Posts Tagged ‘Gastric Acid’

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Highlight

April 7, 2008

I’ll refrain from talking about my morning ritual, it’s the same everyday. I did some work in the morning and went, with a headache, for Physiotherapy with my new shoes. Wilfred spotted them immediately and had to laugh. The shoes are high and difficult to take off so I decided to skip the massage. So 15 minutes on a home trainer (that went well) was followed by learning the basics of walking.

How to step forward with and without looking at my foot (difficult) and how to step forward with a bend knee and then stretch that leg (very difficult!). Wilfred wants me to put down the heel of my right foot first and then roll the rest of my foot forward in a controlled way. I have not that much control over this foot-ankle system with the result that after I put down my heel the controlled roll is actually a loud ‘flap’. That causes a strange sound effect “FLAP flob FLAP flob”.

Wilfred will take care of postponing my Physiotherapy (last treatment 21st of April) and he will talk to my Rheumatologist to discuss my participation in this hospital’s dedicated “Neurology Team”. I hope that a holistic approach (Rheumatism and Neurology) will maximize my chances that I will recover any functions that I may have left. I guess though that recovery and revalidation of my functions related to the functional area for Speech and Emotion will also need attention. Today I have no idea about the scope of the “Neurology Team”.

The Dexamethosone has an effect similar to Enbrel (Etanercept) on my Psoriatic Arthritis although it for sure is not as effective. I had to stop with the Naproxen to avoid the build up of too much Gastric Acid and I am therefore afraid that when the treatment with Dexamethasone against the Edema stops (I’m still taking 2 x 4mg daily) I’ll be right back where I started with the Rheumatism. Perhaps at that time I can restart with Naproxen again but I would prefer going back to Enbrel.

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Dexamethasone but no CT Scan

March 31, 2008

Lots of pills to takeSuper Nurse just called. She asked how I was doing and referred to my voice mail. She had spoken with the Neuro-Surgeon and they agreed that in case the headache would have become less (disappear) that I can reduce the Dexamethasone. That is however not the case. To minimise the side effects of the Dexamethasone (without knowing I have several: thick feet, desire to eat more, feeling tense and hyper) she gave some advise on how to counter them:

  • Put my feet up in bed
  • Take the Dexamethason around 18:00
  • Don’t drink tea and coffee in the evening but warm milk (forms a protective layer in your stomach)
  • Don’t eat too much
  • Take up to 6 paracetamol per day against the headaches

I asked her for an additional CT scan but it seems that makes no sense. The CT scan will not reveal anything in more detail as long as the edema is there. She understood my concern about the grade 3 Glioma but explained that although a grade 3 grows faster than a grade 2 it will not be an explosive growth. She will contact me again on Thursday the 3rd of April to discuss my situation. If the headaches have become worse or I have started to throw up (especially during the night) I have to call the hospital immediately.

I have decided to now start regularly take two (harmless) homeopathic drugs my mother suggested me to use:

  • Cinnabaris (D6) which helps very well against Sinusitis to avoid confusing the headache caused by the edema
  • Zincum Valerianicum (D6) which helps to calm down a bit
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Endema?

March 31, 2008

Today will be a busy day and it started with a lousy night. Although I didn’t drink anything last night (coffee, tea, water) after dinner and went to bed around midnight did I wake up every hour of the night to go the toilet. I have a numbing headache (it’s always there but not really painful, a kind of permanent pressure)  on top of my head on the left side.

My gastric acid levels are still high, the pain in my stomach has not become less. Again, it is not unbearable at all but just an indication that I probably should do something about it. During my working period in Italy have I learned to appreciate espresso and although I already cut down on it (max. two cups per day) do I now think I should not drink it at all in the evening. Every evening my sweetheart Monling prepares a dish with different kinds of fresh fruit for me. Thanks baby, I love it!

I would like to have another CT scan made and have it compared with the CT scan of the 22nd of March. I suspect that the endema has not become better and if that is the case this could mean something for the activity of the Glioma. I’ll try to approach this positively, believe that as the 24th of April draws closer that also psychosomatic factors are going to play a roll but I need to know. Enough is enough. I left a voice mail with Super Nurse.