to invest in a funding solution that will bring PKU care in the province up to national, and international, standards and best practices. The B.C. government has been screening every newborn baby for PKU since the 1960s,1 to allow treatment to begin immediately after the disease is detected; however, many treatment options aren’t accessible to PKU patients who need them.

Today, at the annual B.C. PKU Day, families and patients living with the rare, inherited and brain-threatening metabolic disorder gathered to reconnect with the community and learn about developments in PKU treatment and care from international experts. But the issue top-of-mind for many attending the meeting, including Sparwood, B.C. resident Nicole Pallone, is the government’s refusal to fund the basic treatments needed to protect the brains of PKU patients like Pallone’s five-year-old daughter, Rosie.

“We are shocked and appalled that the B.C. government continues to put the health of our community at risk by denying patients access to evidence-based, proven treatments that are the standard of care in most developed countries,” says Pallone, who is Vice President of CanPKU. “For the past three years, the B.C. Ministry of Health has not only turned its back on PKU patients, but has deliberately and systematically avoided providing basic treatment for PKU patients in this province – the same treatments that other governments right here in Canada provide to their citizens.”

Standard of PKU treatment in B.C. stagnant for 50 years

Despite exhaustive efforts by the PKU community, British Columbia is the worst province in Canada for access to PKU treatments. The only public funding that B.C. PKU patients receive is for special low-protein formula,which has formed the basis of the complicated and highly-restrictive PKU diet for the past 50 years. 3

Numerous provinces provide access to medical foods for PKU patients – a key treatment necessary to prevent devastating neurocognitive, psychiatric and physical symptoms caused by the disease. However, B.C. only provides the bare minimum of coverage for the medical foods necessary to manage PKU – a nominal $40 monthly stipend, available only to PKU patients on social assistance.2

Three years ago, when Health Canada approved Kuvan (sapropterin) as the first and only drug therapy for this brain-threatening disease,4 CanPKU began calling upon provincial and territorial governments to fund the treatment for the 20 to 56 per cent of patients who respond to it. While there has been positive movement towards funding agreements in some provinces, such as Ontario where Kuvan will be publicly funded as of February 28, 2013, B.C. is the only government to walk away from negotiations with the drug’s manufacturer.

However, the B.C. government does fund Kuvan to treat BH4 deficiency (originally called malignant PKU), and as a diagnostic tool to determine whether newborns with high Phe levels have PKU or BH4 deficiency.

“There is no question in my mind that PKU patients who have access to the treatment combination of formula, medical foods and medication have the greatest likelihood of healthy, productive lives, with minimized negative health impacts,” says Dr. Barbara Burton, director of the PKU Clinic at the Ann and Robert H. Lurie Children’s Hospital inChicago, who addressed B.C. PKU Day delegates on Saturday. “Many countries around the world have accepted the body of clinical evidence and professional consensus on the sustained health benefits of Kuvan and medical foods, and are making those treatments accessible to patients.”

Call for investment in Comprehensive Brain Protection Strategy

Faced with the B.C. government’s continued indifference and non-responsiveness to CanPKU’s requests for funding, CanPKU has taken a proactive approach by developing a policy paper to demonstrate to government the minimal investment required to make a tangible difference in the lives of PKU patients.

In a policy paper titled, A Comprehensive Brain Protection Strategy for People with PKU: Getting BC from Worst to First, CanPKU has asked for an annual $2.8 million investment by the B.C. government to improve treatment and care for PKU patients. Submitted to the Premier and the Minister of Health on Friday, February 22, the paper is composed of cost-effective, sustainable and realistic solutions to ensure those British Columbians living with PKU have access to all the necessary resources and treatments.

With this modest investment, CanPKU proposes that B.C.’s medical food subsidy be brought up to standards comparable to Alberta, Saskatchewan, Quebec and Ontario. It would also allow for the government to provide dedicated funding for proven, innovative therapies, like Kuvan. Additionally, the investment would enable a full-time psychologist, PKU Clinic Coordinator, nurse and a part-time dietitian to be added to the PKU/metabolic clinic team at B.C. Children’s Hospital.

“We want to show that we’re still willing to cooperate with government to ensure protection for patients from the devastating health impacts associated with PKU, while respecting budgetary constraints,” says John Adams, President and CEO of CanPKU, whose adult son has PKU. “There is nothing unreasonable about our request – in fact, we think it’s a no brainer. This investment would represent about 0.1 per cent of the $2.4 billion in new health care funding over the next three years that was just announced in B.C.”

If approved, funding for the Comprehensive Brain Protection Strategy would be phased in over a three-year period to allow the government time to more easily absorb the costs. CanPKU hopes that the 170 British Columbians living with PKU would then finally have access to all the available resources and treatments that will improve their health outcomes and quality of life.

Adams adds that the longer funding is delayed, the longer the government is needlessly putting the brains of PKU patients – from infants to adults – at risk.  “The time is now for the Premier to make good on her stated commitment to ‘Families First’ by working with us to bring treatment for PKU patients in this province from worst to first.”

