Nurses battle against Multiple Sclerosis

$10,530 of $100,000 goal
Given by 91 generous donors in around 9 months

Lets gets Jenny to Russia for life changing treatment for Multiple Sclerosis, so that she can continue her amazing work as a nurse and Mum.

Canterbury

Hi, my name is Jenny

I have Multiple Sclerosis (MS) and I am traveling to Russia for HSCT (hematopoietic stem cell treatment) in November 2018 with the hope of getting my life back on track and preventing the MS from causing any further damage.

My wonderfully supportive husband Hayden and our two beautiful children, Harry (5) and Georgia (3), are very active and I would like nothing more than to be able to participate in outings and activities as a family without the MS holding me back.

I had my first two attacks and diagnosis in 2012 when I was 28. The first attack was the Lhermittes sign (a buzzing sensation from my neck to my limbs). The second attack occurred while I was pregnant with Harry and the entire left side of my body was affected by altered sensation and weakness. After Harry was born I had a post-partum attack affecting my balance and the strength in my legs. Since that attack my legs never recovered fully and I struggle to walk for very long or far without stopping to rest and recover.

I have had three attacks since my diagnosis, two of them while on drug therapy. I am on a drug called Fingolimod currently but I feel it’s not stopping the MS progression. The stem cell treatment in Russia offers me a good chance to stop the disease progression and hopefully reclaim some of my mobility back.

The Goal: To save my mobility so that I no longer struggle with walking and remain free from mobility aides. I have adapted to all the other symptoms I have been given by MS but the fatigue in my legs has the largest impact on my life.

Along with being a busy Mum I am also a third generation registered nurse and love being able to care for patients and be a part of their recovery from illness/injury. Due to my reduced mobility I now struggle during busy shifts when I am unable to rest and recharge my legs and I do not want to let patients down or be a burden on my workmates. I love my job and want to continue helping others and do not want the MS to take this away from me.

The Treatment: HSCT has been performed for many years in a number of countries around the world with the purpose of improving the lives of people with MS and other autoimmune diseases. Dr Fedorenko at the Medical Surgical Centre in Moscow, Russia, is said to be the best in the world.

In brief, the treatment is like an immune system reboot. It involves harvesting the patient’s own stem cells, storing them during a short but intense week of chemotherapy, then reintroducing the stem cells to build up the immune system again but without the memory of MS. There is a 70-90% chance of success at stopping the disease progression and regaining quality of life back.

I have been booked to start treatment on 6th November 2018. The treatment takes between four and five weeks before I can fly back home. Once I am back home there will be a three month period of recuperation while my immune system rebuilds.

The treatment comes at a cost though - $100,000.00. Any funds raised will go towards the airfares and cost of treatment.

I believe the odds are in my favour to get my life back, I just need some help getting there.

Thank you.

Kimberly McLachlan's involvement (page creator)

Jenny is a cherished nursing colleague, and a wonderful Mum to her two children Harry (5) and Georgia (3). We would love to help achieve her goals in seeking treatment in Russia for her MS and to stop the progression of this debilitating disease. This would mean Jenny could continue her wonderful work as a nurse and have the ability to be more active in her role as a Mum.

Use of funds

All funds raised will go towards airfares and the cost of treatment in Russia, which comes at a cost of $100,000.

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Latest update

Hello from Moscow!  13 August 2018

The stem cell collection needed to be done over two days as I got about 60% required from the first collection and then the same again the next day. The Apheresis process wasn’t anywhere near as bad as I was expecting so two days of collection was the easy part…. So far!

Next up was four days of Chemotherapy infusions which was fine for the first two days then the effects really started hitting. No major sickness, just off food and feeling below average. However, to protect my kidneys from the chemo the flushing infusions meant for rather frequent Loo trips! So fair to say that I’m sick of the inside of the loo!

One rest day after chemo then the BIG day – 08.08.18 Stem cell transplantation! What an experience… very hard to put into words what an all-encompassing feeling such as reinfusion of my stem cells was. I will remember the strong smell and taste of tomato paste as they were being put back in though!

The whole process literally wiped me out cold. It started at noon and I didn’t really come around again until 4pm when my worried husband rang to check up on me! It was Lucky he did because I was able to then join in on the celebrations with two others who received their stem cells back that day. We each got an Iris pin symbolising new life, got to spill some liquid nitrogen, and share in some cake.

The very next day I started isolation – no mucking around! So daily bloods and infusions, regular vital signs and all that jazz. Not really impressed with the isolation clothing though – feeling like an inmate in white pyjamas! Isolation can last anywhere between 8-12 days and I’m currently at day 4…

I’ll be doing my best to keep occupied in the routine of isolation. Cross your fingers that my numbers are remarkable enough that I’m at least allowed out of my room in ‘mask mode’ by day eight!!

The countdown is definitely on and I’m itching to get home to my family!

Xx Jenny

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Latest donations

Guest Donor
Guest Donor on 21 Aug 2018
$50
Greg
Greg on 02 Aug 2018
All the best Jenny, Hayden and family
$50
Guest Donor
Guest Donor on 30 Jul 2018
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Amanda
Amanda on 19 Jul 2018
$50
Stoddarts
Stoddarts on 17 Jul 2018
Thinking of you Jenny. Wishing you all the best x
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Who's involved?

Kimberly McLachlan's avatar
Created by Kimberly McLachlan
Jenny Sincock's avatar
Paying to a verified bank account of Jenny Sincock
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This campaign started on 30 Jan 2018 and ended on 1 Nov 2018.