Silent No More: The Urgent Need to Connect SCA Survivors

When a heart suddenly stops beating, and life is brought back from the brink, the journey is far from over. As the trustees of Sudden Cardiac Arrest UK, we’ve witnessed the profound impact that peer support can have on survivors and their loved ones. Today, we want to share why our mission to reach every sudden cardiac arrest (SCA) survivor in the UK is crucial and how you can help us make it happen.

The Silent Struggle After Survival

Imagine waking up in a hospital bed, confused and scared, with no memory of how you got there. That’s the reality for many SCA survivors. While medical professionals save lives, they often lack the resources to address the complex emotional and psychological aftermath of such a traumatic event.

Our members consistently tell us that joining our support groups has been life-changing for their recovery.

Why?

Because they’re no longer left in the dark, struggling alone with questions, fears, and challenges that only fellow survivors can truly understand.

More Than Just a Facebook Group

Photo of a We Have More Signage

Sudden Cardiac Arrest UK started as a simple Facebook group for sharing experiences. Now, with over 3,000 members, we’ve evolved into so much more:

  1. A community of understanding: Where survivors and co-survivors can connect with others who’ve walked in their shoes.
  2. A source of vital information: Providing resources on recovery, lifestyle adjustments, and navigating the healthcare system.
  3. A platform for advocacy: Raising awareness about SCA and pushing for better support systems.
  4. A beacon of hope: Showing life after SCA can be fulfilling and meaningful.

The Power of a Simple Leaflet

Our “Effective Peer Support” leaflets are more than just pieces of paper – they’re lifelines. These leaflets:

  • Introduce survivors and their families to our organisation at a critical time
  • Provide essential information when it’s needed most
  • Guide people to our online communities and resources
  • Offer reassurance that support is available
SCA_Leaflet_Oct_2023_V5

The Challenge: Reaching Every SCA Survivor

Here’s where we face a significant hurdle. While we’ve built a strong online presence, we know we’re only scratching the surface. Many SCA survivors, especially older individuals or those less comfortable with technology, might never find us through social media alone.

Our goal is ambitious but vital: we want our leaflets in every hospital and cardiac centre where SCA patients might receive care. This means:

  • Printing thousands of leaflets
  • Distributing them to over 250 locations across the UK
  • Regularly replenishing supplies to ensure constant availability

The Reality: It Takes Resources

Silver and Gold Coins on White Printer Paper

This crucial outreach effort comes with challenges:

  • Printing costs: Producing high-quality, informative leaflets isn’t cheap
  • Distribution logistics: Getting materials to hundreds of locations requires careful planning
  • Ongoing maintenance: Ensuring a steady supply demands constant attention
  • Volunteer time and effort: Our dedicated team puts in countless hours to make this happen

Why It Matters

Every day that passes without our leaflets in these hospitals is a day when a survivor or family member might feel lost and alone. It’s a missed opportunity to provide comfort, guidance, and hope at a critical moment in someone’s recovery journey.

How You Can Help

We need your support to make this vision a reality. Here’s how you can get involved:

  1. Spread the word: Share this post to raise awareness about the importance of peer support for SCA survivors.
  2. Contact your local hospital: Ask if our “Effective Peer Support” leaflets are available for cardiac patients.
  3. Volunteer: We’d love your help if you have skills in logistics, printing, or healthcare connections.
  4. Donate: Every contribution, no matter how small, helps us print and distribute more leaflets.
  5. Join our community: If you’re an SCA survivor or co-survivor, join and contribute to our cause.

Together, we can ensure that no one faces the aftermath of sudden cardiac arrest alone. Let’s get our life-changing support into every hospital and cardiac centre in the UK.

Will you join us in this mission?

If so, contact us and get some leaflets in your hospital.

Please share your thoughts in the comments below, and let’s start a conversation about how to make a difference for SCA survivors and co-survivors nationwide.

3 thoughts on “Silent No More: The Urgent Need to Connect SCA Survivors”

  1. Paul,
    You continue to amaze me with the good work you do. Not sure exactly what I can do from the US, but let me know.
    Also, I am happy to talk anytime.
    Steve

    Reply
    • Hi, Steve.

      Although I live in London, UK since 1975, I am a US born native of New Jersey. Where are you from? Always glad to hook up with folks from the old country!

      Reply
  2. I’ve realised that I only sent a message to Steve because he’s a fellow American. My own SCA journey is beginning to cause me more worry. I think it’s because I have survived for so long; it’s been 30 years since my first arrest. Whilst I have come through fairly successfully and have the best care available via Harefield who have been absolutely fantastic, I am aging and slowing down a bit (I am 76, after all); my cardio team know that I’m a very aware patient and always want full explanations of everything. No question I ask is ever batted away, etc. I think the key to my being able to cope with all of it is to be of help to others. Several of the regulars on our site will already know me as one of the “oldies” who has been around the block a few times. I really feel that the best thing for my sense of well being is to be there for the relatively recent survivors who wake up in a cardiac unit wondering what the hell has happened. That’s how I can volunteer most effectively. My only limitation is that my driving licence has just been suspended for the statutory six months after my ICD paced me 2 weeks ago during the worst of several VT events since the Summer. My docs are trying me out on an additional medication to get me back to something approaching normal. Also, November is going to include several diagnostic investigations and a major followup with my cardiologist. We shall see.

    Reply

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