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 16-06-2007 06:49:06 AM
Ann
Ann
From: United Kingdom

From time to time I come across articles where people suffering this condition are asking what other treatment there is other than steroidal injections or removal, which has complications.

I was diagnosed with Morton's Neuroma about 18 months ago, and I think you have to experience it yourself to believe how excruciatingly painful it is. It is a small lump on the sole of the foot and in my case I was told it was caused by wearing narrow, high heeled shoes. Yes, this was probably true!

At the hospital I was offered 6-monthly steroidal injections. I said no thank you. The doctor then said, 'oh, you want to go straight for surgery?' I said, 'no.' He then said, 'well what are you saying?' I replied, 'I'm saying no thank you to both - I'll find another way.' He was incredulous, saying there were no other options, but I still said I would find another way.

24 hours later I found my answer in Serrapeptase, which is a natural supplement derived from silkworm. I contacted the author of the book, Robert Redfern, and he told me it would cure any inflammatory condition including Morton's Neuroma. He advised taking it for two months, but after six weeks, I knew it had disappeared. I did continue, though, for another two weeks.

I had barely been able to walk anywhere without being in absolute agony, so could only wear trainers everywhere :( but not any more!!!

Serrapeptase doesn't just treat people but also animals, and the testimonials backing this natural supplement are staggering. The helpline telephone number is 0870 225 2530. If I can have helped just one person suffering from Morton's Neuroma by recommending this, then that would be good!!!!!

Ann x


The follow-up appointment at the hospital six months later left them absolutely staggered that it had vanished, and still it has never returned.

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 21-11-2007 02:01:52 PM
Ann
Ann
From: United Kingdom

I just wanted to let you know that I have just received an email via my website, from someone in America, whose daughter had seen this post on mortons neuroma.

This lady has really expressed how much Serrapeptase has helped her, and said that it is the only treatment that has worked.

I have never met anyone in my life that has had this problem, or even heard of anyone with it. Why is it that one of my very best friends has just told me she has it?? The odd thing is that we are like twins. We are both Leo, we look sort of alike, we are the same height and figure, we have exactly the same sense of humour and laugh the same way. There are barely any differences between us! I can't get my head around why she has this.

Anyway, I did say that if my post could have helped one person then that's great - it really is.

Ann :) x

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 22-11-2007 01:30:31 AM
Jon
Jon
From: New Zealand

Great stories Ann, Thanks.
What website????????????????????????????????

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 22-11-2007 03:09:58 AM
Ann
Ann
From: United Kingdom

I hope it will be useful to you and people you know Jon. http://www.serrapeptase.info/

You are very lucky to be living so close to this organisation! I wish they were over here http://www.soyonlineservice.co.nz/

Ann :)

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 22-11-2007 11:27:03 AM
Ann
Ann
From: United Kingdom

I have just had some news!!

Apparently in California I am referred to as St. Ann!!! This Mortons Neuroma thing is getting me famous!

I hope that when dealing with me in future, you will address me as St. Ann. Thank you. :D

Last edited: 22-11-2007 11:27:29 AM

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 22-11-2007 12:11:56 PM
Jon
Jon
From: New Zealand

Thanks for those sites St.Ann. I will have a search around them tonight.

Last edited: 22-11-2007 12:12:22 PM

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 23-02-2008 01:57:08 PM
Jocelyn
Jocelyn
From: United Kingdom

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 19-04-2008 02:23:41 PM
Jocelyn
Jocelyn
From: United Kingdom
Jocelyn wrote:

Last edited: 19-04-2008 02:24:06 PM

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 19-04-2008 04:06:31 PM
Jon
Jon
From: New Zealand

Good point Jocelyn.....I think.

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 20-04-2008 12:18:42 PM
Ann
Ann
From: United Kingdom

Well you can't argue with it!

:D x

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 21-04-2008 03:27:24 AM
Jon
Jon
From: New Zealand

Oh, I don't know St. Ann, maybe we can agree to disagree though.

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 21-04-2008 08:36:18 AM
Ann
Ann
From: United Kingdom

I think the many complex issues that were raised require a full debate!!

P.S. Thank you for honouring my title Jon - I do love a bit of respect :D x

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 21-04-2008 11:43:34 AM
Angela
Angela
From: United Kingdom
Jocelyn wrote:
Jocelyn wrote:


Hi

I'm a reflexologist and have had plantaar faciitis twice. Once in each foot! No steriod injections for me thanks!

I did physio and reflexology. I had a lady client with it and I helped her get rid of it - I believe that tight calf muscles pull on the achilles tendon which in turn pull the fascia.

Why not find a reflexologist for your husbands foot problem Jocelyn???
I'd love to have a go:))

If the foot is mobilised - loosened up, the tendons and nerves would be freer. There is mot much flesh in this area and scarring would cause more trouble.

Last edited: 21-04-2008 11:48:15 AM

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 21-04-2008 02:38:13 PM
Helen
Helen
From: United Kingdom

I don't know how you know that Jocelyn had plantar fasciitis, Angela - both her posts, for me, are blank! :) And they were a couple of days ago too!

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 22-04-2008 03:25:19 AM
Jon
Jon
From: New Zealand

Helen, that was the point of my and St. Ann's comments. Sorry, the sublety, but IMO, sarcasm is fun.

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 22-04-2008 05:47:36 AM
Asif
Asif
Moderator
From: United Kingdom
Jon wrote:
Helen, that was the point of my and St. Ann's comments. Sorry, the sublety, but IMO, sarcasm is fun.

Some would say Sarcasm is the funniest form of wit...

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 25-06-2008 06:14:41 PM
maxam
maxam
From: United Kingdom

Hi Anne,

Have you heard of other people curing Morton's neuroma with serrapeptase since the last posts? I have this condition and you are offering me hope.

Maxam Magnata

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 26-06-2008 03:12:48 AM
Ann
Ann
From: United Kingdom

Hi Maxam,

I don't know any one else with the condition I'm afraid, but my friend had opted straight away for the steroidal injections.

They didn't work, so she has just had surgery and is on crutches at the moment for a few weeks.

Mine had measured 7mm but still there has been no return and it is fine. I would recommend you speak to Robert Redfern who is very helpful and he will tell you the best dose. I seem to remember he told me to take it for about two months, but it went in 6 weeks.

Perhaps give it a try at least.
Ann :)

Last edited: 26-06-2008 03:13:37 AM

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 27-06-2008 04:25:50 PM
maxam
maxam
From: United Kingdom

Hi Ann,

I spoke with Robert thanks. I am definitely hopeful that this will work. There almost no info on curing this naturally which is my total inclination. Did your feet have any numbness or just pain? Could you actually feel the neuroma decrease when you felt the area between your toes on the top? I really appreciate you having posted your experience.

Cheers,

Maxam

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 28-06-2008 05:21:18 AM
Ann
Ann
From: United Kingdom

Hi Maxam

I don't remember any numbness, but ooh....I do remember the pain!!! Excruciating at times.

It didn't so much decrease in size I don't think, but just disappeared, so that if you touch that area, it felt and feels just normal.

Be sensible though in the next couple of months, and rest it as much as possible, rather than walk. Whilst taking the Serrapeptase I think it helps to heal quicker, the less you walk on it.

My friend didn't give up her high heels all the way through to the last minute, but I took Robert's advice and wore those dreadful trainers mostly!! Even, then it used to hurt walking.

Anyway.....lets hope you get rid of it quick!
Ann :) x

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