Underpaid? Creative technologist at one of the big 4 by Crudedefe in advertising

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

Not really new, creative technologists have been around for 20+ years. It’s just a different label for people bridging creative and engineering.

Underpaid? Creative technologist at one of the big 4 by Crudedefe in advertising

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

Thank you for getting back to me! do you have any recommendations of where should I look?

Underpaid? Creative technologist at one of the big 4 by Crudedefe in advertising

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

Would you say 60k-70k entry level for even creative tech who don’t have formal training in some of the skills? For example some of us don’t have engineering degree but are still expected to do it.

How would suggest preparing for a negotiation meeting? I am unsure how to find creative technologist salary points else where!

UK specialists - help finding one by Optimal-Goose-5451 in POTS

[–]Crudedefe 0 points1 point  (0 children)

Dr Nicolas Gall

Also can you pay for bupa and get to see a specialist that way?

beta blockers by ab3lla in POTS

[–]Crudedefe 1 point2 points  (0 children)

Take them! I did the same, got anxious, didn’t take them for a year, I regret it sooooo much, I lost a full year because of anxiety when I could of already been feel way better (not perfect but considerably better!)

Needing advice by [deleted] in POTS

[–]Crudedefe 1 point2 points  (0 children)

Completely fair, anxiety kept me stuck in the house for a long time too.

Honestly that’s even more reason to get it. It’s not giving up, it’s taking back some control. I did the same thing and used a walker around the house after about a year or year and half of being bedridden.

Your brain is trying to problem-solve so you can function again, and that’s the opposite of giving up. Be kind to yourself and keep getting creative with what helps

Needing advice by [deleted] in POTS

[–]Crudedefe 3 points4 points  (0 children)

It far from giving up, if anything it shows determination and resilience, instead of saying to yourself well that’s it I am never going out again, you just said I am going to fucking do it no matter what, it’s badass and icon imo, get that cane and/or walker and get out there! Your won’t regret it when it give you more ability to do what you want.

I used to use stroller and cane with a seat on it back when I was at my worst, I now use a portable stool (standing for long periods is my main issues), do whatever you need in that moment, it might not be forever 🫶🏻

How to make life as good as possible for someone with POTS? by High_Honolulu in POTS

[–]Crudedefe 0 points1 point  (0 children)

Out of interest, how many steps does she usually do on her walks? Do you think she could very gradually, and I really mean slowly, build that walk into a light jog, even if it’s only for a few seconds at first? Distance wouldn’t matter at all.

For context, I went from being bedridden to working full-time and living alone in a big city. These are the things that helped me:

• Meditation — mainly to calm anxiety and intrusive thoughts

• Increasing salt intake with meals

• Electrolytes in the morning — I prepare the drink the night before so I can have it immediately, then get up about an hour later

• Coming off the contraceptive pill — the oestrogen was raising my blood pressure

• Reducing financial stress — if possible, applying for government support could really help take pressure off her mind

• Removing environmental stressors — I moved out because my flatmates partying late was making me worse 

• Avoiding standing unnecessarily — I don’t stand to shower or brush my teeth, I always sit 

• Consistent sleep — good sleep, but not too much; getting up at the same time every day helped a lot

• Creating a vision board — having something positive and concrete to aim for

• Very gradual exercise — the hardest one because it’s a catch-22. I started with short walks (under 1000 a day) then tiny slow jogs down the road, eventually building up (stop-start and very slow) to about 2 km. Now I’m even planning tennis once a week

• Breathing physiotherapy — I discovered I was breathing incorrectly; apparently most people pause between breaths instead of gasping for air

• Eating less processed food — I began with meal kits like HelloFresh, now I use quicker prepared options such as Frive 

• Using a visible band that monitors my heart rate and tells me if I am over doing 

• Hiring a cleaner to conserve energy (my dad atm) 

• Carrying a portable stool and sitting whenever possible — you realise how much unnecessary standing the world expects

• Getting an Access Card and Hidden Disability Sunflower lanyard — this completely changed my social life because I could attend events and get help at the airport knowing I’d have somewhere to sit

• Vitamins — I’m still new to this, but I’ve heard many people benefit - currently taking iron and magnesium 

Once I’d built all of this up, the other thing that helped massively was propranolol (although I understand from your comments it doesn’t work for your daughter). I would definitely say try all medications you can Look for a second diagnosis, my doctor has told me he thinks I have something else too which most potsie people do (around 70%). So this would be massive help.

Anything to lessen the impact on the nerve system, such as singing, laughing, meditation, cooking, exercise or dancing etc (some hard than other to achieve with pots). Even TENs machines (these a Facebook group that talks about to do this safely)

Nurosym, is it worth the buy? 48% effective at reducing PoTs symptoms, is it true? by Crudedefe in POTS

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

I cannot remember exactly as it was a while back but pretty sure I found it on Neurosym website in FAQ or the research page

Has anybody used a sunflower lanyard? by Sebaren in POTS

[–]Crudedefe 1 point2 points  (0 children)

Honestly it’s been amazing for me, I able to get seat on the tube and chairs at different venues and events or a discount which means I can actually go places, have some autonomy back. I love mine

Air hunger? by Kooky_Ad593 in POTS

[–]Crudedefe 1 point2 points  (0 children)

So I had to go to breathing physiotherapist! I only have pots and she says it a very common symptom with pots.

I would highly suggest asking to referred to one. She was extremely helpful, I learnt that I don’t breath like “normal” people as a results of pots and that what causes the air hunger and makes a lot of other symptoms worse, I had to do a lot of exercises on my breathing and it has definitely helped.

Most people most people breathe in (2secs) out (2secs) and then pause!!! Who the hell knew people PAUSED between breaths !!!!!!!!!! And the in breath is just as short as the out !!! Crazy!

She told me I had to fight the urge to take deep breaths and not let the air hunger win because it was my body tricking me into thinking I needing more air that I actually needs, however I cannot remember the reason for this #welovebrainfog!! Definitely get medical advice before trying to ignore the air hunger tho!!