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Provincial and Territorial Resources

Accessing Health Services

Below is a list of directories and websites where you can search for health care professionals and services. Other strategies for finding providers with experience with Long COVID are:

  • Word of mouth from other people with Long COVID–people you know personally, people you meet in peer support groups, people who are social media content creators, etc.

  • Word of mouth from providers, through their professional networks. 

  • Guest speakers of Long COVID educational webinars or events or names of providers in this material (see Our Favourite Long COVID Websites for some examples of educational webinars and events).

 

You can ask providers if they have experience with long COVID or ME/CFS. See also Navigating the Health Care System topic.

Primary care and Long COVID care

  • Long COVID Web offers a directory of Long COVID clinics across Canada from (look under “Finding Support and Getting Help” tab). This webpage also contains directories of other healthcare providers (such as physiotherapists and counsellors) who have experience treating people with Long COVID. Please check the list for your province.

 

Occupational therapy and physiotherapy

 

Mental Health Resources and Supports

These resources are for anyone who needs emotional support or mental health support. See Mental and Emotional Health topic for strategies for feeling positive and increasing emotional energy.

General mental and emotional health support

 

Coaching

  • BounceBack is a free skill-building program managed by the Canadian Mental Health Association (CMHA). It helps people of all ages manage low mood, mild to moderate depression, anxiety, stress, or worry. The program is delivered over the phone with a coach or through online videos.

  • Grieving Together is a resource and service by Alberta Health Services to help people impacted by loss.

 

Crisis lines and help lines

  • Suicide Crisis Helpline 9-8-8: Call or text 9-8-8 to reach a trained responder.

  • Suicide.ca is a suicide crisis helpline for anyone thinking about suicide or worried about someone. Call 1-866-277-3553 or text 535353 to connect with a counsellor.

  • Hope for Wellness Helpline is available 24/7 to all Indigenous Peoples across Canada. Call 1-855-242-3310 or go to the website to chat with someone online.

 

Resources for Caregivers

 

Support and general information

  • #MEAction Caregivers’ Support Group is an international Facebook group for caregivers to support one another. 

  • Canadian Centre for Caregiving Excellence is a nation-wide website that offers information and free virtual sessions.

  • Young Caregivers Association website offers virtual workshops and information for young people who are caring for someone with a chronic condition.

  • Care Options is a 4-page info sheet on how caregivers can support the person they care for developed by the Government of Canada.

  • Loving Someone with ME/CFS by SolveME is a 3-page infosheet on how to help someone you love who has myalgic encephalomyelitis/chronic fatigue syndrome, which has many similarities with long COVID. 

  • Family Caregiving by Healthexperiences.ca offers a series of video interviews with caregivers. The stories include experiences related to self-care, the impact of caregiving on their own health, support from family and friends, and more.

  • The Caregiver Space is a website that offers articles and resources relevant for caregivers.

  • Caregiving Matters is a website that offers a resource directory for caregivers by category.

  • Family Caregiver Alliance is a caregiver service based in San Francisco. The website offers online tips and resources for caregivers.

  • Caregivers Alberta offers support, coaching, and resources for caregivers in Alberta, as well as information for employers to support caregivers in the workplace.

  • Caregiver Connections is a program of the Canadian Mental Health Association in Alberta to provide peer support for parents and caregivers of people with mental and emotional health concerns. 

  • Patients4Change is a grassroots initiative to connect patient/family advisors and advocates.

 

Financial information

  • Canada caregiver credit is a non-refundable tax credit for someone supporting a spouse or common-law partner, or a dependent with a physical or mental impairment.

  • EI caregiving benefits provide financial assistance while you are away from work to care for or support a critically ill or injured person.. 

 

Advocacy

  • Carers Canada is a national coalition dedicated to increasing recognition and support for caregivers

 

Finances and Return-to-work

Information for your employer

 

Returning to work

 

Disability benefits and claims

 

Other

  • Donate A Mask is a volunteer-run charity that aims to supply high quality respiratory protective equipment for all Canadians. It offers free masks for people facing financial barriers, as well as an online retail store for masks and other supplies which helps to fund their work.

 

Where to next?

Review the  Tools and Worksheets, Navigating the Health Care System, Mental and Emotional Health topics of MyGuide.

Our Favourite Long COVID Websites

These websites provide general information about Long COVID and resources.

  • Long COVID Web is a Canada-wide network of researchers, health care professionals, people with lived experience, decision makers, and industry representatives with the goal to support and conduct research on long COVID. The website includes a list of resources by province, put together by people with COVID with the support of researchers and doctors.

  • Long COVID Education and Awareness Hub is an initiative of St. John’s Rehab Research Program at Sunnybrook Hospital (Toronto) and the University of Toronto that supports educational and awareness-based resources to support long COVID care and rehabilitation across the continuum of care.

  • The Health Experiences is a research initiative led by academic and clinical researchers. It provides free, evidence-based information about Canadians’ experiences of illness to help inform others and support better care, including for Long COVID, such as video clips of interviews of people with long COVID, organized into 25 topics.

  • Canadian Guidelines for Post COVID-19 Condition (CAN-PCC) is an initiative of Cochrane Canada and McMaster University to produce high-quality guidelines on long COVID that are based on up-to-date scientific evidence and developed with input from clinicians, policymakers, equity-seeking populations, and other members of the public. CAN-PCC also provides plain language recommendations for the management of Long COVID symptoms that are easily accessible to the public.

  • Long COVID Physio is an international advocacy, education, and peer support organization led by physiotherapists living with Long COVID. The website contains general information and videos about long COVID for people with Long COVID and their allies, and these videos have been well received by the long COVID community. The organization also provides peer support to allied health professionals with long COVID via a Facebook group.

  • Long COVID The Answers is a physician-led website (company based in North Vancouver, Canada) that provides information about Long COVID, symptoms and relief strategies, treatments, as well as conferences, webinars, and podcasts. It also includes podcasts that are accredited for physicians for their continuing professional development.

  • Patient-Led Research Collaborative is led by people with Long COVID and other associated illnesses (like myalgic encephalomyelitis/chronic fatigue syndrome, or ME/CFS for short, and postural orthostatic tachycardia syndrome, or POTS for short) who are also researchers. The website contains information and resources for people with long COVID, for clinicians, for researchers, and for the general public.

  • Dysautonomia International is a U.S.-based advocacy and education group for dysautonomia, which is a symptom of Long COVID (see Dysautonomia in this My Guide for more information about this symptom). The website contains information and resources on dysautonomia for patients, researchers, physicians, family and friends, and employers.

  • The Bateman Horne Center is a U.S.-based clinical care, research, and education non-profit that focuses on ME/CFS, fibromyalgia, and other related illnesses. The website provides information for people with Long COVID, health care professionals, and family and caregivers.

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