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Wednesday, June 8, 2011 (No. 5)

Questions

The complete list of questions on the Order Paper is available for consultation at the Table in the Chamber and on the Internet. Those questions not appearing in the list have been answered, withdrawn or made into orders for return.

Q-1² — June 6, 2011 — — With regard to corporate taxation, what is the total amount of deferred corporate taxes for the tax years 2005, 2006, 2007, 2008, 2009, and 2010?

Q-2² — June 6, 2011 — — With regard to corporate taxation: (a) how many corporations in Canada paid no tax in each of the last ten years; and (b) for each corporation identified in (a), what were its revenues and its profits in each of the last ten years?

Q-3² — June 6, 2011 — — With regard to the expenditures of the Department of Indian Affairs and Northern Development as identified in the 2011-12 Main Estimates: (a) what programs are funded under the lines (i) Northern Land, Resources and Environmental Management (page 191), (ii) Contribution for promoting the safe use, development, conservation and protection of the North’s natural resources (page 194), (iii) Contributions for promoting the political, social and scientific development of Canada’s three territories (page 195), (iv) Contributions for promoting regional development in Canada’s three territories (page 197), (v) Canadian Northern Economic Development Agency, Community Development (page 196); and (b) for each program identified in (a), what are the names or identities of each individual recipient of funds from each program and what amount of funding was provided to each recipient?

Q-4² — June 6, 2011 — — With regard to the PROminent FUNCtionaries of the Communist Party (PROFUNC), run by the government between 1950-1983: (a) when requested by an individual who believes his or her name may be on the PROFUNC list, will the government disclose whether or not that individual's name is on the list; (b) what was done with the names on the PROFUNC list once PROFUNC was discontinued; (c) were any of the names or was any of the information about individuals named on the PROFUNC list ever turned over to the Canadian Security Intelligence Service (CSIS), or any other security agency, at any time after 1983; (d) were any of the names or was any of the information about individuals named on the list ever shared with the Government of the United States or any of its security, policing or military bodies; (e) did any of the RCMP personnel who helped compile or maintain PROFUNC work for CSIS or other security agencies following the end of the program; and (f) what other materials were created by individuals working for PROFUNC between 1950-1983 (i.e., minutes of meetings, reports filed by security agents, other documents)?

Q-5² — June 6, 2011 — — What is the total amount of government funding since fiscal year 2009-2010, up to and including the current fiscal year, allocated within the constituency of Vancouver East, identifying each department or agency, initiative and amount?

Q-6² — June 6, 2011 — — With respect to the Veterans Burial Regulations and the Corporation named by the Department of Veterans Affairs Act to administer the Veterans Funeral and Burial program, specifically the Last Post Fund (LPF): (a) what is the annual amount of financial support and funding provided by the Department of Veterans Affairs from 2006 to 2011 inclusively; (b) what is the statistical information, provided to the minister, on reimbursements provided by the LPF to assist in payment of funeral and burial costs for the estates of (i) First World War veterans, (ii) Second World War veterans, (iii) Korean War veterans, (iv) estates of veterans who received a disability benefit from Veterans Affairs Canada, (iv) estates of allied veterans; (c) what are the details of the annual administrative and operating costs of the LPF from 2006 to 2011 inclusively; (d) what are the details of the annual program costs of the Veterans Funeral and Burial Program from 2006 to 2011 inclusively; (e) what are the details of the annual salary costs for LPF staff from 2006 to 2011 inclusively; (f) what are the details of how frequently business plans, operating budgets, capital budgets and performance reports are submitted by the Corporation to the Minister; (g) what are the details of any departmental analysis concerning the raising of the means test for eligibility for support through the Veterans Funeral and Burial program; (h) what are the details of any departmental analysis concerning the extension of eligibility for a funeral and burial to all estate-tested Canadian Forces (CF) and RCMP veterans; (i) what is the estimated financial cost of extending eligibility to the Veterans Funeral and Burial program to all estate-tested CF and RCMP; (j) how often does the department conduct an assurance audit of the LPF; (k) when was the last time the government conducted an assurance audit of the LPF; and (l) when does the department plan to conduct the next assurance audit of the LPF?

