Free fertility support

Cmhc-LqWYAAWk88In recent years, there has been a huge increase in the numbers of people offering fertility support services – often at premium prices from people who have no relevant qualifications and limited knowledge or expertise. What many people don’t realise is that the national charity, Fertility Network UK, provides an amazing range of support services which are all completely free.

The Fertility Network Support Line, run by a former fertility nurse, Diane, offers a unique fertility support service. Diane has a wealth of experience and has worked for the charity for more than 20 years, She can help not only with minor medical questions but provide you with the help you need based on her years of experience, and all calls to her are in complete confidence.

The Support Line has often been described as a ‘lifeline’ by those dealing with fertility issues. It is very normal to feel isolated, out of control, lonely or depressed when dealing with infertility, and Diane is there to help. No question is too trivial to ask and even if you just want to talk you can give her a call on 0121 323 5025 between 10am – 4pm on Monday, Wednesday and Friday, or email her at support@fertilitynetworkuk.org.

Of course, that’s not all the charity has to offer. You can find a wide range of support groups right across the UK, an online community, a Facebook page and masses of information. Do check it out now at fertilitynetwork.org and save the money you were about to spend – or perhaps consider donating it!

“Tea-cember” for fertility support

800px-fairy_cakes_close_up_on_trayThose in the Jewish community who are experiencing fertility problems will almost certainly have come across Chana, an amazing charity offering help and support to Jewish couples with fertility problems.

They run a helpline and counselling service, organise information events and provide medical information – and now they are organising their fifth fund-raising “Tea-cember” event, where people can raise funds for the charity by organising tea parties – there’s an article about the event here and there is a lot more details about how to get involved on the Chana website.

It’s a great way to get together with friends, and also raise money to support a fabulous charity which provides a very special service to help people who are experiencing problems getting pregnant. Late year apparently more than 2,500 people took part in more than a hundred events – so why not join them this year?

Interview with Julia Leigh, author of AVALANCHE

7432976-1x1-700x700We spoke to Julia Leigh, author of Avalanche, at the start of our National Fertility Awareness Week and began by asking her what she thought of the idea.

It’s a wonderful idea which I hope will focus more attention on under-reported fertility issues. Also, it’s a special way to bring together those whose lives have been touched by infertility.

Do you think we are too reluctant to speak openly about fertility issues?
There’s no reluctance on the part of the multi-billion dollar worldwide fertility industry to promote this area of medicine. For example, this month [October] the American Society for Reproductive Medicine Scientific Congress & Expo took place in Salt Lake City, Utah. Exhibitors represented at the Expo included a fertility clinic network; a myriad of ‘bio tech’, ‘health technology’, ’genetic screening’ and ’diagnostic solutions’ laboratories; biopharmaceutical manufacturers; food and vitamin supplement manufacturers; pharmacists; surrogacy and donor organisations; laboratory equipment suppliers; attorneys; insurers; cryobankers and cryoshippers; marketing and brand strategists; a big data analyst; specialist software providers; and a joint venture partner who promised to turn growing medical practices into successful businesses. There’s also no reluctance on the part of the media to report successful ‘miracle’ births. There is a reluctance, however, to talk openly about the plain fact that most treatment cycles fail. To give some perspective, about 80% of treatment cycles fail. There’s also a disturbing reluctance to talk openly about the physical and emotional harms of treatment. It’s almost as if patients and doctors and others in the fertility world are so bewitched by the beautiful possibility of a ‘live birth’ that they turn a blind eye to the real harms.

Your book Avalanche about your own story is intensely personal – was it difficult to be so open in public?
At the time of writing I felt that I’d already lost so much I didn’t care about losing face – and that afforded me an enormous freedom. My heart goes out to anyone who is doing treatment now.

What made you want to write the book?
I wrote an Author’s Note for my publishers and I think it gives the best idea of why I wanted to write the book. Here it is:
A writer contemplating whether or not to begin a new work asks herself – Is this truly a story worth telling? Avalanche felt necessary. I’ve tried to tell an intensely personal story about a common experience that has largely remained unspoken. I wanted to offer a ‘shared aloneness’ to anyone who has desperately longed for a child. I hope I’ve brought into the light the way the IVF industry really works – and I could only do that in non-fiction. I wanted to transmit what it feels like to be on the so-called ‘emotional roller-coaster’, to deeply honour that complex experience in all its detail. Ways of loving, the mysteries of the body, the vagaries of science, the ethics of medicine – the material raised so many questions. I started writing it very soon after I made the decision to stop treatment because I wanted to capture my strong feelings before they were blanketed by time. I wanted to write something for all the women who are contemplating IVF, or currently undergoing it, or who have stopped or who are thinking about stopping (it’s so hard – the decision to ‘give up’). I wanted to speak to their family and friends. I wanted to speak to young women who in a misguided way might be relying on fertility treatment as a kind of back-up. And I wanted to speak to the policy-makers too. Since there is so much IVF failure I wanted to provide an alternative voice to the miracle stories we frequently see in the media. I wanted to counter the push – yes, the push – of the worldwide multi-billion dollar IVF industry.

