When I think back to this time last year, I
was backwards and forwards to Grimsby, visiting Jess in hospital. Now, I am
travelling to Sheffield to visit her at university, as she has a full calendar
and struggling to find the time to be able to come home.
I never thought that life would ever be
normal again, but here I am, a year later, doing the things a parent does with
their child- taking her clothes shopping, enjoying a meal out and going food
shopping with ease- simple pleasures that were impossible this time last year.
It is lovely to see my daughter full of
life, glowing, socialising and most of all being happy with life. As a parent,
nothing compares to that feeling of witnessing your child healthy and content.
I do not have any concerns about her- she
is healthy. However, if I am worried about anything I can ask her now and we
can discuss it rationally- without the flaring temper and out of character
behaviour. Just a few weeks ago, I expressed to Jess that I was concerned about
the lack of physical monitoring she was having following her transition to the
new doctor’s surgery in Sheffield. Without an argument or defensive response,
she agreed to visit the doctor the following day and explain her medical
history so that she could be seen regularly.
I have also noticed changes when Jess does
visit home. On the rare occasion that she came home for the weekend, I was able
to cook her tea on the Friday and Saturday night without her lingering in the
kitchen, observing how I prepared the meals. This time last year, Jess would
have scrutinised every move that I made, leaving me no choice but to allow the
Anorexia to win even myself over. I know that I should not have let this happen,
but you have to understand just how powerful this illness is and the control it
takes over the whole family of the sufferer, not just the sufferer themselves.
Every day I felt like I was walking on eggshells, unsure of how Jess or the
Anorexia was going to react to anything that was said.
We still have days of uncertainty, but
nothing compared to the level that we experienced before, and when this happens
we just talk through it- we can be open and honest with each other. I notice
that Jess is still not confident with her own perception of herself, with the
odd questions about how she looks and if she still needs to gain weight. But
before I have chance to answer the question, she responds herself by confirming
that she needs to be a comfortable healthy weight that is not on the borderline
of being underweight.
As Jess has been so open with her illness
and written this blog, she has had a lot of people contacting her not only from
the UK but also around the world, to which she responds with no hesitation and
is only too willing to help. I obviously would have never wanted this illness
to happen, but in some ways it is now leading Jess’ path in life. Obviously
there has been a lot of heartache over the last few years, but it is strange
how things turn out and that some good can come out of it. She is able to help
other people in various ways, and ultimately wants to make a difference so that
there is further help out there for other sufferers and carers.
As I have said, this time last year Jess
was in hospital. If anybody had have said to me that next year your daughter
would be living a fulfilled life again, and even climbing the highest mountain
in England, as much as I would have wanted that to be right, I would have never
believed it could be true.
BUT IT IS!
I could not be any happier or prouder of what
she has achieved.
Wonderful xx
ReplyDeleteSo happy for you and your family and I hope things continue to go from strength to strength x
ReplyDeleteI can't imagine what it must have been like for you and your husband, but I know that your lovely Jess wouldn't have managed to get through this without you two and your balanced, loving support.
ReplyDelete