Showing posts with label Long COVID. Show all posts
Showing posts with label Long COVID. Show all posts

Friday, 20 March 2026

Long Covid Can’t Be Ignored Anymore. Now Action Must Follow

During March which is Long Covid Awareness Month, the UK COVID-19 Inquiry has delivered a long-overdue reality check: COVID-19 spreads through the air, and the early responses got it wrong.

For many, this confirmation isn’t new. Patients, clinicians and researchers have been raising the alarm for years, particularly around how COVID-19 spreads through the air. 

Now, it’s official: initial guidance failed to properly recognise airborne transmission, potentially allowing avoidable infections, and long-term illness, to take hold.

The Inquiry also acknowledges something equally important: Long Covid is real, serious, and for some, life-changing. 

If you’re unfamiliar with the condition, understanding what is Long Covid and how does it affect the body is key to recognising its impact.

Millions across the UK have lived this reality. Many have faced delayed diagnoses, inconsistent care, or worse, not being believed at all. 

The report admits that why healthcare access varies across the UK remains a major issue, with patients experiencing a postcode lottery in treatment and support.

Research gaps continue to be a concern. While studies into the long-term effects of COVID-19 on health are ongoing, funding has been scaled back at a time when answers are urgently needed.

Perhaps most concerning is the impact on younger people. There is growing awareness around supporting children living with Long Covid, as the condition continues to disrupt education, development, and daily life at a critical stage.

This isn’t a problem that’s gone away. Long Covid is not a legacy issue, it’s ongoing, and remains a public health concern affecting individuals, families, and communities across the UK.

Every infection still carries risk. And every preventable infection risks long-term consequences. That’s why understanding symptoms of Long Covid explained can help people seek help earlier and avoid worsening health outcomes.

Advocates argue that recognising airborne transmission must now lead to meaningful change. If the virus spreads through the air, then prevention strategies must reflect that reality — especially in healthcare settings where vulnerable people are most at risk.

Right now, protections remain inconsistent. Patients continue to face challenges around support available for Long Covid patients in the UK, with gaps in services and long waiting times still common.

The message from campaigners is clear: recognition is not enough.

What’s needed now is action, including stronger airborne infection controls, better access to protective equipment, and renewed focus on how health policy affects patient outcomes.

There’s also a broader issue at stake. Many people are still learning about coping with chronic illness in everyday life, often without adequate guidance or support.

The Inquiry has taken an important step by acknowledging both airborne transmission and the reality of Long Covid.

But without decisive action, the same mistakes risk continuing.

Long Covid isn’t slowing down.

And neither should the response.

https://www.longcfoundation.org/long-covid-awareness-day-and-month

Friday, 20 February 2026

Rebuilding After “Superflu”: Restoring Stamina, Strength and Well-Being

A tough bout of flu, or something more serious such as some strains of COVID-19, can leave you feeling drained long after the fever fades. 

Fatigue, weakness and breathlessness are common. The key to recovery is gradual progress, good nutrition and sensible exercise.

Start Slowly

Before structured workouts, begin with:

Gentle stretching

Short walks around the house

Light mobility work

Slow, steady breathing exercises

If symptoms worsen the next day, ease back. Recovery should feel progressive, not punishing.

Using a Home Treadmill Wisely

A treadmill offers controlled, weather-proof exercise, ideal for rebuilding stamina steadily.

Weeks 1–2

5–15 minutes walking

Flat incline

Comfortable, conversational pace

Weeks 3–4 (if symptom-free)

Extend to 20 minutes

Add short brisk intervals

Avoid rushing into running

Monitor breathlessness and next-day fatigue. Consistency matters more than intensity.

Rebuild Basic Strength

Illness reduces muscle mass quickly. Start small:

Bodyweight squats

Wall push-ups

Resistance band exercises

Two short sessions weekly is enough at first. Rest between sessions.

Nutrition for Recovery

Focus on:

Protein (eggs, fish, beans)

Wholegrains for energy

Healthy fats such as olive oil

Hydration

Small, regular meals can help if appetite is low.

Supplements: Keep It Sensible

Some people consider:

Vitamin D (especially in the UK winter)

Vitamin C and zinc

Magnesium

Omega-3

Avoid high doses and check with a GP or pharmacist if unsure.

Don’t Neglect Sleep

Quality sleep supports immune repair and muscle recovery. Keep a regular bedtime and limit late-night screen use.

When to Seek Advice

Consult a professional if you experience:

Ongoing chest pain

Severe breathlessness

Heart palpitations

Extreme fatigue lasting months

Final Thoughts

Recovery from “superflu” isn’t about pushing hard, it’s about rebuilding steadily. Gentle treadmill walking, basic strength work, balanced meals and sensible supplementation can help you regain stamina safely.

Progress may be gradual, but it will come.

Monday, 19 January 2026

Cost-Saving Shift to Social Prescribing Lacks Essential Safety Data for M.E.

As the UK government accelerates its national transition toward non-pharmacological treatments (NPTs) and social prescribing in 2026, social enterprise ME Foggy Dog is highlighting a critical lack of oversight regarding patient safety. 

While these community-based interventions are being promoted as a "personalised care" solution, the organisation warns that the shift is primarily driven by cost-saving measures rather than clinical safety data. 

Since 2020, the UK has seen a surge in M.E. (Myalgic Encephalomyelitis), Long Covid, and other post-viral conditions. In response, the 2026 policy direction leans heavily on "low-cost" alternatives to biomedical research and pharmaceutical interventions. 

However, ME Foggy Dog argues that this financial strategy overlooks the biological reality of energy-limiting conditions. "NPTs are being scaled nationally because they are inexpensive, not because they have been proven safe for the M.E. community," Sally Callow, Founder of ME Foggy Dog, told That's Health. 

"Biomedical research and specialist care require significant investment, but diverting patients toward community activities without clinical safeguards is a false economy that risks long-term health deterioration." 

Despite the rapid rollout of social prescribing, there remains no mandatory training for link workers or community providers regarding Post-Exertional Malaise (PEM), the core symptom that makes many physical or mental activities potentially harmful for M.E. patients.

Crucially, while patients have reported health setbacks through PALS and individual NHS clinics, there is still no national system to centrally record harms caused by non-medical interventions. This lack of data was highlighted during the 2021 NICE guideline review and remains unaddressed in 2026.

Through the Shake It Up campaign, ME Foggy Dog is calling for:

National transparency: The urgent creation of a national harm-reporting system to track the impact of NPTs.

Evidence-based policy: An end to ill-informed policymaking, ensuring that any expansion of social prescribing is informed by recorded patient outcomes.

"We are at a critical moment where policy is being built without a safety net," Callow continues. "If the government wants to expand these programmes, it must commit to tracking the consequences. We need influence, policy insight, and amplification to ensure the M.E. community is protected, not sidelined by budget-driven decisions."