Breakspear Medical in the UK

Jenny

Jenny

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Skyline said:
I happen to be near Breakspear Medical (http://www.breakspearmedical.com/files/chronic.html) and became aware of a high profile recovery story from their clinic with Clare Kerr (took 5-7 years).

It doesn't seem like there are any threads on this clinic - has anyone got any information on them or had experience with them?

Their approach is very much 'immune' focused, which I am not up to speed on, although I see similar ideas to those used by John Chia and others about the issues with immune response.
Click to expand...


I've done almost every treatment they suggested over a period of about 4 years - lots of different long term abx, CO2 rebreathing mask, low-dose immunotherapy, 30 different supplements. None made any difference at all. I was told I had Lyme but then after 3 years of abx, told I never had it; I was told that I must have food intolerances or allergies as 'everyone with ME had them', and I had thousands of pounds worth of tests which no-one could properly interpret. Each time I went I had to wait between 30 and 90 minutes to see a doctor and they rarely apologised. (I was barely able to sit up at that time and had to ask for a bed to lie on while I was waiting.)
 
T

TheChronicSituation

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85
Thanks for the feedback about this everyone. I wasn't really intending to do LDI in the first place, but if I had any doubts I certainly won't be doing it now.
I've had all my test results back at this stage, and have a new appointment with Dr Munro next week to see about treatment options. I will be posting on my blog again then with an update, if people are interested...
http://thedamnchronicsituation.blogspot.ie/
 
T

TheChronicSituation

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maryb

maryb

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Or - you could buy yourself a far infrared sauna, get some liposomal vits to start with and order artesunate from the internet. See how you feel after doing those for a month.
 
T

TheChronicSituation

Messages
85
maryb said:
Or - you could buy yourself a far infrared sauna, get some liposomal vits to start with and order artesunate from the internet. See how you feel after doing those for a month.
Click to expand...


Yeah, interesting, you're not the only person to suggest the far infra red sauna. Have you tried any of these options, Maryb, or anyone else out there tried them? I'm trying to decide whether these treatment options are for me and have a bit of a knowledge deficit.
 
maryb

maryb

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I'm actually looking to buy one but don't know which - the sit in one or the blanket - I have a chronic back condition so not too good sitting but its only for a short time soooooo? My problem might be the energy needed to shower immediately - sometimes, make that a lot of times I don't have the enrgy to shower. I was thinking of starting a thread to see what others experiences were.
 
EnduringAngel

EnduringAngel

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I use a blanket I don't get to use it often as don't have much space. But when I do it's great.
I hope one day to move and get a bath as epson salt baths are awesome.

A x
 
B

brenda

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I have now received the supplemental treatment regime from B/S and looking through the long list, there are quite a few items I cannot take.

Their nutrient and b complexes have methylb12 and methylfolate in them and at present I cannot tolerate either due to my CBS mutations. They cause a huge increase in histamine and interstitial cystitis which I cannot bear. I am already taking folinic acid and hydroyb12 in small doses.

Also the liver detox they want me to take contains milk thistle and I could not take that in the past.

They don't have a b complex in without methyl donors apart from one from BioCare which has magnesium strearate.

A number of PWME trying the methylation protocols also have trouble when taking methyl donors, so I am wondering whether B/S really do have enough experience to treat the highly sensitive and therefore worst sufferers.

Their answer for sensitivities is to have the immune therapy but I am very cautious of that as I had it done before somewhere else and even though they say at B/S that they use a different method, I have already read of one person who says they relapsed with it.

But anyway that will not help with my CBS mutations and the methyl donors.

As I am being funded, I could ask if I could order the supps I need from somewhere else and have them refunded but I don't know whether they will do that as the pharmacist I spoke to said they like to work with supps they are familiar with. So, I don't know how it will go from here.

I might have reached a dead end.
 
maryb

maryb

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thanks for posting about your experiences - can you tell us what the anti/virals you were prescribed were and how long for?
 
Little Bluestem

Little Bluestem

All Good Things Must Come to an End
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brenda, I am sorry to hear that you have hit a roadblock. I hope they will work with you to get you supplements that you can take.
 
B

brenda

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Little Bluestem said:
brenda, I am sorry to hear that you have hit a roadblock. I hope they will work with you to get you supplements that you can take.
Click to expand...

Thanks. I spoke to the pharmacy and nutritionist and was able to substitute some of the supplements for example. I ordered sunflower lethicin instead of egg and pea protein powder instead of whey protein. I had to cancel about half of the supps though as they contained either iron, folate, calcium carb, sulphur, ALA, milk thistle, chlorella, or mag. strearate. I don't think that I am unusual in not being able to, or desire to, take these substances.

I was prescribed ribose and seem to be able tolerate it so far which is good for my heart but the pea protein from Lambards upset my stomach and then I decided that I would not like to take a non organic highly concentrated substance like that. Lambards who are supposed to be a good UK company were very unhelpful when I asked about how pescticids are removed or what was the allowed level so I ordered an organic one from somewhere else. My leg muscles seem to be coming back after introducing an extra source of protein which is not animal.

Good so far but I don't know whether what I am taking will be enough to repair my mitochondria which is the aim of the treatment.
 
D

denlander

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85
I am curious to know how what is the list of tests that they performed.
I need a UK lab to perform HHV-6 virus study on my UK patients, was this test on their list?
What it what is their treatment protocol?
Regards
Derek Enlander M.D.
www.Enlander.com
 
ukxmrv

ukxmrv

Senior Member
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4,413
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London
Dr Enlander, you could maybe consider this Lab who list 2 HHV6 tests. Dr Hyams used that lab when he was in London

http://www.tdlpathology.com/test-information/a-z-test-list/h

Human Herpes Virus - 6 (IgG/IgM) Ab
Code Sample Reqs Turnaround
HSV6 B 2 days

Special instructions Referral lab
Micropathology Ltd

Human Herpes Virus - 6 by PCR
Code Sample Reqs Turnaround
HHV6 A 5 days

Special instructions Referral lab
Micropathology Ltd
 
maryb

maryb

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UK
A friend had one done recently (April '13) they used Ummunosciences Lab Inc. LA
I had one done a few years ago (2009) then it was The Doctor's Laboratory. London.

I'm sure for a fee they would draw blood here for Dr Enlander's patients, process it and send it off.
They run the clinic as a business after all, and Dr Monro would help I'm sure of it.
 
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