Q-7² — June 6, 2011 — — With respect to Canadian Forces veterans trying to obtain an end to the deduction of Pension Act disability payments from Service Income Security Insurance Plan (SISIP) Long Term Disability benefits: (a) what is the total amount of money spent by all departments and agencies, excluding the Department of Justice, from March 2007 to 2011 inclusively, on the defence against the SISIP class action lawsuit; (b) what is the total amount of money the government has spent to hire outside legal counsel, from March 2007 to 2011 inclusively, on the SISIP class action lawsuit; and (c) what is the total amount of money spent by all government departments and agencies on the SISIP class action lawsuit, from March 2007 to 2011 inclusively, including all costs associated with the work of the Department of Justice?

Q-8² — June 6, 2011 — — With regard to veterans’ long-term care facilities and veterans’ contract beds in community care facilities: (a) what are all facilities, by province and territory, that are under contract by the Department of Veterans Affairs to provide veterans' beds; (b) for each facility identified in (a), what is (i) the number of beds, (ii) the average cost of a veteran’s bed; (c) when, by facility and province or territory, does the department expect to close veterans' beds based on the declining population of its Second World War and Korean War veteran clientele; (d) what are the details of any departmental analysis concerning the expansion of the definition of eligible veterans for admittance to veterans' health care centres; (e) what are the details of any departmental analysis concerning the government’s payment for veterans' beds at long-term care facilities or community care facilities for the spouses of Second World War and Korean War veterans; (f) does the department have any estimates of the cost of paying for veterans' beds at veterans’ long-term care or community care facilities for the spouses of Second World War and Korean War veterans and, if so, what are they; (g) what, if any, are the plans for the long-term care of modern-day Canadian Forces (CF) veterans who require long-term care and do not meet the criteria for admittance to veterans’ beds at veterans’ long-term care or community care facilities; and (h) is the department engaged in any discussion of the development of specialized medical centres for modern-day CF and RCMP veterans?

Q-9² — June 6, 2011 — — With regard to the Veterans Review and Appeal Board (VRAB), legislated by the Veterans Review and Appeal Board Act: (a) who are all permanent and temporary members of the Board, broken down by province and territory, appointed by the Governor in Council since 2006; (b) has the government considered disbanding the VRAB; (c) has the government considered modifying the VRAB; (d) has the government considered implementing a policy to ensure that VRAB appointees by the Governor in Council must have (i) military or RCMP experience, (ii) medical experience; (e) what were the total annual federal funds provided to the VRAB from 2006 to 2011 inclusively; (f) what is a breakdown of the annual spending of the VRAB, from 2006 to 2011 inclusively, as it relates to (i) program costs, (ii) administration costs, (iii) salary costs of the VRAB board members, (iv) travel costs for the VRAB board members, (v) VRAB staff costs, (vi) VRAB staff travel costs; (g) how many reports has the VRAB chairperson made to the Minister with respect to the use of resources allocated to the Board from 2006 to 2011 inclusively; (h) when was the last time the Department of Veterans Affairs completed an assurance audit of the VRAB and when is the department planning to conduct the next audit; (i) how often does the department conduct assurance audits of the VRAB; (j) has the department planned an extensive review of the administration of the VRAB; (k) does the Department of Veterans Affairs regularly analyze the reasons why pension decisions are overturned by the VRAB in favour of the client with regard to the interpretation of (i) legislation, (ii) medical issues, (iii) legal issues; (l) has the VRAB provided information to the department on how many pension decisions, made since the VRAB's inception, have been in favour of the veteran client using the benefit of the doubt clause (section 70); and (m) how many pension matters or cases has the VRAB referred back to the Minister for reconsideration, by year, from 2006 to 2011 inclusively?

