And not too lazy also!

That’s what a second opinion should be all about.

Razvan Mesteriuc its always recommended to get a second opinion

Why would they be? It’s a big fuck you to the other doctor. I’d love to let them know they fucked up.

@@user-jb7tq7ko7e Some doctors won't go against another Dr's diagnosis.

Try keto instead. All these symptoms indicate a metabolically disease

I have have asked doctors specifically for a medication I researched based on my allergies and contraindications, 4 times now they send the prescription that violates all of my needs. And a few times the pharmacy dispensed generic which also was contraindicated, they say because the rx did not say not to substitute. My mom and I have been poisoned a couple times.

@@beverlyanne5699 do you have Eds or a hyper mobility spectrum disorder? Because there some co morbidities that often go along with it. Being on the autistic spectrum… But also mast cell activation disorder…I have loads of allergies too. Another is dysautonomia and POTS postural orthotic tachycardia syndrome. I’ve self diagnosed myself on Eds and pits…arguing to be sent to specialists. Both times I was told that’s very rare, you won’t have that! There was a nurse practitioner who also said it’s mast cell, she’s left. That’s my next battle! She also agreed it was PITS, I’d fallen for years, but in different ways. I got shrugged shoulders, until I smashed my face on a kerb and almost broke both wrists. The a & e dr knew about Eds, did loads of x rays, several ecg because my bp etc we’re going nuts and referred me to find out why I was blacking out. All I want is help to manage them. I don’t want a long list of conditions, I rarely tell anyone or give a brief description of hyper mobility.

This includes vaccines, the most lucrative product made by pharmaceutical companies.

Louise Cramer i have a diagnosis of hEDS and that definitely sounds like eds! I really hope you find a specialist who takes you seriously on it. So many people don't get diagnosed until they're in their 40s or later and it means that a lot of people end up with long term damage that could've been prevented.

So much that. My friends doctor forgot to tell her that a contraindication of her medicine was that her contraception wouldn't work. She found out on her own in time, but it was a close one.

This is true with Lupus as well. I’ve had some people swear on everything that “such and such” cured them, and someone else say that made them worse. I’ve been on injections that helped my pain and exhaustion but caused nausea and rashes. It’s so frustrating but you have to have faith you’ll find the right treatment.

Tracy Watson have you had your calcium oxalates tested? Get them tested darling. It's oxalates that are giving you the issue. Please follow through with that. Carnivore diet all the way. Heal your gut.

I’ve also got Crohn’s disease as well as Granulomatosis with Polyangitisis (GPA) and its symptoms started with purple spots of my legs and elbows.

I have Crohn’s disease too and have had both Erythema Nodosum and Pyraderma Gangrenosum. Since taking bio similar medication - my disease is in remission and no skin issues in over 12 years.

@@catlover6801 That’s awesome. Congratulations. Stay well.

She looks a lot like Catriona Balfe.

Hello how are you doing 👋👋☺️😀

@Debbie's Dilemmas my darling please get your calcium oxalates tested. Please. You're shedding oxalates through your skin. And as well through your intestines and that's causing the inflammation. Oxalates cut. Only 5% of us make kidney stones. The rest of us can have calcium oxalates all throughout our body our organs our muscle fascia and our skin. Bless you on your journey. Carnivore diet all the way. Please have your calcium oxalates checked. It's going to blow your mind. Good luck and Godspeed. I think you're going to be feeling really good sooner than later. Please see the work of Elliott overton. Many blessings

do you mind sharing if the skin lesions match in severity with your GI symptoms? bc my doctors are trying to diagnose crohn’s and i’ve had really strange fluctuating acne/rash type lesions that don’t respond to acne treatments, but i haven’t had GI symptoms in a long time and still getting those rashes so i’m wondering.

Just wondering if you have an update.

Hello how are you doing 👋👋👋☺️

Hello how are you doing 👋👋😀👋

You're so sweet.

Since her issue is autoimmune, she really won't until we find a permanent fix for autoimmune diseases, but knowing is half the battle and we can hope she responds well to her medications.

Wouldn't this be covered in the UK under their universal health care ? We don't pay for dermatologist appts if we get a referral from a gp.

@@cc3184 The clinic you see Emma doing here is "private" which means that you pay to see her. She also works for the NHS (which is "free" at the point of need) Seeing a consultant privately is much quicker and has many more benefits than the cattle market that is the NHS.

