Відео

Thanks for sharing your story dude !!! I’ve been on it for 3 weeks now and today is the first time I’ve started feeling good !!! I had some bad side effects but now I feel like calm waters if that makes sense !!

Hey thanks man , I’m a doctor in India , just confused of taking surgery speciality and I have psoriasis for 2yrs and now I’m getting that click sound and morning stiffness , so I have a doubt that I might have develop psoriasis in future and I just want to know whether this click sound is the starting stage of Arthritis or not , now I’m sure I won’t take surgical speciality as hands are more important for that job , thanks Man U really helped me

How long before your scalp psoriasis disappeared ? I've asked twice now.

Could you please share your ESR and CRP levels? Additionally, I’d like to know if you’ve encountered any difficulties in preventing infections.

Hi bro was just wondered how it took to work for you.I had my first injection last Wednesday and initially felt great but this week the pains coming back and has left me wondering if it will be effective for me

Starting mine in a couple of weeks 🙏🏻

MashAllah good brother

MashAllah good brother

20 years now and I'm still undecided..just don't drink with it..may make you a bit bland.

I love and hate it at the same time.. look into the benefits of eating coconut oil.. it's helping so much.

The loss of erection and sex drive is a real downer for me

Got diagnosed with cyclothymia today.

Ive just started my humira injections and im feeling better thanks to your inspiration which is something to be proud about.many thanks for your videos and merry xmas

Trt injection cured my depression

How about the psoriasis you mentioned on your scalp? How long before that disappeared?

Thank you for making this video. Please how do i combat this depressive episodes i keep having

Hi... I watched your video on SSRI's because my husband takes Prozac. I checked out your channel and found that you also have arthritis. I have rheumatoid arthritis. I take herbs and supplements because pharmaceuticals are not something I want in my body. I haven't watched your arthritis videos, so I don't know if your meds are working in that area. If they aren't working, then the following herbs and supplements work. 1/4 tsp Glucosamine Sulfate 1/4 tsp Chondroitin Sulfate 1/4 tsp Hyaluronic Acid Protein Powder or Bone Broth Powder and or 1.5 tsp Bovine Gelatin 1.5 tsp MSM 1/4 tsp Magnesium Malate 1/4 tsp Turmeric 1/4 tsp Milk Thistle I buy these herbs and supplements in bulk powders, but you can probably buy pills. Anyways, I am concerned for you spiritually and would suggest and hope that you might watch my video trailer on my channel about my personal testimony, which I hope and pray may enlightening you. 💓

thanks for the info can you give a link to the amazon page for that carry case for the humira !

I have also been diagnosed with cyclothymia and often overthink, just like you. I would add that my overthinking varies depending on the episode. During depressive episodes, I often revisit the past and overanalyze what happened back then. This usually leads to self-criticism and a decline in self-esteem. During hypomanic episodes, I overthink about the future. I constantly plan and re-plan upcoming meetings, conversations, my movements, and facial expressions.

Do you take it every month or after some time its better to inject it maybe once every 3 month or when signs of symptoms begining to come back ? Thanks

This guy is really knowledgeable. He is so brave and courageous to share his experiences and education.

Good job, fella. I respect this. Enjoyed it. You’re right on.

Thanks for your review!

i started getting tiny bumps near my eyebrows dunno what to use for it :/

Thank you for the candid review. I have PsA and removed myself from Biologic treatment about 10 months ago and experienced my first flare. So will give this book a go and see how I can get myself back on track with my diet. I have adjusted my diet to reduce dairy, red meats, gluten and I can say it definitely works!

Can’t thank you enough for sharing man. Your videos are super helpful. Please keep making them!

Well done bro, thanks for sharing. 🙏🙏

Looking good mate and glad you're feeling well. Pretty much the same story here since taking Humira starting April this year - pain completely gone, dry skin gone, lifting heavier than ever and sleeping better, more mobile, everything improved. Complete wonder drug and life changer for me. Stay well and thanks for your updates.

Thank you for your informative video. I worked out too and thought it had something to do with that. I was having pain even on the days i didn't work out. I was just diagnosed yesterday with psoriatic arthritis. It took awhile for this diagnosis, but now i can make lifestyle changes and meds to help.

Ive been on biologic and have had huge results. 90% symptoms are gone.