Q-10² — June 6, 2011 — — With respect to the full process currently being undertaken by the Canadian Institutes of Health Research (CIHR) regarding chronic cerebrospinal venous insufficiency (CCSVI), including the August 26, 2010, meeting of the Scientific Expert Working Group (SEWG) and the CIHR’s “knowledge synthesis review”: (a) what is the accepted operating definition of “conflict of interest” for the CIHR, (i) why was no disclosure statement made by all participants who attended the August 26, 2010, joint meeting of the CIHR and the Multiple Sclerosis Society of Canada (MSSC), (ii) are there plans to provide an opportunity to declare possible conflicts of interest subsequent to the meeting; (b) what are the details of all information produced and circulated by the CIHR in January 2011 regarding follow-up care for multiple sclerosis (MS) patients and to which organizations was the information sent; (c) will the disclosure statement to be signed by members of the SEWG at its next meeting in June 2011 include specific reference to any (i) consultancy, (ii) grant support, (iii) membership on advisory councils, (iv) speaker’s bureau, (v) other sources of funding a member might have; (d) how does the CIHR plan to ensure that all members of the SEWG have the same understanding of private or personal interests that could influence decision-making; (e) will all disclosure statements in (c) be made publicly available and, if so, when, and, if not, why not; (f) which, if any, of the SEWG’s members have been trained in Dr. Zamboni’s methods and by whom were these members trained; (g) which, if any, of the SEWG’s members have watched diagnosis and treatment of CCSVI and, for each member identified (i) where did this observation take place, (ii) under what guidance, (iii) how many images and treatments were studied by the member; (h) which, if any, of the SEWG’s members have undertaken diagnosis and treatment of CCSVI and, for each member identified, (i) where were these actions performed, (ii) under what guidance, (iii) how many images and treatments were performed by the member; (i) does the CIHR recognize the emerging scientific discipline of neurovascular disease; (j) does the SEWG include any members of the International Society for NeuroVascular Disease (ISNVD) and, if so, who are these members, and, if not, why not; (k) which, if any, members of the SEWG have attended any of the ISNVD’s conferences, specifying for each such member the conferences that he or she attended; (l) does the inclusion of investigators of the seven MS Society-funded studies in the SEWG comply with the CIHR’s operating definition of “conflict of interest” and, if so, what are the reasons that explain this compliance; (m) regarding the “knowledge synthesis review”, (i) what is the protocol for the review, (ii) how is research deemed to be, or not to be, pertinent, (iii) who specifically is undertaking the review, how were they chosen, and what expertise do they have to undertake the review, (iv) why has the CIHR decided to have them undertake the review, (v) what are the CIHR’s reasons for not having the SEWG undertake the review, (vi) what is the cost of the review, (vii) what is a comprehensive list of abstracts to be reviewed, (viii) what additional material, people, or other sources will be consulted, (ix) will the review include scientific evidence presented at all the major scientific conferences on CCSVI to date, namely, Hamilton (February 2010), New York (July 2010), Washington (October 2010), Katowice (March 2011), Bologna (March 2011), Chicago (April 2011), and San Diego (May 2011), (x) will the review include contacting the leading experts in the field, asking for their unpublished data, visiting their laboratories and operating theatres, (xi) if the answer to (m)(x) is in the affirmative, what, if any, protocol has been established for each contact, and what, if any, weighting will be applied to this evidence; (n) how does the CIHR plan to weigh or asses the seven MS Society-funded studies and the “knowledge synthesis review” in its establishment of any future policy, particularly in its deliberations on whether to undertake clinical trials for CCSVI in Canada; (o) which , if any, members of the SEWG have attended any CCSVI conferences, specifying for each such member (i) what conferences he or she attended, (ii) in what capacity, (iii) who paid for the trip or attendance at the conference, (iv) what written evidence did he or she report to either the CIHR or SEWG, (v) if no written evidence was reported, why not; (p) which members of the CIHR have attended any CCSVI conferences, specifying for each such member (i) what conferences he or she attended, (ii) in what capacity, (iii) who paid for the trip or attendance at the conference, (iv) what written evidence he/she reported to either the CIHR or SEWG, (v) if no written evidence was reported, why not; (q) why has the CIHR decided not to further investigate CCSVI through clinical trials; (r) why has the CIHR decided not to follow recommendations made by the Ontario Association of Neurologists, the Canadian Society of Radiologists, the Canadian Society of Vascular Surgery, the American Society of Interventional Radiology, and the International Union of Phlebology regarding CCSVI; (s) what does the CIHR consider an “appropriate pace”, a term used in its May 18, 2011, e-mail to Dr. Kirsty Duncan, Member of Parliament for Etobicoke North, for the introduction to Canada of any potential new medical treatment for any medical condition, and how much evidence does the CIHR consider is required before a treatment should undergo clinical trials in Canada in terms of (i) the number of procedures undertaken, (ii) the number of countries undertaking the procedure, (iii) scientific evidence presented in academic peer-reviewed journals, (iv) scientific evidence presented at academic conferences, (v) scientific evidence presented at academic conferences for conditions that are progressive diseases, especially progressive diseases for which there are limited or no options for treatment; (t) what is the CIHR’s accepted protocol, including all necessary steps, for bringing a new treatment to clinical trials in Canada, (i) when was the protocol established, (ii) what treatments have undergone clinical trials as a result of the protocol, (iii) which treatments have been rejected to date; (u) is the creation of a SEWG a standard step in the CIHR’s protocol for bringing a new treatment to clinical trials in Canada, and, (i) if so, since the creation of the protocol, what are all new treatments and their associated SEWGs, (ii) if not, why was this step deemed necessary for approval of clinical trials for CCSVI; (v) what are the last five medical treatments for any medical condition accepted by the CIHR for use in Canada and, for each treatment, what are the details of all evidence required by the CIHR in its decision to have the treatment undergo clinical trials, including, but not limited to, the number of procedures undertaken, the countries undertaking the procedure, and scientific evidence presented in both peer-reviewed journals and academic conferences; and (w) with regard to the MS registry announced March 23, 2011, (i) who specifically is collecting the information, (ii) what precise information is being collected, (iii) what consent will be necessary from patients for any data collection, (iv) when will information begin to be collected, (v) what specific information is being collected regarding the treatment of CCSVI, (vi) what information is being gathered or tracking is being done of individuals who have chosen to have the liberation procedure outside Canada?

