Archive for the ‘rants’ Category

Intermittently

August 21st, 2010

So I am sitting here up to my eyeballs in new craft stash that I have purchased for myself over the past week. I am so loving my new Mimi/bluebell stamps from penny black! I have one inked up in front of me and I have my promarkers to the ready. I have some seriously drool worthy papers from MME.

The boys have been shuffled over to the Grandparents with daddy as per usual Saturday style, so the house is quiet. I have no housework to do , I have already eaten (and pooed!) So I am good to go!

But I have no inspiration whatsoever..

Typical.

2+2 Makes Five

June 8th, 2010

The breastfeeding debate; To nurse or not to nurse.

To nrse in public or not.

A 16 year old decides to start an anti breastfeeding group on facebook. She gets slammed and spammed and threatens to commit suicide over it. What would a 16 know about breastfeeding?

Grown women get very prickly over this subject. Probably because they are embarrassed because they were unable to provide for their child.

I am seriously Pro-Breast Feeding myself, and woman who don’t even try are pathetic beings. ” Oh I didn’t produce any Milk” ” I was too tired and my boyfriend wanted to feed the baby as well”

Every sad excuse under the sun. The truth of the matter is that they do feel inadequate,

As for breastfeeding in public , I have without any problems. Well only one from my own Mother.

She was embarrassed. She thought it was “wrong and a hippy thing to do”. My elder sister told anyone who would liisten that she was going to breastfed because it was natural and would go on to speel the benefits. She lasted 3 days, and quit before her milk even came in. Of course my mother sang her praises about breastfeeding and even when she quit it was the ‘best thing to do’

Five years later I gave birth and I was a ” Hippy and a nasty freak” When my son self weened at nine months, she was overjoyed. When I gave birth to another son nearly two years later. She positively hit the roof when I fed him over 18 months. To avoid anymore arguments over it when I visited her home when he was about nine months I brought a bottle of expressed milk. She fed him and all the while she was telling me that it was great that I had switched him to bottle. When I told her iit was indeed breastmilk and I had expressed ,she nearly had a heart attack. Needless to say I have not spoken to that woman in nearly two years.

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Yes, I know this is your website, which includes your opinions and ideas and beliefs. I understand that you are a pro for breastfeeding in public. I am, as well. People have feelings and if you wouldn’t say all of this offline then don’t say it online. Or if you wouldn’t say it in this manner offline, don’t say it in this manner online.

“Which means that women doing everyday real-life things (like feeding a baby, or otherwise having a physical, usable body in a non-sexual way) are “gross” and deserving of a putdown. (‘Cause being a mom is so non-sexy! Eewww! :-P )”
Breastfeeding a baby is natural. ?

“Well done. Your mother risked nipple confusion because she was a prude. Nipple confusion, caused by the totally different suckling method between bottles and the breast, that can cause a baby to totally reject the breast. And what happens if she rejects the breast? No more breast milk. Yay, score one to the formula companies!”
No need to say it so condescendingly. There are ways to un-confuse your baby and let them breastfeed. But even if you don’t like the breast pump. You can do it once a week for about 3 hrs so that if you have to go out to a restaurant or the library or any place you can take a bottle with you. That is what was done with me when I was a baby and that is what I am doing with my child. If Erin (my daughter) gets confused between the bottle and my nipple and wants to suck on the bottle more then I’ll start bottle feeding her at an early age. There is no problem with that. It is completely natural and there is no harm to the baby besides needing braces when it grows older. What is so bad about formula’s anyway? There are some formulas out there that have the nutrients and vitamins a baby needs to develop. Eventually, you’ll have to stop breastfeeding because either the kid gets to old or you just are tired of breastfeeding the kid. So, no matter what, you’ll never get rid of that frustration you and your baby will have when switching from breast to bottle.

“Have you ever tried to make an infant hold in their pee? It’s like asking them to wait for milk. It’s impossible. They have the need and the desire to urinate (or drink) now now now. They are not adults. Applying adult logic such as “suck it up, I’m to prude to watch you pee!” to a baby or a small child is just as stupid as “suck it up, I’m too prude to watch you eat!” hence why babies have diapers (nappies). So, while you can hold your full bladder, or your empty stomach for “a few short hours”, a baby cannot hold it for that long.”


