Welcome to the enthralling universe of a filmmaker turned parent, where poetry meets marketing, and stories come alive. Embark on this journey with me as we delve deeper into the human psyche, narrate compelling stories, and illuminate the craft of storytelling. As an artist fueled by passion and parenthood, I offer a distinct perspective on life. Hit the subscribe button for unique insights, immersive content, and a refreshing outlook on life through my lens. Join me in this creative journey as we weave tales that resonate, inspire, and connect.
I am 71 years old, and have stuttered since early childhood. Based on my own experience and a very large amount of reading about stuttering over the years, I would say the following. In many instances, children who begin stuttering in early childhood (age 4), for reasons not fully understood by experts in this field, will permanently cease stuttering WITHOUT speech therapy. In my opinion, it depends in part on the parenting abilities of the parents, the degree to which they have educated themselves about raising children who stutter, overall conditions within the home, bullying at school, and the severity of the biological basis of the child’s stuttering. If your child’s stuttering does not improve AND IF it becomes a problem, I recommend speech therapy. If the child seems to “be ok” with his stuttering, it is probably best to not obtain speech therapy, just try to be a good parent. If you do decide to obtain speech therapy, try VERY strongly to find a speech therapist who has been trained how to treat stuttering, and few of them have. A better option is an approach that does not treat the stuttering, but the child who stutters. This is sometimes call the “holistic” approach. The “holistic” approach may also be helpful as a young adult. If a person has stuttered since early childhood and still does by his early 20’s, the continued stuttering and related stressful experiences may have caused mental health disorders. No type of therapy will be effective until those disorders have been adequately addressed. The disorders may be depression, PTSD, generalized anxiety, or some type of personality disorder regarding having normal relationships with other people. If so, he needs help from a psychologist or even a psychiatrist. In either case, try to find one who has patients who stutter. I "have been there".
The story of California City doesn't have an end, because after several decades, it's still beginning. Build 21st century infrastructure, and good things will happen. CC would make a great location for tech industries, as the coastal cities become unliveable. No lawns or golf courses, vertical farms for local food production, everything powered by renewable electricity. The future is still bright, if the will is there.
I remember he was on a ship and was trying to get back somewhere, I don’t remember him being a genie, but I thought he played Sinbad the sailor, apparently he didn’t do that either lol 😂
Hi mate it’s my 3rd day with bells parsley I’ve started to take steroids what do I do? I’m not sure if I want to go to work or stay at home till I get better please advise my me greatings from the uk
Thank you so much! Maybe you cannot see my comment, but I still want to say thank you, I was diagnosed with Bell's Palsy 9 years ago when I was 21, and now I'm thirty, and I hate myself, every day when I see myself in the mirror It keeps reminding me that I cannot smile like normal people, there is no one I can talk, but recently I found I do not care about this so much like before, I know I need to move on eventually.
It's been 7 years for me. I got partial movement back, but my smile will never be the same. Synkinesia is absolutely the worst and I wish a doctor told me how I can prevent it. My face distorts when I use my mouth.
I got Bells Palsy 4+ years ago and my face still isn't like it used to be. It's unfortunate. 😮💨 Friends say they can't tell, but it still bothers me. Your video was the most relatable and reassuring because I'm not alone in this. Thank you for sharing your story. Bells Palsy needs to be talked about more.
Same. No one says they notice it but i do. I have a very mild mild case but i can tell most in pics i take of myself just to see if anything has changed for the better everyday. Been about 3 yrs now for me. Even if no one else can see it, i can and its embarrassing sometimes to even look at my spouse knowing at any given moment it could be spotted by her and then she sees im not the same as i used to be. Even tho i know she wouldnt see my flaw like that. Its my hardest struggle yet that i have ever had. Everyday i wake up hoping and praying to see change but i dont. At least not yet☹️
@@emillymiranda7148 I did not get the shingles vaccine prior to this onset. I was always a little concerned about getting the vaccine. I did test positive for Covid though three days before. I have been trying some new therapy low level laser to reduce inflammation. Arnica massage oil for daily massage. 20 minutes daily over infrared red light therapy on my face. And I just started a series of acupuncture. I am getting movement back a little faster. It’s not gonna go away overnight. I know that, I think it’s the first thing we have to come to terms with. I’m just trying to lessen the residual nerve damage and be patient with the process.
I can see your right eye still get affected. I got BP 4 months ago after giving blood donation. My stamina was down and the herpes took over nervous system. Luckyly It's medium condition cause i went to doctor on the 2nd day and got medication prednison, acyclovir and few vitamin melcobalamin, b6, b12, D3K2, magnesium and Zinc. My right eye can do fully closure after 3 ½ months. I still do self massage on my face, chinese acupunture once a week. Stil my right sphere of upper dan below lips still sleeping, imbalance with the left sphere. When i get tired, stil having headache at the back of my head. i hope you can have fully recovered of your face, love your body and be happy.
We lost a lot of medi during the VHS TO DVD transition irrelevant of this being real or not, loads of things never made it to the Yahoo search engine let alone google
I remember watching Kazzam and thinking it was mediocre even as a child. But I also remember Shazaam with Sinbad but unfortunately don't remember much from that film. However, I distinctively remember even as a child thinking that it was funny how 2 films about a genie were released around the same time. Very bizarre...
I've been dealing with Bell's palsy for 5 years as well. And I definitely tear up from eating certain foods usually from something that is vinegary, sweet, or sour I definitely saw results from acupuncture. I did it for at least five or six months, and I stopped because my insurance wouldn't help me cover the cost. I currently still have Bell's palsy, but it has improved. I use a TENS unit 2 days a week. It has a chart for facial paralysis on certain tens units brands. To anyone that struggling with Bell palsy as you read, I'm praying for emotional support in your life, I know it's hard to accept the way you look now but in order to start healing you have to. just don't settle in your condition even though you've accepted how you look. Always have hope that you will get better and that healing is happening even though it doesn't look that way. Prayer Works 🙏 run to God 🏃♀️
