crying

  1. J

    Thanks

    Really did not know where to put this so here goes. Thanks.... For being great compasionate friends For lifting me up when I was down For laughing and crying with me For sticking by me when close friends and family have failed me For truly caring For still caring Love to you all♥
  2. pscheffel

    Do the crying spells ever end?

    I mean for me.....not my Mom who has been stricken by this horrible disease. I don't know if it is the meds she is on or the FTD she has, probably a combo of them both. She has very little emotions going on. I ask her all the time......However, I am amazed at how many emotions I can go through...
  3. B

    I felt very awkward today

    I took my son to an open house at a new school. Sitting in the auditorium, I noticed lots of fathers with their sons. One in particular was three rows down and hugging his son. My son became very agitated as the speaker enthusiastically went on about fundraisers. I was upset with him because...
  4. N

    Speech Devices

    Hey all, I'd like to start by mentioning how glad I am that a community like this exists out there. Reading stories on this board somewhat comforts me. Both the perseverance of many of the posters here in fighting this disease and their optimism is incredibly admirable. So, before I get to my...
  5. pscheffel

    Not fair

    Well, yesterday I woke up and got ready for work, Mom didn't stop by at 7am like she normally does. So I called her and no answer. I find out shortly after that Mom's sister (the fake one who is milking the disability system and cares only for herself) has picked her up at 5am so they can take...
  6. IhavePLS

    Acute exacerbations of symptoms

    Hi to everyone, I apologize for not having had been on the forum for quite a while, but I've been awfully busy (no excuse, as I also need to support other with my insights on this nasty disease). Therefore, mea magna culpa. What are your thoughts concerning acute exacerbations of PLS...
  7. M

    I am mad today

    I am mad my dad is not here to celecbrate his wedding anniversary with my mom. I am mad I can't call and wish you "happy anniversary". I am mad that I am not going to hear about where you went to eat. I am mad I won't hear about what you ate. I am mad. I'm so mad I can't stop crying. I guess I...
  8. T

    New CAL Here...Hello

    Hi Everyone! I'm new here and can't express enough how glad I am to find all of you. My sweet man (fiancee) was diagnosed Dec 2011 and has progressed since then to a PWC with no use of arms, hands or legs. I have felt so completely alone until now. I think I stayed in denial until this past...
  9. B

    In Memory of My Dad

    He was like a younger, more sarcastic Santa Claus: While the rest of Sacramento slept, Dad would tumble (sometimes literally) out of bed to deliver the morning newspaper to every half-hidden house nestled within the unpaved Delta wetlands. He would come home at sunrise, smelling of coffee and...
  10. L

    Feel like I'm getting closer to an answer...

    After all my worry of ALS, I've decided to put it on the back-burner and look at things like EBV/Lyme/CMV. I've been feeling a bit better over these past weeks (dry gross taste gone, smelling is back), still have some joint pain, burning, and twitching. Still do get very hot sometimes but my...
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