Tuesday, February 9, 2010

20 Facts for Caregivers

20 Facts  about being a Carer for someone with severe ME.

Greg and Linda Crowhurst 9th Feb 2010

(permission to repost)

1 The   relationship between you and the person with severe ME, must
be be a priority in your life. You may be caring for decades, as there
is currently no treatment, no cure and limited validation.

2 You need to understand the illness , what it is and how it affects the person.

3 This is going to take time; it will not happen overnight. Tt may
take years, even to identify the symptoms and understand their impact.

4 It is going to be painful, as you try and understand the complexity
of  severe ME and  its  bizarre nature ; in relation to  you as a
carer, trying to help the person and the impact it has upon your

5 The person with severe ME is not living in the same experience of
the world as you are; this is so hard to understand and to deal with.

6 You are most likely going to have to work this out alone.

7 Until you understand it, can cope with it, know how to deal with
it,know  how to maintain your relationship, despite difficult
interactions, you will not be able to convey the severity and effect
of severe ME  to  family, friends, professionals.

8 You are going to experience isolation from normal things because the
person with severe ME cannot do normal things.If you stand by their
side, your life wil become more limited too.

9 You are going to enter into some of the aspects of the person's
experience; the disbelief, the disappointment, the negativity, the
misunderstanding, the misinterpretation, the rejection.

10 You are going to have to become aware politically of what is going
on, in order to survive.

11 You are going to have to fight your corner and the person's corner,
even to get basic needs met.

12 You will have to become an advocate for yourself and the other
personbecause it is a poorly understood illness, often treated as a
psychiatric illness rather than a true neurological, multisystem,
dysfunctional disease.

13 You really cannot assume that you are going to get the
understanding, the acceptance, the medical and  social support from
family and friends that  you would expect and should be entitled to
and would get with any other illness.

14 If you are going to be the main carer for the person with severe
ME, you have to make the choice between work and poverty and quality
of life and your relationship with the person.

15 These are big decisions that have  a huge impact upon the person
and they result in losses that need grieving and understanding. Most
importantly they need accepting.

16 You need to accept the choices you make and look for the benefits
you gain in loving and caring for that person.

17 The person with severe ME is not going to fit into standard
procedures and practices, do not expect that it is going to be easy
and expect that formal agencies are  going to reach out and

18 There is a tendency, on behalf of professionals and well meaning
others   to be quite divisive and to "client-ise"  patients and
carers, rather than offer a holistic approach and understanding  to
what their need is.

19 Do  not give your power away to social workers, nurses, doctors,
anybody. You work, live with the person, you do know better and trust
has to be earned.

20 You will become greater than you ever thought possible, because you
really do have to reflect upon what is important to you in your life
and how to be empowered.

1 comment:

Bad Caregiver said...

Most of these points could be condensed into 2:

1. You can either take on the entire responsibility of caring for your ME sufferer yourself, sacrificing your own life in the process, or you can let the ME sufferer fend for him/herself. There is no middle ground.

2. Sucks to be you.

I'm sure the Crowhursts are trying to be helpful here, applying a little tough love and all that. But throw us a bone? The magical empowerment I'm supposedly going to feel someday, as per #20, ain't gonna get me through the rest of my life.