Q-11² — June 6, 2011 — — With respect to depleted uranium (DU), military service, and Veterans Affairs Canada (VAC) benefits and programs: (a) what are all potential sources of DU to which Canadian Forces (CF) members and veterans might have been exposed between 1990 and the present; (b) what are any operations between 1990 and the present that might have brought CF members and veterans into direct or close contact with DU, including, but not limited to, operations in which Canadian personnel seconded to other military forces were involved; (c) did any CF member or veteran serve between 1999 and 2003 in areas assessed by the United Nations Environment Programme (UNEP) to be DU areas; (d) what, if any, DU munitions, vehicles made with DU, or ships carrying DU munitions, were used by CF between 1990 and the present; (e) what are all possible exposure routes for each source of DU identified in (a), (b), and (d); (f) what, if any, field measurements were taken around any DU source identified in (a), (b), and (d) and, if such measurements were taken, what was the level of contamination of the environment for each site, for each time sampled; (g) what, if any, studies were undertaken by the Department of National Defence (DND), or any other federal government department or crown corporation, from 1990 to the present, regarding DU environmental contamination linked to the military and what were the chief findings of each such report, including (i) whether it identified a need or made a recommendation to work with caution in DU contaminated areas, (ii) whether it identified a need or made a recommendation to do policy work regarding DU contaminated areas; (h) what follow-up took place concerning the chief recommendations of each report identified in (g), as well as concerning the issues identified in each of (g)(i) and (g)(ii); (i) what, if any, clean-up operations were undertaken in impact zones between 1990 and the present, and, if such operations were undertaken, why was each clean-up operation deemed necessary, and what national or international recommendations were followed in each clean-up; (j) which, if any, experts were consulted to determine any possible DU contamination between 1990 and the present, and, if experts were consulted, who were they, and in what field or fields did each expert work; (k) what, if any, specific training, equipment and guidance was given to CF members and veterans who were required to work in areas of DU contamination or to conduct any DU field assessments and clean-ups; (l) what, if any, specific radiation field measurement and health and safety equipment was provided to CF members and veterans, including equipment used to determine the presence of DU, and what specific training was provided concerning the use of any such equipment; (m) what, if any, training, equipment and guidance was given to CF members and veterans concerning the handling of both intact and damaged weapons previously used to fire DU munitions; (n) from 1990 to the present (i) what was the CF’s policy regarding transportation, use, exposure, risk mitigation, and testing of DU from 1990 to the present, (ii) how did or does the policy comply with all relevant guidelines and regulations for the protection of the environment and personnel, including, but not limited to, those established in the Canada Labour Code, by the Canadian Nuclear Safety Commission, and through the Workplace Hazardous Materials Information System, (iii) were the guidelines and regulations identified in (ii) followed during CF operations abroad, (iv) how was the policy elaborated in (n)(i), enforced during CF activities both in Canada and abroad; (o) is there a protocol accepted by the government for urine testing for DU and what are its details, including, but not limited to, (i) who should be screened, (ii) following what exposures should screening occur, (iii) which laboratories were or are used for the screening, (iv) what criteria have been used to select the laboratory that conducts the screening and how can quality assurance in screening processes and results be ensured, (v) the maximum acceptable delay between DU exposure to initial screening, (vi) the screening method and how that method was chosen, (vii) the screening schedule, (viii) any follow-up mechanisms, (ix) how screening is documented, (x) when this protocol was accepted; (p) what, if any, screening procedure exists for potential DU exposure for CF members and veterans, including, but not limited to, (i) an exposure questionnaire, (ii) a 24-hour urine collection test, (iii) a detailed physical exam, (iv) clinical tests of organ systems function; (q) what, if any, DU follow-up program or similar program intended to screen and monitor health problems associated with DU exposure is available to CF members and veterans; (r) what, if any, CF members or veterans have been identified and tracked following potential exposure to DU through situations related to (a), (b) and (d), and what was involved in the tracking procedures, specifying whether the tracking included (i) urinary uranium determinations, (ii) clinical laboratory values, (iii) psychiatric and neuro-cognitive assessments, (iv) other forms of tracking; (s) what, if any, summary statistics are now available for cases identified in (r); (t) what, if any, CF members or veterans have been identified and tracked following exposure to (i) vehicles hit with friendly fire, (ii) burning vehicles, (iii) fires involving DU munitions, (iv) the inspection or salvaging of damaged vehicles; (u) what, if any, information is given to CF members or veterans who might have been exposed to harmful DU conditions, and, specifically, how is this information relayed; (v) can CF members or veterans who might have been exposed to harmful DU conditions ask to be screened for DU exposure, if not, why not, and, if so, (i) what procedure do they follow, (ii) who does the testing, (iii) what is the cost of the testing; (w) what are the potential health effects from (i) external exposure to DU, for both low and high dosages, in both the short term and the long term, and (ii) internal exposure to DU, for both low and high dosages, in both the short term and the long term; (x) what, if any, CF members or veterans have applied for compensation associated with DU exposure during military service, specifying (i) the number of requests, (ii) whether compensation was awarded, (iii) whether compensation is pending, (iv) whether compensation is in appeal, (v) how many appeals have been made; (y) have any of DND’s medical or surgical members ever identified a possible link between a CF member’s service or a veteran’s service, exposure to DU, and particular health effects, and, if so, (i) how many times has such a possible link been made by DND’s medical or surgical members, (ii) what follow-up occurred as a result of any identified possible linkages; and (z) does the government have plans to convene a working group to review the latest research on hazardous materials exposure, including, but not limited to, exposure to DU, and possible health effects and, if so, (i) what is the planned scope of the review, (ii) who is to convene the working group, (iii) how are experts to be chosen, (iv) how are conflicts of interest to be avoided and declared, (vi) what is the timeline for the review and the review’s milestones?