I'm praying that you have a diagnosis and are feeling better. Peace

Any updates? Do you also have Chrons?

I still don’t have a proper diagnosis for my skin and was also just dismissed and called a picker. I recently changed my diet to do an elimination diet for GI reasons and my skin COMPLETELY cleared. Clearly being a “picker” is something Drs say because they don’t have a real diagnosis and want to blame the patient.

@@zenbound33 glad you are looking into diet, you will figure out what you react to. I had 2 years of dermotographia hives, turns out it was all the stewed veggies. Once I stopped them it cleared up. I now do low carb, mostly beef, eggs, cheese, butter, bacon. So many health issues, gone now. My RA has gotten better. Bless you, stick with it and find what you can tolerate.

@@nancy9478 I just looked up dermotographia hives-I had no idea that could happen. Really happy to hear you got it all sorted!!

You should consult her.

Go to a different doctor or report the ones who will not refer you

Why not just go to a dermatologist that will accept cash payment or switch primary care doctors. Your current doctor is treating you in humanely.

Uh… Dr Lee has only done that for one patient. All others she had treated as other doctors would.

@@myahill7475 Then let me dumb it down for you. 1) "telling them it’s all in their minds, like what Dr. Pimple does"; Dr Lee has only had one patient that she's told that to and even that person she prescribed medication to help ease the symptoms 2) All other patients that Dr Lee has treated have been given antibiotics and a treatment program. That dumbed down enough for you?

That was clickbait, she clearly explained that there was a psychological 'cause and that it didn't mean the patient was crazy.

@@RomeroRomeral well, the episodes I watched was what I gathered from it.

Yes definitely looks like a goiter I hope she gets that checked out.

Yeah, she could have one. I wouldn't say it's a massive worry unless she's symptomatic. Some people just have goiters but their thyroid functions perfectly and they have no complications. But it would be good to check out in case, especially having an autoimmune disorder. I funnily enough have clinical hyperthyroidism and a toxic multinodular goiter. It's not visible at all. My thyroid is even inflamed at the moment. But I would definitely swap for a harmless, visible goiter. The symptoms are horrible :/

You can really see it at 1:27

@@browniehartz i laughed

yeah its super noticeable at 9:24

I was really hoping she would mention what they were too!

Be sure to have them biopsy. This is how they finally confirmed for me. Took three years.

Amen to that! Glad you got a second opinion! I have multiple health conditions and over the years I’ve had 2 separate 2nd opinions. 1st when I was a teenager and was diagnosed with Chairi Malformation (which I do have) but my surgeon was saying I just had to live with the awful, debilitating, symptoms which basically confined me to bed most of the day. We found a new surgeon on the other side of the country (uk) and my health improved immensely! Second time was just recently when I came down with mysterious neurological symptoms, neurosurgery said it there wasn’t anything wrong so I was passed to the neurologist, 2 years later between the 2 departments I still hadn’t had an MRI or even a blood test and did have and so I found a new DR. I had a diagnosis within 6 months. Crazy!

I am so happy for you That sounded crazy painful.

I am pretty sure I have ichthyosis myself. I've had horribly dry skin all my life, with eczema in areas (depending on stress levels!) My grandfather also had pretty much identical skin. I always described it like "peeling sunburn" because doctors, beauticians, etc never could understand how my skin actually acted - it literally sheds too fast. The advice from everyone (medical and in salons after a massage, etc) is to drink more water and moisturise more. But the way I describe it to them is that once sunburn/tan has started to peel, no amount of moisuturier/lotion/anything will make it "restick" and stop being that dry, flakey skin that is peeling off, and my skin is exactly the same. Once it "starts" to go, the only option is for me to exfoliate it and literally scrub it off. When my skin gets dry (say I shower and don't moisturise) if you look closely, it literally looks like little scales similar to snakes! My doctor has always just told me I have "dry skin" and over the years I have mostly figured out how to cope with it (minimal showering/baths, moisturising after all water contact, exfoliating fully once a week, given up on any attempts at fake tans or getting a tan on hols, etc). But watching an episode of Doctor Pimple Popper she had an older man with legs that looked just like my grandfathers' legs did (and that mine would if I didn't follow my "routine") and it was ichthyosis according to her. When I looked it up online, I ticked pretty much all of the boxes for it. It kinda was a relief to (unofficially) have a name for it, rather than my skin just being "weird" or "dry". When the world settles down I might push my doctor to refer me to a dermatologist, but even then I'm not sure I'll bother because I don't think they can do anything for me as I have a fairly good grip on it as long as I stay on top of my little routine!

