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Happy New Year and Welcome to my 80 Million Stem Cells
We have just returned from the most AMAZING experience of our lives in China for Norman’s Stem Cell Implants. Here’s a brief summary of what we did in those four weeks.
On arrival at Beijing Airport we were met by Diana who was our assigned co-ordinator for our stay at Beijing Phuha International Hospital. Each family is assigned a co-ordinator who helps with anything you need during your stay that the hospital.
Norman and I both stayed in the same hospital room. He had a proper hospital bed and I slept on a sleeper couch. The hospital does not provide any meals which we found very strange, and we had to do all our own cooking. Our room was equipped with a small “toaster”, fridge and microwave. Luckily China has lots of take-out food places, and we found the most yummy pizza restaurant. We had lasagne for a fair amount of meals.
Norman's daily routine was very intense and normally went something like this :
- 07:30 Wake up, shower and dress.
- 08:30 Speech Therapy with Anna
- 09:30 Daily drip infusion
- 10:30 Physio Therapy with Jason
- 11:30 Occupational Therapy with Samantha
- 12:50 10 minutes for lunch
- 13:00 Acupuncture – 30 needles per day
- 14:30 Hyperbaric Oxygen Chamber
- 17:30 Speech Therapy again with Anna
The above happened every day except for the four days that he had medical procedures done. He had two Lumbar Puncture Stem Cell Implants and two implants directly into his brain – via the Femoral Artery in his groin. The latter were quite painful procedures. After each procedure he had to lie flat on his back for between 4 and 7 hours to allow the Stem Cells to circulate throughout his body. The Stem Cells take between 3 and 6 months to mature, so he is looking after his New Chinese Babies very carefully.
The doctors, nurses and international staff were all wonderful. There was nothing that was too much trouble for them to help us with and we are so privileged to have made friends with these fantastic folk. Every detail was fully explained to us and during each procedure there was an English speaking person in the theatre with Norman that explained what the doctor was doing. His procedures were also videoed and put onto a DVD disc for us to take home.
The other patients and their families were so inspiring. The whole atmosphere was one of positivity and healing. We all that the same goal – to get better! We’d like to say a special thanks to Alp, Mahpare, Can, Mete who came from Turkey. Can had the foresight to get a VPN internet connection so we were very briefly able to communicate on Facebook. Merzaan, Isabella and Jaco were our South African friends there and we thank them for many laughs and pieces of cake. Betsy and Phantom George were from Montenegro and their positive attitudes kept our spirits high. George is a screen writer who wrote “Runaway Train”, and is busy with “Billy the Kid”. He was not fazed about the lack of computer connectivity in China as he wrote everything out by hand – old school style. Sam and his parents from Australia were an inspiration and we loved chatting to them. Nomshado and her family were also from South Africa. Although they were only there a short while we enjoyed having some ‘home contact’ with them. It’s amazing how much I missed pap and sauce over in China, and the smells coming from their room just reminded me of home. Marion and Jack were from the UK and arrived only a short time before we left.
To all these very Special Families we would like
to encourage you to keep positive,
look after your Chinese Babies and
GET BETTER.
I have noticed a difference in Norman’s speech and forearm movements already, but suspect that this is due mainly to the therapies and not yet the Stem Cells which take between 3 – 6 months to mature.
A very big THANK YOU to all our friends who donated money to help Norman get over to China. We truly believe that this is cutting edge medicine and will make an enormous amount of difference to Norman’s physical improvement.
May 2012 be a year filled with love, laughter, health and happiness.
Lots of love,
Sue, Norman, Roland and Hayley.
Ps. The only hiccough during our whole stay was that Sue got sick and ended up in the hospital bed next to me for the last four days. She had a gall stone which was very painful and was treated with drips, drips and more drips, lots of painkilling injections, sonar scans, x-rays and Chinese massage. She started getting pains on the day that I had my last procedure and when I complained about my procedure she told me to wind my neck in. I said that she was just playing the sympathy card – then I realised that she was really sick. They whisked her off to the surgical hospital and she was gone for about 6 hours. I felt so helpless. The staff and other patients and their families who were staying at the hospital were wonderful and looked after both of us.
Pictures from China
Read Norman's story from 2011
PLEASE NOTE: NEW BANK DETAILS FOR ANY DONATIONS - THANKS
| Account Holder: |
Norman Mann |
| Bank: |
ABSA BANK |
| Branch Name: |
Booysen, Johannesburg |
| Branch Code: |
334105 |
| Account Number: |
3330144555 |
| Reference: |
DONOR’S NAME |
*** DON'T FORGET TO READ NORMAN'S LATEST RANGER STORIES ***
LATEST STORY .... READ BELOW
“He ain’t heavy, he’s my brother”
This is not my story. I write this story because he can’t.
Qualified Professional Hunter, Game Ranger, Educator, Commercial Pilot, Soldier, Patriot, Husband and Father. A man who lived to its extreme has his life changed inexorably forever while in a strange land and whilst doing the most mundane chore.
Based out of Johannesburg he travels the world. This time he is in the Far East promoting South Africa its Lodges and its wildlife. He works closely with the South African Tourism board in Japan and is passionate about South Africa and his work with “African Anthology”. On this occasion he has been in Japan for his company “African Anthology” attending travel expo’s meeting with adventure tourism travel agents and Japanese Travel Indaba’s. And then disaster strikes.
This is his story and he’s my brother.
Not too long ago you could have been a visitor to Sabi Sabi in the Kruger National Park or Mvuu lodge in Malawi, or maybe a safari in the Luanga valley in Zambia. And if you were, perhaps it was me who was your guide.
