Personal independent Payment (PiP) Support

  • How is PiP assessed?

    PIP is based on how your condition affects your ability to carry out daily living and mobility activities.

    Assessments consider:

    • Safety
    • Reliability
    • Repetition
    • Time taken
    • Assistance required

    The question is not:

    "Can you do it once?"

    The question is:

    "Can you do it safely, repeatedly and reliably?"

  • How Can Sickle Cell Affect PIP Eligibility?

    Relevant symptoms may include:

    • Pain crises
    • Chronic pain
    • Fatigue
    • Brain fog
    • Breathlessness
    • Reduced stamina
    • Mobility difficulties
    • Anxiety
    • Depression
    • Frequent hospital admissions

PIP Application Tips

  • Keep A Symptom Diary

    Track:

    • Pain episodes
    • Fatigue
    • Sleep disruption
    • Mobility difficulties
    • Hospital visits
    • Days you need support


    Real examples are often more powerful than general statements.

  • Focus On Impact

    PIP is not assessing your diagnosis.

    It is assessing how your condition affects your daily life.

    Think About Your Worst Days

    Many people accidentally describe their best days.

    If symptoms fluctuate, explain:

    • How often bad days occur
    • What happens on those days
    • How independence is affected
  • Gather Evidence

    Useful evidence may include:

    • Consultant letters
    • Hospital discharge summaries
    • Pain plans
    • Medication records
    • Occupational Health reports
    • Appointment history
    • Symptom diaries

Coming soon...

PIP Application Support

Practical support sessions designed to help people:

  • Understand the questions
  • Identify relevant evidence
  • Describe their difficulties accurately
  • Avoid common application mistakes


Please note: The Sickle Cell Care Collective will aim to provide application support and guidance and would not provide regulated welfare advice or guarantee benefit awards.