Yes! The cold weather determines how severe my ME/CFS will become not only for the cold months but how it will permanently affect me moving forward. My doctors have a hard time for some reason understanding how the winter affects ME/CFS, which I cant figure out what is so hard to understand. I live on a farm with black angus cows in the US. We own chickens, but I can no longer have eggs. I will admit when you have so much eggs you do get sick of them so I don’t miss eating them.😅
Really enjoyed another travel vlog! This sounds like such a lovely short vacation and definitely something I'd want to do down the line - I've been trying to make a list of vacation sites in the uk we can go to and have a nice time. This seems like it would fit our vibe nicely
Fantastic! As always, thanks for sharing! I hate it when I get dizzy too. As you said, not very often, but I've had the whole world turn sideways on me a few times.
@@LifeOfPippa "Grim"... yeah. Once I was on a solid wooden bench, leaning forward with both arms on the table, and the house flipped on its side. Nobody else was concerned, so I knew it must be just me. I froze, knowing that as long as I didn't move, I was secure in my seat, and would be safe.
Lovely place. Glad you had fun! 😊 I'm also currently going though that difficult adjustment period with worse ME symptoms and lower energy that comes with autumn/winter 😞 I thought it was only me who experiences this marked change...
Aah loved this vlog. Love seeing the autumn colours and the Highland cows. I find too that the start of colder weather is hard on the ME. I can relate also to dizzy spells. Did you buy any books?
Thanks Michelle! I didn't buy any books this time - as much as I hate to admit it, it was quite a battle to move around and have a proper look in there!
That was lovely!!! ❤ I do love animals and those highland cows are so adorable!!! 🥰 This past winter (southern hemisphere) was incredibly painful for me and I just kept dreaming of winning lotto and moving somewhere warm! 😭 But heading towards summer soon and Spring weather has been a lot easier. Probably my energy levels were affected too, but it's hard to tell as I was already declining. It's only been 15 months since symptoms started, so a lot of learning to do. Thanks so much for sharing your adventure in the Scottish country! 🙏❤️
Im 65 got me 5 yers ago, probably moderate, can walk a bit, need a wheelchair. I was refused PIP and Blue Badeg 2 years ago. Should I apply again as I think I am currently not eligible for VAT relief?
Yes! The cold weather determines how severe my ME/CFS will become not only for the cold months but how it will permanently affect me moving forward. My doctors have a hard time for some reason understanding how the winter affects ME/CFS, which I cant figure out what is so hard to understand.
I live on a farm with black angus cows in the US. We own chickens, but I can no longer have eggs. I will admit when you have so much eggs you do get sick of them so I don’t miss eating them.😅
Really enjoyed another travel vlog! This sounds like such a lovely short vacation and definitely something I'd want to do down the line - I've been trying to make a list of vacation sites in the uk we can go to and have a nice time. This seems like it would fit our vibe nicely
This looks like a perfect place for me to chill and rest while mum cycles and explores the area. Website gives no indication of prices per night.
I'm struggling too in this cold weather
Whenever the weather changes... Auch! Everything hurts.
Oof, agreed - I'm especially feeling it today! Sending love!
❤❤
Fantastic! As always, thanks for sharing!
I hate it when I get dizzy too. As you said, not very often, but I've had the whole world turn sideways on me a few times.
It's such a grim feeling isn't it?! Thank you for watching!
@@LifeOfPippa "Grim"... yeah. Once I was on a solid wooden bench, leaning forward with both arms on the table, and the house flipped on its side. Nobody else was concerned, so I knew it must be just me. I froze, knowing that as long as I didn't move, I was secure in my seat, and would be safe.
Lovely place. Glad you had fun! 😊 I'm also currently going though that difficult adjustment period with worse ME symptoms and lower energy that comes with autumn/winter 😞 I thought it was only me who experiences this marked change...
Every year I think the same! But you're not alone 💜
Aah loved this vlog. Love seeing the autumn colours and the Highland cows. I find too that the start of colder weather is hard on the ME. I can relate also to dizzy spells. Did you buy any books?
Thanks Michelle! I didn't buy any books this time - as much as I hate to admit it, it was quite a battle to move around and have a proper look in there!
That was lovely!!! ❤ I do love animals and those highland cows are so adorable!!! 🥰
This past winter (southern hemisphere) was incredibly painful for me and I just kept dreaming of winning lotto and moving somewhere warm! 😭 But heading towards summer soon and Spring weather has been a lot easier. Probably my energy levels were affected too, but it's hard to tell as I was already declining. It's only been 15 months since symptoms started, so a lot of learning to do.
Thanks so much for sharing your adventure in the Scottish country! 🙏❤️
Really hope much kinder days are on their way to you! 🫶🏻
Im 65 got me 5 yers ago, probably moderate, can walk a bit, need a wheelchair. I was refused PIP and Blue Badeg 2 years ago. Should I apply again as I think I am currently not eligible for VAT relief?