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Improving breathing, facial muscle function and pain with Progressive Bulbar Palsy (MND)

Being diagnosed in 2021 with progressive bulbar palsy (MND), this has been devastating and the hardest 3 years of my life. The NHS told me to go home and sort my finances out there is nothing they can do for me accept palliative care.


So the research started and I have tried loads of alternative therapies but now I have found these 2 amazing, intelligent, caring human beings, I know I am in the right place to get the help I need. There are no false promises, only the promise to work with me to help with some of my most concerning symptoms.


After 3 sessions, I have improvements from several awful symptoms:


1) A nerve in my face is now, no longer pulling, making my top lip snarl, it feels normal after 3 long years.


2) My top lip is moving, it's weak but it now moves. 3) My ability to deep breathe has improved.


4) The pain inbetween my shoulder blades has improved .


5) My saliva flow has reduced, I no longer sit with a tea towel on my chest catching the drips.


I am very hopeful that they will continue to improve and will make my life more bearable.


Sarah and Rob - Keep doing what you're doing helping all of us to improve our quality of life. You are both amazing


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The information, including but not limited to, text, graphics, images and other material contained on this website are for informational purposes only. No material on this site is intended to be a substitute for professional medical advice, diagnosis or treatment. Consult your healthcare provider or medical advisor if you are seeking medical advice, diagnosis or treatment.


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