Hi All, Had my qufora training today my insides feel totally battered, I know once I get used to it and my system is cleared out it should be a positive and make life more beneficial but feel like it is something else that MS has taken away from me, I’m 34 and it sucks something else have to think about when go on holiday, have to do on a daily basis. I would never discussed my bowel movements with anyone now it seems a frequent conversation. I just want to cry and run away from everything I know it won’t stay behind if I did I really hate life at moment. Barney
Hi Barney. Really sorry to hear you’re having such a rough time. I’m sure we can all relate to some degree, even if not experiencing the same problems exactly. MS is certainly a roller coaster. I definitely wasn’t prepared for all the surprises it comes with! I hope you do see benefits from the Qufora soon. Take care, Kaz x
Thanks Kaz. A roller coaster is a good description. But I do like going on rollar coasters. Just trying to organise a visit to a theme park with a friend. Not sure how it is going to work with my reduced mobility but feel I need to try. Barney
Fantastic! You won’t know until you try it buy I see no reason why you shouldn’t have a brilliant time 
Kaz xxx
Hello Barney
I wasn’t quite sure what qufora meant…watched a clip on you tube…it’s a bit like colonic irrigation, yes?
I can imagine at first it must feel quite upsetting to face something like this…I know I would be upset.
I hope once you get the hang of it, you’ll start to appreciate the benefits.
I know what you mean about always seeming to talk about bowel movements…I’m getting a bit preoccupied with mine.
Please don’t hate life Barney. One of the excitements of life is that you never know what’s round the corner…lot’s of good things happen too. Become an expert at this qufora, so that you can get it done quickly when your on holiday and have a really good time
Lot’s of ((((((hugs))))))
Noreen xx
H Barney, I hadnt heard of quofora either, so Ive just watched a video of it being used.
Yes, it`s another indignation for us, but having had enemas and rectal examinations for sluggish bowels, I see it as another aid to our difficult lives.
Im sorry you feel bad about it now, but after a few sessions, youll see the pluses, I hope.
I expect i`ll need something like it somtime.
luv Pollx
It has been a tough few months and everything has taken it’s toll. I’ve been trying to battle through and it’s all got too much. Been to drs today who has told me I need to rest, so contacted work and they’ve told me to take the rest of this week off to rest. I shouldn’t try to battle on but I don’t want to feel I am giving in always been one to battle through but realising how much I have to rest when not well and don’t let myself get to the point that just collapse in a heap. MS fatigue is unexplainable to people, who haven’t experienced it. Hoping sorting out my bowels is going to make me feel more comfortable and being a less exhausting exercise, I have had to lie down for at least 2 hours after trying to get them to move. I suspect it will just become a part of my routine that don’t notice in end just like injecting myself daily. Hope everyone is being able to enjoy the weather. Barney
It has been a tough few months and everything has taken it’s toll. I’ve been trying to battle through and it’s all got too much. Been to drs today who has told me I need to rest, so contacted work and they’ve told me to take the rest of this week off to rest. I shouldn’t try to battle on but I don’t want to feel I am giving in always been one to battle through but realising how much I have to rest when not well and don’t let myself get to the point that just collapse in a heap. MS fatigue is unexplainable to people, who haven’t experienced it. Hoping sorting out my bowels is going to make me feel more comfortable and being a less exhausting exercise, I have had to lie down for at least 2 hours after trying to get them to move. I suspect it will just become a part of my routine that don’t notice in end just like injecting myself daily. Hope everyone is being able to enjoy the weather. Barney
It has been a tough few months and everything has taken it’s toll. I’ve been trying to battle through and it’s all got too much. Been to drs today who has told me I need to rest, so contacted work and they’ve told me to take the rest of this week off to rest. I shouldn’t try to battle on but I don’t want to feel I am giving in always been one to battle through but realising how much I have to rest when not well and don’t let myself get to the point that just collapse in a heap. MS fatigue is unexplainable to people, who haven’t experienced it. Hoping sorting out my bowels is going to make me feel more comfortable and being a less exhausting exercise, I have had to lie down for at least 2 hours after trying to get them to move. I suspect it will just become a part of my routine that don’t notice in end just like injecting myself daily. Hope everyone is being able to enjoy the weather. Barney
It has been a tough few months and everything has taken it’s toll. I’ve been trying to battle through and it’s all got too much. Been to drs today who has told me I need to rest, so contacted work and they’ve told me to take the rest of this week off to rest. I shouldn’t try to battle on but I don’t want to feel I am giving in always been one to battle through but realising how much I have to rest when not well and don’t let myself get to the point that just collapse in a heap. MS fatigue is unexplainable to people, who haven’t experienced it. Hoping sorting out my bowels is going to make me feel more comfortable and being a less exhausting exercise, I have had to lie down for at least 2 hours after trying to get them to move. I suspect it will just become a part of my routine that don’t notice in end just like injecting myself daily. Hope everyone is being able to enjoy the weather. Barney
It has been a tough few months and everything has taken it’s toll. I’ve been trying to battle through and it’s all got too much. Been to drs today who has told me I need to rest, so contacted work and they’ve told me to take the rest of this week off to rest. I shouldn’t try to battle on but I don’t want to feel I am giving in always been one to battle through but realising how much I have to rest when not well and don’t let myself get to the point that just collapse in a heap. MS fatigue is unexplainable to people, who haven’t experienced it. Hoping sorting out my bowels is going to make me feel more comfortable and being a less exhausting exercise, I have had to lie down for at least 2 hours after trying to get them to move. I suspect it will just become a part of my routine that don’t notice in end just like injecting myself daily. Hope everyone is being able to enjoy the weather. Barney