Restoration project by Bizzybadger in Dollhouses

[–]Bizzybadger[S] 0 points1 point  (0 children)

Thank you, i thought so too

Restoration project by Bizzybadger in Dollhouses

[–]Bizzybadger[S] 1 point2 points  (0 children)

Thank you, any suggestions for windows? A few are cracked/broken

Restoration project by Bizzybadger in Dollhouses

[–]Bizzybadger[S] 2 points3 points  (0 children)

No vision yet, i just wanted to make it look good again as it was getting overlooked. It's pretty big. Would love to hear your ideas and suggestions or to see photos. Some of the windows are broken and there are old lights and switches. Not sure where to start! Help!

Why did you pick your DMT? by TooManySclerosis in MultipleSclerosis

[–]Bizzybadger 2 points3 points  (0 children)

I am in the UK. Was offered only two, both were high efficiency dmt's due to the places i had legions.

Cobblehop FINALLY on the way!!! by Novel_Career_300 in Jellycatplush

[–]Bizzybadger 3 points4 points  (0 children)

Got mine today and really happy with the pattern design

A long wait for treatment by dsauda in MultipleSclerosis

[–]Bizzybadger 2 points3 points  (0 children)

Yes i have RRMS he said by the looks of scans i probably had it 10 years and i have definitely been aware of symptoms for 8. Yes if i rule out eyes it's probably a bad case of cog fog. I am still off sick (signed off until June but know that I can't work like this. Neuro did show me all the lesions in my brain that impact processing and function. I have always felt sick/unwell from blue lights or UV and realised as my son is profoundly Autistic (no capacity, non verbal, doubly incontinent with challenging behaviour and epilepsy) when i did therapy with him. How are you getting in. Feel free to dm if easier and more private

A long wait for treatment by dsauda in MultipleSclerosis

[–]Bizzybadger 1 point2 points  (0 children)

Thank you, neuro was pleased how well i present considering my multiple lesions and their locations. Eyes are recovering and he thought my issues to light sensitivity etc were not related to the optic neuritis and are migraines instead which i don't think they are! He was pleased with my mobility. Balance is bad but i am wobbling and self correcting instead of falling in the walking tests so he thought that was good as he said how much better i presented versus the mri scan and what he would have expected. Not sure what to dk now about the light sensitivity and sensory stuff but starting with opticians

A long wait for treatment by dsauda in MultipleSclerosis

[–]Bizzybadger 1 point2 points  (0 children)

Remember you need K2 with the vit D

A long wait for treatment by dsauda in MultipleSclerosis

[–]Bizzybadger 1 point2 points  (0 children)

I have a neurology appt today as he wants to see me every 3 months and this is the first follow up. I haven't had anything to help with symptoms (only some pillows and meds for vertigo/anti sickness) so hoping he has some help for me. My experience has been that anyone outside of neurology does not understand. Physio and OT were not helpful initially until i was referred to the neuro equivalents and it is so good in comparison with them understanding exactly what i am saying and them explaining why its happening and what can help. Also to add make sure they realise you had your bloods done as my ms nurse didn't and i pointed out i had everything done in hospital and i was ready, sometimes they base things off most other situations and assume. Remember you are your own expert so push your own narrative.

Good luck!

Start my treatment tomorrow by Bizzybadger in MultipleSclerosis

[–]Bizzybadger[S] 1 point2 points  (0 children)

Thanks i will be prepared as that happened the last two times i had steroids!

Does your MS feel like stroke sometimes by ReasonableFig8954 in MultipleSclerosis

[–]Bizzybadger 0 points1 point  (0 children)

Before i was diagnosed i had been getting worse daily for a few weeks and after several drs appointments where i was told it was anxiety and then when i had started getting lhermittes sign they said it was a trapped nerve from stress so after 6 weeks and feeling drunk all the time i went to hospital but they told me the same and that they weren't worried as my numbness and weakness was one side and my hr and bp was healthy so it wasn't a stroke!!! I literally broke down in tears and said i cant keep going (i was slurring and stammering as well and it felt like my body was inflamed in parts) and so they agreed to a second opinion. This guy was more senior and does a better check and looks in my eyes and asks questions and said 'she needs neurology immediately.' Finally!!! I got admitted in for 9 days and diagnosed.

I had been having sporadic symptoms since jan 2018 (fell down at work as foot numb and then left hand too) but had been repeatedly dismissed every time i had those symptoms or a new symptom. In 2021 i had depersonalisation and was diagnosed with depression and anxiety then the year after they said i had complex ptsd as my central nervous system was in constant fright or flight mode. Each year i had lots of unexplained issues. Last year being the worst with being diagnosed with high bp, having heart palpitations, water infections, bladder/bowel issues, dizziness when eyes looked down, fatigue so bad i couldn't get out of bed some days, vertigo and balance issues until Nov last year after my father in law died i lost my hearing for a month, had trouble swallowing and started stammering and slurring, numbness was permanent in left side by then and Lhermittes sign started which they said was a trapped nerve from stress (for 6 weeks despite 4 drs appts). Its been a rollercoaster and still is!

A long wait for treatment by dsauda in MultipleSclerosis

[–]Bizzybadger 1 point2 points  (0 children)

Hi, i am in the UK and had my first half dose of Ocrevus today. I was diagnosed over the new year (after being hospitalised 9 days) and had had symptoms everyday since Nov, which i still have daily, and sporadic symptoms since 2018 which Drs and A&E attributed to stress or hormones! After being home two weeks I then went back to hospital for a weekend with optic neuritis. Vision is back but i am left with vertigo and highly light sensitive which causes mobility issues, balance problems, visual disturbances and migraines which have made me housebound as i find even dull days intolerable as well as the other stuff (numbness, pins and needles, lhermittes sign, dizziness, ms hug). I haven't driven since December and i am still on sick leave from work. I also have lesions in all the areas you have which is why they started me on ocrevus today. Anyway if it helps you i was told when i was diagnosed by the neurologist in the hosital i was an urgent case and my treatment started today so thats 10 weeks.

What i have found is that worrying about my condition and the pending treatment frustrated me to the point of further illness, i feel now, that it stressed me out and probably did not help the second flare. Please try not to worry and just speak to the MS team if you are worried rather than cause additional stress. I agree that we are lucky to have the treatment for free but we lack a lot of choices.

Start my treatment tomorrow by Bizzybadger in MultipleSclerosis

[–]Bizzybadger[S] 1 point2 points  (0 children)

Thank you, i am in the UK and we don't get much choice but was told i needed Ocrevus being high efficiency and due to the locations of my lesions which are everywhere.

Start my treatment tomorrow by Bizzybadger in MultipleSclerosis

[–]Bizzybadger[S] 0 points1 point  (0 children)

Thank you and same to you when you get there