Vlogmas Day 1 : The one with the Cheeky Labrador

/ Myalgic Encephalomyelitis / By
Labrador hits the jackpot on Vlogmas Day 13

Vlogmas Day 1 : The one with the Cheeky Labrador

Having a cheeky Labrador to help when opening parcels can backfire and as he knows that I can’t run after him he has lots of fun 🙈

Join us on our very first Vlogmas video The one with the Cheeky Labrador 😂

Through all of my videos I hope that I can raise awareness of Myalgic Encephalomyelitis and how it affects our lives while giving tips as well as giving advice that may be useful to others with disabilities 🫶

So please enjoy this video of Alfie being a cheeky monkey and I hope this brings a smile to your face the way he makes me smile every day 🫶🫶🫶

Please help me get this video out by sharing it with others with Myalgic Encephalomyelitis or to people who could do with a giggle.

We have lots more to come this Christmas 🎅

This Christmas season has been a whirlwind of house projects, from decorating to new carpets and kitchen flooring. While my home is transforming, I’ve yet to embrace the festive spirit with decorations or wrapped gifts. 🎁 Despite my lack of Christmas cheer, your support has been a shining light.

Thank you for being a part of my community and for following my endeavours, especially on my YouTube channel. Your encouragement means the world to me, and I appreciate the time you take to engage with my content.

As we approach the end of the year, I’m filled with hope and excitement for what the future holds. If you haven’t already, I invite you to check out my YouTube channel, where I share my journey and experiences with Myalgic Encephalomyelitis, Endometriosis, Steatohepatitis, and De Quervains Syndrome. Your support there would mean a lot.

Wishing you a Merry Christmas filled with joy, warmth, and the company of loved ones. Here’s to a new year filled with positive changes and continued connections

The 1st Day Of Vlogmas: The One With The Cheeky Labrador

 

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Related Posts

What is Myalgic Encephalomyelitis

According to the NHS Website, Chronic fatigue syndrome (CFS) is a long-term illness with a wide range of symptoms. The most common symptom is extreme tiredness

For more information please visit https://www.nhs.uk/conditions/chronic-fatigue-syndrome-cfs/

People with ME/CFS have fatigue that is very different from just being tired. The fatigue of ME/CFS:

  • Can be severe.
  • Is not a result of unusually difficult activity.
  • Is not relieved by sleep or rest.
  • Was not a problem before becoming ill (not life-long)

Worsening of ME/CFS symptoms after physical or mental activity that would not have caused a problem before illness. This is known as post-exertional malaise (PEM).

Sleep problems.

Many but not all people with ME/CFS have other symptoms.

Pain is very common in people with ME/CFS. The type of pain, where it occurs, and how bad it is varies a lot. The pain people with ME/CFS feel is not caused by an injury. The most common types of pain in ME/CFS are:

  • Muscle pain and aches
  • Joint pain without swelling or redness
  • Headaches, either new or worsening

Some people with ME/CFS may also have:

  • Tender lymph nodes in the neck or armpits
  • A sore throat that happens often
  • Digestive issues, like irritable bowel syndrome
  • Chills and night sweats
  • Allergies and sensitivities to foods, odors, chemicals, light, or noise
  • Muscle weakness
  • Shortness of breath
  • Irregular heartbeat
Information is taken from The CDC Website https://www.cdc.gov/me-cfs/symptoms-diagnosis/symptoms

Myalgic Encephalomyelitis does not have a cure.

Find a Dr or Consultant who listens to you is the first step

It is a manageable condition and depending on the severity of your symptoms the more difficult this can become.

I advise learning to listen to your body and what it is telling you. If you feel tired rest and if you feel pain find a solution to reduce that pain, this could be through pain medication prescribed by your Dr.

I am not saying that finding a Dr who listens or listening to your body is going to be easy as this illness is incredibly complex for some and manageable for others.

Having a Dr who listens to you or reads about the latest drug that sufferers are recommending can take a lot of unnecessary stress and anxiety from the sufferer.

It would be best for me to point you to the above question What is Myalgic Encephalomyelitis? 

Most pages list the illness as ME/CFS or Myalgic Encephalomyelitis/Chronic Fatigue Syndrome or sometimes even Systemic exertion intolerance disease (SEID).

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