Cntacting folk new on to & not new back on to DS
Hi. I have comented on my last profile about lack of comunication on DS to e random memebers ect. One member replied saying I could try reading folks profiles & then maybe see if they have any thing t all in comon with me. When it comes down to it wwee all do. We arre human with human feelings ect weaknesses & so on. But that said. I do contact folk on here. I welcome new folk And eriginal folk back on to DS when I see them. As isaid ion a past jurnal I do not let my contact with rthem depend on if they have any thing in comon ect with me or not. We never know the future. This is waht I say to new folk. Ho and a big worm welcome to what moste folk on here even me wouldcall & see as being the DS family. You are now one of us if you want to be.. Bla Bla Bla. Take care.. Graham from Scotland If I am not sure if some one is new or not then I say If you are new to here then A veery big warm welcome to BLBLA BLA. Take care . Graham from Scotland. If its some one who I know is an eriginal then I say Welcome back. Long time no see. How are you?. Bla Bla Bla.. Take care.. Graham. I replie when & as soon as I can to any one who contacts me new or not. I have been joining more suport groups relvent to me. But also relevent to my epileptic friend Mike. One that aplies to him is the Epilepsy Group. I have left a coment on there about him & me as his carer. I feel that it is & would be a good thing for groups to have or invite carers on to them as they have to deal with the disabilitys ect of the person who has suffered or is suffering from what ever it is.. I do not suffer from Epilepsy but that is nor relevent & does not mean I should not & can not be part of a group such as the epilepsy one. Maybe there should be a group set up on here for carers of folk with alld is abilities ect. A bit like an on line carers suport group. even where carers can suport carers ect. People who help others in any way some times need help too.. Not always or juts from relevent departments. Who knows better than a carer about what is needed ect even for the person needing the care ect?. Experience is a wonderful & a best teacher. Like riding a bicke . Once learned never forgoten most of the time. This is my third jurnal today.Some of us get help ect from families but some of us are not that lucky . I am one of the m who dont get help even from relevent departments who try to dige doing so at all costs ect giving all invalid excuses ect. My epileptic friend does give me morall suport & I do feel good doing what I do for him.so in thease small ways I get soemthing back. I do not look for repayments as its not about that. Thank you all & take real good care .. Graham from Scotland
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