Motor neurone disease
Posted: Mon Jan 14, 2008 7:41 am
From: Jean Doherty [mailto:clellyd@bigpond.com]
Sent: Monday, 14 January 2008 5:27 PM
To: Lesley Lee
Subject: Request for assistance in Motor Neurone Disease
A colleague has asked for help..
Dear Jean,
I have a new client, who strangely enough I am seeing both at the ILC and in my clinic – that was by co-incidence – and he has motor neurone disease, the type that starts with muscular atrophy in the head and neck. He can still walk but his head rests right down on his chest as he does so. He was referred by a dentist from Sydney, who has “heard of my work” and who has a very alternative approach. I have taken his photos and done a facial analysis as well as taken his case history and have repertorised the case. If am wondering whether you or anyone in your list serve has had any success with a patient with this diagnosis. I have told him that I don’t know whether I can help but that I think it is worth a try. Therefore, with a case like this, any help would be much appreciated.
Many thanks
Lesley
I looked up muscular atrophy in Rep Virosa and found a match to Tick bite but it is motor neurone which does not show there . lso asked what was going on at the time illness started. 2nd letter.\>>
Not really. I do wonder whether it was a vaccination issue, as he has had a flu vax each year but there is nothing solid to be sure about that. His mother was dying at about the time he was diagnosed. There is some evidence of heavy metal stuff I think with this condition but he has had all amalgams remove after the diagnosis. I am going to do some dousing and ALS shows Plumb as a big one and he fits into that miasms photo-wise. I am going to read it more thoroughly. It is such a dreadful condition – they are about ready to give him a peg and looking at him, I think that is wise.
I will ask him about a tick bite – it really can be very nasty – but he didn’t mention it in the history.
3rd letter >>>His wife rang to cancel both the appointments – here and at the ILC [Lesley works there as an occupational therapist ]- as he is in hospital. He saw Dr xxxxx for lung condition and he referred him to a sleep clinic – that is another possible clue – extreme insomnia over the past several years. It is hard getting information, as he is unable to talk. He communicates by writing on paper – but as he can’t see and his hands don’t work well it is hard to work out what he is writing very often. He also writes on his hand and his wife can read what he is saying usually. However, it is all very frustrating for all concerned. It is such a diagnosis of doom, that I do wonder whether anyone has had any success with it, and since I have stopped being on the list serve I was on, thought Minitus may be able to help. I am looking into hair analysis too. I have always meant to get into that but never have.
Love Lesley
Thank you Jean
Sent: Monday, 14 January 2008 5:27 PM
To: Lesley Lee
Subject: Request for assistance in Motor Neurone Disease
A colleague has asked for help..
Dear Jean,
I have a new client, who strangely enough I am seeing both at the ILC and in my clinic – that was by co-incidence – and he has motor neurone disease, the type that starts with muscular atrophy in the head and neck. He can still walk but his head rests right down on his chest as he does so. He was referred by a dentist from Sydney, who has “heard of my work” and who has a very alternative approach. I have taken his photos and done a facial analysis as well as taken his case history and have repertorised the case. If am wondering whether you or anyone in your list serve has had any success with a patient with this diagnosis. I have told him that I don’t know whether I can help but that I think it is worth a try. Therefore, with a case like this, any help would be much appreciated.
Many thanks
Lesley
I looked up muscular atrophy in Rep Virosa and found a match to Tick bite but it is motor neurone which does not show there . lso asked what was going on at the time illness started. 2nd letter.\>>
Not really. I do wonder whether it was a vaccination issue, as he has had a flu vax each year but there is nothing solid to be sure about that. His mother was dying at about the time he was diagnosed. There is some evidence of heavy metal stuff I think with this condition but he has had all amalgams remove after the diagnosis. I am going to do some dousing and ALS shows Plumb as a big one and he fits into that miasms photo-wise. I am going to read it more thoroughly. It is such a dreadful condition – they are about ready to give him a peg and looking at him, I think that is wise.
I will ask him about a tick bite – it really can be very nasty – but he didn’t mention it in the history.
3rd letter >>>His wife rang to cancel both the appointments – here and at the ILC [Lesley works there as an occupational therapist ]- as he is in hospital. He saw Dr xxxxx for lung condition and he referred him to a sleep clinic – that is another possible clue – extreme insomnia over the past several years. It is hard getting information, as he is unable to talk. He communicates by writing on paper – but as he can’t see and his hands don’t work well it is hard to work out what he is writing very often. He also writes on his hand and his wife can read what he is saying usually. However, it is all very frustrating for all concerned. It is such a diagnosis of doom, that I do wonder whether anyone has had any success with it, and since I have stopped being on the list serve I was on, thought Minitus may be able to help. I am looking into hair analysis too. I have always meant to get into that but never have.
Love Lesley
Thank you Jean