Questionnaire

You have two choices when filling in the questionnaire. Either use the form below or download a document to print off and post.

Personal
Name:
Date of birth:
Address:
Phone number:
Email address:
Gender: Male
Female
Place in family: (ie eldest of three, etc)
Height:
Colouring: (fair, dark, etc)
Colour of eyes:
What childhood diseases/illnesses did
you have, and at what ages?
History of your condition
When do you think the lesions first
appeared?
How old were you then?
What made you see a doctor about them?
Have you ever been diagnosed as having
pityriasis lichenoides chronica or pityriasis
lichenoides et varioliformis acuta
?
When/where were you diagnosed,
and by whom?
If possible, can you say what tests
were done to confirm the diagnosis?
How many lesions did you have when
first diagnosed?
Have you kept a count since? Yes
No
Where are the lesions?
Do they itch? Yes
No
When, especially?
Do they range in size and appearance?
Can you describe them?
What treatments have you had/are you
having? Please give dosages if possible.
Are any of them effective?
Ulceration of lesions
Have any lesions ulcerated?
If so, where?
Are they lesions which have joined
together?
What treatment do you have for these?
How often are they dressed, and with
what kind of dressing?
How long do they usually last before healing?
How would you describe the pain from
these ulcers? (ie sore, sharp, severe,
neuropathic (nerves affected)
What medications have you needed to
control the pain?
Family history
Is there a family history of skin problems, circulation problems (eg raynaud's syndrome, cold feet and hands, etc), thyroid problems, hormonal imbalance, or any other which you think may be relevant?
You again!
Does cold weather affect you? If so, how?
Would you rather be hot or cold? Hot
Cold
No preference
Do you travel much? If so, how?
(eg, car, coach, bus, air, etc) how often?
Have you made any long-haul flights
before or after your diagnosis?
Do you see any patterns in the appearance of
your lesions? (eg in groups, along nerve lines,
more on the right or the left of your body, etc)
Although stress is subjective and therefore very
hard to quantify, do you think stress has
played a part in your development of Degos?
Do you think any other organs are affected
apart from your skin?
If so, how long after your skin
was affected did the other symptoms appear?
Organ: after years and months
Organ: after years and months
Organ: after years and months
Organ: after years and months
How well do you feel?
Are you working? If so, what do you do?
What is your theory about what may have
triggered this condition in you?
Do you have any other theories/thoughts you
could share about how this condition came to
affect you?

Page last modified on 14 July, 2009

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