10 November 2012

Finally some answers from the Rick Hansen Institute

Compared to getting answers from the Rick Hansen Foundation, the Rick Hansen INSTITUTE gave us some answers after only a few emails and some back and forth on facebook (still too slow in my opinion). 

I'm happy that they gave us answers and that the answers were quite detailed, but I have to admit that in my opinion, the answers clearly show that they are doing nothing, or very very little, to deal with a cure for chronic spinal cord injury.

RHI's advertising makes it look like they are dealing with a cure for chronics. Have a look at http://www.rickhanseninstitute.org/images/header/trudeau_oneday1.jpg and see as one of their own board members, Marie Trudeau who was injured at eighteen, says that, "One day...I hope to run on the beach." This is a clear statement that they are committed to a cure for chronics; I just wish that their research showed the same commitment.

Another good point is that they have agreed to talk. We are in the midst of trying to organize the first talk between myself and Mr. Bill Barrable, RHI's CEO. I'll keep you all posted about the progress.

Now without further ado, I will let you judge for yourself about the amount of RHI's work on a cure for chronic spinal cord injury.


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Legend
Blue: Our questions to RIH
Black: RIH answers
Green highlighting: our highlighting of the main part of the answers
Red: Our thoughts and/or questions
You can also download this document at http://www.scribd.com/doc/112757536.
___________________________________

Q: What percentage of your budget went to research (basic or translational) for a cure for chronic spinal cord injury in 2009, 2010, and 2011?

A: RHI hasn’t and doesn’t invest in basic or discovery research.
I guess that translation and not basic research is their mission, but whether this is correct or not is a different story. Regardless of this we need to find out what basic and pre clinical research they are looking at for chronics. Since they are involved in translation, they should be on the lookout for prospective research aimed at chronics.

The cost of basic science research continues to increase, with the funding required to do pre-clinical research on a potential SCI therapy in the multi-millions. In conversation with our NIH partners, RHI was advised to focus on the areas of research that are essential to translating research from the basic science discovery to the patient's own bedside,
Including their answer about ICORD below, we now know who is responsible for basic research and who is responsible for translational research.

where funding is generally harder to come by.  Large public research funders like the Canadian Institutes of Health Research, the Natural Sciences & Engineering Research Council, and the National Institutes of Health (USA) fund this type of research,
Again, if they can name the institutions responsible for basic research, what research is RHI currently following for chronic spinal cord injury?

whereas there are few logical funders for health services research, best practices implementation (to improve and standardize SCI care), clinical trials networks, and other forms of capacity building for SCI clinical research. 
Thus, RHI has been directed to invest our federal funding in these areas that are essential pieces of translational research (patient registry and research platform, clinical research network and standardizing SCI care and outcomes across the country) that are unlikely to receive support from other funding. I
These are three things they do.
Patient registry and research platforms: how does it apply to chronics?
Clinical research network: Yes, can be used for chronics but is a whole network really necessary.
Standardizing SCI care and outcomes: Outcomes must be their registry. Important for acute cure but I don’t see the benefit for chronics.
In a sense it’s like putting the care ahead of the horse.

in this way, RHI is ensuring we are good stewards of our public funding, avoiding duplicating what is being done by our discovery science partners at ICORD. Following this strategy, RHI/RHF also contributes to seed funding for our SCI research partners at ICORD, in order to enable SCI academic researchers to do the preliminary research necessary to obtain research grants. 
Any seed funding toward a cure for chronic SCI? Again, not naming it in this document makes one doubt that there is any seed funding for chronic SCI. If they can do seed funding for ICORD it does mean that they are involved in basic research by financially supporting the work at other organizations.

Now, onto where we spend our time. About 20% of our projects deal with reducing paralysis, and another 40% or so aim to enhance physical function. Unfortunately, it is next to impossible to calculate accurately how much of our budget was spent on a cure for chronic SCI, as many of our projects target more than one expected outcome. For example, our Rick Hansen Spinal Cord Injury Registry (RHSCIR) collects data on people in Canada with an SCI,
Reducing paralysis: is not cure and often reducing paralysis is dealing with outcomes immediately after injury.
Enhancing physical function: by doing what? How do you enhance physical function of a complete chronic injury without regeneration?

Registry: important for measuring outcomes in acutes. But what I’ve heard of the registry it doesn’t follow people past two years. I’ve also heard that includes a lot of demographics without follow up at different stages.

