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Autoimmune expert and MS researcher, teaching the world how to restore health and vitality. #wahlsprotocol
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I also want to say this…

I want to acknowledge that she is still suffering, clearly. And yet her doctor congratulating her for not having MS despite her saying her symptoms are worsening?! Tone deaf. I can understand why that would leave her grieving. Shame on that doctor.

But after all these years, the fact that she feels like she’s starting over because the label was removed? That is telling to me. And it just makes me sad for her. 

I was there once. I just didn’t allow myself to stay there. 

Listening to her speak on her MS podcasts over the years, I felt like I never heard her speak of empowerment over MS. Maybe I’m totally wrong. If she was fighting like hell for her health, please correct me. 

But when I listened to her, the energy I perceived was that she was allowing MS to have power over HER. And I’m a firm believer that the words you speak over yourself, thoughts and energy matter more than people realize.

I no longer say “I have MS.” I say “I was diagnosed with MS” because it is no longer a part of me because I don’t allow it to be. 

And yes, I have been privileged to be able to be able to functional testing and surgery to help me heal, but honestly, what made the biggest difference in my symptoms were free. 

•sleep
•meditation/mindset work 
•nutrition (arguably not free but most have a choice in what they eat)
•movement 
•hydration 

And we are at the age where we have access to so much information! Maybe too much information? But it really comes down to mindset and what you’ll DO with your diagnosis and the knowledge you seek. 

Your doctor sucks? Just wants you believe you’re powerless? Find a new one. Build your team. 

Will you let the diagnosis take over or will you fight and keep asking why? 

I hope Christina continues to fight. I hope she finds the right people to empower her and help her find her root cause. 

I’d love to hear your thoughts too. Let’s discuss. 

Accounts to follow for MS healing empowerment: 

@mathew.embry 
@beatingmyms 
@drterrywahls 
@medicalmedium 

#MultipleSclerosis #ms #autoimmune #chronicillness #lipedema
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Will this day ever just become another random day? Maybe. But I’m just not there yet and that’s okay. 

Sharing this in the hopes of spreading awareness + a cute lil looksie into my psyche as an ms girlie of 8 years. 🧡

If these words resonate, hi welcome. I’m glad we can relate to one another but I also wish it was under different circumstances. Send this to someone you think may benefit from reading + save for yourself as a reminder that it doesn’t rain forever and to meet yourself exactly where you are without judgement. Ilysm

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#MultipleSclerosis #ThisIsMs #MsDiagnosis #MsAwareness #MultipleSclerosisSupport ChronicallyChILL ChronicallyChILLClub MultipleSclerosis Ms ChronicIllnessSupport ChronicIllness  ChronicIllnessAwareness MultipleSclerosisAwareness MultipleSclerosisWarrior ChronicIllnessWarrior AutoimmuneWarrior MsStrong KeepSmyelin Autoimmunediseases Lupus Diabetes POTS Rhuematoidarthritis Fibromyalgia Endometriosis InvisibleIllness ThisIsMs vasculitis MsSupport Spoonie SpoonieSupport Dysautonomia GravesDisease Disability ChronicIllnessAdvocate
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I know only too well how bad MS can get.
But, I also know how good it can get. 

My book shares with you the journey of navigating it all these past 15 years.
Where it now finds me 'Better than Before' as the title suggests. 

My book  is now available to order and the Foreword is provided by the hugely inspiring  @drterrywahls.

Dr Wahls was the first person I knew of who was improving her health, diagnosed with MS.
She inspired me to do the same.

I provide my framework using the principles of Functional Medicine called my 'Hopeful Approach' where I break down in each chapter what I did, that enabled me to change the trajectory of disease.

Comment 'Better' below to get your copy today.
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#drterrywahls #functionalmedicinehealthcoaching ##multiplesclerosis  #wahlsprotocol  #ms_trust
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