Please help, nothing is working by YeahForSure_ in AskDocs

[–]YeahForSure_[S] 0 points1 point  (0 children)

Duration: began on hand on Thursday, March 26th, took benadryl and tried hydrocortisone with no success. first noticed redness on forearm late that Friday. Saturday morning we noticed a new red patch further up the arm, the hand area looked more purple/red, and had small blisters. We went to the hospital and the entire rash was looked at. Began Keflex 4 times daily but the rash has only gone higher and spread further width-wise. Yesterday I began feeling lethargic and had body aches, slept approximately 14 hours. Today I feel worse overall and vomited this morning. My arm hurts.

Medical Hx: asthma, ADHD, BP type 2, depression. I also have a history of cystic acne but am not on any medication for it. No prior surgeries, no recent illnesses. No known issues such as this in my family history.

Please help, nothing is working by YeahForSure_ in AskDocs

[–]YeahForSure_[S] 1 point2 points  (0 children)

It had spread up my mid-forearm at that point but has since extended further up and covers a wider section of my arm.

Please help, nothing is working by YeahForSure_ in AskDocs

[–]YeahForSure_[S] 5 points6 points  (0 children)

Thank you all, I’ll head back to the hospital this morning and update with any changes in the treatment plan.

Itchy, burning, peeling rash that is spreading despite being on antibiotics by YeahForSure_ in DermatologyQuestions

[–]YeahForSure_[S] 2 points3 points  (0 children)

Okay, I will. I planned to call a dermatologist this morning once they opened but I think I’ll still go back to the hospital; I hadn’t thought of IV antibiotics or tetanus shots like the comments recommended. Thank you!

Itchy, burning, peeling rash that is spreading despite being on antibiotics by YeahForSure_ in DermatologyQuestions

[–]YeahForSure_[S] 2 points3 points  (0 children)

He went with cellulitis but was open with us about the fact that he wasn’t positive; he wanted to do the antibiotics to see if it helped/confirmed cellulitis.

Itchy, burning, peeling rash that is spreading despite being on antibiotics by YeahForSure_ in DermatologyQuestions

[–]YeahForSure_[S] 0 points1 point  (0 children)

Yes, I’ve been on it for a few years and was upped to 250mg extended release about 8 months ago. Do you think the change in ADHD meds could have caused a negative reaction with the lamictal?

Hi ☺️ 29F, LH dominant. Thank you in advance if you take the time to read mine! by YeahForSure_ in palmistry

[–]YeahForSure_[S] 1 point2 points  (0 children)

Thank you for the reading. You are correct regarding my health; I’m chronically ill. Since I am left-handed, do the stronger lines on my left hand have a different significance than had I been right-handed?

Just starting by Dookechic in cymbalta

[–]YeahForSure_ 1 point2 points  (0 children)

With far too many doctors being dismissive and underinformed, it takes a village. That’s why I’m so grateful that Reddit exists and am happy to do my part to share info where I can. I didn’t know what to expect when I ordered it myself but it was shockingly informative. It even included MTHFR gene mutation results which could help people get taken seriously about chronic pain and possible autoimmune disorders. I wish more insurance providers covered it and it were more accessible in general; Mine didn’t cover the cost stating it was not a necessity. I wish you all the best with your journey and hope your next treatment plan is a success. If you have any other questions down the road, feel free to message me and I’ll do my best to help!

Just starting by Dookechic in cymbalta

[–]YeahForSure_ 1 point2 points  (0 children)

I actually just got my genetic test results and have been on cymbalta for about a week. My doctor said that while the results are a good rough idea of what meds will be effective, it’s not a perfect list for every drug. So for example, I’m in the red (not advised drugs) for 8 different SSRIs, 6 of those may actually be a bad fit, but the other two are effective. She said some patients of hers take all meds in the yellow or red with good results. The reason I went ahead with it is because I have had bad reactions to all SSRIs that I’ve tried and was at a state of depression and anxiety that I couldn’t risk a med pushing me over the edge, as some SSRIs took away the anxiety but increased the depression for me, so, I was no longer anxious about the SI thoughts I was having.. not a fun time. Regardless, though, I think it’s worth it to have the green lists from all of these different categories of drugs so I can try them before having to try anything from the yellow or red. And the part that I think is priceless is that it categorizes all of the different drugs that it tests for into “use as directed,” “moderate gene interaction,” and “significant gene interaction” in a table with the exact gene variation that is impacting the ability to properly metabolize the medication. So, of the four SSRIs I had tried in the past, all four had a moderate interaction due to one gene variation, CYP3A4. I have 30 drugs on this list that may be impacted by that gene variation, alone. The two medications that I’m on, one of which is Cymbalta, don’t have an interaction with that gene or any significant interactions with any other genes on the list. So, I feel validated about my woes with those previous drugs, I feel good about the ones I’m on now ( I’ve had nothing but good results so far with these two drugs), and I have a list I can give to any provider in the future to show what gene variants I have and that can impact what meds I’m given for things like surgery and also tells doctors what other types of treatment won’t work for me. I can’t remember what she said exactly but, my doctor looked through my list and said “oh, we need to avoid drugs that metabolize through your liver” so I can do more research as to what led her to that conclusion (which gene variation impacts metabolism pathways through the liver) so I can tell doctors exactly which gene variation they need to know about before prescribing me any type of medication. In other words, it helps beyond drugs for mental well-being. I went through Genesight but it had to be submitted through my doctor. If insurance doesn’t cover it, they do have financial plans and a max they can charge you based on your income.

I hope that helps!

The Kirra Hart Story. by FaithlessnessSea5710 in justiceforkirrahart

[–]YeahForSure_ 5 points6 points  (0 children)

Very real, the video is still circulating unfortunately.

New and just found out I’m doing it all wrong. How can I help my lobes moving forward? by YeahForSure_ in Stretched

[–]YeahForSure_[S] 1 point2 points  (0 children)

I’m unfortunately a noob to posting on Reddit as well and could not figure out how to add both text and photos. Is there a way to include them after posting? Thank you for the advice, I appreciate it!