Helen's Hope

Helen's Hope: February 2013

Tuesday 26 February 2013

February 26 2013

Helen was having her meds when I arrived.  Up, washed and dressed.  Helen looked in my direction when I went in. The nurse said that she had been ok that morning.  The tray for the wheelchair has arrived and in situ.  

Her feed regime has been changed to Jevity 50 & Osmolite.  Hopefully this will help to stabilise her blood sugars.

Went upstairs for OT with Judi.  Helen was learning to press the large red button to make a sound. Judi was also testing her reflexes by touching her face with a tissue and then moving it to her eyes.  She occasionally closed her eyes before the tissue touched her eye lashes but was not consistent.  She is getting better with closing her eyes to command but again not consistent.
She should be starting hydrotherapy soon, the risk assessment still has been done.
Judi has asked for a power pack for wheelchair but not sure it will be approved.  Fund raising goal ?
Physio again today 2-3 with Sam.  Helen has been on tilt table "standing" again.  After all the excitement she was back to bed at 1615.
Put more money in her account.
The hairdresser is visiting tomorrow.  I have asked for Helen's hair to be cut to one length all over.  It will be so much easier for the nurses to deal with.

Wednesday 20 February 2013

February 20 2013

Visit with Dad & Sammie.  

Spoke with the OT.  Helen's wheelchair hasn't been ordered yet.  Berkshire Wheelchair Services have no record of an order, despite Basingstoke Hospital measuring her and ordering it.  Judy has now measured Helen and ordered a wheelchair with tray.

The OT has started a record sheet to be completed by anyone visiting.  They need to note if they notice any sort of response from Helen.  She is also working on closing her eyes to command. However, Judi is not sure about her sight, whether she can see or not.

Wednesday 13 February 2013

February 13 2013

Helen sitting out in wheelchair.   Her head is leaning to right again. She seems quite sleepy today.  I checked her feet as usual and they are ok.  Cream put on.  Brought some more socks, blanket, DVDs and slippers.
She went back to bed approx 1845.
Need to buy some more body/hand cream and foot cream and remind nurses to shave toes as well as legs!!

Tuesday 5 February 2013

February 5 2013

Put £40 in Helen's account for chiropodist, hairdresser, etc.  

Helen in bed on arrival watching music channel.  Very dry lips!!  Put lip salve on.  Even though she isn't breathing through her mouth she still gets very dry.  Her finger nails have been digging into palms.  Especially right palm.  Small mark on right palm.

The OT said that Helen has been out of bed every day and has been in the tilt table, "standing".  She has been doing sensory work with her.  The SALT is visiting later today to try some swallowing.
Her catheter has been removed.  Urine passing fine.  This is very good news as it is one less route of infection for her.
I asked Daniel (nurse) if they would do Helen's insulin in two sites because 80 units in one site is a lot for her. Even when she was only having 20 units she would inject in two sites! Helen visibly winced and almost looked as if she would cry when Daniel did it.  He said she was going onto pens when these vials had finished.
Carol (executive) visited me.  Said they were having their goal meeting.  Everything was going well.  Goals would be as simple as head control, sitting out for longer.  She said that lots was in Helen's favour - young, in rehab early and traumatic injury rather than hypoxic.
Dr McLusky will visit later.  Carol will ask him to prescribe something for Helen's acne as she isn't known to be allergic to anything.  Dr Someone came later and is going to prescribe antibiotics for acne.  He will arrange a blood test for hormone levels because of acne and hairiness.  Botox will be arranged for all limbs.
The physio spoke to me about Helen's goals.  All goals are person specific.  Each goal has a scale from 2 to -2 with 0 remaining the same and 2 being a big improvement, ie prevention of complications - if everything stays the same then 0, if improvement in 1 area then 1, if deterioration in 2 or more areas then -2. Goals are reviewed very month.
Goals to be achieved by 1st March:
  • No deterioration in any of the following areas: pressure sores, diabetes, uti, rti, dvt or contractures.
  • Aim to get trachy changed to uncuffed trachy with a view to weaning.
  • Increase sitting out time to 5 hours.
  • Decrease contractures and increase range of movement.
 
Meeting on 9th April with PCT, staff and us to discuss future funding and progress, etc. Nothing to worry about, it's just routine.
Hydrotherapy was discussed as possibly starting soon.  
Judi asked for any information about Helen (likes, dislikes, etc) so they can talk to her about them, avoid anything she doesn't like and find ways to stimulate.  I started a list and it can be added to as we go along.