Q-12² — June 6, 2011 — — With respect to chronic cerebrospinal venous insufficiency (CCSVI), the liberation treatment, and multiple sclerosis (MS): (a) what consensus documents have been published regarding the diagnosis and treatment of CCSVI, (i) by whom, (ii) on what dates, (iii) what were the recommendations, (iv) were they reviewed by the August 26, 2010, meeting of the CIHR in collaboration with the Multiple Sclerosis Society of Canada (MSSC); (b) why were Canadian members of the International Union of Phlebology (IUP), who were part of the consensus process regarding the diagnosis and treatment of CCSVI, not consulted during the August 26 meeting of the Canadian Institutes of Health Research (CIHR); (c) what are the details of any plan the government has or is developing to collect evidence regarding the diagnosis and treatment of CCSVI, for example, through clinical trials or the creation of a registry; (d) what percentage of surgical procedures in Canada have been double-blind tested over the last 40 years and, for this percentage, (i) what is the risk of complication, (ii) what is considered an acceptable risk of complication, (iii) how do physicians judge acceptable risk and convey this risk to their patients, (iv) what actions do physicians take to reduce risk if the patient chooses to undertake the procedure; (e) when a medical treatment appears to be potentially effective, is its approval ever fast-tracked by the relevant Canadian authorities and, if so, (i) what are any examples of this in Canada over the last five years, (ii) has this ever happened with respect to MS, (iii) if so, who advocated for a fast-tracking and when, (iv) what process was followed to allow the treatment, (v) who made the decision to proceed, (vi) why was fast-tracking deemed necessary, (vii) what were the known risks at the time of the request, (viii) what, if any, negative impacts resulted; (f) what are the reasons for the length of time it has taken the relevant Canadian authorities to implement clinical trials or to develop a registry; (g) why did no member of the August 26 group declare any conflicts of interest, either real or perceived; (h) how many liberation procedures did the August 26 group estimate have been undertaken, (i) which countries were undertaking the procedure, (ii) to which countries were Canadians travelling, (iii) were the practitioners considered to be sufficiently trained, (iv) were the procedures in these countries found to be safe; (i) which people, labs and operating theatres had undertaken the diagnosis or treatment of CCSVI in Canada prior to the August 26 meeting; (j) why did the August 26 meeting not include Canadian experts in the imaging or treatment of CCSVI and for what reasons was Dr. Sandy McDonald not included as a participant; (k) why did the August 26 meeting not include international experts in diagnosis and treatment of CCSVI, data presented at international scientific conferences or site visits to labs and operating theatres, which were or had been undertaking diagnosis or treatment; (l) what is a comprehensive explanation of why the inclusion of CCSVI and liberation experts might have biased the sample of the August 26 group and whether such selection is an established practice at all CIHR meetings; (m) what are all the names of the group members who had spoken out against diagnosis or treatment of CCSVI or the liberation procedure prior to the August 26 meeting, what were the details of their positions, and what are their publically-available comments on the matter; (n) who were all the members of the August 26 group and, for each member, what were his or her stated or declared conflicts of interest or perceived conflicts of interest; (o) what was the August 26 group’s assessment of and comments concerning all reviewed published papers, including both positive and negative observations; (p) did the August 26 group find it unusual that two of the reviewed papers had been accepted for publication in only six weeks, (i) did the group review whether this is a common practice in medicine, (ii) did the group consider how and why this might