Gathering is done till next year.
Well Folks the Gathering is over. I met a few new people and made some new friends. Some people dropped out and there were others that …
I work in community inclusion and recreation for people with developmental disabilities. I am married and I have lovely wife and two beautiful daughters. I also have Neurofibromatosis. Don't feel sorry though. I don't.
I work in community inclusion and recreation for people with developmental disabilities. I am married and I have lovely wife and two beautiful daughters. I also have Neurofibromatosis. Don't feel sorry though. I don't.
Well Folks the Gathering is over. I met a few new people and made some new friends. Some people dropped out and there were others that …
This is it folks. The NF Gathering is this weekend. Come one come all. You can come for the day or stay the whole weekend. There are dozens of …
We are in the last week before the Gathering. There is still time if your are going to go. You can just show up for one day if you like. It is …
The NF Gathering continues to move forward. The news of the gathering has been posted on the midwest NF, Indiana, Illinois, and …
Things are moving along quite smoothly. An email blast with a link to my Gathering website was sent out to people on the midwest NF mailing …
Thank you so very much. My husband and i are also suffering deeply in financial problems. We are looking for work but there is nothing out there. our income is deeply critical. We are living on $680 a month. his part time job is cutting hours starting monday to 21 hours a week. i do not understand why the president does not do somthing for our country. We need it desperately. i am so so sorry i have not been on my illness is taking a big number on me. i am waiting to see from my meeting i had with heritage health services if they will get me on social security, because social security did not believe all my doctors medical reports. I hope everything is well with you. I am so sorry to give you bad news about me it is even worse, i need tro write it all out in my journal so everyone can read it. Please take care and stay in contact with me. Thanks again for the prayers. HUGGLES Kyndra
I am getting excited about the NF gathering. I am looking forward to meeting you and your family.
Read your response to the bumps post. What a story you have and what a great attitude to take!
i completly agree with you. ppl with nf shouldnt feel bad when they go out in public. we get alot of stares bc my baby has it and you can tell hes a little different bc hes trached and his tumors disfigure his face and i cant stand it when ppl stare at him but ive learned how to handle it,it doesnt bother me as much as it use too. i had a lady follow us around in walmart one time staring at will and i finally turned around and asked her if i could help her with something
i think that is great.
I have Nf and two daughters age 2 and 4 who also have nf1. Want to know more? You'll have to ask.
I have sleep apnea
I'm a new foster parent in Toledo, OH. I have not had my first placement yet. I just finished jumping through all the hoops.