A Cuddly Labrador, A Sneezy Labrador and a Funny Labrador

/ Chronic Illness, Disabled blogger, Myalgic Encephalomyelitis / By

A Cuddly Labrador, A Sneezy Labrador and a Funny Labrador it must be Vlogmas Days 14 & 15.

📆 This video was published on or around 17th December 2023

Welcome to my enchanting world, where the holiday spirit dances in each frame, somedays🎅✨

The bad days show no sign of letting up It is times like these that I am so thankful for Alfie, Alfie is always ready for cuddles.

My poor little Alfie is still suffering with his ears a little, I’m hoping that we have had the worst of it now.

I’m sure he loves getting extra cuddles and being spoilt.

Every day with Alfie makes me feel like I won the lottery. He is just amazing 🥰

I was sure that I had talked about my amazing coffee maker before but I can’t seem to find it anywhere so here is a fabulous Christmas Gift Idea for you.

By subscribing to Lavazza you are able to get one of their amazing coffee machines for just £1!!!!

You do need to subscribe to have your coffee delivered by Lavazza but as this was something I would have done anyway this was a big win for me.

🎄Today we have opened 2 days together in the hope of catching up on Alfies Advent Calendar 🎄

🎄In this, my very first year of Vlogmas, join me, Alisha, as I navigate through the festive joy and share snippets of my daily with Alfie my Black Labrador 🎄

🌟 Spread the Joy: Vlogmas Days 14 & 15

Let’s make this season brighter together! Don’t forget to hit the like button, subscribe, and ring the bell to stay tuned for more inspiring content.

Share your favourite holiday traditions in the comments below; I’d love to hear from you!

Join me on this journey, and let’s raise awareness together.

Every view, like, and share contributes to making a difference.

🫶Thank you for being a part of this festive adventure! Let’s create a community of warmth, understanding, and positive change.

Together, we can make a difference.🫶

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 advice that may be useful to others with disabilities 🫶

#Labrador #BlackLabrador #Disabled #AlishaVlogmas #Christmas #FamilyChristmas

#funnydogvideo #funnylabrador #myalgicEncephalomyelitis #italiancoffee #Christmas #Lavazza

A Cuddly Labrador, A Sneezy Labrador and a Funny Labrador for Vlogmas Days 14 & 15

Vlogmas Days 14 & 15

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Black Labrador wearing red pyjamas with reindeers on them

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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