Actually registries done by EMSCI and NACTAN are enough to monitor the evolution of patients with SCI? Why is work being duplicated as no one can see the difference between people with SCI in America or Europe.

which is anticipated to help answer a number of research questions related to the cure, to alleviating secondary complications, and other areas. As part of RHSCIR, a survey of people with spinal cord injury was conducted to assess their readiness and willingness to participate in stem cell clinical trials. So this one activity within RHSCIR was aimed at the cure for chronic SCI, but it is not possible to budget this out as it is part of the larger RHSCIR project.
This was a survey, not “aimed at the cure for chronic spinal cord injury.” Also, a lot of work is going on without cells. Why the focus on cells?
What was the point of a survey like this? How can you ask people if they would like to undergo some non-defined procedure? Who would agree?


Similar types of activities are carried out within other RHI projects, such as our Access to Care and Timing project and others.
Important, but in no way aimed at chronics.

__________________________________


Q: What research was done in regards to question one above?

A: We define cure as reduction of paralysis and restoration of physical function post injury.
Very broad definition of cure. Any little improvement is not cure.CDRF is also involved in this kind of thinking.
The definition of cure is very simple; after medical treatment, the patient no longer has that particular condition anymore. http://kidshealth.org/teen/your_body/medical_care/curable.html 
You cannot redefine the meaning of cure so that even moving a toe becomes cure. That is not cure, it is moving a toe.

If we are strictly talking about neuro-regeneration and neuro-protection, we currently only have a handful of projects. Based on our definition of cure(s), more than half of our projects deal with reducing paralysis and enhancing physical function. Specific projects include: Access to Care and Timing, CAMPER, FES and ReJoyce, for example, could fall within the category. In addition to time into surgery and stem cell transplantation, RHI’s activities in fiscal year 2011-2012 oriented towards reduction in paralysis also included support for two multi-centre trials examining potential neuroprotective agents: riluzole and minocycline. In fact, since 2007, RHI has supported fully half of the Canadian-sponsored clinical trials on SCI.

OK. In your handful of  projects which ones deal with neuro-regeneration and why didn’t you mention them here.
Reducing paralysis and enhancing physical function is not cure. Specifically, how does Access to Care and Timing, CAMPER, FES, and ReJoyce cure chronic spinal cord injury? None of these are a biological answer to cure and only offer very limited functional improvement, if any, in chronics.
Both of riluzole and minocycline are 100% for acutes.
Yes of course they have done clinical trials, but saying “clinical trials” is not the same as “clinical trials for cure for chronic spinal cord injury. Adding this just confuses the situation especially is not one clinical trial aimed at chronics is mentioned.

We are strictly talking about a cure for chronic SCI which means recovery of functions like breathing, hands, bowel, bladder, walking..

__________________________________


Q: What are your future plans for both spending and research for a cure for chronic spinal cord injury in the near future.

A: RHF and RHI have recently received a commitment from the Canadian government for the continuation of its programs. RHI has submitted a new five-year business plan to guide activities towards meeting its objectivesusing these new funds. 
Since our questions are about chronics, why is there nothing mentioned specifically about chronics?

Given all the work conducted by RHI and others, Canada has a unique opportunity to host clinical trials for SCI, due to greater consistency in SCI care across the country. By supporting a network of clinical researchers, creating an infrastructure for clinical trials in SCI, standardizing care, enabling standard measurement of patient outcomes, and creation of a patient registry, RHI is making it possible to trial new treatments for acute and chronic SCI as they are ready for clinical trials, which is the goal we’re all working towards.  
Great. A lot of leg work may have already been done to get clinical trials going, but now the clinical trials have to start.
Standardizing care is not part of this for chronics. It’s just added in and again confuses the situation.
Measurement of patient outcomes. Is this through the registry? I don’t understand the importance of this for chronics, especially complete chronics.
There will be very few clinical trials for chronic SCI in the future because very few labs are doing chronic SCI research and that is also because orgs like RHI/RHF failed to direct founds restricted to chronic SCI research.

(RHI’s fiscal year ends March 31, 2013, so we’re currently wrapping up a number of projects started as far back as 2007. Details on new projects will be available in the new year).

28 October 2012

More reasons to support Working2Walk and Unite2Fight Paralysis

Irvine, California  1-3 November
Today I'm doing a follow up from my last post about the Working2Walk (W2W) conference being held in Irvine, California on 1-3 November. In my last post, "Working2Walk - I'll be there in spirit an pocketbook" I talked about some of the reasons why we should support this conference even if we can't attend and how I made a small donation to Unite2Fight Paralysis (U2FP), the conference's main sponsor.


