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Which nervous system exercises u did to improve symptoms?

Where do you buy the knot tightener tool?

Oh my goodness. I have PRAYED for this. Thank you dear woman for sharing your experience. Exactly what program of Luanne’s did you do? I see the kickstart course, brainfood, ect and they all look great. I’m feeling hope slowly returning. I’ve just been so sick for so long.

Happy for you but I have to say the title was a bit misleading. It sounded as though you were going to share how you healed your mcas, sadly no info on what you did specifically. Felt more like a promotion for signing up for a program to find out.

My child has the symptoms of constipation, bladder issues and Ehlers-Danlos Do you recommend having appointments with this Doctor, or just to do the nutrition program?

So it was mould illness?

Is Cromolyn only a nasal spray or can you take it orally?

What happened to the sound..daughter has this. Mm someone plz help with the sound/ program

So what did you do? Was it a combo of eating differently, breathe techniques, movement? I read your description but I’m not fully understanding..

🙏💖🦋

How are you doing these days?

Thank you very much❤❤❤

Where do you buy your contacts ?

Ok so what if you react to the meds??

Nice video. Thanks. Keep in mind that gluten hydrolysed by acids. I have messed a couple of bread doughs due to acidic sourdough. What i mean is that in high acidic environment (stomach) gluten degrades rapidly. Whatever left is degraded by proteases during metabolic process. It is the imbalance of enzymes perhaps that causes discomfort rather than the gluten itself.

Would like to see you demo using French Wire

Oh my dear Angela. Wrapping an arm around you. You’re taking such good care of yourself. 👏🫂 Thanks for sharing, being so brave and modeling love and care for your family and others.

My issue with H1 blockers are that even the non-drowsy kind lower my blood pressure insanely and cause severe tiredness and mild paralysis of my breathing muscles. I also have a severe allergic response to both sugar and wheat, which is almost every food there is. Sugar lowers my blood pressure almost as soon as it hits my stomach. It becomes impossible to breathe. Potato-based foods cause mild paralysis for me of my fingers and gastrointestinal tract. I have dips that come and go, sometimes I even feel fine. But I cannot exercise with my heart going wild. I worry with the EDS that I will cause one of my arteries to dissect. I have all these things to try to combat my condition (colostrum, quercitrin, cetrizine, pepcid, bromelain, diamine oxidase, etc) but I'm afraid they'll make it worse or just flat out not work. And that's not something I want to know... I don't want to know how screwed I am. I live on mozeralla cheese, and tortilla chips. Last year I lived on potatoes and chicken, but a vaccine I had gotten made my condition go insane and then it messed up my liver and had to get my gallbladder taken out. I don't know how to even approach this condition. The reactions I have to sugar and absorbable materials like vitamins and medications makes it SO hard to start combating this. I should have done this before. I'm only 29, but it feels like I'm at the end of my life. My body is completely shredded inside.

This was so helpful for me to hear how to identify and acknowledge those feelings/beginning symptoms. I get those, but never realized what they are. It was so helpful to see how you work through them. Thank you so much 🙏

You are the only person I see that answers the comments. Bless you and your family. I am so glad you survived. 🙏

I've missed hearing more from you. Its great to have you back on sharing what helps you and all of your followers and family. ❤❤❤

Just wonderful. God bless !

Thank you very much, Angela, you give me hope 💛

What size needle please?

So what changes did you make? Was it all diet? I don’t have any money at all for a program.

What kind of string or thread do you use?

I had a flashback quite a few years back and I can remember a surreal environment with a touch of what I can only describe claustrophobia and being able to hear sounds very close up. it wasn’t dark but red like the light was able to penetrate an opaque layer.

For more content like this, come join me on IG: instagram.com/heartsong_renewed

Is there a kit that we can buy to restring our real pearl necklaces ? If so ..what is the name of it and where can we buy it ? TY

Always so grateful for your posts. ❤

Yea its dark and reddish pink, I also remember being born and the layout of the room, the grey tiles, and everything being blurry and loud, I then blacked out before I almost died from perforated lungs, then Into an incubator for 9 days, I sleep with a fan to this day because I find white noise calming

I signed up for the brain food rebuild your ns thats the right one? The one you did? I just want to do the one you did to heal.

Wow, good show! You are devoted and disciplined with a goal of choosing. Awesome!

Could you please share the information for your practitioner and recommend websites? Thank you.

Did you start to eat vegetarian or vegan ?

Make sure you have B12

GREAT info for mcas/pots/eds on the Turnto app too

Hi Angela! I was curious how did you start following her diet if you were tube fed and not able to eat?

Thank you for this video 💛 Gives me hope!

Wow Luanne and Angela this is so inspiring ! I wish you both well in all you do to help others.

There's info here I never knew. It would be wonderful if children could be assessed for these things because it could completely change the outlook for their life in everything from coping at school to making personal life decisions, and especially how they experience trips to the ER. It could also be incredibly helpful for the mental health. I really do hope change for the better is possible here. I didn't know hip displasia was only a thing for EDS, but that sounds like it would be one of the best signs to pick up on from birth. Thankyou for sharing your story and insights.

You healed paralyses, mcas, ect without change in the nutrition?😊

Immediate chills the minute you let your voice exit your lips. WOW.. PRAISE OUR ALMIGHTY KING JESUS🙌🙌🙌

Thank you so much for posting this video! I have exactly the same issues as you, in my case it really started drastically 7 months ago after I was given an antibiotic that damages the nervous system and was then thrown in psychiatry by my own family who of course have been traumatizing me since I was young but also aren't aware of Mast cells and EDS and POTS etc. Doctors would not believe me, it was a nightmare. Anyways, I am working really hard on my nervous system. I was Als diagnosed with small fiber neuropathy which is common with people with EDS but also is caused by this antibiotic. I have a brain on fire, inflammation, antibodies attacking my own nerve sheets and dopamine receptors. I am 33 yo. I always had difficulties with my nervous system and regulation (unsurprisingly with the family I have). The only thing is that I have had signs of EDS since I was a teenager, but also, they have found the hEDS gene now. I don't think I have hEDS, I think I have classical type, but my very amazing doctor I work with now, an actual MD, says that I should be able to go back at barely having any signs of EDS if I can heal my nervous system and start being active like I used to. And that's a lot as right now, my posture severity according to my X-rays and scans at the nucca was 28. 15 is considered severe. 28 is double that. I never had any issue with my posture until given this antibiotic and being traumatized by family and psychiatrists for months. Now it's at 2.5 after adjustment. But I have no muscle tone at all anymore to hold my back and my connective tissues are sh*t. I really pray this can go away and that I can get my life back. Thanks again for sharing all of this with us. 🙏❤️

Super : ) thank you !!!

You are amazing. So blessed. I am at the end of my hope. My body has hurt for 15 years with many of your issues. I start palliative care this week. God bless you and stay well.

while i was at the peak of being chronically ill my hair got matted, its really thick, i recently cut my hair up to my chin, it was super long.

Do you ever share the actual solution to your problems or is this some affiliate ad

Do you have to eat low histamine for the rest of your life now?

This is scary how similar our stories are *not just the video but the comments* and I am finally figuring things out and excited to start working on it. Thank you for the video and thank you to the commenters ❤️ May we all find more spryness lol and lots of relief. Hang in there. I know we are all in good company.