It was great to see Sally and know she is doing well. It give me hope I could be at the Stage were I’ve worked out how to be a better n me. Thanks Sally andAlex have a joyful 2022
Awwwww! It was SO good to see how Sally is doing!! Thanks for the update, Alex and Sally. I think it's amazing that Sally decided to look for, and accept a new job. Good on her! Too many ppl stay in a stressful and/or, toxic job environment for far too long. I think she'll see a huge difference in her health being at home, with her doggies, with no drama and too much 'business,' going on around her. I wish her all the best. So very sorry to hear about this ongoing cruelty when it comes to her stepdad. I'm in utter disbelief every time I hear a new update. I really hope her stepdad can eventually see the pain he has caused both her and her brother. It's absolutely heartbreaking what he's done. 😪 I hope the celebration of life for Sally's mum is precious and cathartic. All the best for 2022, Sally. I hope you go from strength to strength. 💪 ❤
I can identify with the brother who lives in the mother's house (after she's gone into aged care). Pays no rent, self appointed manager of all my mother's things, just trying to get rid of everything right down to clothes. I can feel Sallys pain. At least she got the ashes. My mother still has my father's ashes after 20 years. He has no resting place and nowhere I can go on his birthday to say hello Dad.
I so needed to hear the part at the end where she talks about the old her would have felt down on herself for moving to a new job and the new her is taking charge of her life. I was at home for almost 9 years and I have tried going back twice. I have cried and been so hard on myself about failing at going back to work because I thought working again was the last piece of the puzzle in putting my life back together. But it’s not the final piece. My life is getting back together and I am just as good of a person even if I am not working. I am working so hard on myself and that is what is important at this point in my life.
I've watched your whole playlist of your journey with Alex and the clinic. Thank you so much for sharing your struggles, being so vulnerable and showing us your recovery 🙏 Yes!! You should be proud of yourself. Love Beki x
It is so lovely Sally has some very good friends to support her through her grief. Thankyou Sally for sharing your story( to the world). Your story and therapy with Alex has been so inspiring. Life is so very tricky for us all managing the best and worst of humanity. Love wins and Sally you are such a lovely special person and your goodness and kindness has shone for us all. Wishing you all the best Sally on your healing journey you have done so well. I am very grateful to have been a part of your journey., it has been so very helpful for so many of us witnessing and sharing your ups and downs. Thankyou so very much. Bless you.💔
Alex , is part of your reset programme - diet and exercise? Also I notice the participants are so pale…they need some sun ☀️ or vitamin D ? New Zealand is experiencing the wettest year ever and it is depressing. The sun ☀️ lifts energy.
so did Sally how she her cfs symptoms were then ? so two years of therapy and still dealing with physical fatigue and pain symptoms ? Genuinely curious . I can see she is growing psychologically but has she got well after two years ? Did any of the supplements actually help ? It seemed in the previous videos she went up and down with symptoms but did not get really well ? This is why the NhS will dish out pills and not pay for therapy, because therapy takes a long time and costs a lot of money.
‘Really poorly still’ - try having CFS, Fibromyalgia AND MANY OTHER CONDITIONS for decades!!!! And try not being able to work AT ALL, and having to rely on benefits!!!
CONGRATULATIONS SALLY AND ALEX YOU ARE HONESTLY GREAT! 🔻 🔸 🔹I am following your channel! I follow your journey closely 🔻 ! Also to everyone who is seeing this comment I want you to know that it doesn't matter which black hole you are in, you can come out stronger then before and achieve every goal you decide to achieve. But if you decide to, don't stop when things get uncomfortable.🖐 🖐 I promise at this stage it can just get better ! Love You ! Happy holidays !!
It was great to see Sally and know she is doing well. It give me hope I could be at the
Stage were I’ve worked out how to be a better n me. Thanks Sally andAlex have a joyful 2022
Awwwww! It was SO good to see how Sally is doing!! Thanks for the update, Alex and Sally.
I think it's amazing that Sally decided to look for, and accept a new job. Good on her! Too many ppl stay in a stressful and/or, toxic job environment for far too long. I think she'll see a huge difference in her health being at home, with her doggies, with no drama and too much 'business,' going on around her. I wish her all the best.
So very sorry to hear about this ongoing cruelty when it comes to her stepdad. I'm in utter disbelief every time I hear a new update.
I really hope her stepdad can eventually see the pain he has caused both her and her brother. It's absolutely heartbreaking what he's done. 😪
I hope the celebration of life for Sally's mum is precious and cathartic.
All the best for 2022, Sally. I hope you go from strength to strength. 💪
❤
Well done Sally. Not easy to manage the loss of your mother's clothes and personal belongings. I hope the grief eases.
Yep, she's come a long way. It's great to see.
I can identify with the brother who lives in the mother's house (after she's gone into aged care). Pays no rent, self appointed manager of all my mother's things, just trying to get rid of everything right down to clothes. I can feel Sallys pain. At least she got the ashes. My mother still has my father's ashes after 20 years. He has no resting place and nowhere I can go on his birthday to say hello Dad.
fantastic thank you both x
I so needed to hear the part at the end where she talks about the old her would have felt down on herself for moving to a new job and the new her is taking charge of her life. I was at home for almost 9 years and I have tried going back twice. I have cried and been so hard on myself about failing at going back to work because I thought working again was the last piece of the puzzle in putting my life back together. But it’s not the final piece. My life is getting back together and I am just as good of a person even if I am not working. I am working so hard on myself and that is what is important at this point in my life.
I've watched your whole playlist of your journey with Alex and the clinic. Thank you so much for sharing your struggles, being so vulnerable and showing us your recovery 🙏 Yes!! You should be proud of yourself.
Love Beki x
It is so lovely Sally has some very good friends to support her through her grief. Thankyou Sally for sharing your story( to the world). Your story and therapy with Alex has been so inspiring. Life is so very tricky for us all managing the best and worst of humanity. Love wins and Sally you are such a lovely special person and your goodness and kindness has shone for us all. Wishing you all the best Sally on your healing journey you have done so well. I am very grateful to have been a part of your journey., it has been so very helpful for so many of us witnessing and sharing your ups and downs. Thankyou so very much. Bless you.💔
Love this information. You should be doing a Netflix series you deserve even more support !
It would be lovely to see how Lauren is doing. Such an eloquent person
She had verbal diarrhoea
Alex , is part of your reset programme - diet and exercise? Also I notice the participants are so pale…they need some sun ☀️ or vitamin D ? New Zealand is experiencing the wettest year ever and it is depressing. The sun ☀️ lifts energy.
so did Sally how she her cfs symptoms were then ? so two years of therapy and still dealing with physical fatigue and pain symptoms ? Genuinely curious . I can see she is growing psychologically but has she got well after two years ? Did any of the supplements actually help ? It seemed in the previous videos she went up and down with symptoms but did not get really well ? This is why the NhS will dish out pills and not pay for therapy, because therapy takes a long time and costs a lot of money.
Umm ❤❤
‘Really poorly still’ - try having CFS, Fibromyalgia AND MANY OTHER CONDITIONS for decades!!!! And try not being able to work AT ALL, and having to rely on benefits!!!
CONGRATULATIONS SALLY AND ALEX YOU ARE HONESTLY GREAT! 🔻 🔸 🔹I am following your channel! I follow your journey closely 🔻 ! Also to everyone who is seeing this comment I want you to know that it doesn't matter which black hole you are in, you can come out stronger then before and achieve every goal you decide to achieve. But if you decide to, don't stop when things get uncomfortable.🖐 🖐 I promise at this stage it can just get better ! Love You ! Happy holidays !!