About PKU 
PKU (phenylketonuria) is a rare inherited, brain-threatening metabolic disorder, observed when the body is unable to process phenylalanine (“Phe”), an essential amino acid found in dietary protein.  The resulting accumulation of Phe in the blood is toxic to the brain, and if left untreated, symptoms can range from mild cognitive impairment to severe mental retardation.5,6 Approximately 1 in 12,000 to 15,000 infants in Canada is born with PKU.7

About Canadian PKU and Allied Disorders Inc.
Canadian PKU and Allied Disorders Inc. is a non‐profit association of volunteers, dedicated to providing accurate news, information and support to families and professionals dealing with PKU and similar, rare, inherited metabolic disorders. Our mission is to improve the lives of people with PKU and allied disorders and the lives of their families. By allied disorders we mean other rare, inherited metabolic disorders also detected by newborn screening. For more information, visit www.canpku.org and our new comprehensive resource for patients and families, PKU and the Brain.

Please join the conversation!
CanPKU on Twitter – follow our Tweets during our event today! #canpku
CanPKU on Facebook
CanPKU on YouTube

_____________________________
1 Canada lags on newborn screening. Canadian Medical Association. Available athttp://www.cmaj.ca/content/173/1/23.1.full. Accessed on January 18, 2012.
2 Canadian PKU and Allied Disorders Inc. Coverage for PKU Diet Formulas & Medical Foods – May 2012. Accessed on January 29, 2013. Available at: http://www.canpku.org/images/pdf/coverage-pku-2012.pdf
3 Singh RH, Quirk ME. Using change in plasma phenylalanine concentrations and ability to liberalize diet to classify responsiveness to tetrahydrobiopterin therapy in patients…, Mol. Genet. Metab. (2011), doi:10.1016/j.ymgme.2011.09.009
4 Kuvan [product monograph]. Toronto, ON: BioMarin Pharmaceutical (Canada) Inc.; 2010.
5 Leuret O, Barth M, Kuster A et al. Efficacy and safety of BH4 before the age of 4 years in patients with mild phenylketonuria. J Inherit Metab Dis, 2012; DOI 10.1007/s10545-012-9464-3.
6 Martynyuk A et al., Epilepsy in Phenylketonuria: A Complex Dependence on Serum Phenylalanine Levels. Epilepsia. 2007, 48(6):1143-50
7 Arnold GL. Phenylketonuria. 2009; http://emedicine.medscape.com/article/947781-print

Video with caption: “Families appeal for access to treatments for Canadian PKU patients”. Video available at:http://stream1.newswire.ca/cgi-bin/playback.cgi?file=20130223_C7794_VIDEO_EN_23995.mp4&posterurl=http://photos.newswire.ca/images/20130223_C7794_PHOTO_EN_23995.jpg&clientName=Canadian%20PKU%20and%20Allied%20Disorders%20Inc%2E&caption=Families%20appeal%20for%20access%20to%20treatments%20for%20Canadian%20PKU%20patients&title=CANADIAN%20PKU%20AND%20ALLIED%20DISORDERS%20INC%2E%20%2D%20PKU%20Families%20ask%20Premier%20to%20invest%20in%20Comprehensive%20Brain%20Protection%20Strategy&headline=PKU%20Families%20ask%20Premier%20to%20invest%20in%20Comprehensive%20Brain%20Protection%20Strategy

Image with caption: “Poster – Premier Clark: To Harm or Protect? (CNW Group/Canadian PKU and Allied Disorders Inc.)”. Image available at: http://photos.newswire.ca/images/download/20130223_C7794_PHOTO_EN_23980.jpg

PDF available at: http://stream1.newswire.ca/media/2013/02/23/20130223_C7794_DOC_EN_23985.pdf

PDF available at: http://stream1.newswire.ca/media/2013/02/23/20130223_C7794_DOC_EN_23986.pdf

PDF available at: http://stream1.newswire.ca/media/2013/02/23/20130223_C7794_DOC_EN_23987.pdf

PDF available at: http://stream1.newswire.ca/media/2013/02/23/20130223_C7794_DOC_EN_23988.pdf

PDF available at: http://stream1.newswire.ca/media/2013/02/23/20130223_C7794_DOC_EN_23996.pdf

SOURCE: Canadian PKU and Allied Disorders Inc.

For further information:

Beth Daniher
Cohn & Wolfe
 416-924-5700 ext. 4070 (office)
 416-417-8093 (mobile)
beth.daniher@cohnwolfe.ca

 
BC Residents and news, CanPKU, News

February 24th

Live Twitter updates during BC PKU DAY 2013 yesterday. 

  1. snap shot from #BCPKUDAY2013 . my phone is dying so thanks for following my tweets on the event. photos to come later!