Do you think people need more emotional support when they are going through treatment?
It’s difficult to discuss treatment with family and friends but in so doing a patient can lighten the emotional burden. There’s also the counselling option. In my case, the clinic offered free in-house counselling as part of the very expensive treatment package…but I would advise seeking an outside independent therapist. I say this because the decision to stop treatment, to give up, that incredibly painful decision, sits uncomfortably with the fact that clinics are making money from their patients. In my case, when I was 44, using my own eggs, and I’d already done 2 IUI’s and 6 egg collections plus subsequent transfers, my doctor suggested I try once more. It was my sister who had the courage to tell me firmly that I needed to stop. I feel an independent therapist would be well-placed to basically warn patients of the emotional pitfalls that can lay ahead. Is there such a thing as pro-active counselling? Identifying the traps for new players and advising how best to respond to them…identifying the tricks of the mind that don’t serve patients well…I think a therapist who was familiar with the IVF world, who had experience in this area, would be best.

And do you think there is adequate support when treatment doesn¹t work?
There was little to no follow-up from my clinic after I decided to stop treatment. I can’t recall exactly – there may have been one phone call. I saw an independent therapist.

Here in the UK, the individual success rates for individual clinics are collated and published by the fertility regulator, the HFEA, and are broken down by age too. Do you think access to information like this would have made a difference to you?
Yes I would have loved to see results for my individual clinic. That would have helped. But I also want to note that I did see the graphs on my clinic website which used our ANZARD data and clearly showed how fertility dropped away with age. (The ANZARD report collates data from all clinics in Australia and New Zealand but doesn’t identify individual clinics). And when I was 40 my first doctor at the clinic said I had about a 20% chance of ‘taking home a baby’. BUT as it happened, at age 43, when I was transferring a thawed 5 day blastocyst, using my own egg, I asked my new doctor what my odds were of being pregnant (please note, pregnancy not live birth). Even though I’d seen the fertility graphs I figured my chances would somehow be better than the average because unlike some patients my age I was both responding to drugs and producing blastocyts: “Pollyanna Juggernaut could do amazing things with the numbers.” In reply to my question about odds, the doctor said “A Day 5 blastocyst has about a 40% chance.” I took that to mean I had a 40% chance of being pregnant – but later I discovered the 40% figure was for women of all ages. I hope that illustrates how statistics can be malleable…

What changes do you think we could make to try to ensure that fewer women suffer the kind of anguish you went through?
That’s a good question and I don’t have any easy answers. I wonder if there couldn’t be a buffer between women – especially older women – who are prepared to do almost anything to have a child and the clinics who are prepared to put patients through almost anything even though there is no guarantee of a successful outcome, far from it. In Australia a well-respected doctor put a patient through 37 cycles. 37! He had no qualms about that since she did end up with a child. But what if she hadn’t? I’m not sure what happens in the UK but in my case it was my General Practitioner who referred me to the fertility clinic. My GP never asked how my treatment was going. I wonder if GP’s could step in as a buffer, walk patients through the facts and figures, help decide whether or not to do an experimental protocol advocated by the clinic that will cause physical harm but has limited evidence of benefit, to basically serve as a ‘reality check’. There’s a great deal clinics can do to change…For example, during an embryo transfer my doctor pointed to an image of the blastocyst on the ultrasound screen and said ‘That’s the baby’. At the time, I thought it generous and I was touched that the doctor might be the only person in the world who would ever refer to ‘my baby’ but in retrospect the comment – that’s the baby – only heightened my intense desire for a child.

The Fertility Show goes to Manchester

the-fertility-show-london-logoIf you missed the Fertility Show in London at the weekend, you may be interested to know that there will be a second Fertility Show in Manchester for the first time this year. There will be the same wide range of seminars and exhibitors with lots of information and advice.

The Manchester Fertility Show will take place on March 25 and 26 in the Exchange Hall at the Manchester Central Convention Complex in Windmill St in Manchester. Tickets will go on sale in January 2017 and you can find out more on the Fertility Show website.

Finally, for those of you who came to my talk in London and are looking for the notes on my talk, I am hoping to put them up on the blog later this week so you will be able to find out all you need to know about choosing a fertility clinic!

