Dearest Relapsing Remitting ms (RRms) family. Today is my Monday, whatever day it is for YOU as always look at it with a smile. Go forth with strength and determination. This is your day, treat it as your day. Your day of strength, boldness determination and learning. What will happen will happen YOU have no choice, how YOU react to it is up to YOU though. RRms can be a very long journey, there is no cure, so try not to make every day a struggle and fight,
Be at ease with yourself and have a great day,
Royce 👍
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RoyceNewton
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My day has been quite productive! I had to get bandages and toilet paper out of the linen closet, which requires me to balance on the edge of the bathtub while opening the closet door and then stepping inside into a space that's barely big enough for my feet. I found everything I needed and got back down without any catastrophes. Usually I manage to bring a stack of towels down with me...
oh so well said ..i do believe we do make our happiness and what is to happen will happen and we will be fine ...love and happiness for all and to believe in your self ...love is contagious...hahha..be happy and it can help so many around you...
I had a somewhat productive day yesterday! First, I got a call from my guy at Kia, telling me my car will be ready on Monday 7th, so cue me having to go sorting my FIL out with getting him on my designated drivers list, telling my husband that it'll be alright because he doesn't have to get out of work early, to then realise I've got bloods to be taken at half 4 that day, so would need him to drive me. Then, the plasterer for the room that's becoming a wet room got in contact with me, saying how much it'll cost (pretty cheap, given its nearly the full room) and will be coming on Wednesday. The was my appointment with an epilepsy nurse, who had a student nurse with her. I learned how I should be taking folic acid, but my GPs haven't prescribed it to me! 😤 the nurse did tell me of a medication I could get if I were to go into another status epilipticus. Well, someone would have to do it 😅 it's called buccal medazilam, and thankfully they'd only need to put a syringe in between my gums and inner cheek and squirt it in. Sounds pretty cool, given the number of times I've had a status epilipticus from 2021 to earlier this month. But, the nurse couldn't prescribe it, as she's not a nurse prescriber/practitioner, so will have to wait until I see my neuro 😅 Later on, husband gets home at his usual time at 6, barely sits down to have his brew, then he gets a call from the guy buying his car, saying he's ready for him to take it round. Cue us hunting around the house for (I can't remember the name of it, but it's an important document showing you own the car), finally finding it in a drawer in the dresser in our bedroom, him taking it to the guy, and the guy driving him back home with the £150 he sold it for!Not mad, really. The car is an '06 ford fiesta. All the repairs and the MOTs cost more than it's worth. But, will miss Bessie, the nickname I gave it, from Disney's Mulan and mushu telling the horse, "down Bessie!" 😂 so currently no car, no folic acid, and a naked room 🤣 all on a Monday 😜 next Monday's just as busy! Pick the car up, then go to hospital to get bloods done before the ocrevus infusion on Thursday. Will either need husband to finish early, or his dad to take me and bring me back home 🤔 oh well 😁 the wicked never rest 🤣
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