  • a yearly conference sponsored by U2FP since 2006 to bring together scientists, practioners, paralysis survivors and family members for a dynamic exchange of information and strategies
  • with a jam packed agenda of the best science to cure paralysis
  • presented by leading world scientists and others involved in raising money and advocating for a cure for spinal cord injury
  • having a live blog to read about the events as they happen (2011 W2W)
  • putting the main speakers up on the web so we can see the good news about the main scientific cure breakthroughs (2010&2011 W2W). These videos have been seen in over 50 countries.
And the things that U2FP does for the spinal cord injury community outside of the W2W conference.

These are the the first hand benefits that we all get from this conference and this organization, and why I made a donation to support their work.

But there is a more personal side because U2FP's work IS personal. 

U2Fp understands firsthand the challenges and issues that accompany an SCI. They aren't driven to our work by a paycheque. They are driven by the love they have for the people who are injured. Everyone on the U2FP board either has a SCI or a child with one. They're passionate about moving therapies forward and witnessing recovery in our lifetimes. 

The researchers they work with, recognize this and partner with them to better understand the science and work with us to advance it.  The scientists and researchers understand the value of this partnership and commit year after year to participating at W2W. U2FP needs more people to support their work, so that they can develop additional strategies to support the researchers work and move us all closer to recovery. 

So, even if you can't attend, you do get a benefit and I hope that you can join me in supporting U2FP's wonderful work.

19 October 2012

Do I smell or something?

I'm starting to get the distinct feeling that the people at Rick Hansen Foundation and Institute don't want to answer questions from the public. Not even questions from their own constituents.

I asked,
1. What percentage of your budget went to research (basic or translational) for a cure for chronic spinal cord injury in 2009, 2010, and 2011?

2. What research was done in regards to question one above?

3. What are your future plans for both spending and research for a cure for chronic spinal cord injury in the near future.

And they answered.
////////////
Hi Dennis,

Thanks for writingus again with your questions.

We share your passion in accelerating progress towards a cure for paralysis after spinal cord injury, although we may not always agree on the meansto get there.

We're a young organization (created in 2007) now enteringour next five-yearwork phase.
We're currently wrapping up many of our olderprojects and about to embark on some exciting new initiatives in our three core areas: cure, care and collaboration.

In the meantime, our FAQ page (http://www.rickhanseninstitute.org/what-we-do/faqs#percentage )providesa breakdown of projects by core area,ourwork in the cure sphere, someprogress, funding sourcesand where we're heading.

Regards,
The Rick Hansen Institute
Rick Hansen Institute
6th Floor, Blusson Spinal Cord Centre
6400 - 818 W. 10th Avenue, Vancouver, BC V5Z 1M9
t: 604-707-2100
e: info@rickhanseninstitute.org
www.rickhanseninstitute.org

A world without paralysis after spinal cord injury.

Follow us:
facebook.com/RickHansenInstitute
twitter.com/rhinstitute
/////////////////

Follow the whole conversation between me and the Rick Hansen Institute

1. To Rick Hansen Institute: we don't need paper heroes - http://stemcellsandatombombs.blogspot.com/2012/09/to-rick-hansen-institute-we-dont-need.html?m=1

2. Pants on firs - http://stemcellsandatombombs.blogspot.com/2012/10/lxxx-lxxx-pants-on-fire.html?m=1

3. Copy and paste the answers. Thanks. - http://stemcellsandatombombs.blogspot.com/2012/10/copy-and-paste-answers-thanks.html?m=1

Dennis Tesolat

www.StemCellsandAtomBombs.blogspot.com

BlackBerry from DOCOMO

14 October 2012

Vote for your favourite image

Ask most people that I work with and they will tell you that I love my work to be constructively criticized. It's what makes the end product better.

There was some criticism of the image I chose of the woman dancer (image 2). Some believed that she looked like a stripper and maybe that it wasn't the most positive image that I could have chosen. I truly believed the woman to be a dancer and didn't even consider the fact of what others might have thought. A friend of mine told me that it couldn't be a stripper because strippers dance in heels and my image was clearly a dancer, but I guess we all have different eyes and I truly do appreciate the comments.

So, what I'm going to do, because I believe that most people have good sense, and the last thing I want to do is divide us over an image, I will let those who follow my blog, my facebook friends, your facebook friends, anybody, vote to decide what the best image is.

I think people can chose an image that won't insult most people. 

It's up to YOU to chose. I've picked five that I like, at least that were free and not stolen, and I'll leave it to you.

You can vote in one click below to pick the image that I will use for our current Rick Hansen Lobbying campaign. For more information about the campaign, please see here.

IMAGE 1

IMAGE 2
IMAGE 3


IMAGE 4


IMAGE 5




The vote is over and image 3 wins the race. Thanks to all of you who voted.