You can train the baby to go for hours at a time if you ignore the cries for food when you just fed them 3 hours ago. Yes, it hurts as a mother, but it is also easier when the baby can go to 5-6 hours without needing to be fed. It was frustrating for me at first to do this, but after I was finished, I am happy at the result. Erin will sleep for 5-6 hours at a time without needing to be fed. Which lets me sleep 5-6 hours without being woken up by a whine or a cry from her. We are sleeping better which is improving our moods.

“My baby’s needs are more important to me than your stupid, immature objections to a woman breastfeeding.”
If that is so, then just ignore it. That is always an option. Although, you cannot take back what you have posted you can apologize for being so condescending about this. I mean, just because you are for breastfeeding in public doesn’t mean that you should just yell at her. I mean that never changes anyones mind. What if you were Jennifer? Would you like this? Probably not. Please, think of it in both shoes. I am not saying I have not gotten into stupid fights like these but I am saying that you can resolve this by saying you are sorry in your last blog and closing comments on this blog (maybe even deleting this blog entirely). There are other options than fighting about things. I know you know this, but please, take them into consideration when replying to comments and other blogs that people write. Jennifer was never there to be the butt of ridicule neither were you. Now, she has stopped posting about you and you need to stop posting anything about her as well. If you just unfollow her on twitter and delete her on facebook and just stop looking on her website, you guys will be fine. You are not forced to talk to anyone. It was an option you had from the beginning.

“If you don’t like it, look away.”
I totally agree with this statement. I think that people should look away if they don’t like watching something. But, at the same time, they shouldn’t have to. Like Jennifer said, breastfeeding and sex are both natural. What if people were allowed to have sex in public. We would probably be having this exact same conversation. You and I would be against it though. She (Jennifer) wasn’t saying that people need to have sex NOW NOW NOW. She was just saying that sex would be opposed if it were allowed in public, as well. I totally agree with some of the things that she has said as well.

Maybe you should drive?

May 17th, 2010

Monday the 24th of May at 11 am… The phone rang at exactly 9.06am , Daddy and the boy has already left for school,so it was just myself and the small yoke.

She was her usual saccharin sweet self and by the power of the gods does that woman make my skin crawl!

I can’t stand her, I really can’t she is the most horrible two faced woman on the planet. I mean no one, no one is that nice and sweet in a utterly soul destroying manner.

I would not spare a thought for her if she were to burn alive in a horrendous car crash. Nasty,Nasty cow.

I wonder if I could be reassigned another MS nurse or are they all hideous? Probably but never matter. Thankfully I will only have to set eyes on her wretched face for two days. Then I am allowed to inject myself-aren’t I all growned up!!

If the NHS insist on giving me ten grand worth of drugs ,free, on yearly basis who am I to argue? I have tried to refuse it but no-one wants my opinion so being the good little disabled girl that I am, I will sit quietly and allow the well meaning able-bodied people to seal my fate.

Once they give me the drugs they cannot take me off them unless my condition deteriorates to the point where DMD’s no longer work for me. LDN costs £180 a year but it can’t be prescribed for use in treating MS because there are no conclusive clinical trials out there. Why? Money of course..

The powers the be ie the pharmaceuticals who hold the ring when it comes to the CRABS and they do not want any contenders in their little dominion regardless if it actually helps the patient a damn sight better than their offering.

Small Victories

May 1st, 2010

The small victories
The cankers and medallions
They keep me thinking that someday
I might beat you
But I’ll just keep my mouth shut
The little nothings
It shouldn’t bother me
But it does
IF I SPEAK AT ONE CONSTANT VOLUME AT ONE CONSTANT PITCH
AT ONE CONSTANT RHYTHM RIGHT INTO YOUR EAR, YOU STILL WON’T HEAR
You still won’t hear
You still won’t hear
You still won’t hear
You still won’t hear
You still won’t hear
You still won’t hear

