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I have such crazy random symptoms and my doctor won't consider things like MCAS, pots or EDS. She thinks I'm crazy 😭😭😭

This is a very frustrating diagnosis & condition. Thank you for the video.

Thank you for all the support you provided last year!

Вау, it's si good, very good❤🎉

Always always get a second opinion and if that doesn’t work third, fourth…It can get exhausting but you are the only person who knows that’s that there is something seriously wrong happening with your body. It’s scary how patients get dismissed or sometimes made feel inadequate when asking for help.

I’m acc sobbing listening to this. I’m 19 and going through similar, undiagnosed. It’s so difficult.

Merry Christmas!

Merry Christmas and thanks for all your hard work and support you provide for us all ❤xxx

One day they will find its not so rare after all, just under diagnosed...and even harder in Canada to be recognised.

She's lovely and understands restrictions. You don't need to do the movement as the relaxation is enough if we struggle.

Hi Jen, just found your videos. Definite positive shift after doing this exercise. Thanks 🙏

Can psychiatric drugs, antibiotics, h pylori infection, COVID and COVID vaccine injury cause these?

What about multiple chemical sensitivities? Odors and Volatile organic compounds?

What kind of exercise can one do improve mast cells behaviour.? Thank you.

What kind of testing can be useful to diagnose MCD, please, ,thank you. Histamine and tryptase came back as ok . I am suffering from symptoms that you described. Very desperate to get diagnose.

Brilliant information,thank you.

Hi. I really have a problem with closest people at home ,, how can you react to everything,, .....what do i do , relationships are at very very strugle. Thank you.

Yes hope and positivity I like that ❤🎉😊

🎉❤the lovely Deborah 💕😍😊

Have did you get diagnosed with MCAS, struggling to get diagnosis. Thank you.

Great!

You help me so much with this video. They always ask me to do exercises and I always feel sick. I had given up but I learned important things here. I am going to try. Thanks a lot

Big hugs. We mirror in our story, as most of us with EDS, MCAS and POTS. I had a fever of 102 for 4 months and ran every test in the book. Now, I know long-term fevers are indeed a thing. It’s exhausting and utterly debilitating. By hearing the stories of others who share my conditions helps me see myself outside of my eyes, and assists in self-compassion. And you are so right, stability is so important along with medication maintenance.

Thank you, brilliant information.

Fantastic info. Detoxing is crucial in this toxic and polluted world. Thank you.

Hi, thank you so much for very useful information. I would be most grateful, if it is possible to contact you as i am absolutely desperately need help with mcas symptoms. Please.

I've had a very, very similar experience with medical professionals. The favourite 'diagnosis' was anxiety.

Thank you SO much for sharing your story, it was incredibly encouraging to me.

I've bought squishmallow penguin 😊

So deep in that you feel some drip out 2 days later

Id det up because cant take ot anymore..as soon as i enter your flower the seed is ready to explode

I have to fingers to spread the flowee so my tongue drink all of the nectar

Then ask you spread wide open..and i get right there so i can drink you sweet nectar

I could feeling squeeze me from the inside as you start flow as well

Tell him to go deep

Yes

Let me see both in your eyes when your filling starts

I kiss you and hear you whisper in my ear telling me that you want the seed buried in your wet soil

The flow continues

Here we go! Look in my eyes and feel that explotion

Are you ready? Im pulsing so it might be overflow

Id be all the way down while pinch your button

When the knot pulls out, im going right in you.

Here i go!

Have to drag you to the other room while we are coneccted

If i wait i will have get you tied myself ❤

Are ladies close? Im going to wait until you are ready

Im still flowing. I was not expected that

Yes!❤