I’m on hydroxi and MTX 25mg injections for psa I have a feeling that the MTX isn’t gonna get me to where I need. I feel at around 80% Any advice on how to get on Humira? Did you suggest it or was it just suggested to you?

Congrats on the pr! I just took my first dose on Friday, I hope I have the same experience as you. Wishing you the best!

Thanks for sharing pal.

I’m currently in a massive flare and I’m unable to walk. Can not wait to start biologics hope by December. Your videos have given me the confidence to start them

I hope I don't come off insensitive but do you take meds? No judgement either way x

So jealous of your travels…How do you manage all your travel? Is it part of your employment? Or just lucky and make it work with your goals? Anyway so glad you are living life to fullest and your PsA is so well controlled!

thank you currently i am in the process of getting diagnosed my psychologist suggested i have cyclothymia and i am still not sure so looked for people with cyclothymia experiences and yours helped me the most up till now

Question: that metotrexate is weekly, by injection right? I've noticed that when I take it on a Friday, then by the next Thursday it already starts to wear off and symptoms become more severe. Like weekly is not enough and it should be half the dose twice per week. I don't know if anybody ever tested the hypothesis that this is more efficient.

Glad mtx is working for you! There’s a lot of fear around taking a gets basically a chemo drug I was on it two years for PsA on the max recommended dose (9 pills/week). Worked great and really brought my inflammation numbers down. The first year was great and I felt like I was starting to return to some semblance of normal The second year though… not so much. I started to see the liver enzymes climb and I was starting to have digestive issues because of it. And I was getting sick a lot. My rheumatologist noted this and lowered the dose. I went into another flare, which I expected. But when it didn’t let up after four months, I felt I was back at square one. After much research, I determined mtx wasn’t the answer for me. I have a very physical job and couldn’t afford joints that were too swollen and painful to even twist a doorknob. I felt like I was 80, not 50! My rheumatologist wanted to put me on an expensive biologic instead, which didn’t sit well with me. So I quit him. Quit my mtx too. Cold turkey. It was scary but it felt right for me. I know several people who are treating autoimmunes naturally, including seronegatives arthritis, so I decided to try that route while searching for a new doc. I became more strict with my gluten free diet, went grain free following a paleo/lower carb plan, then added in daily CBG/CBD… wow was all I can say. I’m feeling better now than I did when on the max mtx dose. Better than I have in decades. My gut was more f-ed up than I realized. I’ve been off mtx since last January… and no flares, no swelling. I can do my job without an Advil (which I DEFINITELY couldn’t brag about when on mtx) Not advocating ditching a doctor or meds, but i do encourage everyone to look outside the limited box rheumatologists work out of. Question any change in your bloodwork. Keep track of the trends, and correlate that with how you feel. And be your own advocate if something feels off. Not once was diet change recommended as a path, and my rheumatologist completely shut down the medical cannabis conversation when I brought it up. Sad really… Enjoyed hearing your journey. Hopefully your treatment will continue to work for you and not have any serious negative effects. Blessings!

Make videos on the psoriasis part of your journey. If you can share anything useful for us long-term suffers of psoriasis

I’m going onto in December. First video I’ve found of yours. Gonna do a deep dive now thanks for the hope

Hi! I'm starting methotrexate tomorrow and I am petrified about taking it. Iv had anxiety about taking it for the past two weeks since my last Rheumatology appt. I will be taking 6 15mg in one go every Sunday then folic acid the following day for a 3 month course. I'm worried about the side effects, i have 3 young children and really concerned. Thank you for your videos I feel a little better about things. Kind regards 💙

Your voice is so soothing and calming.

Quality mate glad all is good.. meant to be having these injections in the next couple weeks, just wondering about gyms? I train in a sweaty mma gym and am worried about infection.. do you go to the gym and if so have you had any issues? Cheers

Your psoriasis was ve ry mild. Mine is horrible and im wbaiting t o see if my insurance approves it

I will be taking my first dose of Methotrexate tomorrow. I am very nervous but after watching your video I am feeling more positive. Thank you.

Ive watched all your videos, theyre inspiring,and helpful to everyone having to go on these drugs. Thanks pal.

For me Adalimumab worked only for 3months

Well done! Have you consider reducing methotrexate yet? My son is symptom free and started a Biologic end of July. I would like him to reduce the methotrexate as it does seem to have a mild side effect on him the next day - tiredness and mood

I have borderline personality disorder. So totally relate to this.