I got a call from the Neurologists secretary yesterday. Apparently ‘Adrian’ can’t prescribe the LDN, so he said no to that. Oh well, I already have it ‘sir’ and my doctor is willing to keep me on it and monitor my usage, so tough titty said the kitty but the milk’s still good..
After that little episode I have decided to get rid of the Neuro..
The GP wrote to inform my Neurologist , and basically the wank-stain Neuro said no, he wants me to go down the Rebif route and I’m pissed at him. So bye bye Neuro!! I can pay for my LDN if I need to and well, what does the Neuro do for me anyways? Fuck all in the past ten years is what. A couple of MRI’s since he diagnosed me, and squat all since then. So in short, he is gone-shot out of my life. I am not wasting twenty miles worth of diesel to go see him anymore. I will take my LDN and my GP will monitor me. Game Over.
Compared to a lot of MS’er it is virtually nothing, he waited nine years -NINE YEARS- before he decided to start me on DMT’s , I know of folks who have been diagnosed just a year ago and they are already on DMT’s for almost the same length of time.

Make it so..

April 27th, 2010

I’m feeling that my journey on the MS meds cycle should begin with LDN. I have never been truly comfortable with the whole CRAB (Copaxone, Rebif, Avonex and Beta Interferon) thing if I am to be perfectly honest. I’m not one to throw drugs down my throat for any other minor (non MS) related illness to begin with ,so it does fit in with my own thoughts regarding the subject.

I don’t know if any of the CRABS would work for me anyhow, I have no real explanation it is just a hunch! And I have seen my cousin start on the Interferon’s about five years ago and she is now paralyzed from the waist down, wheelchair, bedridden, carers the works. Yes MS is progressive and it does effect ever MS’er differently and all that garbage but I don’t know ? It just doesn’t sit with me at all.

The only thing that my cousin and I share is the fact that we both have Multiple Sclerosis. I have a different mindset to her in every way. She is what I would call a ‘squealer’ she would moan about everything and everyone then maintain that because she had MS she was ‘special’.. Yeah okay.

People expect you to behave in a certain manner when you mention that you have MS. Like it automatically makes you a wheelchair user. I’m sorry that I don’t fit the mould ya know. Yes, I do have it, no I am not faking it ( I have three MRI scans and a Lumbar Puncture to prove it) I am not one for sprouting all the positives about the disease -MS sucks. Big time. You suck it up and get on with it. I work full time (online) I’m not a benefit fraud, I am not currently in receipt of any, Yes I get working DLA because of the daily issues that I have because of the MS.

MS is not only an illness that effects mobility, it is a lot more than that- go and google it- have fun!

I like my life,sorry. I am married to a wonderful man whom I still adore nearly 11 years later two incredible boys that I am so fortunate to have and we live in a tidy not so little bungalow (that we own). We are happy more-so I am happy with my lot. It does suck to know what maybe in store for down the line, but I don’t and won’t dwell on it. The ‘worst’ might happen then again, it might not..

I have MS..tough. You do not have MS but you are still an idiot, at least I have a viable excuse

Shot down in flames

March 31st, 2010

YEAH

Go ahead and live your life as an MS sufferer for just one day,and you would soon enough change your prospective.

The UK Governments official response to MS patients requesting that the procedure being available in the United Kingdom.


The Government is aware of Dr Paolo Zamboni’s findings.  However, as this is the only piece of research on the link between CCSVI and MS that is currently available, it is important to approach such findings with caution until a further review of the research has been conducted.

A number of medical advisers to the MS Society have read the papers published by Dr Zamboni, and have heard him lecture on the subject.  The advisers have provided the following statement about the alleged link between MS and CCSVI:

We are not convinced by the evidence that blockages to draining veins from the brain are specific to people with multiple sclerosis, or that this explains the cause of multiple sclerosis at any stage of the condition.

We are all agreed that people with multiple sclerosis are not likely to benefit by treatments that dilate blood vessels and consider these procedures to carry risks with no evidence for benefit.

The treatment for CCSVI is not available for patients with multiple sclerosis in the United Kingdom because there is no convincing evidence to suggest that it is safe or beneficial to people with MS.

The Government is determined to make the UK the best place in the world for health research, development and innovation and to invest its substantial health research budget in the best possible way.

