1 year ago
Wednesday, 19 May 2010
Weight loss update
I lost 1 1/2 lbs this week and I was relieved as I have not been 100 % on plan. Now I must focus..
Wednesday, 12 May 2010
First week results on slimming plan
Well I have to admit I struggled to organise myself to get back on this plan, but I think I am getting there.
I lost 2 1/2 lbs :)
Long may the loss continue.
I lost 2 1/2 lbs :)
Long may the loss continue.
Saturday, 8 May 2010
MRI
I am having an MRI on Monday morning, this will be looking to see if I fall under the criteria for Tysabri. I will not have the results for a while.
I have peace with it all as it is all in my mighty Lord's hands. He is in complete control of all things, so why should I be worrying?
I have peace with it all as it is all in my mighty Lord's hands. He is in complete control of all things, so why should I be worrying?
Tuesday, 4 May 2010
Re- joined slimming world..
Well as I haven't mentioned my weight recently means that I have been steadily gaining not loosing over the past year or so. So today I joined slimming world to shed those pounds..My dear hubby isnt going to the class but will be on the eating plan with me.
I feel quite positive and determined to stick with it.
If I cannot exercise the weight off I sure can attack on the dietry front.
So watch this space....
Update on my husband- He has been to the lung clinic today and got showed how to wire himself up for an over night sleep study. So that should be interesting tonight, then he will go to the hospital and get an indication on the results. .
I feel quite positive and determined to stick with it.
If I cannot exercise the weight off I sure can attack on the dietry front.
So watch this space....
Update on my husband- He has been to the lung clinic today and got showed how to wire himself up for an over night sleep study. So that should be interesting tonight, then he will go to the hospital and get an indication on the results. .
Wednesday, 28 April 2010
Course of treatment?
Two posts in a week is unheard of from me lol!
Just wanted to share what direction my treatment is going.
I went to see my neurologist on Friday and he agreed with me that my daily injections of capoxone (stopped now) were the cause of my breathing problems and site reactions. Seems I have most probably become hyper-sensitive to the drug.
So we discussed what direction and course of treament we should be looking into.
We are looking into a drug called
I will have a MRI scan in the next few weeks to see if I need it.
Here is a little bit of imformation about it.
Who is it for?
People with relapsing remitting MS. It is available on the NHS for people who have had two
or more disabling relapses in a year and have signs of new MS inflammation on a recent MRI
scan.
How is it administered?
Intravenously by infusion into the vein once a month
How does it work?
Natalizumab is an antibody that works by attaching itself to cells of the immune system and
preventing them from getting into the brain and spinal cord, where they normally cause
damage in MS.
The most common side-effects experienced after taking natalizumab are, joint pain, fever,
tiredness, a runny or blocked nose, sore throat, feeling nauseous, headache and dizziness.
In addition, skin reactions to the infusion are experienced.
One serious and often fatal side effect is a condition called progressive multifocal
leukoencephalopathy (PML). This is caused by a viral infection in the brain. The risk of
developing this is about one in 1000 for people who have received natalizumab for more than
12 months. The risk of PML with natalizumab use increases after 2 years of therapy. Patients
with MS should be informed about the risks of natalizumab, including PML, both before
treatment and again after 2 years. People taking natalizumab are monitored regularly to
identify PML and other potentially serious side effects as early as possible.
As of 10th March 2010 there have been 41 reported cases of PML of which 9 resulted in
death. However, the risks of developing PML remain at 1 in 1000.
I would value prayers at this time . As it would be a huge decision.
Just wanted to share what direction my treatment is going.
I went to see my neurologist on Friday and he agreed with me that my daily injections of capoxone (stopped now) were the cause of my breathing problems and site reactions. Seems I have most probably become hyper-sensitive to the drug.
So we discussed what direction and course of treament we should be looking into.
We are looking into a drug called
Tysabri (natalizumab)
Tysabri (also known as natalizumab) is a drug used to treat highly active forms of relapsing-remitting MS. It is proven to be effective at reducing relapses by approximately 65 per cent in people with the condition .I will have a MRI scan in the next few weeks to see if I need it.
Here is a little bit of imformation about it.
Who is it for?
People with relapsing remitting MS. It is available on the NHS for people who have had two
or more disabling relapses in a year and have signs of new MS inflammation on a recent MRI
scan.
How is it administered?
Intravenously by infusion into the vein once a month
How does it work?
Natalizumab is an antibody that works by attaching itself to cells of the immune system and
preventing them from getting into the brain and spinal cord, where they normally cause
damage in MS.
The most common side-effects experienced after taking natalizumab are, joint pain, fever,
tiredness, a runny or blocked nose, sore throat, feeling nauseous, headache and dizziness.
In addition, skin reactions to the infusion are experienced.
One serious and often fatal side effect is a condition called progressive multifocal
leukoencephalopathy (PML). This is caused by a viral infection in the brain. The risk of
developing this is about one in 1000 for people who have received natalizumab for more than
12 months. The risk of PML with natalizumab use increases after 2 years of therapy. Patients
with MS should be informed about the risks of natalizumab, including PML, both before
treatment and again after 2 years. People taking natalizumab are monitored regularly to
identify PML and other potentially serious side effects as early as possible.
As of 10th March 2010 there have been 41 reported cases of PML of which 9 resulted in
death. However, the risks of developing PML remain at 1 in 1000.
I would value prayers at this time . As it would be a huge decision.
Friday, 23 April 2010
The sun is shining.
Just wanted to share how blessed I feel.
We at home are having a roller coaster ride of health issues but I am so at peace about it all. It is impossible to put into words how I feel. I have no worries or stress about any of it.
God has been so good to me and Us as a family.
We all at times can be so unthankful for Gods mercies towards us. We too quickly forget God is in control of all things. .
I am sitting here this morning reflecting on the past week and it has been so blessed and Gods love is so evident throughout.
I thankyou for the prayers and most importantly I thank God for loving a sinner such as I.
We at home are having a roller coaster ride of health issues but I am so at peace about it all. It is impossible to put into words how I feel. I have no worries or stress about any of it.
God has been so good to me and Us as a family.
We all at times can be so unthankful for Gods mercies towards us. We too quickly forget God is in control of all things. .
I am sitting here this morning reflecting on the past week and it has been so blessed and Gods love is so evident throughout.
I thankyou for the prayers and most importantly I thank God for loving a sinner such as I.
Sunday, 28 March 2010
Quick update on my husband.
Jonathan went private in the end as its was a 2 month wait for a scan.( Thankyou parent in law xx who payed for it.)
He has been diagnosed with sleep apneoa and will have a scan in the future (on NHS) to double check on things.The scan is not urgent hence going back to NHS.
Futher tests will be done and I will keep you updated.
He has been diagnosed with sleep apneoa and will have a scan in the future (on NHS) to double check on things.The scan is not urgent hence going back to NHS.
Futher tests will be done and I will keep you updated.
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