MS MuSings

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Who Live with MS,

Multiple Sclerosis

 

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Real Life Stories

Meet Our Newest Writer!

Dave Halkyard

Profession: Quality Assurance Engineer

Age: 54 Years

Nationality: English

Diagnosis: Secondary Progressive Date of Diagnosis: 1992

I love Golf and used to play off 5 handicap now I will be lucky if I can play to 20 Handicap, using my golf cart but still love the game. I retired early due to my disabilities, but still keep myself busy with my faithful PC, writing the odd poem and the like. I also have 3 grandchildren (all girls) two live in Ontario with my daughter and her husband.

I am not a negative person and believe I will walk a reasonable distance without sticks in the future, it may be a while away but nothing worth waiting for comes easy.

In 1990 I was involved in a motorcar accident and believe this was the trauma that triggered the beginning of my Multiple Sclerosis attacks.

During the year of 1991 I started to tire quite quickly and my left foot began to drop. Theses were my first MS symptoms. Later I could not flex from the ankle. I could not lift my foot from the knee or hip. My left hand was claw like and weak and I could not straighten my arm in an upward direction. I had no energy or stamina and walked with the aid of a stick. My walking distance was approximately 25 meters

The only treatment I could receive here in the UK was steroid after an exacerbation. I was anxious because I was aware there was no know cure or effective treatment available to date (1997).

After chatting with a email friend Gary Shane from USA he told me of his visit to a Dr in Athens who prescribed low dose Mitoxantrone. So after my own research I went and had this treatment for about 30 months from October 1997 to March 2000, it meant a trip to Athens every 3 months. I stopped deteriorating and improved from 3.5 to 2.5 on the EDSS scale. Of course I have now reached my maximum dose.

Since stopping the treatment I have again deteriorated and currently about 4.5 on the EDSS scale.

I hope to start Beta Interferon in April of this year, if the NHS have the funding in place. If that fails to work for me then I am considering a stem cell transplant.

In the mean time I try to keep fit doing various stretches, use a electrical muscle stimulation and exercises with assistance. I also have a regime of vits and mins designed by a nutrition advisor.

Dave’H

A little more info

Stuff I have tried – as you can see we are easy prey for people promising they can help us. All the treatments below tallied to £42,000+ including the mitoxantrone which is the only treatment that helped me.

1992

MRI Scan  

1992 -1993

Homeopathy Good intentions: medication & diet principal as per books read, but a bit to extreme, all organic and she had me allergic to most things I had a very restricted diet. No real improvement. Medication included B12 injections.

1992

Steroids RVI Newcastle

1992-1993

Osteopathy?? No improvement at all

1993-1994

Spiritual Healer No improvement at all

1993-1994

Spiritual Healer No improvement at all

1994 & 1997

Acupuncturist ‘Chinese’ Needles in foot, arm & hand + she recommended I see a neurologist

1995

Hypnotism Made no change to my condition at all

1995

Carri Loder Treatment No improvement at all

1995

Spiritual Healer No improvement at all

1995

Masseur Helped my muscles, but not MS condition

1995

Reflexoligist Feel an improvement, and I believe it helps, but not until a few days after the treatment and only lasts a short period, a few days maybe.

1995

Osteopathy Joints manipulated, & cortisone injections in the back of left leg, but no improvement

1995-2002

Vits & Mins  Still take them

1995-1996

Decompression -chamber Helps but only for a short period

1995-1996

Acupuncturist Needles in head, neck, foot, arm & hand + medication Felt a little better on occasions but not convinced it was because of this treatment

1996

Spiritual Healer No improvement at all

1996

Amalgam Fillings removed All amalgam fillings removed and replaced with none toxic white fillings. Made no difference

1996

Osteopathy Joints manipulated, no improvement

1996

Allergy Testing (on going) Helpful copy of results received

1996

Spiritual Healer No improvement at all

1996

Aromatherapist Felt terrible for days after, maybe 3 different treatments all in the same session

1996

Spiritual Healer No improvement at all

1997

Steroids no help this time

1997

Chiropractor Joints manipulated, no improvement

1997

Tai Chi Class much To advanced for me. More personal tuition required if tried again I think there could have benefits

1997-1998

Weight Training (on going) Helps keep muscle tone were you still have some strength and movement

1997-2002

Swimming baths Stopped in May 2002 allergy to chlorine

1997-2001

Mitoxontrone /Imunoglobulin I am improving, the only treatment I have tried to date that is worked 2.5 years complete and had an affect now stopped because of life time dose limitations

1997-2001

physiotherapy  Helps

1998

Cacey Treatment - Diet No Help

1998

MRI Scan Carried out at Darlington, check lesion size after Mitoxantrone, maybe reduced but difficult to assess conclusively

2001

Plastic foot support No Good to restrictive and gave me pins and needles

2002

Steroid intravenous No help – no more steroid treatment

2001-2002

Chiropractor Joints manipulated, no improvement

2001-202

Massage No change

2002

Natural Health California Tablets L-Threonine- Moducare-Bovine myelin and cytlog Allergy to bovine myelin NO HELP AT ALL made me feel sick

2002

Bee Sting Therapy Felt stronger after !st 3 sessions but spasicity worse. Then left leg got infected and cellulites was diagnosed. Hospitalized on IV anti-biotic. I believe it is one of the reasons I have worsened over the past 6 months

Sept

Naltrexone Took for one week made me weak and spastic felt awful so stopped

 

Reach Dave by email to comment: davehalk@dh85xr.fsnet.co.u

Dave is in our Gallery on Page 5!

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