The Government’s research strategy ‘Best Research for Best Health’ is resulting in an expansion of the Department’s research programmes and in significant new funding opportunities for health research.  The National Institute for Health Research programmes support high quality research of relevance and in areas of high priority to patients and the NHS.

Tee'd off? Me? Never!

March 8th, 2010

I’m sitting here in the games room in disgust. I have the new table in position and the PC and desktop perched on top of it. My crafting paraphernalia is currently gathered in the centre of the room in what I can only describe as a dirty great big mess..

I am not happy. Apparently the pool table will not fit in the space that Will decided that it would occupy. My rather large PC desk ,which had about 50% of my storage in it has already been dismantled and dumped and my storage cupboard which I used for the remainder of my stash has also been removed, hence why all my crafting goodies are all over the floor.

Not happy, Not happy at all!

Oh and with regards to the Magnolia Ink magazine- Just because I may post to the same forum as you do, does not mean that I know you and should therefore not “charge a pal” how many times have you spoken to me let alone responded to any of my posts. The second copy of the mag is also listed on eBay and is at £21 with almost two days to go.. I know what I have and I now know the going rate for a copy-why do you expect me to settle for less? If you want it, you pay for-simple as that.

Crapoids

December 22nd, 2009

So we did it again. I wish Christmas would hurry up and get here because this is starting to get ridiculous.We went to Smyths today -to get batteries and walked out £142 lighter…

A storage unit at £40 quid, a 66cm plush Mickey Mouse, three more trains,more track and a little windmill thing set for the Thomas job and a handheld thing for DS1 At this rate we mght as well keep half the stuff back and save it for next year! We left the boys with the grandparents, thankfully. I think if we had of taken them with us we wouldn’t down that obviously. We just strolled around the shop going “ah DS1 would like that” and “Oh that is perfect for DS2”

BLAH

We are idiots.

Tomorrow we have to go do the Christmas grocery shop..Another £150 no doubt.

Christmas better hurry upand get here because we are going to be penniless otherwise!

Next year ,I am going back to last minute mommy.We started in early October this year-and look what happens!!

Oh  and we forgot the batteries!

Back to me!

September 18th, 2009

My eyesight has thankfully returned to semi normal! It still goes a bit wobbly when I get tired but other than that- I CAN SEE STRAIGHT!! Joy oh Joy!!

I have been busy getting my Christmas stash together, which has been fun. The postie has brought me a package every day this week, much to DHs’ disgust..It hasn’t been that much to be honest about £30 in total, but still he sees “packages of rubbish that I will never use” coming through the door at an alarming rate. It’s Christmas..almost

I have noticed that a lot of UK online retailers that I have used previously, have doubled their online prices to Northern Ireland. It does not cost £6.95 to send a magazine to Northern Ireland, and it certainly does not cost £10 to send a few ribbons and a packet of clear stamps over here. Of course it is their loss in the end , because there are hundreds of crafty retailers out there to shop with. Out of principle I would never cough up over £3.95 for postage, I understand that the Royal Pants have increased their prices and retailers have to adjust accordingly, but be reasonable people..

As I said, your loss and I will take my money elsewhere.

Been there,done what?

September 9th, 2009

I have barely been online.. The MS relapse that I currently have going is stretching into three months now, my longest to date. My eyesight is basically with shot to pieces doublevision. Optic Neuritis, which simply translates to “swelling of the optic nerve” is fairly common with MSers with around 30-40% suffering an episode.

Life is a bitch and all that..I can take steroids to help it clear ,but that is something I want to avoid at all costs. 90% of people get through the bout within about 5 weeks without steroid intervention and I am approaching week three ,so hopefully I can get things back on track.

I haven’t been reading anything at all and that , for me,  is worse that anything I have ever experienced. October/early November I have  about four new releases out from the likes of Kelley Armstrong with the eagerly anticipated ‘FrostBitten’  and Lora Leigh with ‘HeatSeeker’ then Nalini Singh with ‘ Blaze of  Memory’ and that is just what I can recall of the top of my head.

It all goes to hell in a  hand basket doesn’t it ?

I guess the Open University will not be getting me back as a student come October..