@@LovelyLawla i'm sorry you've had to go through that all your life. Ichthyosis seems to be often hereditary from what i read but i didn't have any family history of it. Your routine sounds pretty similar to what i was doing when my skin was at its worst. It was very time consuming but it had to be done. I would soak in epsom salt baths and use a natural pumice stone to lightly scrub my skin, moisturise straight after a shower or bath, use only certain soap free bodywash and fragrance free moisturisers. My derm dr recommended a lactic acid cream to help soften and remove the dry, flaking skin. There are differentvstrenghs so maybe check with a dr first so you don't use to strong of a cream. I tried a urea cream and it hurt so much i cried and had to washnit straight off. If you do decide to go to a dermitologist they may wan't to do a skin biopsy to confirm ichthyosis (just a little fyi). Thats what i had to get done. Again, from what i read, there is no cure but they may be able to tailor a treatment routine to help manage it. Hope you find some relief and answers soon :)

If you can fine the right doctor the first time.

How would you know if they're the right doctor or not before you've seen them? We all make appointments hoping that the doctor will be able to help. My thoughts on this are, don't stick with a doctor who is not helping or isn't listening to you. Get a second opinion, or find another doctor altogether.

I'm sad to say that I have zero faith in G.P's anymore. Dr Emma shows you what CAN be done if you have the means to pay for it and refer yourself to her privately.

Unfortunately, I also don't trust most doctors anymore - even specialists. Too many bad experiences with terrible consequences, being ignored, not believed, not listened to - even though I know my body and can tell when something's off... I'm terminally ill now when I didn't have to be, and it makes me both sad and angry.

@@marinam.2293 Sorry to hear that Marina. x

Yes Kathy, I noticed that too. At age 23 my thyroid gland killed itself off via an auto immune process called Hashimoto's. It took two years to be diagnosed and it almost took my life as i went into a myxedemic coma, my heart rate was 24 beats a minute, I suffered severe angina due to oxygen deprivation.. I tend to always look out for thyroid swelling now on others because I'd hate to see someone else go through the agony and pain of what I endured for 4 years. I hope this young lady goes to a thyroid specialist, pref someone who deals with holistic healing with natural hormone replacement.

@@ozgal6929 oh dear that is awful for you. My Step Sister and Step Brother also have what you have. After my second Baby was born and I lost all the weight I found a golf ball sized lump in my neck. It was a benign adenoma. I had surgery to have half of my thyroid removed alas it has all grown back and is full of nodules. I now have multi nodular goitre! Like you I notice when someone has a puffy neck and suggest they have it checked. Most thank me after they have treatment or surgery. Ever the watchful Empath...🤗🤗🤗

@@katmauriks thanks for your beautiful reply hun. Yes get your entire thyroid removed asap as it does not sound like it's doing you any good with all the growths and you don't want it to turn cancerous. Best of luck in your treatment hun..

I noticed too... I’ve got hypothyroidism and the symptoms of crohn’s, as well has about 10 different skin diagnoses... but underlying all is something called MCAS. Makes a HUGE difference to treat the underlying causes.

LMAO 🤣 "BitChute is a video hosting service known for accommodating far-right individuals and conspiracy theorists, and for hosting hate speech.[a]" "Med Bed technology has been “suppressed” and hidden from the public for a long, long time. Fortunately, due to the planetary shift from 3D to 5D happening at this time, and the increasing demand for transparency by the human collective consciousness, an increasing number of courageous people are coming forward to disclose what they know has been hidden for decades, even centuries, and most likely for thousands of years. Two of these courageous souls are Ileana the Star Traveler (her internet name) and Jared Rand."

Topical*

I was on Azathioprione. For goodness sake. WHY?

I don’t imagine doctors have missed that and not tested it. I had a cystic thyroid that was becoming a goiter. It was not visible, and they noticed it while feeling my neck and glands during an annual check-up. Her meds could be causing her thyroid issue. Steroids can really cause some people to swell in weird ways/places as well.

There is no treatment for hashimoto's. Just treatment to correct the thyroid hormone irregularities

@@frankied.roosevelt6232 it’s an AI so u follow an AI protocol diet among other things

@YeshuaMyKing no. No there isnt any AI diet that treats hashimotos. Its genetic.

That’s not politically correct