     

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  2. @canpku press conference at #BCPKUDAY2013 to raise awareness & ensure patients get the treatment they deservepic.twitter.com/Mc6o4irtlN

     Retweeted by Amanda Cosburn

     View photo

  3. Honoured to introduce internationally renowned #pku expert Dr. Barbara Burton. #BCPKUDAY2013 http://www.canpku.org/pku-news/190-2-harm-or-protect …#bcpoli

     Retweeted by Amanda Cosburn

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  4. Dr. Burton says we can do beter for #pku patients. I agree!#BCPKUDAY2013 #bcpoli

     Retweeted by Amanda Cosburn

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  5. DR.BURTON was the first doctor to treat PKU with kuvan ever!!#BCPKUDAY2013

     

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  6. Dr. Barbra Burton is our next speaker on optaimizing outcomes in pku! Very exited to here from this expert! #BCPKUDAY2013

     

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  7. I am so happy and enjoying #BCPKUDAY2013 this year! Great experience :)

     

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  8. Just had a fabulous visit socializing with pku families over a low protein lunch atv@BCPKUDAY2013

     

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  9. @canpku at press conference at the #BCPKUDAY2013 to raise awareness & ensure patients get the treatment they deserve pic.twitter.com/TghTf7CBKg

  10. DR.Syliva stockler head of the bc children’s clinic is our next speaker of the day. #BCPKUDAY2013 #bcpoli

     

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  11. Congratulations Wyoming on there new coverage of PKU formula! Signing later this week. Big news from #BCPKUDAY2013 #BCPOLI

     

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  12. So interested in karis maternal pku talk. Never met a pku adult with a pku baby! #BCPKUDAY2013 #bcpoli

     

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  13. are you following my live tweets for #BCPKUDAY2013 on Twitter? ?

     

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  14. Kari”s pku story is so familiar to me! Love hearing from other adults#BCPKUDAY2013 #BCPOLI

     

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  15. @christyclarkbc I have PKU! Its time you policy “famlies first” includes famlies like mine. #BCPKUDAY2013 #BCPOLI

     

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  16. @pmharper can myslef and other PKU patient’s get a re tweet to support #BCPKUDAY2013 today at chan center BC children’s hospital. #bcpoli

  17. Kari kilmer @canpku #BCPKUDAY2013 . Would love to ask her all my questions! Inspiration! #bcpoli pic.twitter.com/efGM7R8x7y

  18. So excited to here guest speaker kari kilmer pku adult and mom to a pku little girl. #BCPKUDAY2013 #BCPOLI

     

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  19. RT @canpku PKU FAMILIES ASK @christyclarkbc TO INVEST IN BRAIN PROTECTION STRATEGY!!! #BCPKUDAY2013 #bcpolihttp://lnkd.in/Pwu3P2 

     Retweeted by Amanda Cosburn

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  20. It is time to extend BC Premier @christyclarkbc commitment to “Families First” to PKU families #BCPKUDAY2013 #BCPOLIhttp://www.canpku.org/email_premier/ 

     Retweeted by Amanda Cosburn

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  21. I am working to host a pku walk a thon in kamloops on june 1st for@canpku to raise funds for #bcpkuday2013 #bcpoli

     

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  22. Today’s the day. #BCPKUDAY2013 is about to get started! #bcpoli#raredisease

     Retweeted by Amanda Cosburn

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  23. Today is the Canadian PKU and Allied Disorder’s BC PKU Day!#BCPKUDAY2013 Visit the CANPKU website to learn more!http://ow.ly/hToWp 

     Retweeted by Amanda Cosburn

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  24. Arrivd in Vancouver yesterday&droped off @canpku policy doc to Min@DrMacDiarmid constit office #bcpoli #bcpkuday2013pic.twitter.com/iaqBRIq3e7

     Retweeted by Amanda Cosburn

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  25. @canpku president and me at the #BCPKUDAY2013. Shaping up to be a great day! #bcpoli #raredisease pic.twitter.com/7gdKzT9D7K

     Retweeted by Amanda Cosburn

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  26. Looking forward to hear Dr. Barbara Burton speak about#pku today at #BCPKUDAY2013#bcpoli #raredisease

     

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  27. Today’s the day. #BCPKUDAY2013 is about to get started! #bcpoli

     

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  28. almost there. thank you cole for driving us and coming to the event with me every year! happy this year to have… http://fb.me/271mKnHzh 

     

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  29. we are on our way to bc pku day dont forget to follow me on twitter today hashtag #bcpkuday2013 for live tweeting during the event.

     

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  30. Dont forget to bring your pennies for pennies for pku #bcpkuday2013penny drive!

     

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  31. Good morning tweeters! We are on our way to #BCPKUDAY2013. Are you excited as I am. Thank you @canpku for hosting this wonderful event!

     

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  32. I will be live tweeting during tomorrows event with the hashtag#BCPKUDAY2013. Follow me on twitter at @Project_PKU

     

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  33. 2 new blog posts tonight! Be sure to check them out!

     

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  34. made it to vancouver at 12:00 pm had lunch, went to clinic had a good check , stopped to get low pro food now at the hotel :)