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Vicsta (11/13/09)
Sending you a big hug! Well for you and the babbie. I just saw your status... you can talk to me if you need to.
Also I was reading your journal entry the other night and some of it resounded with me. I was diagnosed with PCOS when I was 19/20 and it was around the time that a lot of my symptoms that I had since a child either worsened or I got new ones. It's hard to look back and see how your childhood was totally altered by something out of your control and not in a positive way. I work so hard to not let myself be bitter about it and not let myself get consumed by looking back, but it's really difficult and sometimes I just want to give into the pain and hurt I feel. Having things to keep your mindset in the present and the future helps so much I think.
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kissxxes (11/09/09)
Hi Long lost twin :-) Welcome to the group, it's been a great support for me over the last few months. You have a beautiful little boy, which gives me such hope that maybe one day i will be able to add to my family. You have had a hard journey but im glad to hear you have found someone to love and care for you now, how lucky we are really. our stories are very similar, great to see someone else feeling the same feelings, at least now we know we're not mad lol
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Vicsta (11/08/09)
Hi fellow Vicky/Vikki :o)
Thanks for adding me as a friend. If you are interested, then please read my journal, you will get up to speed on where I am at: am basically awaiting an endo appointment to test for acromegaly.
Your little baby looks so cute. I'm loving the pics! Keep them coming.
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orit (11/08/09)
Hi, sending you a rainbow with love & light. also give lots of xxx.. to you baby for me he is so so sweet.
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mctrjt (11/08/09)
This is so amazing..I saw your posting on facebook...and shared with with flouncy and what do you know...next thing I know you have joined us here how great is that....!!!! welcome to our little not so little family...
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flouncy (11/07/09)
hi thanx for adding me, i have been diagnosed for about 3 years now and would like to have a baby. the nedo and doctors have been ohhing and arhing for months and have now said its ok. would love to chat to see how things went for yourself and what you had to go through. much respect to you for having a little one and this disease!!!! you must be wonder mum, i found it hard with my little boy when i found out i had acro i had been struggling for months without anybody knowing what i had. welcome to the world of ds
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Jen564 (11/07/09)
Welcome to our support group. You will find a lot of supportive friends here.
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nanleigh (11/06/09)
here's a hug back. your son look wonderful. i have a 7 month-old. the doctor is doing some more bloodwork. it's not back yet. i'd love to know how you're dealing with all this, and with a newborn to boot. is it easier with your son to talk on the phone or e-mail? i'd call or e-mail, whatever you're comfortable with. thanks so much for writing me. nancy
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