It’s hard to believe that in
less than 24 hours my beautiful wife and I will be on a plane heading for India, it seems
I’ve been waiting for this moment for an awfully long time! I’m very happy that the time has arrived but not
very happy about the time it will take to get to our destination. Our flight time to Amsterdam is over 8 hours; we have less than
two hours before our next flight to Mumbai which will take over 9 hours! Once we land the clinic will be there to
drive us to Pune which I’ve recently been told is over a 5 hour drive which was
completely unexpected! We leave on March
26th and don’t arrive at the hospital until March 28th,
that’s like two days of travel! Not
including time changes, our journey will take well over 24 hours of continuous
travel, that is going to be extremely hard on me but no one said this was going
to be easy.
I know that my experience in India will be very different than the stem cell
treatment I had in China. The stem cell transplants were spread out
over 6 separate procedures and I was in the hospital for a month. The program in India is condensed into 2
procedures and only 2 weeks in the hospital.
I will have the “Liberation Procedure” first and stem cells injected
into my jugular veins at the same time.
The next procedure is the actual stem cell transplant which is done in
one operation rather than 6. In China I was
given an average of 15 million stem cells each time totalling less than 100
million cells. This time I will receive
200 million stem cells but all in one shot!
This is the maximum amount allowable and they will all be cultured from
my own body. A vastly different approach
than what I experienced in China
but there will be some similarities for sure.
Some of the possible side effects that have been explained to me are the
same but possibly intensified. For
example, in China
I had to lay immobilized flat on my back for 6 hours after each transplant,
that was very hard on me! Well I’m in
for a shock because I must be immobilized for 48 hours after the transplant in India! I have to be lying down with my feet above my
head for the entire time other than getting up for bathroom breaks and
eating. I'm not too sure how this is
going to work out but I’m definitely not looking forward to it! In China I had free time between
treatments that allowed me to leave the hospital and go touring around,
shopping etc. Not this time, I’m told
that my days will be full the entire time but if I feel up to it the staff will
take me out during the final days for some shopping and sight seeing. Lorelei will likely have time to experience
more but in the end we are there for one purpose, to undergo medical treatment
and not vacation.
Having been explained the
possible side effects I know that I will have some pretty tough days. Although I got through most of my transplants
in China
without incident, there were some extremely uncomfortable and painful post
reactions. The side effects range in
duration and severity but I’m told the most critical can be post-dural-puncture
headaches. I experienced this in China
and looking back at my blog from the time it was extreme pain, the only time I
could recall in my adult life crying from physical pain. I just pray that things don’t go down that
road in India!
The headaches can be very brutal
as the central nervous system (CNS) adjusts to pressure changes after
cerebrospinal fluid is momentarily drained by lumbar puncture. 200
million stem cells are then injected into the spinal canal and the cerebrospinal
fluid is then returned and pushes the stem cells up the spinal canal and into
the brain. This creates great changes in
the hydrostatic pressure of the CNS but it is impossible to know how severe the
headaches will be and this can occur several hours or even several days after
the lumbar puncture. At least I’ll have
my honey there to console me if problems do start!
Other noted side effects will
vary depending on the level of ones disability.
For example, patients who are paraplegic may experience the return of
rigid and spastic muscle tissue from a contractured to a flaccid state which is
a normal response to the neural pathways making reconnections. One patient that I spoke with experienced
this, he was used to his legs being very spastic and his knees locking so he could
stand up. He was shocked post procedure
when he tried standing and like a limp noodle he collapsed to the floor! I’m glad that I have stayed active exercising
my muscles to avoid muscle atrophy so hopefully this transitional phase will be
easier on me. It can be difficult to
distinguish between side effects from the treatment and what some sceptics see
as disease progression. So far in every
case patients have reported that this spasticity disappears once they return
home. Some patients have reported being
very tired and feel they have regressed sometimes up to a month after returning
home. However it is now understood that
what some patients see as regression is actually the spasticity relenting as the
neural pathways are being reconfigured to the brain. If certain muscles have not been used in a very
long time they will need to develop muscle tone again and be able to handle the
new loads as they are now available to the nervous system again. Some patients report being very tired as this
goes on but it is just the body needing rest as it goes through a new nerve
growth phase.
It is difficult if not
impossible to know how each individual will react post procedure and results
will vary. The normal period of noticeable
recovery begins between 60 and 120 days post procedure. No one really knows what to expect exactly
but I’ve been told to accept the fact that I will not experience straight-line
recovery. The actual fact is that no one
knows how I’ll react and recover, no one but God that is. Time will tell and I must be patient, stem
cells have shown to have continued improvement for over a year. Again no one really knows but the cells are
not like batteries, they just don’t fade away and die. It will take a lot of work on my part to
reach the full potential of my recovery but of coarse I’m up for that
challenge! I’ve been told that physical
therapy is key to ongoing improvement, for me that means exercising my body
after I recover to retrain my lost muscle and brain connections.
I’m not sure if I’ll be doing
any blogs while I’m away but stay tuned for future posts and to follow my
progress. In the mean time I would like
to thank everyone that has been and will be praying for me, it means so much to
me.
GOD BLESS
LC
1 comment:
what is your status now.?
please post..
Thanks
juleatkr@gmail.com
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