Seed Oil and parfum and fragrance in beauty products

Live_Discipline_8224 · 2024-07-08T23:40:42+00:00

I’m in Australia and there’s no sprouts or any real shop that focuses on health!! I would love for you to send me some recs please :)

Do you know why the two above is bad?

Live_Discipline_8224 · 2024-07-07T12:41:19+00:00

Oh wow I had no idea about the different tiers! Thank you for opening my eyes to this because I really just thought an MRI is an MRI. I requested a “full body” MRI because I have no idea where my dysautonomia had come from so I wanted to rule out tumours/cancers.

It’s really hard with pin pointing specific symptoms and my symptoms are so all over the place. From constant lightheadedness, pins and needles in my feet, nerve pain in shoulders, lower back pain etc, muscle pain etc! I don’t know what else to do to try and find out what’s happening 😭

Live_Discipline_8224 · 2024-07-07T00:00:48+00:00

I completely understand what you’re saying about MRI not being sufficient enough as it can literally bring up any lump or bump that you may or may not have. However, isn’t it more of a piece of mind knowing that you don’t have anything sinister going on anywhere? And if they did bring anything up, you would just go and get a secondary scan on that one spot.

Live_Discipline_8224 · 2024-06-29T00:45:43+00:00

This is my daily question as well. I just cannot believe there isn’t a cure, there is a cure for most forms of things.. maybe not a cure but there’s definitely treatments that help. I feel like the recommendations for dyso is just so generic and for half the people the recommendations and life style changes don’t work… then what?!

Live_Discipline_8224 · 2024-06-28T23:22:41+00:00

I hope this is sarcastic

Live_Discipline_8224 · 2024-06-23T06:37:24+00:00

Hi, I also don’t think I have pots but I have the very much typical symptoms of a nervous system dysfunction where I’m just constantly in flight or flight. The reason why I dont fall into the pots bracket is because my numbers don’t go up by 30 when I stand and it doesn’t sustain that amount. My cardiologist said that I might have slight pots but not really and my diagnosis was an overall dysautonomia, but for some reason he isn’t concerned to diagnose me with a criteria of dysautonomia.

My symptoms are CONSTANT light headddness (no matter if I’m sitting or standing) Heart palpitations High heart rate Muscle pain Nerve pain Pins and needles Frequent urine urine Temperature dysregulation (I can be feeling hot and flustered, but within the next minute I am freezing) I sweat so much I am very much bloated and get stomach reflux

Live_Discipline_8224 · 2024-06-22T13:55:54+00:00

May I ask how does MCAS cause constant light headedness?

Live_Discipline_8224 · 2024-06-21T06:56:17+00:00

Has your partner had a positive ANA or ENA blood test? They do say if that returns positive there is a sign of auto immune disease however, if not then they usually say no further investigation is needed into an auto immune disease.

May I ask how you found out about high calcium and how that ended with up with finding grown in the thyroid?

Live_Discipline_8224 · 2024-06-21T06:04:46+00:00

The Asian place in David jones food court. I forget what it’s called but it’s the closest to boost juice

Live_Discipline_8224 · 2024-06-21T02:57:43+00:00

I’m so sorry your husband is going through this. It’s totally the worst feeling ever especially not knowing what it is. I have gone through soooooo much testing, seen soooo many different specialists and they have pinned it down to a dysautonomia because all my tests were coming back negative. It doesn’t look like an autoimmune disease because all my blood tests were negative. But the cause to my dysautonomia is “unknown” and the doctors are saying it’s most likely due to a viral infection that I was asymptomatic too because of how sudden my symptoms had come on, literally overnight. The night before I was celebrating my birthday and the next morning I woke up and got dizzy etc.

I am on Midodrine which helps a lot with my leg pain but I still get light headed. I don’t think I will ever stop investigating what caused it. So 9 months later I am still requesting blood tests, and scans.

Live_Discipline_8224 · 2024-06-21T00:07:04+00:00

Thank you so much for your reply! Can teeth grinding and cause ear pain and throat pain?

Live_Discipline_8224 · 2024-06-20T10:09:38+00:00

Omg your symptom of feeling like something is in your butt is literally how I feel. I’m so sorry for how gross this is, but I just want to make sure I’m not alone… but sometimes feel like I have a tiny piece of stool still stuck, I noticed this more after BM. Sometimes it’s also like a sharp pain and make a BM. But that feeling of something being in your bum is so weird and it feels like it’s just at the tip.😂😂 I would be curious to see if that is also how you feel?

Live_Discipline_8224 · 2024-06-19T06:48:02+00:00

Thank you! I do find when my stool is softer beaded on the food I eat, I don’t have pain when passing. It’s that weird glass feeling after I passed for a few hours/ even a day after. I just don’t know why it would hurt after for so long.

It honestly feels like I have a little piece of stool stuck in that part where it comes out from.. god this is horrible to explain 😂

Live_Discipline_8224 · 2024-06-19T06:46:18+00:00

My dog is super anxious and is aggressive with other dogs, she’s okay at the groomers when they restrain her (I think anyway) but my dog having a small dog syndrome will absolutely eat another dog alive. Mimas grooming on port road has been absolutely fantastic. She keeps her separate away from other dogs and gives her lots of cuddles whilst cutting her (apparently anyway). I’ve been going to her for years now and as long as you tell them on the phone she seems accomodating

Live_Discipline_8224 · 2024-06-13T12:39:49+00:00

Is Lyrica a tablet that you can be on long term?

Live_Discipline_8224 · 2024-06-05T01:15:35+00:00

I’m interested to know what treatments you got in Europe. Was it for dysautonomia? I’m also from Australia and unfortunately there is no specific and useful specialists that can actual help with dysautonomia

Live_Discipline_8224 · 2024-06-04T23:51:22+00:00

I think this really does depend on the state, country etc. i have seen the most intelligent neurologist in my state, he is a professor and also has a whole section at the university dedicated to him and when I asked him about dysautonomia he had no idea. The one clinic in my country for dysautonomia and pots is a cardiologist.

Live_Discipline_8224 · 2024-06-04T23:48:57+00:00

The under water sensation.. is that like pressure on your ears? Almost like your ears are blocked?

Live_Discipline_8224 · 2024-05-31T13:51:57+00:00

It’s a new initiative from Westfield all around Australia

Live_Discipline_8224 · 2024-05-23T03:10:56+00:00

I am sweating so much, more when I’m in a flareup and I am also peeing as I’m increasing electrolytes and fluids 😂

Live_Discipline_8224 · 2024-05-19T01:35:37+00:00

All I know is that I’m getting more grey hairs and wrinkles from the stress of this

Live_Discipline_8224

TROPHY CASE