happen, (iii) did the group explore the expertise of those writing the papers, their experience, how their results compared with those of Dr.Zamboni and, if so, (iv) what were the group's findings for questions posed in (iii); (q) which neurologists, present at the August 26 meeting, had followed MS patients who were diagnosed with CCSVI and who had been treated for the condition, (i) how had neurologists followed them (e.g., appointment, EDSS score/another scale, MRI, neurological exam, etc.), (ii) what, if any, evidence did they present of patients' progress following the liberation procedure; (r) did the August 26 group find the reversal in the MSSC's position, who was part of the greater group, unusual, (i) did the group investigate or consider the reasons for this change in position and, if so, (ii) what observations did it make or conclusions did it come to regarding the reversal; (s) did the August 26 group estimate how its decision might impact Canadian MS patients, including (i) impacts on their mental health and how this might impact their disease, (ii) the number of Canadian MS patients who might feel forced to seek help outside Canada, (iii) how air travel, a compromised vascular system, recent surgery, and lack of follow-up in Canada might impact their disease and, if so, (iv) what are the results of those estimations; (t) what consensus documents are forthcoming, (i) by whom, (ii) when will they be published; (u) what is the work plan for the new expert working group which met for the first time on November 23, 2010, (i) who are the panellists, what are their qualifications and what is their expertise in diagnosis and treatment of CCSVI, (ii) how were the panellists chosen and by whom, (iii) what is the group’s mandate and how was it derived, (iv) what is the schedule of meetings, (v) what is the timeline for the group’s work, (vi) what evidence will be reviewed to reach any decision about possible clinical trials, registry, diagnosis, treatment, follow-up care, etc.; (v) what was the agenda for the November 23 meeting of the expert working group, (i) what abstracts, documents, and presentations were reviewed, (ii) which Canadian and international experts, with experience in diagnosis and treatment of CCSVI, were consulted, (iii) what Canadian and international unpublished data were explored, (iv) what Canadian and international labs or operating theatres were reviewed and visited; (w) for what reasons is the new group going to analyze interim and final results from seven studies funded by the Canadian and US MS Societies and why are these studies considered more worthwhile cases for analysis than other studies already completed; (x) when will the November 23 expert panel declare and post any conflicts of interest, following the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS) guide, on the CIHR website to eliminate the possibility of real or perceived conflicts; and (y) further to assurances made by the President of CIHR, Dr. Alain Beaudet, to the Subcommittee on Neurological Diseases on December 7, 2010, that MS patients who have had the liberation procedure would have follow-up, what are the details of how that follow-up will occur, specifically, (i) how will “a message be sent”, by whom, to whom, by when and what will the message be, (ii) specifically, will all patients who travel or travelled outside Canada be assured that their doctors will see them, that appointments will not be cancelled, that tests will not be cancelled, that they will have access to recommended prescriptions, that they will not lose their long-term care and that they will not be berated for making the decision to have liberation, (iii) how will this be enforced, (iv) what action should MS patients take if they are denied care, (v) to whom should they report a denial of care, (vi) what are the consequences for a physician or health practitioner or organization who delivers care but fails to provide follow-up care, (vii) will follow-up include ultrasound or MRI to image the veins of MS patients and, if so, how often will these imaging procedures occur and who will pay for them?

