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Stroke Support Group – 1-2-3 GO!

For the longest of times I have been obsessed with forming a support group for families with stroke patients.    In my conversations with Doctors, Nurses, Physiotherapists, and Social workers one of my predominant questions would be if they know of any families with stroke patients.    If they answer in affirmative, then they would be subjected to a barrage of questions.   What happened? When? Present condition? Who takes care of them? Which Neurologist is consulted?  Which hospital?  And the questions go on.  It usually ends with “May I have their contact number and talk to them myself?” If I do get the number, the families would be asked these and more questions.   In almost all the cases there has been a ready willingness to talk and share.   So now I have around 10 families or so that I talk to on regular basis.  Getting a call from them is a rarity, its usually me hounding them every now and then...

Tooth Fairy

Our father’s lower teeth dentures were missing since the time of his hemorrhage.   They were removable; he was supposed to get them out every night before hitting the bed. We were on the lookout for them.  Well, to be precise my sister was.   She asked everyone -  at the first hospital he was taken to, to the neighbors who took him there,  to any and every staff who came in contact with our father at the specialty hospital where he was later admitted.  No luck.  Dentures weren't to be found.  We got home, months passed, urinary infections visited us a ton of times, my sister still didn’t forget the dentures.  I couldn’t understand what the fuss was all about.  Yes, our father could eat orally, but it was more of swallowing than chewing, so I didn’t see the urgency for tracking down the missing dentures. Bowing to the pressure from his wife and being a dentist himself my brother-in-law took our father t...

MUSIC THERAPY FOR FATHER AND DAUGHTER

One of the persistent recommendations during our father’s ICU days to stimulate the unconscious brain was to repeatedly play his favorite music or a recording our voices.   Trusting a positive response to the music than to our voices, the choice of which to play was an easy one.  We did it in the ICU, later when in a private room, and also when at home. A cousin of ours gave us a CD by one of those new age teachers.   The recommended dosage to play was everyday for one hour and continue this for at least a month.  Did we follow it?  Ofcourse we did.  I read somewhere that classical music helps, especially with a varied tempo.  So Hindustani and Carnatic instruments would rock on in his ears when asleep.     It is beyond doubt for me that music helps and what we did helped.   Although I don’t exactly know how.  This seems to be the conclusion of most of the literature on music therapy  - very effective...

The Mystery of Heavy Breathing – I

It first happened around the third or fourth day after our father was shifted to the ward from three weeks in the ICU.   His usual languid right side, would stiffen up, his right arm all clenched would move to his chest, his facial expression would be that of a person in utmost pain and breathing would be heavy, noisy and rapid.   It was scary to say the least, to watch him have this episode all of a sudden when he was asleep peacefully.   This would recur – sometimes every time 10 minutes, sometimes every half hour and on real fun days every 5 minutes.  The first night it happened, he was moved back to ICU for observation.  Nothing particularly seemed amiss, he was wheeled back to the room next morning.  In our five month stay at the hospital, this happened every so very often.    Some said our father was getting emotional.   Emotional?  So timed, every 10 minutes emotional?  Nah.   He was give...

Heavy Breathing: Cause Figured II

It was an all nighter of heavy breathing on the first night at home.  A night to remember.  A new fumbling bumbling nurse, father breathing like he was possessed, and me just watched them with exhaustion all night.   And there, it stopped in the morning.   After a couple of days of just watching him obsessively, figured he breathed so when passing urine.   However did not know if the heavy breathing caused him to pass urine, or passing urine caused him to breath rapidly.   All I knew was they were connected.   Since IMC was usually done first thing in the morning, there was no frequent heavy breathing during the day.   Ha, there, the explanation why the episodes occurred mostly during the night.   It was because there was so much urine retention in the night and he was struggling to pass it and hence the frequency.  But why was the interval between so timed, I still do not know. So we then started hi...

An Amazingly Simple (Temporary) Solution for Heavy Breathing – III

Unable to bear our father’s suffering any longer, we circumvented the experts and tried inserting a catheter anyway.  It was highly uncomfortable for our father, he started to bleed and few blood clots came out.   It scared us sufficiently, pulled out the experimental catheter.   It must’ve been the wounds from the regular IMC that caused the bleed. Not knowing the next steps, we waited for the wounds to heal – just miraculously. Complications Due to IMC   Source:   http://www.manfredsauer.co.uk/iqcath.asp After maybe like a week or two, my sister was at the temple for a special prayer session and I was rushing out for a meeting.  I would’ve been out of the door in a minute, but our nurse came running to tell me that our father was shivering and had temperature.  Having known the drill of infection, I knew what it was.  Unable to cancel the meeting at the last minute and not wanting to disturb my sister during her prayer, I told...

FOOD ROUTE

Although our father could swallow food in small quantities, he was mainly fed through the ryles tube.  With repeated episodes of him yanking it out due to discomfort and given his chronic cold, we were advised to have a PEG tube inserted in his stomach.    Apparently ryles tube is a temporary solution, not recommended for more than couple of months, if even that.   So we decided to have the PEG in place.  It's a fairly simple procedure, does not take more than 20 minutes.    There was a gastroenterologist in our hospital, whom I will hence forth refer to as Dr. G.  He seemed friendly and we zeroed on him to perform the procedure.  Dr. G, recommended that we get our father admitted a day before the procedure, then stay for another couple of days to monitor him.   Although the expenses for such a stay at this corporate hospital seemed daunting, we opted for it given it was for the greater good! Incidentally in Jul...