At last a comment from other poor soul who has Fibro and migraines, especially with these awful Trigger Points.
Perhaps we can help each other, that's what I am about, finding a way out of this.
If there is anyone else too shy to comment. Please do, at least now you wont be the first.
What is it like to have FMS/CF/ME?
Friday, 7 November 2008
Monday, 22 September 2008
Trigger Points
Friday, 12 September 2008
IBS. Migraine
OK, it does seem no one reads this, so it might as well go.
Before I pull it, one more try to see if anyone has the same problem as me.
Does anyone have IBS and/or Migraine to go with their Fibro (CFS/ME, its all the same)
I would love to know. I cant decide if my migraines are a cause or effect.
And I had IBS for years before either the Migraine, and later the FMS hit.
Last chance....
Thanks.
Before I pull it, one more try to see if anyone has the same problem as me.
Does anyone have IBS and/or Migraine to go with their Fibro (CFS/ME, its all the same)
I would love to know. I cant decide if my migraines are a cause or effect.
And I had IBS for years before either the Migraine, and later the FMS hit.
Last chance....
Thanks.
Wednesday, 3 September 2008
Closing down
Given no one reads this as far as I can tell, and I don't always feel like talking to myself, I think I will shut this down.
I had hoped I might meet some other people encumbered with this crappy illness, but it seems not.
So unless anyone begs me....form a line to the right....to keep this blog.
In a few days, it goes.
I had hoped I might meet some other people encumbered with this crappy illness, but it seems not.
So unless anyone begs me....form a line to the right....to keep this blog.
In a few days, it goes.
Thursday, 28 August 2008
Back again
I cant believe I have pulled my back again. this is twice in as many weeks.
this time it seems to be worse, and what was I doing.....nothing.
this also follows pulling my neck, reading the paper....
this is bizarre not to mention painful.
I guess I have FMS to thank for this, but given I have no medical advice/assistance, how would i know?
Like having brittle bones of the muscles.....
this time it seems to be worse, and what was I doing.....nothing.
this also follows pulling my neck, reading the paper....
this is bizarre not to mention painful.
I guess I have FMS to thank for this, but given I have no medical advice/assistance, how would i know?
Like having brittle bones of the muscles.....
Thursday, 7 August 2008
No weight loss.
I am truly disappointed. We got this Wii machine and although I cant use it every day I have been trying to use it as much as I can.
Everyone has lost weight and lowered BMI except me.!!!!!!
Not an ounce.
Now I wasn't expecting a huge change, but after6 weeks and this providing at the very least more exercise than I was getting......
I don't understand it.
It isnt what I eat, and everyone said "you need more exercise".
Seems that isn't it either.....
Why cant I shift this blob around my middle....
Everyone has lost weight and lowered BMI except me.!!!!!!
Not an ounce.
Now I wasn't expecting a huge change, but after6 weeks and this providing at the very least more exercise than I was getting......
I don't understand it.
It isnt what I eat, and everyone said "you need more exercise".
Seems that isn't it either.....
Why cant I shift this blob around my middle....
Monday, 14 July 2008
Reverse Therapy/Mickel Therapy
These are the wonder treatments for Fibro ME etc.
They work on the presumption that the Hypothalamus is responsible for all our problems. Anyone tried these things....i have and am interested to hear from anyone else who has. So assuming anyone ever reads this blog.....if you have used it, or are just curious, please leave a message after the tone.
They work on the presumption that the Hypothalamus is responsible for all our problems. Anyone tried these things....i have and am interested to hear from anyone else who has. So assuming anyone ever reads this blog.....if you have used it, or are just curious, please leave a message after the tone.
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