13 October 2012

Rick Hansen Foundation lobbying

This below letter was sent by fax and email after reading information about the Rick Hansen Foundation's (RHF) plans to start lobbying to secure government funding for the next five years.

Our goal is to make sure that there is a commitment by RHF to fund basic and translational research for a cure for chronic spinal cord injury. 

The signatories to this letter all want RHF to be successful in their bid to secure funding, but refuse to idly sit by and allow words and phrases like 'cure' and 'a world without paralysis after spinal cord injury' be used to raise funds if there is no effort to fund research for a cure for chronic spinal cord injury, or at least a statement from RHF saying that they do not support research for a cure for chronic spinal cord injury.

We who are currently living with spinal cord injury and our supporters will not be left behind and told to shut up, sit down, clap our hands, and pass the donation bucket.

/////////////////////////////////////////////////////////////////////////////////////////////////////



04 October 2012

Copy and paste the answers. Thanks!

Dennis Tesolat
Japan, Osaka-shi,
stemcells.and.atombombs@gmail.com

5 October 2012

Via FAX & Email


Bill Barrable, CEO
Rick Hansen Institute
6400 - 818 West 10th Avenue,
Blusson Spinal Cord Centre,
Vancouver, British Columbia,
Canada
FAX: +1-604-707-2121
Email: bbarrable@rickhanseninstitute.org


Dear Mr. Bill Barrable,

Thank you for your reply.

I'm sorry if I have missed any answers that RHI or RHF have sent me in the past.
Actually, this is the first time that I have written to RHI and the only other time that RHI 'signed' an email was the very first time. After that, each email was sent from Mr. Art Reitmayer, the past CEO of RHF.

Therefore, if you've already answered in the past, please forgive. This means that you should have the answer at the ready since you have already answered.

So here we go.
1. What percentage of your budget went to research (basic or translational) for a cure for chronic spinal cord injury in 2009, 2010, and 2011?

2. What research was done in regards to question one above?

3. What are your future plans for both spending and research for a cure for chronic spinal cord injury in the near future.

Thank you for your patience in answering my questions. I've tried to find the answers that you spoke of, but failed. If you could just copy and paste the information, it would be well appreciated.

Sincerely,
Dennis Tesolat
www.StemCellsandAtomBombs.blogspot.jp



Dennis Tesolat
www.StemCellsandAtomBombs.blogspot.com
BlackBerry from DOCOMO

Pants on fire!


Mr. and Mrs. Institute must be really ashamed of their son, The Rick Hansen Institute after the letter he sent me. Yes, I received a letter signed, Rick Hansen Institute (RHI). Now either it was signed by Mr. and Mrs. Institute’s son, OR, no one at the RICK HANSEN INSTITUTE was willing to take responsibility for the rubbish that was written in it so no one signed it. I tend to believe the latter as I looked on Canada411 and only found one person with the surname ‘Institute’ but that person was in Toronto.

Let’s go back a second.

Many of you will know that I have been involved in writing to the Rick Hansen Foundation (RHF) about their commitment to a cure for CHRONIC spinal cord injury. You’ll also know that they have NEVER NEVER NEVER answered this question.

You can see the whole explanation at www.bit.ly/HansenFoundation. 

So this time I wrote to the RHI to see about their spending and research since they receive $12 million of RHF’s $13 million that they endow on ‘outside’ organizations. The email I sent to Mr. Bill Barrable, RHI’s CEO, can be found at http://bit.ly/paperheroes. 

I was shocked that he would even dare say, "We believe that we have been very responsive to all your requests."

For one, we have never written asking questions to the RH INSTITUTE. They have only ever been cc'd into the questions. Furthermore, the responses have never come under the name of RH INSTITUTE except for our very first ask. Other than this, we have only ever received answers from the Rick Hansen Foundation and Mr. Art Reitmayer who was the CEO. 

So how can they in good faith write that they have, "always been responsive to our requests."

Are RHF and RHI the same? They must believe so. Well, if they are the same, I think they should stop acting as two separate entities and the costs that it entails  like office space, telephones, and administrative staff. It's starting to sound weird to me.

I'm starting to feel that two groups that can't answer questions about spending on regeneration or a cure for chronic spinal cord injury are somehow hiding something from the community of the chronically injured.

As always, I hope I'm wrong and that they're not answering because they are too arrogant and feel that they don't owe US, the paralyzed, an answer, not because they're not spending on chronic cure.

I guess this means a new campaign. Stay tuned.

By the way, just in case you don't know who I am, I am Dennis Tesolat. I take responsibility for what I write.