I am Norman Robert Mann and I am 42 years of age.
The African bush is my life. I can tell you what that soft whistle is when you listen to it in the middle of the night or the quiet bark or loud huff from the water. I can tell you why a marabou stork’s legs are white. Every bird sound you hear, every smell, I know intimately. Which snakes you can touch and which ones you should not. I am so tuned to the African Bush, I am almost apart of it. I have been this way from a very early age.
I love Africa and she has treated me well.
It never crossed my mind that one day I would not be able to be a part of it and that I would not be able to see Africa perhaps ever again. Not because I am away abroad forever but because I was in Osaka, Japan when I sat down to enjoy a business dinner with Japanese clients and I ate a meal that caused the immediate swelling of my throat. This swelling was aggressive and rapid. Within minutes I was unable to breathe. Fortunately, Takashi my Japanese friend realised what was happening and immediately called an ambulance. In Japan, city emergency response services are stationed within 5 minutes of any location and the closest ambulance was dispatched and arrived within minutes. I stepped into the ambulance but barely being able to breath. While in the ambulance, I collapse, my heart stops and unbeknown to me, anaphylactic shock is setting in. Everything went dark and in effect I was dead.
Emergency response personal gave me a tracheotomy to open the airway passage while others were taking action to start my heart again. The brain requires oxygen to function so the time delay was critical. In my case, it really was too late.
Seconds later I am woken by Stuart, my brother. I cannot not understand it, why the hell is he here? A just moment ago I was at dinner, oh crumbs, what’s that noise? What’s happening? Where am I? I can feel my heart pounding and why can I not see or move? What’s happening?
I hear Stuart, he is calling me from far away. “Norman, Norman can you hear me”
I realise that I am in Critical Care but I can hear. Stuart explains to me the sequence of events that have changed my life.
I was in fact in a coma for a week before he and Wayne Pritchard, arrive in Japan from Tanzania and South Africa. For me it was seconds. The doctors believed that due to the extensive global brain damage, I would be vegetative for life. Stuart did not tell me this. Only he knew that I could hear him because I respond to him by the smallest nod. I still don’t understand what’s happened to me as to make the smallest movement requires all my energy and I can’t see. I feel the tracheotomy pipe in my throat and hear the breathing apparatus keeping me alive.
A week passes by and my left lung collapses. I have no energy making me withdraw from communicating with Stuart. The doctors still insist that I am vegetative and they convey this to Stuart. Frustrated, he tells them that I am communicating but they shake their heads and move on.
Stuart moves close to my ear. He asks, pleads for me to fight this thing, to find the energy and hold on for the family and together we can beat this thing. For the first time, I manage to cry. I cry, Stuart cries. The doctors walk in as this happens and now they know that I am not totally vegetative.
Progress starts and I start to heal rapidly. After two weeks the tracheotomy is removed and I start to breathe through my mouth. The left lung inflates and I get moved to high intensive care. Day, night or time mean nothing to me. I still cannot see.
Stuart leaves for South Africa and my youngest brother John, arrives to take over.
He should not be here as he too is suffering with a serious ailment. John stays with me for two weeks. He encourages me, he entertains me, he is with me for twelve hours a day. I know that seeing me in this condition is causing him stress and just exasperating his own condition.
By now My wife Sue, who stayed with our children and quite rightly stayed in South Africa until I am deemed stronger, arrives after two weeks to relieve John and to monitor my progress so that NetCare911 can repatriate me back to South Africa. Sue is with me in the hospital for three weeks all the while assisting with the physio and other exercises.
I know that Sue is struggling terribly with this and I can only imagine the terrible insecurities that she must have been feeling.
Eventually NetCare911 take me home. They provide a doctor and a nurse for the trip and I come home to South Africa via commercial airline.
I can’t walk, talk, move freely and I am blind......
3 months since my ordeal and progress is slow, but there is progress.
For three months Sue is under tremendous pressure. Her life has changed. She runs me to and from hospitals, physio sessions and all the while trying to have a normal life with 2 young children to care for.
I am no longer in a hospital but I continue to receive physiotherapy as I am still blind and cannot move my arms freely. I can walk although badly and I can talk but you will have to listen carefully to understand what I am saying.
6 months
My wife was unable to cope with our young family and with the enormity of dealing with me on a day to day basis so I have gone to spend time with my Mother and her husband, Guido on their farm outside of Nelspruit. I can readily get the therapy I require in Nelspruit.
I have spent many months with my Mother on her farm and she has driven me to and from the physio sessions. She is 63 and petite but despite her tiny stature, has managed to practically carry me up and down stairs, bath, feed and take care of all my basic needs.
18 months
It is now a year and a half since my Japanese Indaba and the accident. I have returned home from my Mother to my family and home in Johannesburg. I am still blind. I have been through physiotherapy, speech therapy and ozone therapy. I have had an operation on both hands to try and alleviate the spasm and claw hand that was developing. My back has been in spasm for most of the year and a half.
There has also been pain, tears, compassion and love.
In all of this I have discovered new friends, found renewed love in my family and made progress albeit slow. But most of all “African Anthology” have stood by me and my family all this way.
Thank you
Written by Stuart Cogan “He ain’t heavy, he’s my brother”
***** We are still appealing to the travel industry to use the bednights *****
that have been donated to the Trust. If you have any
clients wanting to stay at any of the lodges displayed
on the Website, please contact Wayne Prichard
from An African Anthology and he will advise
how this can be done.
All monies generated by doing this will go towards Norman's rehabilitation.
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