Q-13² — June 6, 2011 — — With regard to the Champlain Bridge in Montreal: (a) what is the volume of correspondence in which a new bridge is requested or complaints are made about traffic congestion as a result of the maintenance and repair of the bridge as received by the Prime Minister, the Minister of Transport, Infrastructure and Communities, or Transport Canada from (i) individuals, (ii) organizations, (iii) elected representatives; (b) what is the total number of petition signatures received from individuals requesting the construction of a new bridge; (c) what are the names and addresses of the organizations that submitted correspondence as per (a)(ii); and (d) what is the government's reason for not funding the replacement of the Champlain Bridge?

Q-14² — June 6, 2011 — — With regard to infrastructure project applications made under Canada's Economic Action Plan: (a) what is the total number of project applications approved, broken down (i) by municipality, (ii) by electoral district in each municipality; (b) what is the total number of project applications rejected, broken down (i) by municipality, (ii) by electoral district in each municipality; and (c) broken down by municipality, what project applications were rejected and, for each, what was (i) the reason for the rejection, (ii) the amount of funding requested, (iii) the electoral district in which the project would have been completed?

Q-15^1-2 — June 6, 2011 — — With regard to the Montreal Port Authority: (a) was the Prime Minister's Spokesperson, Dimitri Soudas, involved in any way in the appointment of the Montreal Port Authority's Chief Executive Officer; and (b) if the answer to (a) is in the affirmative, (i) what are the details of this involvement, (ii) did the Prime Minister consent to this involvement?


¹ Requires Oral Answer ² Response requested within 45 days