Why it’s worth considering a support group

images-2Going along to a support group can seem a bit outdated when so much support is online now, but there is still a place for the old-fashioned way of getting together. The survey released for National Fertility Awareness Week by Fertility Network UK and Middlesex University found that just 17% of respondents had attended a support group, but more than half (52%) would have liked to attend one if they’d had the opportunity.

It isn’t easy to go along to a group for the first time, and the very idea of a “support group” can sound off-putting. I think people often imagine something terribly gloomy and it can take courage to take the first step and commit to going to a meeting. In fact, most people who do get as far as going to a group tend to find it incredibly helpful. There’s something very empowering about being with other people who understand what it’s like to experience fertility problems, to share experiences and to learn from one another. People are often surprised at how upbeat and cheerful the groups can be. Of course, there is sadness sometimes but there is also a lot of laughter and many friendships are forged.

If you have a group near you, why not give it a try – and if you don’t, maybe you could think about setting one up yourself? You don’t need any special training as a group can be a simple matter of arranging a get-together at a local cafe. Those who have done this in the past have found it to be incredibly rewarding at many levels – you may be interested in this article by Fertility Network UK volunteer Ridhi Sahi about her experiences and you can find out more about volunteering as a support group organiser here.

Fertility advice in Wales

Cmhc-LqWYAAWk88If you want to know more about fertility and live in Wales, you may be interested in a fertility information event organised by Fertility Network UK and sponsored by Darren Millar AM.

Held at the Pierhead Building in Cardiff Bay on Saturday 19th November from 10.30am to 4pm, this free event will bring together fertility clinics, practitioners and support agencies from all over the UK and Europe.

There will be the opportunity to have an informal chat and to pick up information on clinical and donor treatment options; fertility counselling; alternative family options; male fertility and local support services

For more information please contact Alice  – alice@fertilitynetworkuk.org

Social media – is it helpful?

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For many of those with fertility problems, social media has become a key source of information and support, but is that a good thing? There’s quite an interesting article in the British Medical Journal on the subject which you can find here (and you can sign up for a free trial for 14 days to access the whole thing).

It is written for medical professionals but is still of interest to patients – one of the points it raises is about concerns that social media may be used to offer “dangerous or unsuitable remedies”. It’s an interesting issue as I know how many times I delete what are apparently “comments” on this blog that are actually people advertising their businesses for fertility patients. One clinic overseas was attempting to post promotional comments on a daily basis at one point – personally, I’d be worried about any clinic that needed to advertise itself in that way (and just to reassure you, I’ve yet to come across anyone who has visited the country for treatment let alone the clinic). Having been an administrator for another fertility group online, I saw how often posts were reported and then deleted because they weren’t from fellow fertility patients but from people offering miracle cures or promoting their businesses.

Despite all this, I think social media can be incredibly helpful and can provide support that may be difficult to find elsewhere – particularly with a problem like fertility which it can be hard to talk about – and that the problems outweigh the negatives – but I’d be interested to know what you think too so feel free to post your comments (but beware, I will delete anything that is promotional…)

Ask A Consultant

800px-Woman-typing-on-laptopIf you’ve got questions you’d like to ask a fertility specialist, you may want to join Infertility Network UK’s online chat session via Skype this Thursday titled ‘Ask a Consultant’.

This month’s guest speaker is Shipra Singh Krishna, Consultant Gynecologist. Shipra will address the most commonly asked questions before those joining the group have the opportunity to ask their own questions during a Q and A session.

The session begins at 7pm and all you have to do to join the group is email your Skype username to hannahtramaseur@infertilitynetworkuk.com

New name and logo for fertility charity

Cmhc-LqWYAAWk88Infertility Network UK, the country’s support charity for anyone affected by fertility problems, is set for a change of name and logo! From mid-August, the charity will be Fertility Network rather than Infertility Network.

It’s a welcome change – the term “infertility” is no longer so widely used and in fact the majority of those experiencing difficulties getting pregnant are sub-fertile rather than truly infertile. The new name also reflects some of the wider interests of the charity, around campaigning for better fertility education for young people for example.  Here’s a preview of the new logo and colour scheme!  A new website will follow and will be launched in the Autumn at the Fertility Show.

How volunteering can help

Please read this brilliant piece for the Guardian Voluntary Sector Network written by Ridhi, one of Infertility Network UK’s volunteers, about how running a support group has helped her cope with her own fertility problems. Ride is an absolute star, runs a hugely popular group and has written a really honest and open piece which I hope may inspire other people to get involved – see here and if you want to volunteer for Infertility Network UK, you can find more details here