I really enjoy SI folk music or string band music.I prefer it over the current popular digital music in that it's more raw,more...." real" I guess.Thanks for putting it up in this channel.
I have something that will help people with that disease, add me on facebook m.facebook.com/carlos.montoya19?ref_component=mbasic_home_header&ref_page=%2Fwap%2Fhome.php&refid=7 and i can talk with someone who is interested on that. Trust me, i like to give people hope with solutions for their health. 😉😉
A Brighter Star there are people in Canada. Dr Elizabeth O'Brien in Montreal, Dr Afsaneh Alavi in Richmond Hill are two off the top of my head who specialize in this but there are also others. Join the FB groups and ask if there are Canadians with good names to share.
My wife has this. So do her mother and sister. She was just diagnosed about 2 weeks ago. She can barely function from the pain sometimes. I hope she gets a good doctor that can help her
I have HS, it’s definitely a terrible thing to go through, I’m a 15 year old in high school so I definitely understand how this poor lady feels! Luckily I haven’t had a flair up in a few months thanks to medications but it’s definitely terrible to go through! God bless this lady🙏🏻
That ugly old bag made me so angry, so upset for Amber. If he has nothing nice to say, she should keep her mouth closed. No Southern manners there, no manners at ALL!!!
With all the medical research ongoing by millions of medical researchers throughout the world it seems someone would have come up with a treatment regime to at least put this horrible condition into remission if not cure it! There has got to be a medication or treatment even if it means continuous scheduled treatments. Maybe Dr Lee can influence colleagues in the research field to establish an international team to dedicate their research solely on HS. Medical discoveries and advances, requests for trial volunteets come out everyday-to those with HS, don't remain silent! Doors will never open if you don't keep knocking.
When dr asked amber if she has ever spoken to anybody about it & she answered NO, I felt that!!!!!!! No lie I cried because I myself have never spoken about it for 10+ years till now. I don't know why this year but I did it & I feel really relieved. HS is no joke
I also suffer from HS, thanks for getting this video out there. Am very happy for her relief at the same time frustrated as many of us cannot travel distances to see Dr Lee. Many doctors in my area won't do anything. But I am in support groups on Facebook so it helps knowing I'm not alone in this.
I suffer from HS and mine was at stage 3. I have been in excruciating pain everyday for the last six months I had to quit my job. I've been treated with multiple antibiotics and pain killers but I was never offered a steroid shot, I was basically told "We can no longer help you, you need surgery". I decided to try the natural way and help myself. I prayed, prayed and prayed. Finally I tried Black Seed Oil and Royal Jelly, I take 2 tsp of black seed and a tsp of royal jelly in the morning followed by plenty of water. I also made an ointment out of the royal jelly and black seed and put it on my abscess after I get out of the shower. I changed my diet and became vegetarian, I also stay away from dairy. I take Zinc, Multivitamins, Probiotics and vitamins C to help my overactive immune system. This has helped me tremendously. I cry constantly because I'm so happy God has blessed me with something that is actually helping, I was beginning to loose hope. I pray for anyone suffering from this condition and I hope my remedy will help.
I've had HS for 30+ years. Only plastic surgery and the cortisone shots have helped. This episode made me cry, and empathize. Dr.Lee is so amazing! Kenolog ( the cortisone) is a game changer !
I have suffered from HS for 16 years. Im in groups on Facebook for hs. It has helped me with questions ive had and good for support. Im really sorry for anyone suffering from this horrible disease.
Titanic Truths I truly hope you get some medical help & support! I don't have your condition, but I do have fibromyalgia. People don't understand the pain & sadness because they can't see it. Best wishes for you!!
So sorry to hear that. I also have HS. You can find support groups on facebook. Just type in Hidradinitis suppuritiva in the search bar and request to join. Ive learned a lot from the wonderful people there and its good for support
