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Looks like they didnt make the beds up very well. Becky

Thank you for your informative stories

Hopton is a lovely site. My favourite x

🧡

Ooh just realised you put the same clip in twice LOL [the bit that says its where you had your ears pierced] ! Loved your 2 part vlog though, you're a lovely lady.

Yeah, "snowflake" disease, different for everybody. With my MS I don't have pain but have tingling and numbness in my feet. I walk like a drunk and have strength issues in my legs. Walk with a cane in public, have a hard time with stairs (need to pull myself up with handrail), stepping up curbs, etc. But try not to use a cane if I can. Try to force myself to walk. I was in college part time this winter, only took 3 classes, 4.0, so don't think I have memory or cognitive issues..... yet! Have fatigue, worsens as day goes on. I worked this weekend, came home went to bed at 9:00 PM slept until 4:00 PM the next day. Have bowel and bladder issues. Mine are similar: I have leakage (bladder) but have trouble going when I think I have to go. Bowel is different: If I feel I need to go soon, I must go! Because there is a point where I cannot hold it. I will maybe have 20 to 30 minutes to start looking for a place to go if I am away from home. I also have speech issue (talk like I'm, drunk), comes on as I get fatigued. I ironically have chronic insomnia too. My vision issues may be unique, not heard anyone else that experiences this. Worn glasses for years, but sometimes still have vision go blurry or double vision that goes away after a few minutes. With glasses on.

Also does it have direct access to the beach? Thanks xx

Hi looking at trying this site normally go caister, does it have a playgroup? Swings etc x

I just stayed at Greenways 72, we loved it!

I hope you enjoyed your stay with us from Alan in Lowestoft a cleaner at Hopton Haven 😊

Is there cross road in the arcade? 😊

Great video. We're heading there tomorrow.

I LOVE this song 😊 great video Tara 👍🏻🙂

My heart broke for you. I deal with the same thing. I find its best that nobody touches me when it happens. I forced my arm to straighten once and it really hurt my muscle after the contraction was done. I have MS which makes it happen. I'm not sure if that is what you have. I have to be on several meds for my nerves and 1 muscle relaxer I take regularly.

I look forward to each of your vlogs, thank you x

Thanks

When were you there please?

Great vlog love watching universal vlogs as never been there before

your eldest is your twin! ❤

Fantastic vlog as always x

I really love the costumes that they are wearing

Lovely vlog as always. You do amazing as its such a physical demand on the body going through the parks even for fit people. Your girls are so lovely. Tilly is your double. In this vlog you were like twins walking through the emporium. Take care and hope you are keeping well.

Have you ever looked at cervical cranial instability (CCI) when neurologists can't find anything wrong it's usually that. the atlas c1 and c2 aren't aligned properly and it irritates the vagas nerve.

I am proud to be one of your subscribers! 😊 As a young woman newly diagnosed with MS who always loved going to Disney every year, I really appreciate hearing your experience! By just sharing your adventures I've learned quite a bit about how I can make another Disney trip possible while protecting my health. Thank you for sharing the highs and lows of a Disney vacation with a disability, it is very helpful and inspiring ❤ Cheers from the US! I hope you and your lovely family are doing well!

Wow 🤩 your 2024 trip , is like a fantasy trip come true !! I cannot wait to see all the wonderful vlogs you will make while on your in LA and Hawaii !! I bet the girls are beyond excited 😆

Looks like you had fun! We were there last week. Fun but exhausting, I feel like I need a vacation from my vacation lol.

We absolutely love Pop Century, the skyliner is the icing on the cake!

Thats my 4th favourite Park as well

I use a heating pad..it really helps.

How long was the flight?

Love the gastons cinnamon roll

Where did you get the waffles from?

Do you have any proper old videos of the layout of the park was like? If you don't mind me asking... They was my childhood memories. It's such a shame they changed it all 😢

Great vlog do you like staying at the Pop hotel , have been looking at staying their

hi , i have this and i want to know too and asked a few , its when im super stressed so i wonder if cortisol, (im like the child in exorcist ) ,,, how u doing ?

Hope you have been able to get some relief since posting this video. I have a long history of similar spasms. Wish I had answers for you. I was first diagnosed with MS, then it was discovered that I have spinal compression. Neither seems to really explain the severity of the spasms. A combination of baclofin, daiazepam, and tizanidine seem to keep it under control most of the time. Of course all can be sedating. I have to try to balance what to take and when. When things are at their worst there is nothing to do but take tizanidine and sleep until my body relaxes.

When you have insomnia and discomfort try some magnesium carbonate called Calm.

Hello, Im your new subscriber. What was your diagnosis in your ms? Where i can message you for privacy

Hi, What causing your heart rate while doing nothing, by stand up or walking?

I’ve been in terrible pain for 30 years with this MS. I was only diagnosed 2 1/2 years ago so it’s been a rough journey. You are brave. Your plea has touched me. I wish I could give you some tips. It can go right into the bones. I hope you find relief. They are full of useless pills, gadgets and declare themselves knowledgeable. They know nothing as you are the one in it. I will have a think….

I've had a lot of what could be MS symptoms over the years, but there have been recent events that are more concerning and the neurologist had no clue. For a period of a few days my legs felt like they were a foot or two in front of my body and it made me feel like I needed to lean forward so I wouldn't fall backward which ironically made me feel like I was going to fall forward. Another scary event was when I got total paralysis and lack of sensation in my leg while lying in bed. It lasted a couple of minutes and I was finally able to kick it with my other leg and it was like the switch flipped back on. I've had lots of numbness, etc. over the years and that was definitely not what this was. The MRI on my brain and spine were done without contrast so I hope they didn't miss lesions. My wife asked me if I maybe had MS and I kind of felt like that could be ruled out because of the MRI, but it makes me wonder how much of it can go under the radar. Thanks for helping in my search for answers.

Would u suggest getting the chicken and donuts when we got to homecomin

Hi I have just come across ur smear video well done you for doing that I was just wondering did you get them results and was I still hpv positive ect sorry o know it was a while ago lol x

Also the Market Chips are the best!

You cannot beat the snail ride! I love Yarmouth and Hopton. I'm off to Hopton on Friday

amazing xxx

I love watching your videos xxxx

that sprinkles cupcake was amazing .

Cardiologist told me its autonomic system dysfunction of multiple sclerosis

How are you