PPI Reclaiming discussion Part III

maxdp

di3004 wrote: »

Hiya Maxdp

Thank you.:A

Yes he has had a lovely birthday, and now out playing bowling with his grand-parents, (my inlaws) and a few of his cousins.....:D , it was good to see him all excited.....:T X

Am sure it was good to see him excited Di. Did you see in the Mail today writer talking about her friend who has a child with Autism. Seems quite bad.

Anyway lots of love to you and yours:D

di3004

marshallka wrote: »

Oh, i thought you meant consultants coming to the surgery, that is who our docs put you under and that is the guidlines, if my BP has been troublesome I have had to go straight to hossie for the meds immediately and on the renal ward. They don't mess around cause its a silent killer apparently. (you can feel well and not know how high it is). If we have 3 reading over the weeks and they are higher than that what is expected again its over to the hossie. I thought all britain was the same and all followed the prodigy guidlines.

My hemo appointment has come through quick too and if we are waiting for ops now its about 16 weeks in all I think. I just think your doc needs to put you in touch with the hopital consultant if things are bad in that you have to go every month for bp:eek: . I suppose we are lucky then cause they do not mess around with it. Its a thing that only takes a short time to take hold. I was told with mine I was a fingers click away from a stroke. It was malignant hypertension...;)

That was me confusing matters again ......:o lol.
Here I have a chart and take my home readings in, they do say if I have a couple that stay high I do have to consult them, other than that, they do a few within a space of time of 20 mins when I have my check up, the readings are up and down, even though I say its whitecoat syndrome, because its hereditary this is another reason for the regular check ups.

I think this is another reason why they monitor every month to keep a check on it, they were going to change my meds the last time, I take 180 XL Adizem for mine, only at one a day, so when I go back the nurse will check it, if its high, its straight into the doctor.

I think you have a good procedure going by what you said with yours and they do keep a close eye on you.

Both my mum and youngest sister had breast cancer the same time, this was only a few years ago, it was in fact mum first then my sister found out 3 months after, then 3 months on my father was diagnosed with prostrate cancer, I was put in touch with the genetics, my result came back as med to high risk, I am still waiting for my mammo appointment to come through, also pestering them but nothing, my sister from Cornwall even though she is a few years older than me, she had her's within a few weeks when her GP referred her....good news though, it was all-clear and so was Christines.;)

Golly your appointment came through very quickly, and that is very good, blimey you were that close to a stroke then........:eek:

di3004

maxdp wrote: »

Am sure it was good to see him excited Di. Did you see in the Mail today writer talking about her friend who has a child with Autism. Seems quite bad.

Anyway lots of love to you and yours:D

Cheers hun.;)

No I didn't see that.....wonder if its online ??

di3004

Yummy Jamie bought us a KFC, no cooking tonight, Dan having food out as well.....:p Back later xx

maxdp

di3004 wrote: »

Cheers hun.;)

No I didn't see that.....wonder if its online ??

Should be Di. Also sorry to hear all your genetic background Also love to you and your patience as usual,:D

marshallka

di3004 wrote: »

Cheers hun.;)

No I didn't see that.....wonder if its online ??

Yeah it is Di. Such a shame too for the kid. He is only young and from what the writer says they have time for nothing at all and even affording a mobile phone is a no no... they don''t even get any help money wise or anything . I think this was written by someone else about this couple and their son....does seem like an extreme case though like maxdp says.

marshallka

di3004 wrote: »

That was me confusing matters again ......:o lol.
Here I have a chart and take my home readings in, they do say if I have a couple that stay high I do have to consult them, other than that, they do a few within a space of time of 20 mins when I have my check up, the readings are up and down, even though I say its whitecoat syndrome, because its hereditary this is another reason for the regular check ups.

I think this is another reason why they monitor every month to keep a check on it, they were going to change my meds the last time, I take 180 XL Adizem for mine, only at one a day, so when I go back the nurse will check it, if its high, its straight into the doctor.

I think you have a good procedure going by what you said with yours and they do keep a close eye on you.

Both my mum and youngest sister had breast cancer the same time, this was only a few years ago, it was in fact mum first then my sister found out 3 months after, then 3 months on my father was diagnosed with prostrate cancer, I was put in touch with the genetics, my result came back as med to high risk, I am still waiting for my mammo appointment to come through, also pestering them but nothing, my sister from Cornwall even though she is a few years older than me, she had her's within a few weeks when her GP referred her....good news though, it was all-clear and so was Christines.;)

Golly your appointment came through very quickly, and that is very good, blimey you were that close to a stroke then........:eek:

Yeah, but medicated now and regular checks but nothing like yours. I have been on meds since 30 and lots of meds....only take one though now since being at home... its just something you live with...;)

marshallka

maxdp wrote: »

Should be Di. Also sorry to hear all your genetic background Also love to you and your patience as usual,:D

Same here with the genetics. We are under Brimingham womens hospital for herditary bowel/stomach cancer. I had my colonoscopy this may last year and hated it... we go every 3 years and they are now testing for something called HNPCC in the genes from something or other... Seems like me and Di have lots in common.;)

marshallka

maxdp wrote: »

I am fab. Are you happy with info from incipidence does it help your case or for you to make a decision.

Think we all ought to join something like google mail so we can discuss between us info we want to share so it is not on here. Do you see what I mean. Know there is facebook but there are others as well MSN Messenger I think

What do others think on here.

I have messenger, I will give you my messanger details although its just the email addy I think...

maxdp

marshallka wrote: »

Same here with the genetics. We are under Brimingham womens hospital for herditary bowel/stomach cancer. I had my colonoscopy this may last year and hated it... we go every 3 years and they are now testing for something called HNPCC in the genes from something or other... Seems like me and Di have lots in common.;)

Must be really worrying. My family have all been farmers and grandparents have all been in their 90 apart from grand parent on dads side. Have felt reall awful with probs (fem stuff) all tests come back excellent) extremely annoying I promise you. Am going to have on my gravestone. I told you I was ill.:rolleyes: